Endometriosis, PCOS (🙋), Ovarian Cancer, etc...All of these diseases are things that plague women, but are rarely talked about. Thanks for taking the time share your story.
These are all hormone related. Endometriosis and fibroids are caused by high estrogen. PCOS is caused by low progestrone and estrogen. I have been dealing with half diagnosed endometriosis and breast lumps for years but I decided to heal my best naturally and with herbs. My diet Is all the way different and I supplement with herbs to boost immunity and stabilize my hormones.
@@campbecy They're not all hormone related, endometriosis is mainly due to a genetic mutation which affects development of the female reproductive organs and the cause of PCOS is for the most part unknown (however the symptoms occur due to higher male hormones in the body). For PCOS one treatment I've seen help is losing weight and taking tablets prescribed by the doctor to help regulate the hormones, it helps to regulate the periods a bit more and helps with the other symptoms
Fed up I think you guys need to do a lot more research. In theory the cause of endometriosis is unknown but it Is strongly linked to estrogen dominance. To my knowledge no one in my family has uterine endometriosis however, I started getting symptoms and all of sudden I had all the signs of endometriosis. I was not fully diagnosed because I denied the surgery and decided to go the natural route and Tia talked about it in her book. I went on a no sugar, no diary, gluten and meat diet and I will seldom have eggs, fish or chicken like every few months. During the journey I found out that endometriosis is also linked to parasites which causes the inflammation. I’ve done parasite cleanses and I have actually seen tons of eggs and parasites. I have been on a protocol to balance my estrogen and progesterone since last summer because my doctor had me on birth control before. The first few months after birth control were brutal but now my periods are regular, 50% less bleeding and wayyyy less painful. 🤗 I forgot to add that I have do not eat high estrogenic foods other than meat like most beans and soy. When I was younger I thought painful cramps and heavy bleeding were normal and would go home from high school to curl up in a ball. The reason why Pcos becomes more under control after dieting is because they are mostly over weight and eat whatever they want. The liver becomes over worked and doesn’t process the hormones well. Read Tia’s book or just research journals on internal inflammation and its link to hormone imbalance.
Te'ylor Beck Do not Take what the doctor prescribes, they’re just bandages for what will be a long term alignment. Someone I work with actually changed her diet but she wasn’t super over weight and she conceived within a few few months. She said she will be eating healthier in general going forward so it doesn’t affect her again in the future. You can also look into calcium d glucarate and DIM. You also need more estrogenic healthy foods like beens fruits and veggies, try for a minimum of 3 months and see how it goes for you. Cheers!
I have endometriosis. I was diagnosed last year and undergone surgery last year as well. my ob removed my left ovary and fallopian tube and she told me i only had 50% chance of being pregnant. but hey, 4 months later, im pregnant.. yassssss
I struggle with it. I feared for years that it would prevent me from becoming pregnant. I'm expecting my first son in two weeks:) Thank you for sharing.
@@TEWMUCH honestly, the only thing that has truly helped has been the right vitamin combination. I recently shared on my channel. It took me years to finds the right combination.
Right! Yes ma’am! I’ve recently been focusing my attention to Takin care of my nutrient deficiencies as well.! I’m hoping that’ll help me accomplish some of my health goals. I’ve experienced with things like veganism and whole food plant based. And I don’t think I did it right cuz I was lackin nutrients and always felt deprived and hungry.
I had endometriosis at 17 and PCOS at 19. I'm now 25 with baby number 3 on the way! Thank you for sharing your story. These are very real conditions and should not be ignored.
Krista Smith did you have to change your diet to lose weight or did you take something to get pregnant . I have PCOS I changed my diet and lost a lot of weight but still haven’t got my period yet
I had surgery at 17 and at 19 and I would drink lots of teas and eat foods that would keep it at bay. I did lose weight but all 3 times I got pregnant I wasn't really trying and I was also on a birth control pill to help keep my cycle regular. Hope this helps!
@@joelkamau1411 you have to change your diet drastically. This helps in any illness... Do research on juicing, raw veggies meals and what food to avoid such as Dairy, sugar, sodas and juice, processed food like canned, frozen, red meat and have occasional organic chicken or beef. Bone Broth is good. fermented foods.... Dont give up. ask God for help and healing anf guidance too
I was diagnosed with endometriosis on December 12th with blocked fallopian tubes I was very blessed to have a very small case of it and I just found out I'm pregnant I'm so happy to give birth to my first child in october.
Courtney Reynolds honey you aren’t alone. I was diagnosed 3 yrs ago and had my 2nd surgery last week and I love this video have to change diets. Take care of yourself
Not sure how is best but contact me. I was diagnosed at 18 started at 15 and now am 32. I was alone, no one I knew understood or even got what a bad period was etc. Xxx
Definitely not alone! I was diagnosed with stage 3 Endo at age 18 after 9 years of so much pain. There are so many of us that spend years in pain before diagnosis. If you want to find more information about being your own advocate and different treatments I definitely suggest reading "The Doctor Will See You Now" by Dr. Seckin. Its very eye opening and doesnt make you feel alone 💛 welcome to the fight, endowarrior.
@@Ps-do2si I am sorry for the pain you are enduring, but if you remove all dairy products and foods that contains gluten it will help.Drinking water is very helpful, room temperature, stop drinking cold water.Drink water first thing in the morning then eatanorange or a banana. Drink water one hour before you eat and even before you shower and before you go to bed.
Me 2 changed my whole Life style😀 have since five years no pain anymore. Did all Things since age of 30. Was 25 five when i was dwaling with it after i stopper with the poll. But i have to watch my eggsquality now cause it has effect on it. Im 38 now.
Hi Tia, I have endometriosis from I was 27 and I am 46 this year, married for 18 years, we didn't get any children. I change how i eat but it didn't happen. The doctors say the old I get the harder, so I have to thank God my husband he gave me. Lately I am feeling some pain. But my God is a healer he can heal anything.
Look up iodine deficiency and endometriosis. Dr. David Brownstein and Dr. Jorge Flechas have done extensive research in iodine deficiency and what it does to the body. You would be surprised at what you find out. Also read "The Iodine Crisis" by Lynne Farrow.
Dear Lydia I'm very sorry about that..I was fortunate I was diagnosed of it @ the age of 14 I'm now 25 years the last time I went to see my gynaecologist I was told it's better now...The day I was told I had it I cried cux the doctor told me I might not give birth I prayed about it and thanks to God my doctor says I'm better now
@@sempfi22 I agree 100%...Thyroid function has alot to do w/ the reproductive sys...Iodine levels are very important for thyroid function, also for the entire body...Iodine is important for T3 & T4 convertion...Iodine solves lots of problems, please research it people...I learned the hard way...
Hi. Hope and wish you recover soon and get healthy. I need to know if one can have a surgery at 4th stage of endometriosis without removing the entire uterus? My cousin, she is almost 40, and she is extremely upset for doctors have told her that she need to remove her uterus because her endometriosis is in 4th stage and any other medication or surgery is not helpful. Can you please find and tell if she still can ho under surgery without removal of uterus, and can have children. She is not getting pregnant and have no child yet
@@qaimkhan2549 My endometriosis is stage 4. I didn’t have my uterus removed. The doctor removed a significant amount and prescribe an IUD, Lupron Injections and Birth Control pills to slow the progression. Your cousin should seek a second opinion. Everyone one is different but I hope this helps.
I just got diagnosed with endometriosis. It is so painful. I eat gluten free and dairy free mostly because I discovered it made my family and me feel better. I am now focusing on doing 100% of the time just to heal and feel better. You are an inspiration to me. Thanks for your support ❤
Omg yes! I’ve struggled with endo for so many years and it keeps me in bed screaming and crying from the pain. I recently had a talk with an older friend who has been with endo for years and she also told me that sugar, dairy, and processed foods would make it worse so last month about a week before my cycle I cut out those things and my period was sooo much better. It’s crazy how food can really affect us.
That’s crazy because I did the exact same thing you did. Just to test it out I ate clean 1 week before my cycle and BOOM!, no more excruciating period cramps! It was so shocking. But it’s changing my life knowing how much meat and dairy can really cause so many interruptions in our bodies. Been vegan/vegetarian ever since! 😆
OMG RESPECT OTHERS HUMAN home food made scratch only cooking for me personally was nutrition eating. Fast food was awarded be generous by getting student with A report card.
Unfortunately it’s too late for me. I had to have a partial hysterectomy and wasn’t able to have children. Thank you for putting this out here for other women. ❤️💪🏾
@@Some1sAuntie Of Course! I was just diagnosed with endometriosis on my right ovary. I have two cyst growth there . And I’m only 26 😞 Hoping for the best !
Thanks for sharing.... I had 10 years of miscarriages and now the last 3-4 years not being able to "get" pregnant. I got diagnosed just last week with a blood clotting disorder and have a docs letter to get me onto fertility treatment. PCO, polops and fibroids 😔😖😫 A long wait of heart ache and loneliness BUT I'm on my way!!! Such a beautiful family you have 💚💚
This is perfect timing. I go in Friday for an ultrasound. The thing that broke my heart most was the chance of infertility. I know I’m only 19, but I’ve always wanted to be a mama, and I want to do whatever I can to fix this. We will all be stronger because of it. Thank you so much, Tia.
I have both Endometriosis and PCOS too. It’s so annoying sometimes. Watching this video kind of made me teary as it’s so relatable. Thank you for making this video - I love hearing other ladies stories 💕
33 and discovered while having uterine fibroids removed that I had stage 4 Endo. I want to have a family of my own some day, so this was very heartwarming to hear. I hope I am just as blessed to meet the right person who will support me and my dreams. 💜
I can’t begin to thank you for sharing your story. I was diagnosed with endometriosis a couple months ago and I have had mild depression due to the thought of one day not being able to get pregnant. Thank you for showing me that there is still hope to have beautiful babies even with our condition.
I was diagnosed with endometriosis at age 27 after having terrible cramps since I was like 14 years old. So I was finally diagnosed at 27 and I was married 7 years at the time to my high school sweetheart. I was told my chances of having kids was really low. I became severely depressed with emotional and physical pain. I no longer felt like a woman and I just felt I was useless. My mother was diagnosed with breast cancer during that time as well so I was going thru a really tough time. Fast forward, I'm 37 now and I have allowed my fear and depression just stop me from further treatment and being the happy person I use to be. My husband and I are now seperated and alot of it was due to me just basically checking out on life. He left and now have a child with someone else. Today I feel alot of hurt and regret because now I have to go at this alone to get my problem fixed. I wish we could have worked thru it but I guess he's happy now. So ladies, if you are going thru Endometriosis, please go to the doctor and get it taken care of and please don't let it control your life. I just don't want no one else taking the route I did out of fear. I have a doctor's appointment coming up so please pray for me. Thanks and Good luck and Blessings to others battling this condition. 🙏💯💪
When man say no God say YES!!! He only put you through that so you can be a living testament and help others that are going through the same thing. I struggled with fibroids and thought I wasn’t going to be able to have kids but God knows what he had in store for me and at age 36 he blessed me with my beautiful baby girl who is now 2 1/2 years old....the BEST gift in life!!!Continue with your healthy journey and blessings to you and your beautiful family always. 😘
Praise God sister 🙌 your testimony is encouraging me to keep believe that God can do the impossible, I have had irregular cycles since a teen and later found out I was diagnosed with PCOS, I'm believing God for my healing that I will soon have a child.
Hey guys keep fighting an enjoying your life don’t give up , I’m a mother of 6 kiddies my kids range from 19-18,16,8 girls & two boys 14 & 10 I’m 39 years old an was diagnosed with Endo! Keep fighting my warriors thank you Tia ❤ Love you need to pick up your book
i have a 15 year old history, i diagnosed it by my self when i realised something is going on. My pain is soul crushing with severe nausea fainting & extreme mood swings. I strongly believe in listening to your body & we should take care of ourselves. After arguing with my family, 100 doctors, 1000 tests & surgeries, now they're telling me, I'm the better diagnostic for my condition instead of the lab tests.
