Jared: “What more can I do to help you?” Literally 8 words I never once heard coming from my husband’s mouth in my 25 years of marriage, and I have suffered with chronic migraines most of my life! If you have to be sick Ellie, be thankful that you have Jared by your side! 😢
Every time I watch a video with a man doing the bare minimum (aka showing the slightest amount of care for his wife) there are always women like you complaining that your husband can't even reach that bare minimum. And I am surrounded by women in partnerships like you. The effect of not being viewed as a human being by the person you've shared 25 years of your life with, risked your life, body and health to birth babies that you assign his surname to, catered to his needs, sleep with must be so demeaning and exhausting. I dream of a world where women don't think another woman is lucky to have someone who kinda cares about her. I dream of a world where women have self respect. I dream of a world where women value themselves more than to live a life like you have. Until women wake up, all we can do is dream...
He is so wonderful, but I think it’s through work and compassion because Ellie does the same for him. They are both so respectful and kind to eachother
Ellie, as someone who is doing this same exact program, I will tell you it has been the best thing I’ve ever done for my health! It’s hard at first not being able to eat hardly anything, but it gets easier and you will see that it’s so, so worth it!! I was diagnosed with hoshimotos and rheumatoid arthritis years ago and I’m amazed at how well I feel since I’ve started this program.
How amazing it is to have a diagnosis! Diagnosis gives SO much validation! ❤️ An empathetic husband is an absolute god-send, also. What a blessing Jared is!
I’ve had coeliac disease since I was 2 years old. I’m 60 now. We didn’t have all the food convenience that we have now. I struggled, not only wth the diet and my own “0h a little won’t hurt” but also having others understand it. BUT it does get easier. Your health is EVERYTHING. You’re going to be just fine AND you have Jerrad to help you - go you!!! You have a diagnosis!!!! You now know what you MUST do. You’ve got this!!!
My mom had Sjogrens and she has had the worst issues with doctors not understanding. Now she found someone an hour away so im so glad you found someone to take you seriously. This is a hard illness related to food. My mom has so much she can't eat and it is one of the worst parts. Hang in there. Praying for wisdom for your docs.
Hi Ellie, I have Mast Cell Activation Disorder which has a lot of similarities to your diagnosis. I have a ton of food allergies/sensitivities too. I see you, it's really hard. I also have fluctuation in my sensitivities. When my body is more riled up, I react to everything. When my inflammation is lower, I can eat way more. But overall diet change is such a hard lifestyle change! I love that you share your journey, I know it's vulnerable but it's also so nice to connect with other people's journeys as a viewer.
How truly wonderful that doctors are finally finding out how to help you. Even though this new diet may be difficult at first it will help you so much especially with those awful migraines and your eyesight. I'm 72 and diagnosed with many of the same issues many years ago but I was told it was something I just had to learn to live with. The Migraines were the worst. I was getting at least 3 per week and had to literally get knocked out with injections every weekend. I'm so happy that you have a way to help you. I recently started my own food plan and I do feel a big difference and so much better. My Migraines went away after menopause but the other things, especially my eyesight which gets worse every year. I have been a bookkeeper my whole life and this year was the worst year with my eyesight. Hang in there, Ellie. You have finally found some help and I pray that you will finally get rid of those Migraines and feel so much better really soon so you can enjoy your life and those adorable kids. Sending g lots of hugs, Love and many, many prayers🙏🙏🙏🙏🙏🙏🙏🙏
Ellie I’m so glad that you FINALLY have a solid diagnosis. Sjogren’s is brutal from everything I’ve learned over the last decade. Following a FODMAP diet is very challenging, but I know you can do it. I was so sad when the docs gave me the lists of what I should and shouldn’t eat. Taking that control can be so empowering. Look at all you’ve endured over the years and know that you can do this!
I’m so glad you both have each other for support!! My husband just went through kidney cancer at 35 years old and as a family we’ve had to change a lot to make sure his health remains a priority ♥️
Thanks for sharing this issue in your personal life. I am older that you, but also struggled with IF, endo and recently diagnosed with auto immune issues. Similar as you... just never feel 100% and am always achy. I will be begining a new food journey also. I have not had food sensitive test done. But, curious now after you mentioned your sensitivities. Please, please, please keep sharing the diet, food, meal planing part of your journey. I think most of us dealing with auto immune issues need to find a support group that can support and share that part of the journey. Also, you may have shared your doctors name, clinic but would you be willing to share his name again? Hang in there, your a great mom and wife!
