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It was challenging and unbearable because of how critical my health situation was. but I am grateful and happy to have ordered Dr Aluda herbal supplements on UA-cam which I used and it shrunk my multiple fibroids completely💯💯💯

Felt like i was going to be sick. Got in the bath tub and soaked in the hot water for 10-15 minutes. It helped

Thank you so much! This video was so helpful

I don't have a uterus anymore so the days leading up to and during ovulation are the worst and it's debilitating. And yet I'm still undiagnosed for endometriosis. Or anything. 😭

This video was so helpful and spot on with everything I’ve been experiencing. I’m so glad to know that I’m not alone in this battle!

I'm just starting to get bloating and all the things you said at 7:25, also the pelvis thing, bowel movements, etc etc I'm 30 and I'm shocked as I've been trying to look wtf is going on, this is the 1st time I've experienced so bad 🥲🥲🥲 Tysm sister, I feel pretty sad tho, but I'm gotta take action

Ive had a procedure bit they werent a specialist. Doc states she found nothing and I just need birth control.

Man being a biological woman sucks. Please just take it out! (They refuse to take it out).

3 cm the line of my endo No symptoms

My wife has debilitating pelvic pain during ovulation. Like she lays in bed and/or the bathtub for 3-4 days. Here’s the kicker, she’s already had excision surgery for her endometriosis and fibroids. The excision surgery helped with her period, but the ovulation pelvic pain before her period has almost gotten worse! PLEASE. I beg of you to help me find out what’s wrong or where to start. Could the doctor have missed something or done something wrong? Please help!

I found one who listens to me and my pain they help me a lots I found out I had endometriosis in 2009 when I come back home to New Orleans after hurricane Katrina in 2005 I have stage 4

I have an iron deficiency and I’m on my period now I came across your video I feel so bad can’t eat I been sipping on water I’m cramping alil bit but I still feel like I want to throw up I’m on day 2 yesterday was very bad 😢 I’m going to try your remedies thank you

I'm going threw the same symptoms of Endoscopy)

I also have Endometriosis & it's very debating to even nearly walk or move physically Ong it's very painful)

👍👍👍👍👍👍👍👍👍👍👍👍 Video)

Every time i have my period. I get nauseous during the day, and sometimes I can't even sleep at night because im so nauseous. Even in the early morning, I will wake up feeling so nauseous like I am about to throw up. It is comforting to know that I am not the only one suffering with this.

I only have very painful periods if I don’t take a pain killer during my periods I think the pain can kill me I have never not taken painkillers so I can’t even imagine but that’s my only symptom do u think I have endometriosis? Cos my period pain can’t be normal

Great points and video, sis. Not overexplaining ourselves and having to justify why we can't/don't want to participate in things is huge when it comes to family and friends. At the workplace, we usually have to share more (and it often makes sense to), but hopefully most of us are surrounded by supportive friends and family who don't mind making the kind of adjustments you mentioned in this video.

Primary Umbilical Endometriosis - the struggle of trying to explain to the docs that it's a thing is REAL! I need help. This video is the pep talk I needed to continue speaking up for myself.

These are all really good points. We have to be SO careful with how we distribute our energy and not taking too much on with endo. Thanks for sharing your journey with us! I've just found your channel.

THANK YOU for saying we don’t have to accept birth control. every time i complain about my pain there’ll always be someone to say “if it’s that bad just go on birth control”. like hello?? the side effects are crazy

I was diagnosed when I was 21 I’m 39 now. 4 laps. 36 miscarriages, yes 36. We kept trying in between children and we are lucky to have a family with four children. My last lap was June 23 it’s now April 24 and it’s back a few weeks with a vengeance. I’m on cerezette back to back and do not have a period so the endo will not grow. But last week I had a breakthrough bleed. It was a substantial amount of blood and came fast. Sorry for the TMI. It was frightening to say the least. My pain is in my right ovary (the knife like stabbing pain) the all over intense cramps are in my abdomen, tailbone and groin. I’m so so tired of this. My Gyne and GP refuses to offer a hysterectomy as “I am too young” I know this won’t cure it all but with having Adenomyosis also (diagnosed last June) I want it removed. They keep saying it will lead to more problems. I’ve seen women very happy after their hysterectomy. What am I missing? 💔😩 I hope everyone here is having a pain free day. But if you’re looking up this like I was you’re probably not. Stay strong. We are in this together. 💛💛💛

Mine was chronic before, as ir is again. no matter my cycle or lifestyle. My sisters was worse during her cycle before both our surgeries

I am so happy for you to be able to share your story, I grew up the same way. 5 years ago my sister was able to find a surgeon for endo. At that time i had spent at least 4 months finding any dr to take me seriously and not think I was a pill popper. Now 5 years later I am going back to the same surgeon even now I moved out of state and I think it is worse. My husband and I will try 1 year to have a child but after that I will have to take some hornones so it doesn't come back again. Thank you for sharing your story, its very special and encouraging for many women.

Happy to share after 10+ years I'm finally getting my laparoscopic procedure on Wednesday!! 🎉🎉🎉

My daughter fast the whole day . And take off from school . In Spain women take a day off for period. Here of cause no😊

You forget infertility and recurrent pregnancy loss. Many of us with endo do NOT have pain with periods whatsoever and aren't diagnosed until we've spent $30-40K and had several failed embryo transfers with IVF.