Tia! I have Endo and honestly it's been a journey and I've been slowly implanting changes in my diet and your book was the first one I bought to help me get started!!! Thank you so much!!!
Welcome back beautiful Tia, Thank you for sharing your journey with endometriosis. There are so many females that have this but are afraid to discuss it. Thank God for your friend Alicia referring you to this specialist. You are abundantly blessed with two beautiful children after having your surgeries . The change of diet is a must! Again thank you for sharing this.❤️🙏🏼
Thank for sharing Tia ... I'm 16year old girl who was diagnosed with endometriosis last year ... ii understand what you went through... 💔😢❤ ... You are my role model / my rock ❤
I love that Endometriosis is being being talked about! Especially by you! You are a sister warrior and I'm so happy that you have a beautiful family. I do want to point out that pregnancy DOES NOT cure or relieve Endometriosis, only suppress it. Every endometriosis case is different but its a big myth from doctors. Many still have the pain and stress about surgeries even after giving birth. My opinion is that it would be very hard to take care of a baby or kid when the mother continues to have debilitating pain. There are many myths out there and many doctors with different opinions with different solution to test on. Some work some don't. But one thing is true... there is NO CURE and NO real reason why endometriosis happens. I totally agree with the diet part since I've experiment it myself.. I get flares up with dairy, meat and alcohol. I think gluten too but I'm still not sure. I'm very interested in you cookbook!! Thank you Tia!!
I found out that I was diagnosed with endometriosis in March but I’m pretty sure I’ve had it for years! I am now urging myself to change my diet because I want to have kids with my husband like you Tia. I had surgery and my right ovary was removed, but my doctor said I can still have children and I’m keeping my faith! I need more advice because it’s a struggle to be in the unknown with endometriosis!
Such a timely video. I got married last year and in the last 4 months I’ve been trying to get pregnant. This past Christmas I felt a swelling on my lower left side of my tummy that was cramping like crazy, went to the hospital , turns out I have ovarian cyst on both ovaries and endometriosis. About 7yrs ago and at least once a year I would have very bad period pain that would literally knock me out (fainting spells). At least I know why I had those terrible pains. I’m literally just coming home from having a blood test at the hospital, and they will be calling me in for surgery in the next few weeks. Thanks Tia for this video, I can start eating better to help myself and there’s hope xx
Thank-you for raising awareness for this condition. Very painful cramps are not normal, no matter how much people try to normalize or downplay it. As Tia says if something feels wrong you owe it to yourself to investigate and get a second or even third opinion.
A couple of years ago.... I went to ER and found out I had uterine fibroids. It has been a long journey. But god is good! I became vegan 6 months ago! Thank you for sharing ur story Tia!
Thank you for sharing. I was diagnosed at age 11 and was told i may not be able to have a child. But God! He's amazing and knows all. I'm now 34 and have a beautiful daughter. I too will share my story as I know so many women are affected by this. Thanks for being brave!!
I had my son at 15 and I’m now 32 he is 17 and I would LOVE to be a mom again I thought it could never happen but you truly give me hope! I have pcos/endometriosis also, Thank you for sharing this!❤️
Thank you for sharing your experience. I bought your cookbook 2 years ago and read your story there. You are absolutely right, food is medicine. Endometriosis, fibroids, PCOS and other issues are related to estrogen dominance based on what we consume, especially dairy since hormones are often injected into cows. I suffer from fibroids and once I started eating better and cut out alcohol (another culprit) it got better.
Hi Tia, thank you so much for sharing your story, you are a great inspiration to me. I also have endometriosis, been diagnosed about 5 years now. It gives me hope knowing that you were able to conceive twice with this disease. I'm about to get married and plan to start a family immediately after, I think your recipe book will significantly help me in this journey to conception. Where can I purchase it? I do not live in the US.
@@kimberleyfrancis6038 Hi darling! Thank you for the love and support ❤️ You can find my book on Amazon! amzn.to/2L8ceDy I hope it can help you on your journey 🙏🏾
Hi Tia, thank you so much for sharing your story. You are helping so many women. I am learning how important diet is. @Marci, it's interesting to read that your fibroids got better after eating better. I am suffering from fibroids myself and it seems that doctors and specialists have no solution for me. Non of them ever said anything about a healthy diet. They only talk about medicines. But I read from different women who suffer or suffered from fibroids that a diet has helped them. I am wondering if this cookbook has helped you in your journey with your fibroids.
Tia! Your story helped to give me life! Thank you! I have a large fibroid and while speaking to my surgeon she said that I could have endometriosis, as well. It has already been so challenging on my body and I have gone to many Gynos who have never caught my symptoms (I was in sports when I was young and everyone told me to suck it up. Ugh!). The surgeon will be taking a sample of my uterus to test for endometriosis during the removal of the fibroid. I'm so happy I don't have to have 2 surgeries! Anyone reading this, please pray for me as this is a very time in my life. But I am also so relieved to be getting answers! It's a God send! Tia, your cook book looks amazing! I can't wait to get it! 💖 love and hugs!
From the age 13 - 21 I went to the doctor/hospital with severe pain and was always told ‘it’s just a heavy period, take paracetamol’ until I was diagnosed last year so I feel ya on the long diagnosis process x
This made me feel like I wasn’t alone! I was diagnosed at the age of 18 and it was scary plus I was young! I found out a couple years ago that you had Endometriosis and I just thought to myself I would have never known that! Thank you for your story!
So thankful for you making this video! I too was able to conceive my miracle son with Stage IV Endometriosis and being told I wouldn't be able to do it. We need more women sharing their stories, that is the only way we will truly find healing. It wasn't until I shared my endo story on my channel that I started to find a support system that helped me figure out my body. The only thing I would add is the right vitamins saved my life and relieved me of my pain!
I have two friends that have been diagnosed by endometriosis and my sister is in the process of finding out whether or not she has it. Thank you for sharing your story. I see how much they go through dealing with it and it makes me feel so terrible that I can’t help. I will be praying for you as well as my loved ones.
I was diagnosed with endometriosis at age 19 I'm now 28 and looking for a new doctor who can do this surgery. I've talked to multiple offices that do not perform the laparoscopy surgery. It blows my mind how unaware or carefree some of these doctors are when it comes to womens health. So, this video is a beacon of hope that something can be done to being more awarness.
Tia, First and foremost, may God continue to BLESS you and your family. I would like to thank you for sharing your journey regarding conceiving with endometriosis. I, too, am struggling with endometriosis. I am 33 years old and is two weeks from my 34th birthday. I have really been struggling emotionally because I really want to have children. My first surgery was at the age of 31 and that’s when I was diagnosed with endometriosis. My doctor said if you get pregnant the symptoms will improve, however the struggle is getting pregnant. As I get older, I’m only human so the thought of conceiving is constantly on my mind but I also struggle with the fact that as you get older the more challenging it is to conceive. I have done cleanses, detox, everything you can think of I have done. Due to surgery as well as additional procedures my doctor, bills are putting a financial strain on my finances. In spite of my circumstances, I will continue to give all the Glory and Praises to GOD. He would never put too much on me that I can not bear. I will continue to hold on to the faith that We will Conceive and there will be resources in place to help those who can not afford medical procedures to assist with reproducing. I thank you again Tia for sharing your story and shedding light on this topic. God Bless You and Everyone viewing this video and those struggling with endometriosis. Respectfully, Tiarra Indiana
Hi Tiarra, It's possible! Don't give up hope... I am 34 and have a 15 month old. I conceived naturally after my doctor told me I would need another surgery to have a chance. You are doing the right thing by staying positive and giving thanks for where you are... Those seeds of thanksgiving will push you to where you need to be! Focus on getting and staying healthy and happy. It is going to happen!! With Love -- Endo Sis
Just turned 26 a couple days ago and I’ve come to terms that I need to take care of my body. I’ve had these ongoing symptoms on and off for the past couple years. And with my recent weight gain they have gotten worse. Thank you for sharing your story! I have hope that I can become healthy again.
I’m 23 I’ve been to SEVERAL doctors. My menstrual is the worst part of my life, I usually go to the bathroom for hours and one day in school my teacher denied me going to the bathroom and I actually ended up having a seizure and urinating on myself and that’s when I’ve noticed ok this is obviously not normal. Every doctor, my family and friends never believed me and said I exaggerate until a friend actually watched me have a seizure I fell to the floor and cracked my tooth. Till this day no one knows what’s going on but my passing out, having seizures and throwing up only occurs on my menstrual. I truly 100000% believe I have endometriosis after doing extensive research but terrified of surgery. Thank you so much for speaking out because we’re all told to take a pill and lay down or just go on birth control
Hi i have endometriosis and had a surgery a few years ago and it has changed my life. The surgery is done via a laparoscopy (keyhole surgery) not a big incision whatsoever. During laparoscopy, the surgeon makes a small cut around 1cm to (0.4 inches), usually near your belly button. After the surgery you feel sore for a day or two, but not that much and once you have healed completely you will not see any scars at all. 🤗
I’m 22 and been dealing with this for 9-10 years now. Feeling the worse pain in my life right now as I’m watching, this is literally how I feel. Watching this has made me smile and feel a little better.
My daughter who is 24 is struggling with this as well. Same exact symptoms and not being able to conceive. 😔 Thank you so much for sharing this! I will def. pass this on to her❤
Far too often females are treated as though they are over reacting. I agree to listen to your body and keep searching until you find someone who will really listen and investigate. Your digestive system houses 70 to 80 percent of your immune system so yes, diet plays a very important role. This was informative and I enjoy your style of delivery.
@@TiaMowrysQuickFix hi tia endometriosis can cause bladder pain I had surgery sep 30 of endo doctor told I don’t have any endo but my bladder is hurting so badly
My mother had a long journey with her diagnosis as well. She was in extreme pain for YEARS, but was ignored and gaslit by her doctors. They accused her of being an opioid addict, even though she's never taken any of those overprescribed medications in her whole life. They made those spurious accusations just based off of the speculation of the previous ob/gyn who also didn't do his job. Until she advocated for herself to the point of tears in the waiting room and hallway (i.e., outside of the exam room) they hadn't even conducted a pap smear. Ignoring women in severe pain is, unfortunately, par for the course in healthcare. I believe the studies show that this exacerbated when that woman is non-White or has a lower socioeconomic status. My mother's actions got her in front of the director of gynecology who LISTENED to her, paired her with two excellent physicians in her unit, and censured the doctors who abused her instead of conducting a routine examination that would've helped to identify the cause of her pain. If you're being ignored and your health is at stake let EVERYONE know and don't give up on yourself.
Dr's are great at ignoring even with proof of test... because so many people do wrong by medication.. I have been fighting it for over 15 years.. when I got fibroid cysts the dr didn't do anything to help.. now the two fibroid tumors have grown together and is the size of my uterus.. drs try to make you feel like you are crazy because the pain ..
Thank you . Because your Mom story was mine . It took 20 years to be diagnosed, 20 years . I was accused of having phantom pain. By the time they conducted a hysterectomy...my ovaries were glued to my walls and twisted . I suffered out of my mind kind of pain.
I’m 22 years old and in a similar situation... I will keep fighting. This has been going on since I was 13 years old. I currently have endo, a massive 12cm ovarian cyst, and pelvic bleeding yet nobody will help me even though they have the results right in front of them. Thank you for the words of encouragement
I have to have my laproscopy in 2 weeks to remove endo and 2 cysts on my left ovary. Did they have to remove your ovary? Did they mention if it would help fertility?
@@backroads227 they didn't remove my ovary, and my doc said it should help out and that I'm "in my prime" for baby making after the surgery. So we'll see...