The video we’ve been waiting for!!! This is so beyond exciting. I am so passionate about this stuff. As someone who was diagnosed with Hashimotos and realizing just how much food is our lifeline…food is information… it’s not just calories. It truly programs our system. I cannot wait to watch your journey ❤
Hi Ellie, I have RA. I was diagnosed 7 months after my daughter was born. That was 24 years ago. I’m glad you finally got some answers. I hope you start to feel better soon ❤
Hi Ellie! ☺ I was so happy to hear that you are finally getting some answers, although they might not be the ones you wanted. I myself was diagnosed with an autoimmune disorder just last week and the biggest part for me is also to change my diet. Meal prep, batch cooking and freezer meals here I come because no way I will have the energy to cook every day, when everything I cook is new and different. Like some others suggested, talk with a dietitian so you get help and support as you and Jared change what you eat so that you don't have to do all the work yourself. It might also be helpful to buy some cookbooks about anti-inflammatory foods and meals. I find that to me that it is easier to absorb than getting sucked into articles online that might have no scientific references. Best of luck with your food endevors! You are doing it together with so many other people 🤗
Doing it together really does make all the difference. One of our sons has an autoimmune disease so we have been looking into a full family diet change but even when he has to do colonoscopy preps and such we all follow to help him too. Well the other boys do get to eat but in hiding and must be something you can't smell 😂 Praying this helps, the start of change is always the hardest.
Ellie I'm sorry about the diagnosis but happy you're finally getting some answers. My daughter in law has just been diagnosed with a super rare auto immune disease that causes her tongue and throat to swell. She's had to be intubated several times to keep her alive. It terrifies me. She has 17,14,4 and 2 year olds that need their mommy and my son needs his wife. She suffers from debilitating migraines too. I am praying for you and your family. Jared I know how helpless you must feel, I know I do. Sending love from Wilsonville Oregon
Keep going guys!!! Thank you for sharing. You’ve been giving me hope for years. Looking at you I want to believe that healthy, trustful and loving relationship can exist!! Thank you so much, Ellie and Jared! I’m sending you my virtual hugs❤God blesses you!
Hi Ellie, I have Sjogrens. I have my ups and downs and it's not easy but with a clean diet and low stress lifestyle it's very manageable. You can do this. You have such a great family and a great support system.
Ellie, April was recently diagnosed with Sjorens as well. You might find comfort in reaching out to her for support. So sorry you're struggling, and you're right it is SO hard. 💛
Autoimmune is definitely rough. I was diagnosed with Crohn’s Disease in my 20s. It’s a daily battle, especially as a mom. Thinking of you guys as you navigate this new diagnosis!
Tommy is providing some comedic relief in that conversation at the end hahahaha I’ll be praying for you guys 💗 I’m so glad you finally have a diagnosis and can finally hopefully start feeling better!!!
Awe Ellie. I had to completely change my eating habits as well when I became a bariatric patient. My husband then decided to become a bariatric patient as well with surgery, and we both changed our eating habits. I have faith you both can make these changes!!! It's hard, absolutely, but having Jared and you both work together.. will make it easier. You got this!!!! Many prayers and love from Canada 🇨🇦
I’m so happy you guys are getting some answers! I can’t imagine going through pregnancy, birth, newborn stage, postpartum all with migraines & no energy. I’m really hoping you will see results ❤
It is a blessing your kids are young so you can teach them about food and health and they will learn to like it all. My kids were newborn and toddler ages when I got diagnosed and have no problem eating vegetables and health food. You crave what you eat
this sounds so exciting!! knowing what is good for YOUR body. the beginning might be hard because of the change but you'll get used to it very quickly and be so happy 💕
I'm graduating from school to become a registered dietitian. In the US we are the only healthcare professional that is regulated to give nutrition advice ethically. I highly recommend seeing an autoimmune dietitian to help you navigate changes that are sustainable for you.
Is your nutritional advice the SAD? That's why Americans have so many autoimmune diseases. A Ketogenic diet put my autoimmune Hashimotos and insulin resistance into remission
My daughter has three autoimmune diseases and her diet is very strict but it helps her and that is a positive. She does have medications and infusions but we always pray for good results and stay positive. Prayers for you Ellie it’s a discovering journey for sure.