I can relate to you 😨😭🥹

This video made me feel so seen❤

I will add that for sciatic endometriosis which can cause the hip or leg pain and numbness and tingling should not be ignored. There are case reports where it has led to paralysis. Personally i use OCP to control the symptoms such as paralysis, numbness and tingling. The pain has reduced but is still there but i apply ice compresses to my waist to also help with the symptoms. Surgery around the nerve to remove the endometriosis is available, but it is expensive and there are only a few experts on it and surgery around nerves comes with risks too. Hang in there. Try to deal with the pain and try to keep walking to make use of your muscles.

is that cause fever and back burning?

Hi I'm going through it now but i can't even drink any water if i do it'll come right back up😭

I have had years of experiencing endo symptoms. It's recently got so bad that I've been in and out the doctors and hospital with UTI, kidney issues, severe abdominal pain, back problems, and long heavy periods. I saw a doctor yesterday that finally believed me. I am now on the waiting list for surgery and have finally felt like there is hope. Although my new doctor does fear it has been left for too long and I could have long-term damage to my organs due to my severe problems over the last 6 months. I can't believe I'm saying this, but I am really looking forward to my surgery. Here is what I have been told by medical professionals over the years, and yes, I remember every word: • I have been told, "It's not possible to bleed for this long." •"The pill will fix it" after years of trying different pills. •"The coil will fix it" after having two different one which don't work. •"It's just IBS, you need to change your diet" even though I have cut out everything that could cause problems and just live on rice and veg. •"It's normal to experience pain in sex just try different positions." Me and my fiancée have just given up as it's too painful for me. • "Your UTI is cause by sex" like I said I have given up. Ladies, don't let these people tell you it's all in your head when you know your body. Don't leave it as long as me who will now potentially suffer with long-term damage. Take Endo seriously and keep fighting for your diagnosis.

This video is so incredibly helpful, thank you so much. I do a few of these things when I'm nauseous on my period. But there are some new ones here that will definitely come in handy!! Thank you so much!!

So I have been having weird pains in my stomach, it almost feels like gas or even like ulcer symptoms I guess. I have heavy periods and bad cramps. But even when not on my period, i have dull aches. I was told i had IBS... I also have a gallstone, but they said its too big to cause anything, also i think i have a hernia...yay me. Anyway, had a vaginal ultrasound and i might have Adenomyosis..

I have been going to the GP for 5 years with symptoms: very painful and heavy periods that last 7 days, back and pelvic pain, ovulation pain, thigh pain during menstruation, constipation or diarrhea, I often have anemia, spotting before menstruation or 4 days before, dizziness and fainting.

I have all the symptoms except painful urination i also have this burning fire sensation in my stomach which hottness can be feeled when you place your hand on my tummy. My husband always discard my complain he said is caused by sugar consumption. For 6yrs + i have been trying to conceive but no positive results. I have never gone to the doctor regarding this issues. Anytime I talk of hospital my husband gets angry. But i have started savings to take my self to the hospital, is my new resolution. Didn't know why i didn't think of this all these while.. please which doctor am seeing and how much will it costs? Am in Africa, Nigeria precisely

I just got results back that I now how another endometrioma from my endometriosis on my remaining ovary. They just removed at 17cm along with my right ovary and tube ten months ago. It is so frustrating to have stage 4 endometriosis as I do, my heart goes out to anyone else suffering from this awful condition.

Plz get help, the pain isn't normal. I wish I would have known this!

more videos please !!

I relate so strongly to this. Developed Hashimoto's and endo as a teen but went undiagnosed on endo for 20+ years because of the Hashimoto's. We arent taught how to manage chronic illness, it's only when it becomes a crisis that we learn, I think.

Ive been looking every doctor to help me with my period the effects im getting for my period is painful pain, sharp pelvic pain, lower back pain, nausea and vomiting sometimes it hurts to pee and poo i am only diagnosed with dysmenorrhea and only been told that its normal

Fffffff the sciatica that has put me out for 6 months 😅

You like to say “lot in life” a lot lol

I’m literally crying. I feel so seen, finally.

i sure do have a lot of irregular periods a lot lately and I never had this irregular period before Usually I have a regular period and track my period but the pain I'm going through my back and everything. now it makes me want to get diagnosed.

It's insanely cruel of them to level such accusations against u when the infertility is NOT UR FAULT.

This was extremely helpful - thank you for your medical advocacy!

Before 1 week my period start, I get abdomina pain, stomach upset, digestive problem, back pain... To painful.. After getting it I feel period pains & vomiting, udiness, only I can get 1 day.. After tht I can free from my period, every time it happening😟🤭😁can you suggest me for my problem mamplzz.. 🤝

I'm literally crying for the whole video I'm 18 and I have been dealing with so much pain and disorder with my body that I can't recognise is anymore Ive been suffering for more than 9 months and still no diagnosis I've started getting digestive problems and my cycle got irregular and got diagnosed with H.P bacteria , got the treatment and still nothing changed or got better I can't do anything and I don't know how I'm going to deal with everything or how do I explain to people when Ihave nothing dignosised or when I tell them no matter what I drink or get as medicines nothing makes it better and it's hard so hard my own mother can't understand it and Ihate it so much I've been dealing with crazy painful periods since my first evenbleeding, very painful periods that had me going to the hospital but it was regular, and I never ever suffered from any digestive problems until the last months Also my mom has endometriosis but she doesn't believe that I could get a higher chance to get sick with it because of her and tells me that she got it in her 30s like before she got birth to me so it wasn't possible for her to be the reason of my suffering now Keep in mind my mom also had crazy periods during her youth