Oh my gosh... YOU are the first person I've watched on UA-cam who has actually been able to really explain what Endometriosis is in such a heart warming way!! It was like you spoke right to my heart! Thank you so much for sharing!!! I used to not know that Endometriosis even existed! Sending you all lots of love and prayers!🙏❤
Bless your heart Tia. I was diagnosed with endometriosis at 17. I'm now 43. I had 6 surgeries and the 7th was a hysterectomy. I was 28. I was blessed with a son before hand (Thank God). I wish I had the information that you discussed in this episode because I would have done things differently. Thanks for speaking on this subject. Appreciate you❤
Wow I had no idea she had endometriosis. I know it affects so many women , but no one talks about it! The pain - simply indescribable and unbearable. It is literally debilitating. Stay strong women are the STRONGEST on earth 💙
I’m 27 years old and I was diagnosed in 2018 after going through 4 different doctors who wouldn’t believe me and 11 years of painful periods, multiple ER visits, crying because I didn’t understand why I was in so much pain. I had my second lap surgery last year and I finally met an OBGYN who wants to help me. I’m getting my third surgery and getting excision instead of ablation. I’ve been at stage 2 for years.
Am finally a mother today , because of fibroids my tubes was block for 6years I and my husband was having issue because of my situation no child when I was Searching online on UA-cam about fibroids I saw a testimony about dr Omo so I write him and place order for his herbal today I have 2weeks old baby now he can help you too Herb's work like magic. Both on Endometriosis x
I had this surgery in Jan, and I have endometriosis as well! Thanks for your transparency, Tia!! I am very much afraid of infertility, but I am trusting God!
Preach sister! I was misdiagnosed for approx 14 months. After missing way too much work to be acceptable and being in the ER every week for severe pain, nausea, etc and being sent home with nothing but a huge bill and feeling like the doctors really were not listening to me I finally had an ER follow up with a general PCP who took one look at me and my records and said "I bet you have endometriosis". I said endo-what?. He wasn't a "specialist" but he was a blessing and a catalyst to have my first laparoscopy to get diagnosed properly. The OB who did my lap tried to schedule me out several weeks and this Dr called her and said he wanted me in surgery within the next 48 hours. Even that OB didn't want to acknowledge my pain or my symptoms. This was back in 2010-11. There is alot more exposure and awareness now . I think the hardest part was the isolation. Feeling alone because you don't "look sick" but you have to cancel plans last minute because you cant even get out of bed. Friends simply don't understand. If I had Cancer (God forbid) then I would get sympathy and understanding but since I have a disease no one understands unless they have it, then I just look flaky and unreliable. My job pressured me once I got FMLA and tried to punish me for calling in (which is illegal and if it happens to you document everything and contact your state Dept of Labor). I found solace being on IG and seeing how many women across the globe also struggle with this disease .. it's like a support system and sisterhood when you feel abandoned by friends and family. I was told I would never have kids and would keep needing maintenance surgeries. I have not had another surgery since 2011, however I am probably due. I was also informed about changing my diet and exercising in order to keep inflammation under control. I declined the Lupron due to the horror stories and side effects I heard. I took myself off hormonal birth control (which made me feel even worse) and just put my faith in my own instincts. I think each woman has to find out what works for her , regardless of what your doctor feels and also get several opinions. I went to approx 8 different Dr's and specialists and each one has their own method and opinion so it gets confusing. Listen to your OWN body just like Tia said. Sorry this is getting long. Best of luck to everyone struggling with invisible illness.
Thanks Abundantly Tia! To God be the Glory for your loving-kindness and willingness to share your story. My 26 year old daughter is doubled over in pain with endometriosis at this very moment. We have seen Doctors previously but was of no help. Please share with us the Doctor or Doctors who has helped you and performed your surgery. We are willing to travel.
Thank you so much for sharing Endometriosis awareness! Endometriosis is an inflammatory disease that can affect many parts of the body. It occurs when endometrium-like tissue is found outside the uterus. The only way to properly diagnose Endometriosisis is to obtain a biopsy-proven confirmation of the disease through surgical pathology; meaning through a Laparoscopy. It is at this time that the Endometriosis Specialist can excise the Endometriosis as well - hopefully through LAPEX excision surgery.
I was diagnosed at 15 with endometriosis and am now 42. After 3 surgeries I was blessed with my miracle baby at 30. My symptoms went away after having my daughter but now 10 years after having her I feel like the symptoms have returned worse than ever! It’s so frustrating the way doctors blow you off when you explain what you are experiencing. I know my body and I know something isn’t right but no one seems to listen! Instead I am made to feel like I over exaggerate and it’s nothing. So frustrating!! Thank you for sharing your story!
I am so happy to hear that you listened to your body and didn't stop until you found the right physician. I had to do the same thing, I had all the symptoms of cirrhosis of the liver, but my liver was normal. My physician knew he had exhausted himself, and he actually contacted a colleague in another state. My insurance would not allow me to see her, but I knew I had to get to her. She diagnosed that I had an blood clot in my abdomen that had been there for over a year. I had numerous procedures to solve the consequences, but couldn't find a doctor in my network to do the surgery to remove the clot. Long story short, I stepped out on faith, bought expensive supplemental insurance. The doctor and her team removed the clot, and now I am healed. We must not let one doctors inability to fix it, stop us from receiving our blessing. Do the work, walk by Faith and God will do the rest.
I grew up with you, watching you on tv following all of the different shows you and your sister were on. I’ve watched this video several times to encourage myself. I was diagnosed at 18 with PCOS (I wanted 4 kids), and it felt like my world crashed around me. Still no kids and I’m about to turn 25, but I’m trying not to loose hope. Thank you for being an inspiration
Thank you for being open about this. I have been pre-diagnosed with this disease. Throughout the years I suspected I had endometriosis....no doctor listened...I finally got a doctor to listen and pre -diagnosed me with it. Ironically, throughout the years before I was "diagnosed" I changed my diet and cut out some sugar, most gluten and all highly processed foods. My symptoms became better but still isn't perfect. I still struggle with infertility. Each day I fight for myself and do the best I can to take care of myself and advocate for myself. I'm proud of you and thank you so much for sharing your story!!!!
I'm 28 yo and after 2 years of marriage i have diagnosed with endometriosis in my ovarium I'm so sad about that, my doctor said that i have to surgery and i want to have my own baby, thank you for sharing
*am filled with joy and happiness with my family today, because of fibroids my tubes was blocked for 5years after using Dr Omo herbal medicine I was able to shrinking my fibroid naturally, I just give birth to a boy🤱🏿last month here*❤️ Dr Omo herbal medicine work perfectly well he can also help you get rid of Endometriosis, Ovarian Cyst, Pcos..
Tia I appreciate you so much for sharing your story about having endometriosis. Like you, I experienced the worst cramps of my life in my early to late 20's I had days that I would ball up in a fetal position on the floor and just cry out in pain. I didn't know why I was suddenly experiencing so damn much menstrual pain whereas no pain meds seems to help. I was literally losing my sanity over it and was dreading every single months that came when it was that time. Like you, I went to my doctor, only to be told the exact same things your doctor told you and none of it worked. I wish I had known to go to a specialist. When I got married and we decided to start a family, that's when I found out not only that I had endometriosis, but that my tubes were far too damaged for me to have any kids because of the years I suffered with it and had nothing done about it. It's been 20 yrs now and I'm still emotionally hurt to this day that I couldn't have any kids for me and my husband to enjoy. I don't really get over it, I just learn to deal with it. I wish someone had told me about seeing a specialist. I figured since my doctor never mentioned it, it was no need to take it further than the things she told me to do. Some doctor huh? I'm blessed to have a wonderful sincere understanding husband who stuck by me through thick n thin, the high ups and low downs. You are blessed Tia and I'm so happy that you were able to have 2 beautiful children. You are an inspiration, I love your truth and honesty. Keep sharing girly. Much love to you ❤💕🌺 🤗
lexdee523 sorry, to hear. Have you tried changing your diet? My husband aren’t trying to have babies right now so I don’t know if there’s any issues with my uterus or now. But I have had horrible cycles for years. I would be so nauseated that I could barely stand. I would be cramping so badly that I would be balled up in fetal position crying and found myself missing school often. I would vomit because the pain was so intense. Once I stopped eating most fast food and frozen foods (other than chick Fil a now and then) and eating mostly cooked food (like grass fed meat, lots of vegetables, fruit, beans, nuts, rice here and there, smoothies with chia seeds) I saw a HUGE difference. The only symptoms I still experience is heavy bleeding and light cramps. My cramps are WAY better than they used to be and sometimes they not last for 1 day. I take blackstrap molasses before and during my cycle and it really does take the cramps away. I would encourage you to change your diet and look into natural remedies like blackstrap molasses.
@@IAmHisBeloved5 Thank you so kindly for your reply. As I had mentioned in my comment, it's been 20+ years now and my tubes were already damaged to the point of not being able to have kids by the time I got married. I know a lot more about it today than I did 20 something years ago. Seems my doctor didn't have much thorough knowledge about it herself to even tell me about diet changing which back then I wasn't into a lot of fast foods or fried foods too much, or to even recommend seeing a specialist about it. I'm more educated about it now so when I hear of someone I know that may be trying to have kids but are experiencing the same symptoms as I had, I come with recommendations that may help. Happy to say, because of my suggestions in cases such as this, a couple of my friends did seek out further help (through a specialist that is) and now have kids of their own. It still makes me sad that I wasn't able to enjoy the experience of motherhood but I'm happy for others I've helped who were able to. I'm in a good place in my life now. Outside of not being able to conceive, I have no regrets. But I do strongly encourage women to research and educate themselves and seek out further help if ever they find themselves in the same situation. I do wish you (and your husband) the best when the time comes that you two do decide to have kids. I would also like to add if I may. If you have any concerns about your tubes or uterus, you can make an appointment with your doctor to discuss having tests done to determine if everything is ok in those areas in the event that you choose to have kids down that road. Good luck to you.
I'm still scared to go to the doctor but the pain is too much already. I hope to get the strength one day to finally know what I feel. Just watching this while in pain somehow gave me a sense of relief and comfort.
Thank you so much for this info. I just got diagnosed with endometriosis. I have one baby and thought that this diagnosis was the end of having babies but you have given me hope.
Hello! 🙋Fellow woman struggling with endometriosis and sharing her journey on UA-cam. I had my laparoscopy one month ago and am in the process of recovering. I want to have children and am scared about the possibility of being infertile. Your story inspires me and gives me hope. Thank you!
Tia, I struggled for five years after my children were born. I was diagnosed with endometriosis early April of this year. I am having a hysterectomy in October, due to endometriosis and other issues. More women need to know more about endometriosis!!!! Thank you for shearing! God bless you!!!
I just discovered your channel and I was hooked within a day! Your energy is infectious and I always end up smiling. However I also love that you keep it real. Thank you for telling us your story and bringing an awareness to this subject that is slowly becoming less taboo to talk about. So many women suffer in silence and live with endometriosis daily. It’s lovely to see you again Tia❤️❤️
It’s crazy that your doc ignored your issues! I’m finding that so many doctors do that mine included. I was so concerned with my issues and my doc literally didn’t care. I had to help myself with a lot of research and trial and error with my own body. Crazy.
Thank you Tia for sharing your experience. The cramps are from a place called hell, and unfortunately you just reminded me! Diet, and issues we grow up with are very, very important. I became a vegetarian, and eat a whole foods diet because of this, and some other reasons. (The hormones and the trauma the animals go through that we ingest and digest when we eat them are transferred to our own beings. Tia, and for anyone who is interested in deeper healing, here are some great resources to look into: - Queen Afua: She has books on female health issues, and healing. - Gary Null: Is the guru on any health issue you want to know about and is into natural healing. - Louise Hay: Her book, YOU CAN HEAL YOUR LIFE, is a great book that explains disease and healing on a metaphysical level. (RIP Ms. Hay!) - Dr. Jewel Pookrum: Specializes in female reproductive disorders (mostly uterine fibroids), and Ethno-Consciousness differences in the human race. Many, many Blessings!
I had doctors tell me I was crazy for 6 years before I was diagnosed with stage 3 endo. Thanks for being an advocate for women who struggle with this disease. You’re bringing awareness to other women who have been silenced, been told “this is part of being a woman”, and passed by.
Thank you so much for this!!! My doctors say I have endometriosis...its on my charts. But they have never tried to help me with it. I've had horrible cramps. I've cried and screamed in pain since 16. I'm 35. Now I will search for a specialist. Thank you!!!