Hi Ellie! I do not have this disease, but I have cerebral palsy, I walk in 2004, I was diagnosed with stage 4 sensorineural deafness. I received a lot of support from my family, I have been married for 2 years, my husband knows about all diseases, he loves me the way I am, I admire you because you gave birth to 4 children, I am watching old videos of the birth of all children, I want to say: Persevere, pray and everything will be OK
Usually you’ll find it’s the foods your body is oriented towards when sick already are the most inflammatory. The gut is imbalanced so it wants you to keep feeding the imbalance. It’s so beautiful to see you Jared change your life to support Ellie.
I am so glad for you Ellie! I know it will be hard for a while, but it will be better! I went through something similar in 2018. Then again in 2021. I had to cut dairy out first. Then wheat. Along side my husband finding out he is a type 1 diabetic. For a while there it felt like all I was able to think about, talk about was food. What to eat and not eat. I don't feel like that anymore though! You've got this you can do it! And you will feel sooo much better!! Remember there are people behind you! Rooting for you!! 💛💛💛
Hi I’m a Coeliac so I fully understand what you’re going through. But honey your going to feel sooooooo much better. You can do this. Just remember your body needs time to heal. You go girl. ❤️
I totally get it Ellie, it is hard. I have tons of food allergies. But eliminating the things that make you sick is so worth it. Hang in there it will get easier, and your family will learn to adapt.
Ellie I’m so happy they’ve finally found what’s been happening with your health. Jared you’re the best support system for Ellie I’m really glad Ellie has you. I wish I could have more of a support system ❤ from Perth Western Australia xx
I have celiac disease and had to complete cut out gluten about 5 years ago (I even have to worry about cross contamination) so it makes vacations and eating out really hard sometimes. It does get easier with time though as you get used to it and it is worth changing your diet to feel better!! Praying for you ❤
Sending you loads of love and strength Ellie. I genuinely hope this is the answer you have been looking for. In the meantime just know we love you and are supporting you from the other side of the world. Loads of love Leisa Western Australia xx😘😘😘😘❤️❤️❤️
I was diagnosed with Fibromyalgia first, then Chronic Fatigue, then Sjogrens and finally Rheumatoid arthritis. These past 4 years have been quite challenging and I haven't found my equilibrium yet. Best wishes for you.
I'm sorry that you have been suffering, but I'm so excited for you to have answers.. It may be difficult to make these changes at first, but I know you guys got this. :D Looking forward to your progress videos showing the changes.
Ellie - I am a long time subscriber, but first time commenting. I am so, so glad that you finally have some answers! I could see how hard this has been for you, but it seems like there is finally some hope. This will bring a lot of change in many ways and will be a learning curve, but all the effort will be worth it in the end to feel better. Sending you lots of prayers and blessings as you (and Jared) navigate all of this! 💛💛💛
I was just diagnosed with Lyme Disease after over 10 years of struggle and the diet is such a central component! There are options out there and I hope it is the same with your diagnosis, but I feel better even after just adjusting my diet! I'm praying for you as you begin this journey - you are not alone❤
You guys really inspire me to do much better in my health. ❤ I've been following you guys since Calvin was a baby . And I'm so so proud of how far you guys have gone with everything.
Hi Ellie! I know it seems overwhelming and scary right now but it gets easier. I have Lupus, Fibromyalgia & majority of the symptoms of Sjogrens. Diagnosed 12 years ago when I was 20. Sending you love! You’ve got this 🖤
My mom has fibromyalgia and my aunt just got diagnosed with all of the above that you have! Is there anything that has particularly helped you? They said there’s nothing to do for my moms fibro
My NP has Lupus . She keeps hers in remission with diet. A food sensitivity test is the best way to know what foods to avoid to stop your body from an inflammatory response like Lupus
I also have lupus vasculitis, rheumatoid arthritis, and fibroymalgia and had three different kinds of cancer starting at age 21. And it's rough, but it will become your normal
Ellie, I have had years of struggling with the same types of symptoms. I hope this works for you!I am going to see a Rheumatologist. Thank you for sharing!