Thank you for sharing this video with us. It is so helpful. I currently have fibroids on both ovaries and cyst. I always had horrible cramps but, I just thought it was cramps growing up as a teen. As I got older I realized something is wrong. It can be very depressing. We as women go through so much. Some days I am good some days I am down. It’s a process. We are survivors! 💖🤧
I just had a hysterectomy for my Endometriosis. I have had this for 10 years, and I agree with you, trust in yourself and don't get discouraged. I have a love/hate relationship with Dr.s. Thanks for sharing! 💜
I just found out that I have it. I been looked and accused of using it as an excuse or making up the pain. I’m so relieved to have an answer because I was believing the looks and comments of disbelief. I’ve just had the laparoscopy but I’ve been struggling for years with difficult periods and nausea,vomiting and more recently constant. I’m really grateful that I’ve had family and friends who believe in me and support me. Thanks Tia for sharing your story. Since finding out that it could possibly be what is going on with me, people have told me that they went through it and it makes me feel less alone. God is good.
I'm here a year after you posted this, but I'm glad that I did. I was diagnosed with Endo in 2017 after having been misdiagnosed with PCOS for 11 years. My situation sounds a lot like yours. My surgery results lasted about w years and I am seeing my specialist again. All of the things that your doctor told you to do are the things that I use to help relieve pain during periods. I have changed my diet to be less inflammatory. Trying to eat a lot more veggies and fruits. Cut out red meats. It has been a journey and I am continuing on it. I think it is so good to hear other women's stories. We should all learn from one another and uplift each other. God bless you.
Thank you for sharing. I am 27years old and I got diagnosed today with the same condition. My period is like a nightmare every month, and sometimes I would bleed for the whole month. I've been to several doctors until finally today I got to know what exactly is going on with me. Thank you for sharing your experience, I was soo scared and is still scared, but at least I know I'm not alone in this!
I'm currently on my menstrual cycle and I just want to cry for you. 😭 It could be from the hormones haha But I completely agree that food intake is an absolute key to better life in general *And Jesus of course❤* But Thank you Tia so much for sharing your story! You are a warrior ❤
Thanks so much I've just been diagnosed with it recently . I am 33 and have no kids. Want to have kids so badly. Thanks so much for your advice I am forever grateful.
This video helped me a lot!! I was officially diagnosed about 6 months ago with endometriosis. But I’ve been hospitalized and have been put on hormones since I was 15. Ive been extremely lucky to have found a doctor that has been very aggressive with my treatment and has BELIEVED me since the very beginning along with letting me know that this isn’t normal. I’m also a very competitive tennis player and I remember being in the middle of practice and have to stop because I just couldn’t walk. Also being in 5th grade and have to go to the bathroom for hours crying because I was in soooooo much pain and the teacher not believing me .I’ve very appreciative that you made this video and was honest about what you have been through. I know I have a long journey ahead of me but this video made it seem possible. Thank you!!
Thank you Tia for expaining some intricacies of Endometriosis Journey. Everything you said was told to me by my doctor. I was devastated and resolved to not have children against my desire. 😔
Thank you so much for sharing this Tia. So many women suffer for years because they’re either not going to the right doctor (see a specialist!) or they’ve never heard of endometriosis or PCOS. I’ve had painful menstruatal cramps since I was 9. I vividly remember laying on my kitchen floor when I was about 12. I was curled in a ball, crying, and ripping my hair out because the pain was so much. I refused going to the mall I was in so much pain! (FYI for the younger viewers, that was a big deal in the 90s!) It wasn’t until my first extensive DnC and a visit to a specialist that I got diagnosed and treated properly. That was after a visit to the ER because I bled through a jumbo tampon and 2 additional pads within an hour. Since then I’ve had issues in which I’ll bleed for almost a month. That’s when I know it’s come back. Ladies, your body is your best gauge for when you need to seek additional help. It’s not shameful. Call your doctor. Get a referral from a friend. Too many of us suffer in silence.
Tia, I can't thank you enough. I've had severe cramp periods for years. My mom always said she always did so I just thought it just was what it was. But one too many periods of having to stay at home from work, going to the emergency room after fainting of pain, and barely being able to drive (like what happened today and how I stumbled upon your story)> I feel my body saying enough is enough there must be something that can be done. So many people have told me I probably have endometriosis but I have barely had enough money for one visit to the doctor let alone a surgery. I am a big firm believer in food is medicine as I've seen it help in my mental health, overall health, etc. My problem right now is sticking to it as I'm so busy and keep using food as comfort from other problems I'm facing in my life. :( Hearing your story, however, has motivated me to really dedicate this time each week on meal planning for my body. I know it may not be the one & only solution as I do need to go to the doctor, but while I'm saving up more money to spend on my health, at least food I can work on as it is a planned expense already. Just needs more time to plan out the meals. So thank you again so much for your courage in sharing your story (and also that you can cheat a little cause I'm all I don't know how I can live without sharing in some foods w/ friends every now & then!!) & helping me feel way less alone - that feeling of being alone is the worst especially when people make you feel lazy when all you can do is lay in bed for hours but it's because the pain is so bad or just exhausted from enduring the pain!!! Praying for all us period-pain-sufferers and so glad that you are no longer in that much pain and giving hope to others!. God bless you & will definitely look into buying your book !! Much Love , Angela PS Just have to say you & Tamara have no idea how much you blessed me + my sister's childhood w/ Sister Sister!! You both are so beautiful inside and out!
Omg I been dealing with this for a while. I can't take it anymore and I don't want to do the surgery but here I am having my consultation on Monday. Keep me in prayer please! I got emotional listening to you .... Thanks for sharing.
Prayers to you. I just had my surgery last week. I had it in my uterus, on my liver and diaphram. I don't regret the surgery because I wanted to know 100%. Be strong you will overcome!🙏
I had the 1st surgery 5 months ago... It's on my colon bladder. Intestines cervix and uterus. 1 week ago I had a hysterectomy. Everyone is different. I'm praying for you.
@@kamilvolz930 how are you now? I have some near my heart and lungs but doctor was to afraid to remove it so I have to see a different one who treats diaphramic endo. It's crazy never thought it could grow anywhere else
@@amandabavender308 omg I'm so sorry. I had to go see an endo specialist in orlando. At winnie palmer. She is hard to get into but my 1st surgeon referred me in. Her name is Jessica Vaught and she the number 1 robotic surgeon at winnie palmer. My hysterectomy has been a breeze. I'm not taking pain meds and literally yesterday was one week from surgery. I feel cramps but not worst than most my life. I see her again monday and hopefully I will get good news about my colon and bladder. I'm sorry you are also experiencing this.
Thank you for sharing this! I just found out I had endometriosis 3 years ago and I’ve been having these symptoms since I was 13. You have convinced me to change my diet, time to go buy your book!
Thank you so much!! I am not yet diagnosed. I suffer from chronic pelvic pain and other various symptoms. My mom had a very severe case of Endometriosis when I was a kid. She was about my age when it got really bad and she finally got diagnosed. It took a long time to be diagnosed and the doctors told her for a long time that it was in her head. They kept giving her narcotic pain reliever to make it look like they were doing something. FINALLY she was diagnosed. I am going to spare you the rest of the details because I don't want to scare anyone....my mom survived but it was a rough road for a while. This was almost 40 years ago and some of the treatents that they have now were not available then. Anyway, I just remember her telling me as a child "if this ever happens to you don't let the doctors tell you that it is in your head and just keep giving you painkillers". So, here I am. My primary doctor believes I likely have Endo. When I saw the gyn for my annual, I shared my concerns. It was a different doctor in the office who I had never seen before. She was not knowledgeable. She pretty much blew me off. However, here I am 6 months later in more pain that is lasting longer. I have also developed other symptoms such as loss of appetite, nausea, and diarrhea. So, I am on a search for a knowledgeable doctor. I will get there. Hopefully, before this gets too much worse. Doctors are very conservative with prescribing pain medication now and I really don't want to be on pain killers like my mom was. I am going to check out dietary changes and your book.
28yrs of painful periods & 3 miscarriages later got diagnosed this year because my sister found out she has it. 1st surgery into March 2020 surgeon went in looking for mild endo came out with severe. Twisted tubes, bowel stuck to uterus, kidney / uterine vein out of place, endo everywhere including diaphragm. The joys of being a women 🙄 have a 2nd surgery booked in for 17th August 2020 for hysterectomy & treatment of endo. 3 surgeons involved not freaking out yet but relieved to be getting this shit sorted. Thanks for speaking out much appreciated 🙏 👍 😊 ❤
Endometriosis, PCOS (🙋), Ovarian Cancer, etc...All of these diseases are things that plague women, but are rarely talked about. Thanks for taking the time share your story.
These are all hormone related.
Endometriosis and fibroids are caused by high estrogen.
PCOS is caused by low progestrone and estrogen.
I have been dealing with half diagnosed endometriosis and breast lumps for years but I decided to heal my best naturally and with herbs. My diet Is all the way different and I supplement with herbs to boost immunity and stabilize my hormones.
@@campbecy They're not all hormone related, endometriosis is mainly due to a genetic mutation which affects development of the female reproductive organs and the cause of PCOS is for the most part unknown (however the symptoms occur due to higher male hormones in the body). For PCOS one treatment I've seen help is losing weight and taking tablets prescribed by the doctor to help regulate the hormones, it helps to regulate the periods a bit more and helps with the other symptoms
Fed up what tablets have your dr prescribed ? Birth control? I have Pcos and wondering ? And what kind of diet have you found works for you?
Fed up I think you guys need to do a lot more research. In theory the cause of endometriosis is unknown but it Is strongly linked to estrogen dominance. To my knowledge no one in my family has uterine endometriosis however, I started getting symptoms and all of sudden I had all the signs of endometriosis. I was not fully diagnosed because I denied the surgery and decided to go the natural route and Tia talked about it in her book. I went on a no sugar, no diary, gluten and meat diet and I will seldom have eggs, fish or chicken like every few months. During the journey I found out that endometriosis is also linked to parasites which causes the inflammation. I’ve done parasite cleanses and I have actually seen tons of eggs and parasites. I have been on a protocol to balance my estrogen and progesterone since last summer because my doctor had me on birth control before. The first few months after birth control were brutal but now my periods are regular, 50% less bleeding and wayyyy less painful. 🤗 I forgot to add that I have do not eat high estrogenic foods other than meat like most beans and soy. When I was younger I thought painful cramps and heavy bleeding were normal and would go home from high school to curl up in a ball.
The reason why Pcos becomes more under control after dieting is because they are mostly over weight and eat whatever they want. The liver becomes over worked and doesn’t process the hormones well. Read Tia’s book or just research journals on internal inflammation and its link to hormone imbalance.
Te'ylor Beck Do not Take what the doctor prescribes, they’re just bandages for what will be a long term alignment. Someone I work with actually changed her diet but she wasn’t super over weight and she conceived within a few few months. She said she will be eating healthier in general going forward so it doesn’t affect her again in the future. You can also look into calcium d glucarate and DIM. You also need more estrogenic healthy foods like beens fruits and veggies, try for a minimum of 3 months and see how it goes for you. Cheers!
I have endometriosis. I was diagnosed last year and undergone surgery last year as well. my ob removed my left ovary and fallopian tube and she told me i only had 50% chance of being pregnant. but hey, 4 months later, im pregnant.. yassssss
I struggle with it. I feared for years that it would prevent me from becoming pregnant. I'm expecting my first son in two weeks:)
Thank you for sharing.
Brianda Pondexter congratulations! Did you have to seek fertility help ?
@@nataliashafaye2741 Thank you! I didn't. I wasn't even trying. It just happened and I'm so grateful.
Brianda Pondexter Wishing you a safe delivery. Blessings xo
How old are you? If you don’t mind me asking
@@TheGorgeousfemme Not at all. I'm 27.
“Take a bath” 🙄🙄 doctors get on my nerves. 😖
#FACTS I swear I got some of the craziest responses from doctors for years before finding a specialities that took my pain seriously.
Wow! I can only imagine! What did U find that helped?