Hey Ellie, I have family with the same diagnosis and also with dietary restrictions including for myself and wow yes, it IS difficult but once you make the change in your diet and find new things to eat it becomes easier and you start to miss those bowls of ice cream less and less! Don’t take this as a punishment!! Eating different foods BETTER foods is a win in so many ways!!
Hi Ellie! I have psoriasis it is also an autoimmune condition! It was very hard for me and sometimes still is to change my diet and eat other things that my family is not use to eating. I also cried at the beginning because I didn’t know how to balance everything. I also struggled because I have a sweet tooth, but for my body it’s a big no. You are strong Ellie and with the help of God and Jered you will come through. ❤
I also have an autoimmune disorder. I was diagnosed in 1999, with Churgg-Strauss Syndrome. It was hard in the beginning, but since I know when I’m getting sick and what to do, to be proactive, is a great help. I have a great rheumatologist and pcp. I feel we are team against my illness.
You're not lying about how difficult managing food is Ellie, planning 3 meals a day & snacks everyday is exhausting. Especially with kids when they most times don't wanna eat what you make lol. I'm praying for you guys through this journey and hope it makes you feel 100 times better ❤️
It’s so awesome you have a Dr willing to help you.I have Hashimoto’s and just recently found out I have Turners mosaic as well at the age of 47 and many dr it shouldn’t have taken so long to get properly diagnosed.
Ellie so glad you have answers this will be hard yet hopefully helpful. Please share what you eat and more along with this journey I believe this information can help many people! Thanks for being vulnerable
I have so many health issues too. After years I finally did a food blood panel and can’t eat Hardly anything. But looking forward to feeling better. Prayers you will too
My spouse has had sjogrens for years and has never been told to change their diet. She uses restasis for dry eye. Dry mouth drops and chewing gum for dry mouth. She also needs to take a nap most days. I hope the diet works for you. It sounds like hard work-one day at a time! So glad Jared is doing it, too. He is such a huge support and so caring.
You finally have a diagnosis! That's ultimately your first step to feeling better. Since you were unknowingly eating many of the foods you were sensitive, removing them from your diet will be a big step to being more healthy and feeling better.
I can't imagine how low and vulnerable of a state you have to be in to state outloud how hard it is to live. I pray you find healing, soon. The mind is powerful and I hope and pray you guys feel well soon. 🙏
Food is habitual. When I went vegan the first three weeks were really the hardest to develop new habits in our meal plans and snacks. It does become normal with time and before you know it it's second nature. I'm excited to see the new creative meals you come up with, and how you feel.
I was diagnosed with my first autoimmune disease in 1998. Rheumatoid arthritis was first, then came Sjogren's, then can psoriasis. I also have Raynaud's. You will live with this for the rest of your life. I am so sorry, Ellie. You are young and have a young family. Once you figure out what is right for you to eat, and how much exercise you need, changes will become a way of life. Hang in there Ellie, you are not alone. There are many of us that fight autoimmune diseases. Sending hugs.
Hi Ellie, you can replace your peanut butter balls with cut up dates, almond butter or sunflower seed butter rolled in cacao powder. They're delicious. Watch oatmeal...many ppl are allergic. If you are, just used crushed chex cereal instead of oatmeal for any recipes
I also have sjogrens syndrome. When I was diagnosed, I was told there's nothing they can do about it and I just have to drink more water. It was extremely frustrating so I'm excited to see how all these changes help you ❤
I’m very excited to watch you both go through this journey! I, too, have an autoimmune disorder and experience bloating/anxiety/difficulty swallowing while taking medication for it. Please share the foods you eat!!
My husband has the same exact issues. He can't eat foods with nightshades in them (potatoes, peppers,tomatoes) he can't have wheat, he can't have dairy...it was so hard at first....but I found recipes, and substitutes, and I changed my diet to help it be easier for him...now he feels wonderful all the time, his mood is better. It will get easier...I promise, and it's all worth it in the end. You'll still crave your old food once in a great while...but it's easy to find substitutes.