@@TEWMUCH honestly, the only thing that has truly helped has been the right vitamin combination. I recently shared on my channel. It took me years to finds the right combination.
Right! Yes ma’am! I’ve recently been focusing my attention to Takin care of my nutrient deficiencies as well.! I’m hoping that’ll help me accomplish some of my health goals. I’ve experienced with things like veganism and whole food plant based. And I don’t think I did it right cuz I was lackin nutrients and always felt deprived and hungry.
Wheat is also bad for you. If you stop with that a lot changes
I had endometriosis at 17 and PCOS at 19. I'm now 25 with baby number 3 on the way! Thank you for sharing your story. These are very real conditions and should not be ignored.
Krista Smith did you have to change your diet to lose weight or did you take something to get pregnant . I have PCOS I changed my diet and lost a lot of weight but still haven’t got my period yet
I had surgery at 17 and at 19 and I would drink lots of teas and eat foods that would keep it at bay. I did lose weight but all 3 times I got pregnant I wasn't really trying and I was also on a birth control pill to help keep my cycle regular. Hope this helps!
please help me i have being suffering from this disease bthat is almost costin my life
@@joelkamau1411 you have to change your diet drastically. This helps in any illness... Do research on juicing, raw veggies meals and what food to avoid such as Dairy, sugar, sodas and juice, processed food like canned, frozen, red meat and have occasional organic chicken or beef. Bone Broth is good. fermented foods.... Dont give up. ask God for help and healing anf guidance too
Thats awesome God bless TC
I was diagnosed with endometriosis on December 12th with blocked fallopian tubes I was very blessed to have a very small case of it and I just found out I'm pregnant I'm so happy to give birth to my first child in october.
You have two beautiful children 😍 telling your story just shows that you have endometriosis, but endometriosis doesn't have you! Welcome back Tia ❤
Thanks darling ❤️
☝️💃🏽💃🏽💃🏽💃🏽🏃🏾♀️🏃🏾♀️🏃🏾♀️🏃🏾♀️🏃🏾♀️🏃🏾♀️👐😉
💯
R
Awesome comment! That's why I decided to share my story as well.
I’m 18 and I was diagnosed last week with endometriosis. I feel a lot less alone knowing I’m not alone.
Courtney Reynolds honey you aren’t alone. I was diagnosed 3 yrs ago and had my 2nd surgery last week and I love this video have to change diets. Take care of yourself
Not sure how is best but contact me. I was diagnosed at 18 started at 15 and now am 32. I was alone, no one I knew understood or even got what a bad period was etc. Xxx
Mine im.bleeding for.month
Soo.scared
Definitely not alone! I was diagnosed with stage 3 Endo at age 18 after 9 years of so much pain. There are so many of us that spend years in pain before diagnosis. If you want to find more information about being your own advocate and different treatments I definitely suggest reading "The Doctor Will See You Now" by Dr. Seckin. Its very eye opening and doesnt make you feel alone 💛 welcome to the fight, endowarrior.
You're not alone..I too am dealing with it for 7yrs
I also suffer from Endometriosis. We will find a cure someday. We can kick Endometriosis out the door for good. I love you Tia ❤️❤️❤️
Your food is your medicine.Changeyour diet.doresearch and see what works for you.
You still have pain? I was also endometriose patient
@@Ps-do2si I am sorry for the pain you are enduring, but if you remove all dairy products and foods that contains gluten it will help.Drinking water is very helpful, room temperature, stop drinking cold water.Drink water first thing in the morning then eatanorange or a banana. Drink water one hour before you eat and even before you shower and before you go to bed.
Me 2 changed my whole Life style😀 have since five years no pain anymore. Did all Things since age of 30. Was 25 five when i was dwaling with it after i stopper with the poll. But i have to watch my eggsquality now cause it has effect on it. Im 38 now.
I am with you!! I hope a cure is found soon, too!!
i just wanna cry for all the pain we women face on a day to day basis . i feel all of you, im praying our lives make a change for the better . Bless
God is faithful, thank you Tia for sharing your experience.
Faith Shaya Amen
🙏🏾
Hi Tia, I have endometriosis from I was 27 and I am 46 this year, married for 18 years, we didn't get any children. I change how i eat but it didn't happen. The doctors say the old I get the harder, so I have to thank God my husband he gave me. Lately I am feeling some pain. But my God is a healer he can heal anything.
Lydia Hutchinson
Look up iodine deficiency and endometriosis. Dr. David Brownstein and Dr. Jorge Flechas have done extensive research in iodine deficiency and what it does to the body. You would be surprised at what you find out. Also read "The Iodine Crisis" by Lynne Farrow.
Do you still cramp bad?
Dear Lydia I'm very sorry about that..I was fortunate I was diagnosed of it @ the age of 14 I'm now 25 years the last time I went to see my gynaecologist I was told it's better now...The day I was told I had it I cried cux the doctor told me I might not give birth I prayed about it and thanks to God my doctor says I'm better now
@@sempfi22 I agree 100%...Thyroid function has alot to do w/ the reproductive sys...Iodine levels are very important for thyroid function, also for the entire body...Iodine is important for T3 & T4 convertion...Iodine solves lots of problems, please research it people...I learned the hard way...
I’m currently recovering from my first surgery and this video made me feel so much lighter and encouraged. Thank you so much ❤️
Hi.
Hope and wish you recover soon and get healthy.
I need to know if one can have a surgery at 4th stage of endometriosis without removing the entire uterus?
My cousin, she is almost 40, and she is extremely upset for doctors have told her that she need to remove her uterus because her endometriosis is in 4th stage and any other medication or surgery is not helpful. Can you please find and tell if she still can ho under surgery without removal of uterus, and can have children. She is not getting pregnant and have no child yet
@@qaimkhan2549 My endometriosis is stage 4. I didn’t have my uterus removed. The doctor removed a significant amount and prescribe an IUD, Lupron Injections and Birth Control pills to slow the progression. Your cousin should seek a second opinion. Everyone one is different but I hope this helps.
I just got diagnosed with endometriosis. It is so painful. I eat gluten free and dairy free mostly because I discovered it made my family and me feel better. I am now focusing on doing 100% of the time just to heal and feel better. You are an inspiration to me. Thanks for your support ❤
Omg yes! I’ve struggled with endo for so many years and it keeps me in bed screaming and crying from the pain. I recently had a talk with an older friend who has been with endo for years and she also told me that sugar, dairy, and processed foods would make it worse so last month about a week before my cycle I cut out those things and my period was sooo much better. It’s crazy how food can really affect us.
Autumn LaShay I’m gonna have to try that.
That’s crazy because I did the exact same thing you did. Just to test it out I ate clean 1 week before my cycle and BOOM!, no more excruciating period cramps! It was so shocking. But it’s changing
my life knowing how much meat and dairy can really cause so many interruptions in our bodies. Been vegan/vegetarian ever since! 😆
@@latinaylove8323 dairy and chocolate are the worst for me
I'm glad those things helped you. Adding in more calories, more whole good carbs, and raw dairy (Weston A Price) and it has helped mine a lot
OMG RESPECT OTHERS HUMAN home food made scratch only cooking for me personally was nutrition eating. Fast food was awarded be generous by getting student with A report card.
Unfortunately it’s too late for me. I had to have a partial hysterectomy and wasn’t able to have children. Thank you for putting this out here for other women. ❤️💪🏾
stay strong.u dont need to give a birth to be a mother.just share yr love with someone else and adapt a baby.
So sorry❤️
You’re still freaking amazing!!!
@@fatimemehdiyeva2439 thank you!
@@Sunflower97095 thank you so much as are you!☺️
@@Some1sAuntie Of Course!
I was just diagnosed with endometriosis on my right ovary. I have two cyst growth there . And I’m only 26 😞
Hoping for the best !
Thanks for sharing.... I had 10 years of miscarriages and now the last 3-4 years not being able to "get" pregnant. I got diagnosed just last week with a blood clotting disorder and have a docs letter to get me onto fertility treatment. PCO, polops and fibroids 😔😖😫 A long wait of heart ache and loneliness BUT I'm on my way!!! Such a beautiful family you have 💚💚
God bless you, I truly hope that God protects, heals you, and blessed you
Please research thyroid, iodine levels, & maca root...Thyroid balance is very important for the reproductive sys...
This is perfect timing. I go in Friday for an ultrasound. The thing that broke my heart most was the chance of infertility. I know I’m only 19, but I’ve always wanted to be a mama, and I want to do whatever I can to fix this. We will all be stronger because of it. Thank you so much, Tia.
I have both Endometriosis and PCOS too. It’s so annoying sometimes. Watching this video kind of made me teary as it’s so relatable. Thank you for making this video - I love hearing other ladies stories 💕
I have endometriosis and pcos and fibroids and ppl still think its all in my head
I have
No baby
33 and discovered while having uterine fibroids removed that I had stage 4 Endo. I want to have a family of my own some day, so this was very heartwarming to hear. I hope I am just as blessed to meet the right person who will support me and my dreams. 💜
I can’t begin to thank you for sharing your story. I was diagnosed with endometriosis a couple months ago and I have had mild depression due to the thought of one day not being able to get pregnant. Thank you for showing me that there is still hope to have beautiful babies even with our condition.
I was diagnosed with endometriosis at age 27 after having terrible cramps since I was like 14 years old. So I was finally diagnosed at 27 and I was married 7 years at the time to my high school sweetheart. I was told my chances of having kids was really low. I became severely depressed with emotional and physical pain. I no longer felt like a woman and I just felt I was useless. My mother was diagnosed with breast cancer during that time as well so I was going thru a really tough time. Fast forward, I'm 37 now and I have allowed my fear and depression just stop me from further treatment and being the happy person I use to be. My husband and I are now seperated and alot of it was due to me just basically checking out on life. He left and now have a child with someone else. Today I feel alot of hurt and regret because now I have to go at this alone to get my problem fixed. I wish we could have worked thru it but I guess he's happy now. So ladies, if you are going thru Endometriosis, please go to the doctor and get it taken care of and please don't let it control your life. I just don't want no one else taking the route I did out of fear. I have a doctor's appointment coming up so please pray for me. Thanks and Good luck and Blessings to others battling this condition. 🙏💯💪
I really appreciate this. The fear of treatment for Endometriosis is taking over my relationship and life. I really needed your advise. Thank you.
I’m praying for you. You are healed in Jesus’ name.
I hope this worked out for you. 🤍🤍🤍
❤
How were you diagnosed? My doctor told me there was no way to know besides surgery? I think I have it
When man say no God say YES!!! He only put you through that so you can be a living testament and help others that are going through the same thing. I struggled with fibroids and thought I wasn’t going to be able to have kids but God knows what he had in store for me and at age 36 he blessed me with my beautiful baby girl who is now 2 1/2 years old....the BEST gift in life!!!Continue with your healthy journey and blessings to you and your beautiful family always. 😘
Praise God sister 🙌 your testimony is encouraging me to keep believe that God can do the impossible, I have had irregular cycles since a teen and later found out I was diagnosed with PCOS, I'm believing God for my healing that I will soon have a child.
Amen and Amen! well said Blessing to you and your family!
Hey guys keep fighting an enjoying your life don’t give up , I’m a mother of 6 kiddies my kids range from 19-18,16,8 girls & two boys 14 & 10 I’m 39 years old an was diagnosed with Endo! Keep fighting my warriors thank you Tia ❤ Love you need to pick up your book
i have a 15 year old history, i diagnosed it by my self when i realised something is going on. My pain is soul crushing with severe nausea fainting & extreme mood swings. I strongly believe in listening to your body & we should take care of ourselves. After arguing with my family, 100 doctors, 1000 tests & surgeries, now they're telling me, I'm the better diagnostic for my condition instead of the lab tests.
Tia! I have Endo and honestly it's been a journey and I've been slowly implanting changes in my diet and your book was the first one I bought to help me get started!!! Thank you so much!!!
Thank you do much for sharing
Welcome back beautiful Tia,
Thank you for sharing your journey with endometriosis.
There are so many females that have this but are afraid to discuss it.
Thank God for your friend Alicia referring you to this specialist.