Ellie! I'm so glad that you finally have answers girl! I have been following your medical journey because our symptoms are so similar. I will keep you in my prayers that this will be an easier transition for you & that you will see the results that you are expecting. 🙏🏼❤🤞🏻 Would it be possible to get your doctor's info. I have been chronically ill since 2012. I have received many diagnoses, but I still have unexplained symptoms that includes a lot of what you have been feeling. Most of my drs say that they feel I have to have an autoimmune disease. I have had bloodwork done, I've seen a couple of different Rheumatologist's & no one can find anything, but I know we are missing something. There are days that I can't even get out of bed. My body is full of inflammation which causes my pain to be worse. Anyways, if you are able to share his contact info please do. I'm in Las Vegas, but very willing to travel to your area. Heck its much closer then UCLA & The Mayo clinic in Arizona where I have specialists that I travel to. Thanks in advance if you are able to share & thanks for sharing the update. ❤
It's very difficult; because of family history and dealing with auto immune and health issues myself, I did actually guess that might be her issue! Hoping things ease up soon!
Hi! I know this sounds hard but I did the same thing and within 6 months my auto immune disorder is in remission AND I got pregnant. Something I never thought I could do. You WILL feel so much better. Just find what works for you!
Who is it that you are seeing now? I have been trying to get answers for years, I have around 13 different doctors/specialists and I feel like I am constantly spinning my wheels. It is so frustrating! Ellie I am so happy that you finally have those answers.
i too have an autoimmune disease so i get it sending a prayer and hug your amazing i now get an injection every four weeks which helps it is sad but all we’ll be ok another great video
I have had to do the autoimmune protocol diet and its misery. You can get to the point when its under control and you are feeling much better. You can do it!
The person I am really concerned about at this point in time is JARED I can see the pain, in this man's eyes and yet it seems as though his health issues can go to the back burner! I have never once, ever seen Jared be anything but 100% supportive and loving and it is my strong opinion right now he needs that from Ellie! As a person who has suffered from an autoimmune disease for over 35 years I empathize with Ellie, it can be and is devastating to deal with a constant life-sucking illness, STILL, Jared is suffering right now I can see it in his eyes....and in his soul, he has even broken down and cried which is NOT like Jared, I pray to Jesus that Ellie will see how much Jared is in need right now and gives to him the love, support, and care he has always given to her!
Something that has really helped me with my inflammation is ginger/turmeric shots. I have trouble digesting food with my hashimotos. I take FRESH ginger & turmeric root & blend them up in my ninja with an orange, some water (i use coconut water) and fresh ground pepper, which helps with the absorption of the curcumen in the turmeric. Then i strain it because especially the turmeric has a lot of pulp. But you don’t have to strain it. I do this every night & literally i can feel my bloating go down. I FEEL FOR YOU BOTH!!! Praying this is the beginning for answers & help in your health journey.
You guys can do it! Once you get past the 3 weeks like Dr Axe said it does get easier. When you start to feel better it will motivate you to keep going. Diet is a huge factor in health and like Dr said it’s what you (we ) can control. Praying you feel better sooner than later so you can enjoy the benefits of everything!
My godmother has shograns and she lives an absolute full and healthy life!!! Im so glad you finally have a diagnosis ellie!!! This is going to change your life for the better!!!
Ellie! I am so sorry. I have a ton of unexplained symptoms of things, but I don't know what causes it. I have never had one overarching diagnosis, but food seems to play a major factor. I also have gotten extreme vertigo as well. I am struggling to figure out where I can find answers. Please continue to share, because I hope it can help me figure out what to do next too.
I’m happy for you Ellie you now have the answer for you to get back to perfect health. I understand that you have a lot to process but with Jared by your side and doing the diet with you will make all the difference. Love you guys ❤❤❤❤❤❤
Jared: “What more can I do to help you?” Literally 8 words I never once heard coming from my husband’s mouth in my 25 years of marriage, and I have suffered with chronic migraines most of my life! If you have to be sick Ellie, be thankful that you have Jared by your side! 😢
She’s so lucky!!! I’m in tears Jared and Ellie are truly soulmates🥹🖤
Same here, my husband hates to see me not feeling well and is total opposite of Jared. Not sure he actually knows how to handle it.
Every time I watch a video with a man doing the bare minimum (aka showing the slightest amount of care for his wife) there are always women like you complaining that your husband can't even reach that bare minimum. And I am surrounded by women in partnerships like you. The effect of not being viewed as a human being by the person you've shared 25 years of your life with, risked your life, body and health to birth babies that you assign his surname to, catered to his needs, sleep with must be so demeaning and exhausting. I dream of a world where women don't think another woman is lucky to have someone who kinda cares about her. I dream of a world where women have self respect. I dream of a world where women value themselves more than to live a life like you have. Until women wake up, all we can do is dream...