You are abundantly blessed with two beautiful children after having your surgeries .
The change of diet is a must!
Again thank you for sharing this.❤️🙏🏼
Hi tia how are I always watch your show an I ave learn alot my name is kerry
Thank for sharing Tia ... I'm 16year old girl who was diagnosed with endometriosis last year ... ii understand what you went through... 💔😢❤ ... You are my role model / my rock ❤
I love that Endometriosis is being being talked about! Especially by you! You are a sister warrior and I'm so happy that you have a beautiful family.
I do want to point out that pregnancy DOES NOT cure or relieve Endometriosis, only suppress it. Every endometriosis case is different but its a big myth from doctors. Many still have the pain and stress about surgeries even after giving birth. My opinion is that it would be very hard to take care of a baby or kid when the mother continues to have debilitating pain. There are many myths out there and many doctors with different opinions with different solution to test on. Some work some don't. But one thing is true... there is NO CURE and NO real reason why endometriosis happens.
I totally agree with the diet part since I've experiment it myself.. I get flares up with dairy, meat and alcohol. I think gluten too but I'm still not sure.
I'm very interested in you cookbook!! Thank you Tia!!
I found out that I was diagnosed with endometriosis in March but I’m pretty sure I’ve had it for years! I am now urging myself to change my diet because I want to have kids with my husband like you Tia. I had surgery and my right ovary was removed, but my doctor said I can still have children and I’m keeping my faith! I need more advice because it’s a struggle to be in the unknown with endometriosis!
Such a timely video. I got married last year and in the last 4 months I’ve been trying to get pregnant. This past Christmas I felt a swelling on my lower left side of my tummy that was cramping like crazy, went to the hospital , turns out I have ovarian cyst on both ovaries and endometriosis. About 7yrs ago and at least once a year I would have very bad period pain that would literally knock me out (fainting spells). At least I know why I had those terrible pains. I’m literally just coming home from having a blood test at the hospital, and they will be calling me in for surgery in the next few weeks.
Thanks Tia for this video, I can start eating better to help myself and there’s hope xx
Hope your surgery went well.
Thank-you for raising awareness for this condition. Very painful cramps are not normal, no matter how much people try to normalize or downplay it. As Tia says if something feels wrong you owe it to yourself to investigate and get a second or even third opinion.
Totally agree!
Exactly! Multiple opinions and we must continue to seek knowledge, get to know our bodies.
A couple of years ago.... I went to ER and found out I had uterine fibroids. It has been a long journey. But god is good! I became vegan 6 months ago! Thank you for sharing ur story Tia!
That is great!!! It was the best decision I ever made !😊
Try yoni detoxing
Did becoming a vegan help with the fibriods.
Yes it has help with fibroids
Praise god! Thank you for sharing 😊
As someone that also has this as well as ovarian cysts and a whole host of issues I can’t thank you enough!!! Such an important message!! 💛💛
Thank you for sharing. I was diagnosed at age 11 and was told i may not be able to have a child. But God! He's amazing and knows all. I'm now 34 and have a beautiful daughter. I too will share my story as I know so many women are affected by this. Thanks for being brave!!
FIRST!!! WELCOME BACK TIA MOWRY-HARDRICT!!!
I had my son at 15 and I’m now 32 he is 17 and I would LOVE to be a mom again I thought it could never happen but you truly give me hope! I have pcos/endometriosis also, Thank you for sharing this!❤️
Thank you for sharing your experience. I bought your cookbook 2 years ago and read your story there. You are absolutely right, food is medicine. Endometriosis, fibroids, PCOS and other issues are related to estrogen dominance based on what we consume, especially dairy since hormones are often injected into cows. I suffer from fibroids and once I started eating better and cut out alcohol (another culprit) it got better.
Diet is everything!!
Hi Tia, thank you so much for sharing your story, you are a great inspiration to me. I also have endometriosis, been diagnosed about 5 years now. It gives me hope knowing that you were able to conceive twice with this disease. I'm about to get married and plan to start a family immediately after, I think your recipe book will significantly help me in this journey to conception. Where can I purchase it? I do not live in the US.
@@kimberleyfrancis6038 Hi darling! Thank you for the love and support ❤️ You can find my book on Amazon! amzn.to/2L8ceDy I hope it can help you on your journey 🙏🏾
Hi Tia, thank you so much for sharing your story. You are helping so many women. I am learning how important diet is.
@Marci, it's interesting to read that your fibroids got better after eating better. I am suffering from fibroids myself and it seems that doctors and specialists have no solution for me. Non of them ever said anything about a healthy diet. They only talk about medicines. But I read from different women who suffer or suffered from fibroids that a diet has helped them.
I am wondering if this cookbook has helped you in your journey with your fibroids.
This has helped tremendously. I’ve recently been diagnosed with Endometriosis and waiting to have treatment. Tysm for sharing:)
Tia! Your story helped to give me life! Thank you! I have a large fibroid and while speaking to my surgeon she said that I could have endometriosis, as well. It has already been so challenging on my body and I have gone to many Gynos who have never caught my symptoms (I was in sports when I was young and everyone told me to suck it up. Ugh!). The surgeon will be taking a sample of my uterus to test for endometriosis during the removal of the fibroid. I'm so happy I don't have to have 2 surgeries! Anyone reading this, please pray for me as this is a very time in my life. But I am also so relieved to be getting answers! It's a God send! Tia, your cook book looks amazing! I can't wait to get it! 💖 love and hugs!
From the age 13 - 21 I went to the doctor/hospital with severe pain and was always told ‘it’s just a heavy period, take paracetamol’ until I was diagnosed last year so I feel ya on the long diagnosis process x
This made me feel like I wasn’t alone! I was diagnosed at the age of 18 and it was scary plus I was young! I found out a couple years ago that you had Endometriosis and I just thought to myself I would have never known that! Thank you for your story!
So thankful for you making this video! I too was able to conceive my miracle son with Stage IV Endometriosis and being told I wouldn't be able to do it. We need more women sharing their stories, that is the only way we will truly find healing. It wasn't until I shared my endo story on my channel that I started to find a support system that helped me figure out my body. The only thing I would add is the right vitamins saved my life and relieved me of my pain!
Songood to hear that .
How did you convince with 4th stage of endometriosis? I need to know please
I have two friends that have been diagnosed by endometriosis and my sister is in the process of finding out whether or not she has it. Thank you for sharing your story. I see how much they go through dealing with it and it makes me feel so terrible that I can’t help. I will be praying for you as well as my loved ones.
I was diagnosed with endometriosis at age 19 I'm now 28 and looking for a new doctor who can do this surgery. I've talked to multiple offices that do not perform the laparoscopy surgery. It blows my mind how unaware or carefree some of these doctors are when it comes to womens health. So, this video is a beacon of hope that something can be done to being more awarness.
i am definitely dealing with endometriosis and i have ever since i was in high school. changing your diet is a must!
Tia,
First and foremost, may God continue to BLESS you and your family. I would like to thank you for sharing your journey regarding conceiving with endometriosis. I, too, am struggling with endometriosis. I am 33 years old and is two weeks from my 34th birthday. I have really been struggling emotionally because I really want to have children. My first surgery was at the age of 31 and that’s when I was diagnosed with endometriosis. My doctor said if you get pregnant the symptoms will improve, however the struggle is getting pregnant. As I get older, I’m only human so the thought of conceiving is constantly on my mind but I also struggle with the fact that as you get older the more challenging it is to conceive.
I have done cleanses, detox, everything you can think of I have done. Due to surgery as well as additional procedures my doctor, bills are putting a financial strain on my finances.
In spite of my circumstances, I will continue to give all the Glory and Praises to GOD. He would never put too much on me that I can not bear. I will continue to hold on to the faith that We will Conceive and there will be resources in place to help those who can not afford medical procedures to assist with reproducing.
I thank you again Tia for sharing your story and shedding light on this topic.
God Bless You and Everyone viewing this video and those struggling with endometriosis.
Respectfully,
Tiarra
Indiana
Hi Tiarra, It's possible! Don't give up hope... I am 34 and have a 15 month old. I conceived naturally after my doctor told me I would need another surgery to have a chance. You are doing the right thing by staying positive and giving thanks for where you are... Those seeds of thanksgiving will push you to where you need to be! Focus on getting and staying healthy and happy. It is going to happen!! With Love -- Endo Sis
Just turned 26 a couple days ago and I’ve come to terms that I need to take care of my body. I’ve had these ongoing symptoms on and off for the past couple years. And with my recent weight gain they have gotten worse. Thank you for sharing your story! I have hope that I can become healthy again.
I’m 23 I’ve been to SEVERAL doctors. My menstrual is the worst part of my life, I usually go to the bathroom for hours and one day in school my teacher denied me going to the bathroom and I actually ended up having a seizure and urinating on myself and that’s when I’ve noticed ok this is obviously not normal. Every doctor, my family and friends never believed me and said I exaggerate until a friend actually watched me have a seizure I fell to the floor and cracked my tooth. Till this day no one knows what’s going on but my passing out, having seizures and throwing up only occurs on my menstrual. I truly 100000% believe I have endometriosis after doing extensive research but terrified of surgery. Thank you so much for speaking out because we’re all told to take a pill and lay down or just go on birth control
Hi i have endometriosis and had a surgery a few years ago and it has changed my life. The surgery is done via a laparoscopy (keyhole surgery) not a big incision whatsoever. During laparoscopy, the surgeon makes a small cut around 1cm to (0.4 inches), usually near your belly button. After the surgery you feel sore for a day or two, but not that much and once you have healed completely you will not see any scars at all. 🤗
Join Nancy's nook endometriosis education facebook group and learn about excision surgery. There is a way out!
@@rubyname8885 Pelvic ultrasound can only diagnose endometriosis if the patient has chocolate cysts.
Add Nancy's nook endometriosis education on FB plzzz
Thanks for sharing! I have these symptoms(vomiting, painful unbearable menstruations, dizzy) I’m so scared I have my ultrasound in 2 weeks 🙏🏾❤️
I’m 22 and been dealing with this for 9-10 years now. Feeling the worse pain in my life right now as I’m watching, this is literally how I feel. Watching this has made me smile and feel a little better.
My daughter who is 24 is struggling with this as well. Same exact symptoms and not being able to conceive. 😔 Thank you so much for sharing this! I will def. pass this on to her❤
Far too often females are treated as though they are over reacting. I agree to listen to your body and keep searching until you find someone who will really listen and investigate. Your digestive system houses 70 to 80 percent of your immune system so yes, diet plays a very important role. This was informative and I enjoy your style of delivery.
Very true! Listen to your body and trust yourself 🙌🏾
@@TiaMowrysQuickFix hi tia endometriosis can cause bladder pain I had surgery sep 30 of endo doctor told I don’t have any endo but my bladder is hurting so badly
My mother had a long journey with her diagnosis as well. She was in extreme pain for YEARS, but was ignored and gaslit by her doctors. They accused her of being an opioid addict, even though she's never taken any of those overprescribed medications in her whole life. They made those spurious accusations just based off of the speculation of the previous ob/gyn who also didn't do his job. Until she advocated for herself to the point of tears in the waiting room and hallway (i.e., outside of the exam room) they hadn't even conducted a pap smear.
Ignoring women in severe pain is, unfortunately, par for the course in healthcare. I believe the studies show that this exacerbated when that woman is non-White or has a lower socioeconomic status. My mother's actions got her in front of the director of gynecology who LISTENED to her, paired her with two excellent physicians in her unit, and censured the doctors who abused her instead of conducting a routine examination that would've helped to identify the cause of her pain.
If you're being ignored and your health is at stake let EVERYONE know and don't give up on yourself.
Dr's are great at ignoring even with proof of test... because so many people do wrong by medication.. I have been fighting it for over 15 years.. when I got fibroid cysts the dr didn't do anything to help.. now the two fibroid tumors have grown together and is the size of my uterus.. drs try to make you feel like you are crazy because the pain ..