Alexa Davis
He is so wonderful, but I think it’s through work and compassion because Ellie does the same for him. They are both so respectful and kind to eachother
Ellie, as someone who is doing this same exact program, I will tell you it has been the best thing I’ve ever done for my health! It’s hard at first not being able to eat hardly anything, but it gets easier and you will see that it’s so, so worth it!! I was diagnosed with hoshimotos and rheumatoid arthritis years ago and I’m amazed at how well I feel since I’ve started this program.
How amazing it is to have a diagnosis! Diagnosis gives SO much validation! ❤️
An empathetic husband is an absolute god-send, also. What a blessing Jared is!
I love how supportive and loving jared is toward Ellie no matter the situation. Sending all my love and prayers to you guys. ❤
I’ve had coeliac disease since I was 2 years old. I’m 60 now. We didn’t have all the food convenience that we have now. I struggled, not only wth the diet and my own “0h a little won’t hurt” but also having others understand it. BUT it does get easier. Your health is EVERYTHING. You’re going to be just fine AND you have Jerrad to help you - go you!!! You have a diagnosis!!!! You now know what you MUST do. You’ve got this!!!
My mom had Sjogrens and she has had the worst issues with doctors not understanding. Now she found someone an hour away so im so glad you found someone to take you seriously. This is a hard illness related to food. My mom has so much she can't eat and it is one of the worst parts. Hang in there. Praying for wisdom for your docs.
May I ask who the dr is & location? Looking for help myself…thx.
God bless your mom❤
Hi Ellie, I have Mast Cell Activation Disorder which has a lot of similarities to your diagnosis. I have a ton of food allergies/sensitivities too. I see you, it's really hard. I also have fluctuation in my sensitivities. When my body is more riled up, I react to everything. When my inflammation is lower, I can eat way more. But overall diet change is such a hard lifestyle change!
I love that you share your journey, I know it's vulnerable but it's also so nice to connect with other people's journeys as a viewer.
How truly wonderful that doctors are finally finding out how to help you. Even though this new diet may be difficult at first it will help you so much especially with those awful migraines and your eyesight.
I'm 72 and diagnosed with many of the same issues many years ago but I was told it was something I just had to learn to live with.
The Migraines were the worst. I was getting at least 3 per week and had to literally get knocked out with injections
every weekend. I'm so happy that you have a way to help you. I recently started my own food plan and I do feel a big difference and so much better. My Migraines went away after menopause but the other things, especially my
eyesight which gets worse every year. I have been a bookkeeper my whole life and this year was the worst year with my eyesight.
Hang in there, Ellie. You have finally found some help and I pray that you will finally get rid of those Migraines and feel so much better really soon so you can enjoy your life and those adorable kids. Sending g lots of hugs, Love and many, many prayers🙏🙏🙏🙏🙏🙏🙏🙏
It's so sweet that Jared is so very supportive and loving to Ellie ❤
Ellie I’m so glad that you FINALLY have a solid diagnosis. Sjogren’s is brutal from everything I’ve learned over the last decade. Following a FODMAP diet is very challenging, but I know you can do it. I was so sad when the docs gave me the lists of what I should and shouldn’t eat. Taking that control can be so empowering. Look at all you’ve endured over the years and know that you can do this!
I’m so glad you both have each other for support!! My husband just went through kidney cancer at 35 years old and as a family we’ve had to change a lot to make sure his health remains a priority ♥️
Thanks for sharing this issue in your personal life. I am older that you, but also struggled with IF, endo and recently diagnosed with auto immune issues. Similar as you... just never feel 100% and am always achy. I will be begining a new food journey also. I have not had food sensitive test done. But, curious now after you mentioned your sensitivities. Please, please, please keep sharing the diet, food, meal planing part of your journey. I think most of us dealing with auto immune issues need to find a support group that can support and share that part of the journey. Also, you may have shared your doctors name, clinic but would you be willing to share his name again? Hang in there, your a great mom and wife!
The video we’ve been waiting for!!! This is so beyond exciting. I am so passionate about this stuff. As someone who was diagnosed with Hashimotos and realizing just how much food is our lifeline…food is information… it’s not just calories. It truly programs our system.
I cannot wait to watch your journey ❤
Hi Ellie, I have RA. I was diagnosed 7 months after my daughter was born. That was 24 years ago. I’m glad you finally got some answers. I hope you start to feel better soon ❤
Hi Ellie! ☺
I was so happy to hear that you are finally getting some answers, although they might not be the ones you wanted. I myself was diagnosed with an autoimmune disorder just last week and the biggest part for me is also to change my diet. Meal prep, batch cooking and freezer meals here I come because no way I will have the energy to cook every day, when everything I cook is new and different. Like some others suggested, talk with a dietitian so you get help and support as you and Jared change what you eat so that you don't have to do all the work yourself. It might also be helpful to buy some cookbooks about anti-inflammatory foods and meals. I find that to me that it is easier to absorb than getting sucked into articles online that might have no scientific references.
Best of luck with your food endevors! You are doing it together with so many other people 🤗
I’m thankful you have a support system Ellie! Your husband and other family. Having an autoimmune disease is sooo hard. Praying for you! ❤
Jared you are so sweet and supportive. Everyone needs a Jared. Wishing you both the best in this journey ❤❤
Doing it together really does make all the difference. One of our sons has an autoimmune disease so we have been looking into a full family diet change but even when he has to do colonoscopy preps and such we all follow to help him too. Well the other boys do get to eat but in hiding and must be something you can't smell 😂 Praying this helps, the start of change is always the hardest.
Ellie I'm sorry about the diagnosis but happy you're finally getting some answers. My daughter in law has just been diagnosed with a super rare auto immune disease that causes her tongue and throat to swell. She's had to be intubated several times to keep her alive. It terrifies me. She has 17,14,4 and 2 year olds that need their mommy and my son needs his wife. She suffers from debilitating migraines too. I am praying for you and your family. Jared I know how helpless you must feel, I know I do. Sending love from Wilsonville Oregon
I have RA and have since I was 8. You got this! Meal prep will be your best friend!
Keep going guys!!!
Thank you for sharing.
You’ve been giving me hope for years. Looking at you I want to believe that healthy, trustful and loving relationship can exist!!
Thank you so much, Ellie and Jared!
I’m sending you my virtual hugs❤God blesses you!
Hi Ellie!! I was diagnosed with fibromyalgia. It’s a struggle but once you take everything out of your diet, it is amazing. Hugs!!
Hi Ellie, I have Sjogrens. I have my ups and downs and it's not easy but with a clean diet and low stress lifestyle it's very manageable. You can do this. You have such a great family and a great support system.
Ellie,
April was recently diagnosed with Sjorens as well. You might find comfort in reaching out to her for support.
So sorry you're struggling, and you're right it is SO hard. 💛
Autoimmune is definitely rough. I was diagnosed with Crohn’s Disease in my 20s. It’s a daily battle, especially as a mom. Thinking of you guys as you navigate this new diagnosis!
Tommy is providing some comedic relief in that conversation at the end hahahaha
I’ll be praying for you guys 💗 I’m so glad you finally have a diagnosis and can finally hopefully start feeling better!!!
Awe Ellie.
I had to completely change my eating habits as well when I became a bariatric patient. My husband then decided to become a bariatric patient as well with surgery, and we both changed our eating habits.
I have faith you both can make these changes!!! It's hard, absolutely, but having Jared and you both work together.. will make it easier.
You got this!!!! Many prayers and love from Canada 🇨🇦
I’m so happy you guys are getting some answers! I can’t imagine going through pregnancy, birth, newborn stage, postpartum all with migraines & no energy. I’m really hoping you will see results ❤
It is a blessing your kids are young so you can teach them about food and health and they will learn to like it all. My kids were newborn and toddler ages when I got diagnosed and have no problem eating vegetables and health food. You crave what you eat
this sounds so exciting!! knowing what is good for YOUR body. the beginning might be hard because of the change but you'll get used to it very quickly and be so happy 💕
I'm graduating from school to become a registered dietitian. In the US we are the only healthcare professional that is regulated to give nutrition advice ethically. I highly recommend seeing an autoimmune dietitian to help you navigate changes that are sustainable for you.
I second this!
I was going to say the same!