Wow God bless your mom!!!! Thank you for sharing this incredible story of strength & bravery! It's SOO true about our healthcare system :( smh
These same people will diagnose you with stage FOUR cancer after ignoring you
Thank you . Because your Mom story was mine . It took 20 years to be diagnosed, 20 years . I was accused of having phantom pain. By the time they conducted a hysterectomy...my ovaries were glued to my walls and twisted . I suffered out of my mind kind of pain.
I’m 22 years old and in a similar situation... I will keep fighting. This has been going on since I was 13 years old. I currently have endo, a massive 12cm ovarian cyst, and pelvic bleeding yet nobody will help me even though they have the results right in front of them. Thank you for the words of encouragement
Had my first endometriosis laparoscopy yesterday, they found it on my left ovary and removed it. This video helped me. Ordered the cookbook too.
I have to have my laproscopy in 2 weeks to remove endo and 2 cysts on my left ovary. Did they have to remove your ovary? Did they mention if it would help fertility?
@@backroads227 they didn't remove my ovary, and my doc said it should help out and that I'm "in my prime" for baby making after the surgery. So we'll see...
Is the surgery done on the novel 😯?cause I think I have one on the right ovary
@@saprice13 were you able to get pregnant?
Oh my gosh... YOU are the first person I've watched on UA-cam who has actually been able to really explain what Endometriosis is in such a heart warming way!! It was like you spoke right to my heart!
Thank you so much for sharing!!!
I used to not know that Endometriosis even existed!
Sending you all lots of love and prayers!🙏❤
I was recently diagnosed with endometriosis.I am glad I watch this video because it gave me hope to be able to have children. Thank you 😊
Bless your heart Tia. I was diagnosed with endometriosis at 17. I'm now 43. I had 6 surgeries and the 7th was a hysterectomy. I was 28. I was blessed with a son before hand (Thank God). I wish I had the information that you discussed in this episode because I would have done things differently. Thanks for speaking on this subject. Appreciate you❤
Hi did u get laproscopy done at age 17??
@@divkuruvHello, I did not. Not until my 3rd surgery. I was 24 at that time. Hoping you are doing well.
@@elliejackson597 when did u have ur son? Also did u use vissane?
@@divkuruvDid not use Vissane. Not familiar with that. I was 24 when I had my son. He’s now 24. 😊
Wow I had no idea she had endometriosis. I know it affects so many women , but no one talks about it! The pain - simply indescribable and unbearable. It is literally debilitating. Stay strong women are the STRONGEST on earth 💙
My doctor just discovered I have endometriosis after 2yrs marriage and unable to conceive and I pray after my surgery I should have my own baby
Miranda Fonge I pray you have a healthy baby love
I pray you have a health baby in god blessed name
You can and You Will Look up Dr Joe Dispenza
Prayers
Sending baby dust your way!
I’m 27 years old and I was diagnosed in 2018 after going through 4 different doctors who wouldn’t believe me and 11 years of painful periods, multiple ER visits, crying because I didn’t understand why I was in so much pain. I had my second lap surgery last year and I finally met an OBGYN who wants to help me. I’m getting my third surgery and getting excision instead of ablation. I’ve been at stage 2 for years.
Am finally a mother today , because of fibroids my tubes was block for 6years I and my husband was having issue because of my situation no child when I was Searching online on UA-cam about fibroids I saw a testimony about dr Omo so I write him and place order for his herbal today I have 2weeks old baby now he can help you too Herb's work like magic. Both on Endometriosis x
I had this surgery in Jan, and I have endometriosis as well! Thanks for your transparency, Tia!!
I am very much afraid of infertility, but I am trusting God!
Preach sister! I was misdiagnosed for approx 14 months. After missing way too much work to be acceptable and being in the ER every week for severe pain, nausea, etc and being sent home with nothing but a huge bill and feeling like the doctors really were not listening to me I finally had an ER follow up with a general PCP who took one look at me and my records and said "I bet you have endometriosis". I said endo-what?. He wasn't a "specialist" but he was a blessing and a catalyst to have my first laparoscopy to get diagnosed properly. The OB who did my lap tried to schedule me out several weeks and this Dr called her and said he wanted me in surgery within the next 48 hours. Even that OB didn't want to acknowledge my pain or my symptoms. This was back in 2010-11. There is alot more exposure and awareness now . I think the hardest part was the isolation. Feeling alone because you don't "look sick" but you have to cancel plans last minute because you cant even get out of bed. Friends simply don't understand. If I had Cancer (God forbid) then I would get sympathy and understanding but since I have a disease no one understands unless they have it, then I just look flaky and unreliable. My job pressured me once I got FMLA and tried to punish me for calling in (which is illegal and if it happens to you document everything and contact your state Dept of Labor).
I found solace being on IG and seeing how many women across the globe also struggle with this disease .. it's like a support system and sisterhood when you feel abandoned by friends and family. I was told I would never have kids and would keep needing maintenance surgeries. I have not had another surgery since 2011, however I am probably due. I was also informed about changing my diet and exercising in order to keep inflammation under control. I declined the Lupron due to the horror stories and side effects I heard. I took myself off hormonal birth control (which made me feel even worse) and just put my faith in my own instincts. I think each woman has to find out what works for her , regardless of what your doctor feels and also get several opinions. I went to approx 8 different Dr's and specialists and each one has their own method and opinion so it gets confusing. Listen to your OWN body just like Tia said. Sorry this is getting long. Best of luck to everyone struggling with invisible illness.
Thank you for this. I read every word. Did ypu end up having kids?
I've been going through the same pain but the doctor has no idea why. Thank you so much I must go see a specialist...I love u so much Tia
Thanks Abundantly Tia! To God be the Glory for your loving-kindness and willingness to share your story. My 26 year old daughter is doubled over in pain with endometriosis at this very moment. We have seen Doctors previously but was of no help. Please share with us the Doctor or Doctors who has helped you and performed your surgery. We are willing to travel.
Thank you so much for sharing Endometriosis awareness!
Endometriosis is an inflammatory disease that can affect many parts of the body. It occurs when endometrium-like tissue is found outside the uterus.
The only way to properly diagnose Endometriosisis is to obtain a biopsy-proven confirmation of the disease through surgical pathology; meaning through a Laparoscopy. It is at this time that the Endometriosis Specialist can excise the Endometriosis as well - hopefully through LAPEX excision surgery.
I was diagnosed at 15 with endometriosis and am now 42. After 3 surgeries I was blessed with my miracle baby at 30. My symptoms went away after having my daughter but now 10 years after having her I feel like the symptoms have returned worse than ever! It’s so frustrating the way doctors blow you off when you explain what you are experiencing. I know my body and I know something isn’t right but no one seems to listen! Instead I am made to feel like I over exaggerate and it’s nothing. So frustrating!! Thank you for sharing your story!
U have two healthy kids that’s blessings from God a miracle, this issue needs to B talk about us women-go though a lot in life changes.
I am so happy to hear that you listened to your body and didn't stop until you found the right physician. I had to do the same thing, I had all the symptoms of cirrhosis of the liver, but my liver was normal. My physician knew he had exhausted himself, and he actually contacted a colleague in another state. My insurance would not allow me to see her, but I knew I had to get to her. She diagnosed that I had an blood clot in my abdomen that had been there for over a year. I had numerous procedures to solve the consequences, but couldn't find a doctor in my network to do the surgery to remove the clot. Long story short, I stepped out on faith, bought expensive supplemental insurance. The doctor and her team removed the clot, and now I am healed. We must not let one doctors inability to fix it, stop us from receiving our blessing. Do the work, walk by Faith and God will do the rest.
I grew up with you, watching you on tv following all of the different shows you and your sister were on. I’ve watched this video several times to encourage myself. I was diagnosed at 18 with PCOS (I wanted 4 kids), and it felt like my world crashed around me. Still no kids and I’m about to turn 25, but I’m trying not to loose hope. Thank you for being an inspiration
Thank you for being open about this. I have been pre-diagnosed with this disease. Throughout the years I suspected I had endometriosis....no doctor listened...I finally got a doctor to listen and pre -diagnosed me with it. Ironically, throughout the years before I was "diagnosed" I changed my diet and cut out some sugar, most gluten and all highly processed foods. My symptoms became better but still isn't perfect. I still struggle with infertility. Each day I fight for myself and do the best I can to take care of myself and advocate for myself.
I'm proud of you and thank you so much for sharing your story!!!!
I'm 28 yo and after 2 years of marriage i have diagnosed with endometriosis in my ovarium
I'm so sad about that, my doctor said that i have to surgery and i want to have my own baby, thank you for sharing
*am filled with joy and happiness with my family today, because of fibroids my tubes was blocked for 5years after using Dr Omo herbal medicine I was able to shrinking my fibroid naturally, I just give birth to a boy🤱🏿last month here*❤️ Dr Omo herbal medicine work perfectly well he can also help you get rid of Endometriosis, Ovarian Cyst, Pcos..
Tia I appreciate you so much for sharing your story about having endometriosis. Like you, I experienced the worst cramps of my life in my early to late 20's I had days that I would ball up in a fetal position on the floor and just cry out in pain. I didn't know why I was suddenly experiencing so damn much menstrual pain whereas no pain meds seems to help. I was literally losing my sanity over it and was dreading every single months that came when it was that time. Like you, I went to my doctor, only to be told the exact same things your doctor told you and none of it worked. I wish I had known to go to a specialist. When I got married and we decided to start a family, that's when I found out not only that I had endometriosis, but that my tubes were far too damaged for me to have any kids because of the years I suffered with it and had nothing done about it. It's been 20 yrs now and I'm still emotionally hurt to this day that I couldn't have any kids for me and my husband to enjoy. I don't really get over it, I just learn to deal with it. I wish someone had told me about seeing a specialist. I figured since my doctor never mentioned it, it was no need to take it further than the things she told me to do. Some doctor huh? I'm blessed to have a wonderful sincere understanding husband who stuck by me through thick n thin, the high ups and low downs. You are blessed Tia and I'm so happy that you were able to have 2 beautiful children. You are an inspiration, I love your truth and honesty. Keep sharing girly. Much love to you ❤💕🌺 🤗
lexdee523 sorry, to hear. Have you tried changing your diet? My husband aren’t trying to have babies right now so I don’t know if there’s any issues with my uterus or now. But I have had horrible cycles for years. I would be so nauseated that I could barely stand. I would be cramping so badly that I would be balled up in fetal position crying and found myself missing school often. I would vomit because the pain was so intense. Once I stopped eating most fast food and frozen foods (other than chick Fil a now and then) and eating mostly cooked food (like grass fed meat, lots of vegetables, fruit, beans, nuts, rice here and there, smoothies with chia seeds) I saw a HUGE difference. The only symptoms I still experience is heavy bleeding and light cramps. My cramps are WAY better than they used to be and sometimes they not last for 1 day. I take blackstrap molasses before and during my cycle and it really does take the cramps away. I would encourage you to change your diet and look into natural remedies like blackstrap molasses.
@@IAmHisBeloved5 Thank you so kindly for your reply. As I had mentioned in my comment, it's been 20+ years now and my tubes were already damaged to the point of not being able to have kids by the time I got married. I know a lot more about it today than I did 20 something years ago. Seems my doctor didn't have much thorough knowledge about it herself to even tell me about diet changing which back then I wasn't into a lot of fast foods or fried foods too much, or to even recommend seeing a specialist about it. I'm more educated about it now so when I hear of someone I know that may be trying to have kids but are experiencing the same symptoms as I had, I come with recommendations that may help. Happy to say, because of my suggestions in cases such as this, a couple of my friends did seek out further help (through a specialist that is) and now have kids of their own. It still makes me sad that I wasn't able to enjoy the experience of motherhood but I'm happy for others I've helped who were able to. I'm in a good place in my life now. Outside of not being able to conceive, I have no regrets. But I do strongly encourage women to research and educate themselves and seek out further help if ever they find themselves in the same situation. I do wish you (and your husband) the best when the time comes that you two do decide to have kids. I would also like to add if I may. If you have any concerns about your tubes or uterus, you can make an appointment with your doctor to discuss having tests done to determine if everything is ok in those areas in the event that you choose to have kids down that road. Good luck to you.
I'm still scared to go to the doctor but the pain is too much already. I hope to get the strength one day to finally know what I feel. Just watching this while in pain somehow gave me a sense of relief and comfort.
Please go to a doctor.
I hope u go soon too I'm 37 and had to really sit down and evaluate September 15 2023
Thank you so much for this info. I just got diagnosed with endometriosis. I have one baby and thought that this diagnosis was the end of having babies but you have given me hope.
Hello! 🙋Fellow woman struggling with endometriosis and sharing her journey on UA-cam. I had my laparoscopy one month ago and am in the process of recovering. I want to have children and am scared about the possibility of being infertile. Your story inspires me and gives me hope. Thank you!
Tia, I struggled for five years after my children were born. I was diagnosed with endometriosis early April of this year. I am having a hysterectomy in October, due to endometriosis and other issues. More women need to know more about endometriosis!!!! Thank you for shearing! God bless you!!!
I just discovered your channel and I was hooked within a day! Your energy is infectious and I always end up smiling. However I also love that you keep it real. Thank you for telling us your story and bringing an awareness to this subject that is slowly becoming less taboo to talk about. So many women suffer in silence and live with endometriosis daily. It’s lovely to see you again Tia❤️❤️
It’s crazy that your doc ignored your issues! I’m finding that so many doctors do that mine included. I was so concerned with my issues and my doc literally didn’t care. I had to help myself with a lot of research and trial and error with my own body. Crazy.
The doctor ignored mines for 30yrs
Thank you Tia for sharing your experience. The cramps are from a place called hell, and unfortunately you just reminded me!
Diet, and issues we grow up with are very, very important. I became a vegetarian, and eat a whole foods diet because of this, and some other reasons. (The hormones and the trauma the animals go through that we ingest and digest when we eat them are transferred to our own beings.
Tia, and for anyone who is interested in deeper healing, here are some great resources to look into:
- Queen Afua: She has books on female health issues, and healing.
- Gary Null: Is the guru on any health issue you want to know about and is into natural healing.
- Louise Hay: Her book, YOU CAN HEAL YOUR LIFE, is a great book that explains disease and healing on a metaphysical level. (RIP Ms. Hay!)
- Dr. Jewel Pookrum: Specializes in female reproductive disorders (mostly uterine fibroids), and Ethno-Consciousness differences in the human race.
Many, many Blessings!
Thank you so much.
Hola, can you please share your diet ?
I had doctors tell me I was crazy for 6 years before I was diagnosed with stage 3 endo. Thanks for being an advocate for women who struggle with this disease. You’re bringing awareness to other women who have been silenced, been told “this is part of being a woman”, and passed by.
Thank you so much for this!!! My doctors say I have endometriosis...its on my charts. But they have never tried to help me with it. I've had horrible cramps. I've cried and screamed in pain since 16. I'm 35. Now I will search for a specialist. Thank you!!!
Thank you for sharing this video with us. It is so helpful. I currently have fibroids on both ovaries and cyst. I always had horrible cramps but, I just thought it was cramps growing up as a teen. As I got older I realized something is wrong. It can be very depressing. We as women go through so much. Some days I am good some days I am down. It’s a process. We are survivors! 💖🤧
Yes we are! Thanks for sharing love ❤️
I just had a hysterectomy for my Endometriosis. I have had this for 10 years, and I agree with you, trust in yourself and don't get discouraged. I have a love/hate relationship with Dr.s. Thanks for sharing! 💜
That's the best way to put it love/hate. I received no counseling or anything and the mental anguish of not bearing a child is worst than the surgery.
omg Tia Mowry you’re are so cute...I love your energy my sis...this video is full of video nd very real ...respect sis
You truly are so beautiful and so amazing.
I just found out that I have it. I been looked and accused of using it as an excuse or making up the pain. I’m so relieved to have an answer because I was believing the looks and comments of disbelief. I’ve just had the laparoscopy but I’ve been struggling for years with difficult periods and nausea,vomiting and more recently constant. I’m really grateful that I’ve had family and friends who believe in me and support me. Thanks Tia for sharing your story. Since finding out that it could possibly be what is going on with me, people have told me that they went through it and it makes me feel less alone. God is good.
I'm here a year after you posted this, but I'm glad that I did. I was diagnosed with Endo in 2017 after having been misdiagnosed with PCOS for 11 years. My situation sounds a lot like yours. My surgery results lasted about w years and I am seeing my specialist again. All of the things that your doctor told you to do are the things that I use to help relieve pain during periods. I have changed my diet to be less inflammatory. Trying to eat a lot more veggies and fruits. Cut out red meats. It has been a journey and I am continuing on it. I think it is so good to hear other women's stories. We should all learn from one another and uplift each other. God bless you.
You have no idea how badly I needed to hear this message. Thank you.
Thank you for sharing. I am 27years old and I got diagnosed today with the same condition. My period is like a nightmare every month, and sometimes I would bleed for the whole month. I've been to several doctors until finally today I got to know what exactly is going on with me.
Thank you for sharing your experience, I was soo scared and is still scared, but at least I know I'm not alone in this!
I'm currently on my menstrual cycle and I just want to cry for you. 😭 It could be from the hormones haha But I completely agree that food intake is an absolute key to better life in general *And Jesus of course❤* But Thank you Tia so much for sharing your story! You are a warrior ❤
Thanks so much
I've just been diagnosed with it recently .
I am 33 and have no kids.
Want to have kids so badly.
Thanks so much for your advice
I am forever grateful.
This video helped me a lot!! I was officially diagnosed about 6 months ago with endometriosis. But I’ve been hospitalized and have been put on hormones since I was 15. Ive been extremely lucky to have found a doctor that has been very aggressive with my treatment and has BELIEVED me since the very beginning along with letting me know that this isn’t normal. I’m also a very competitive tennis player and I remember being in the middle of practice and have to stop because I just couldn’t walk. Also being in 5th grade and have to go to the bathroom for hours crying because I was in soooooo much pain and the teacher not believing me .I’ve very appreciative that you made this video and was honest about what you have been through. I know I have a long journey ahead of me but this video made it seem possible. Thank you!!
Hey Tia welcome back, Thank you so much for sharing your story I pray God continues to bless you and your beautiful family
You’re so strong for this! and your babies are beautiful 🤗♥️
Thank you Tia for expaining some intricacies of Endometriosis Journey. Everything you said was told to me by my doctor. I was devastated and resolved to not have children against my desire. 😔
Thank you so much for sharing this Tia. So many women suffer for years because they’re either not going to the right doctor (see a specialist!) or they’ve never heard of endometriosis or PCOS.
I’ve had painful menstruatal cramps since I was 9. I vividly remember laying on my kitchen floor when I was about 12. I was curled in a ball, crying, and ripping my hair out because the pain was so much. I refused going to the mall I was in so much pain! (FYI for the younger viewers, that was a big deal in the 90s!)
It wasn’t until my first extensive DnC and a visit to a specialist that I got diagnosed and treated properly. That was after a visit to the ER because I bled through a jumbo tampon and 2 additional pads within an hour. Since then I’ve had issues in which I’ll bleed for almost a month. That’s when I know it’s come back.
Ladies, your body is your best gauge for when you need to seek additional help. It’s not shameful. Call your doctor. Get a referral from a friend. Too many of us suffer in silence.
OMG Tia, endometriosis! You are a strong woman doing several surgeries and now you have your beautiful children. You are blessed.
Tia, I can't thank you enough. I've had severe cramp periods for years. My mom always said she always did so I just thought it just was what it was. But one too many periods of having to stay at home from work, going to the emergency room after fainting of pain, and barely being able to drive (like what happened today and how I stumbled upon your story)> I feel my body saying enough is enough there must be something that can be done. So many people have told me I probably have endometriosis but I have barely had enough money for one visit to the doctor let alone a surgery. I am a big firm believer in food is medicine as I've seen it help in my mental health, overall health, etc. My problem right now is sticking to it as I'm so busy and keep using food as comfort from other problems I'm facing in my life. :( Hearing your story, however, has motivated me to really dedicate this time each week on meal planning for my body. I know it may not be the one & only solution as I do need to go to the doctor, but while I'm saving up more money to spend on my health, at least food I can work on as it is a planned expense already. Just needs more time to plan out the meals. So thank you again so much for your courage in sharing your story (and also that you can cheat a little cause I'm all I don't know how I can live without sharing in some foods w/ friends every now & then!!) & helping me feel way less alone - that feeling of being alone is the worst especially when people make you feel lazy when all you can do is lay in bed for hours but it's because the pain is so bad or just exhausted from enduring the pain!!! Praying for all us period-pain-sufferers and so glad that you are no longer in that much pain and giving hope to others!. God bless you & will definitely look into buying your book !! Much Love , Angela
PS Just have to say you & Tamara have no idea how much you blessed me + my sister's childhood w/ Sister Sister!! You both are so beautiful inside and out!
Omg I been dealing with this for a while. I can't take it anymore and I don't want to do the surgery but here I am having my consultation on Monday. Keep me in prayer please! I got emotional listening to you .... Thanks for sharing.
🙏🏾
Prayers to you. I just had my surgery last week. I had it in my uterus, on my liver and diaphram. I don't regret the surgery because I wanted to know 100%. Be strong you will overcome!🙏
I had the 1st surgery 5 months ago... It's on my colon bladder. Intestines cervix and uterus.
1 week ago I had a hysterectomy. Everyone is different. I'm praying for you.
@@kamilvolz930 how are you now? I have some near my heart and lungs but doctor was to afraid to remove it so I have to see a different one who treats diaphramic endo. It's crazy never thought it could grow anywhere else
@@amandabavender308 omg I'm so sorry. I had to go see an endo specialist in orlando. At winnie palmer. She is hard to get into but my 1st surgeon referred me in. Her name is Jessica Vaught and she the number 1 robotic surgeon at winnie palmer.
My hysterectomy has been a breeze. I'm not taking pain meds and literally yesterday was one week from surgery. I feel cramps but not worst than most my life. I see her again monday and hopefully I will get good news about my colon and bladder.
I'm sorry you are also experiencing this.
Thank you for sharing this! I just found out I had endometriosis 3 years ago and I’ve been having these symptoms since I was 13. You have convinced me to change my diet, time to go buy your book!
Thank you so much!! I am not yet diagnosed. I suffer from chronic pelvic pain and other various symptoms. My mom had a very severe case of Endometriosis when I was a kid. She was about my age when it got really bad and she finally got diagnosed. It took a long time to be diagnosed and the doctors told her for a long time that it was in her head. They kept giving her narcotic
pain reliever to make it look like they were doing something. FINALLY she was diagnosed. I am going to spare you the rest of the details because I don't want to scare anyone....my mom survived but it was a rough road for a while. This was almost 40 years ago and some of the treatents that they have now were not available then. Anyway, I just remember her telling me as a child "if this ever happens to you don't let the doctors tell you that it is in your head and just keep giving you painkillers". So, here I am. My primary doctor believes I likely have Endo. When I saw the gyn for my annual, I shared my concerns. It was a different doctor in the office who I had never seen before. She was not knowledgeable. She pretty much blew me off. However, here I am 6 months later in more pain that is lasting longer. I have also developed other symptoms such as loss of appetite, nausea, and diarrhea.
So, I am on a search for a knowledgeable doctor. I will get there. Hopefully, before this gets too much worse. Doctors are very conservative with prescribing pain medication now and I really don't want to be on pain killers like my mom was.
I am going to check out dietary changes and your book.
28yrs of painful periods & 3 miscarriages later got diagnosed this year because my sister found out she has it. 1st surgery into March 2020 surgeon went in looking for mild endo came out with severe. Twisted tubes, bowel stuck to uterus, kidney / uterine vein out of place, endo everywhere including diaphragm. The joys of being a women 🙄 have a 2nd surgery booked in for 17th August 2020 for hysterectomy & treatment of endo. 3 surgeons involved not freaking out yet but relieved to be getting this shit sorted. Thanks for speaking out much appreciated 🙏 👍 😊 ❤