I think she already is. Could be wrong though
Is your nutritional advice the SAD? That's why Americans have so many autoimmune diseases. A Ketogenic diet put my autoimmune Hashimotos and insulin resistance into remission
I third this
My daughter has three autoimmune diseases and her diet is very strict but it helps her and that is a positive. She does have medications and infusions but we always pray for good results and stay positive. Prayers for you Ellie it’s a discovering journey for sure.
Hi Ellie! I do not have this disease, but I have cerebral palsy, I walk in 2004, I was diagnosed with stage 4 sensorineural deafness. I received a lot of support from my family, I have been married for 2 years, my husband knows about all diseases, he loves me the way I am, I admire you because you gave birth to 4 children, I am watching old videos of the birth of all children, I want to say: Persevere, pray and everything will be OK
Usually you’ll find it’s the foods your body is oriented towards when sick already are the most inflammatory. The gut is imbalanced so it wants you to keep feeding the imbalance.
It’s so beautiful to see you Jared change your life to support Ellie.
I am so glad for you Ellie! I know it will be hard for a while, but it will be better! I went through something similar in 2018. Then again in 2021. I had to cut dairy out first. Then wheat. Along side my husband finding out he is a type 1 diabetic. For a while there it felt like all I was able to think about, talk about was food. What to eat and not eat. I don't feel like that anymore though! You've got this you can do it! And you will feel sooo much better!! Remember there are people behind you! Rooting for you!! 💛💛💛
Hi I’m a Coeliac so I fully understand what you’re going through. But honey your going to feel sooooooo much better. You can do this. Just remember your body needs time to heal. You go girl. ❤️
I fought through my autoimmune horror for ten years before my amazing physician. So glad you found Josh.
Who is the dr you recommend & what location - looking for similar help. Thx ❤ God bless!
I totally get it Ellie, it is hard. I have tons of food allergies. But eliminating the things that make you sick is so worth it. Hang in there it will get easier, and your family will learn to adapt.
Ellie I’m so happy they’ve finally found what’s been happening with your health. Jared you’re the best support system for Ellie I’m really glad Ellie has you. I wish I could have more of a support system ❤ from Perth Western Australia xx
I have celiac disease and had to complete cut out gluten about 5 years ago (I even have to worry about cross contamination) so it makes vacations and eating out really hard sometimes. It does get easier with time though as you get used to it and it is worth changing your diet to feel better!! Praying for you ❤
Jared had so much love, loyalty, and support for Ellie. She's truly blessed to have a great husband like him.
Sending you loads of love and strength Ellie. I genuinely hope this is the answer you have been looking for.
In the meantime just know we love you and are supporting you from the other side of the world. Loads of love Leisa Western Australia xx😘😘😘😘❤️❤️❤️
I can’t imagine what this disorder is like. Together, all is possible 😊❤
I was diagnosed with Fibromyalgia first, then Chronic Fatigue, then Sjogrens and finally Rheumatoid arthritis. These past 4 years have been quite challenging and I haven't found my equilibrium yet. Best wishes for you.
I'm sorry that you have been suffering, but I'm so excited for you to have answers.. It may be difficult to make these changes at first, but I know you guys got this. :D Looking forward to your progress videos showing the changes.
Ellie - I am a long time subscriber, but first time commenting. I am so, so glad that you finally have some answers! I could see how hard this has been for you, but it seems like there is finally some hope. This will bring a lot of change in many ways and will be a learning curve, but all the effort will be worth it in the end to feel better. Sending you lots of prayers and blessings as you (and Jared) navigate all of this!
💛💛💛
I was just diagnosed with Lyme Disease after over 10 years of struggle and the diet is such a central component! There are options out there and I hope it is the same with your diagnosis, but I feel better even after just adjusting my diet! I'm praying for you as you begin this journey - you are not alone❤
You guys really inspire me to do much better in my health. ❤ I've been following you guys since Calvin was a baby . And I'm so so proud of how far you guys have gone with everything.
Hi Ellie! I know it seems overwhelming and scary right now but it gets easier. I have Lupus, Fibromyalgia & majority of the symptoms of Sjogrens. Diagnosed 12 years ago when I was 20. Sending you love! You’ve got this 🖤
Same
Acceptance comes in time
My mom has fibromyalgia and my aunt just got diagnosed with all of the above that you have! Is there anything that has particularly helped you? They said there’s nothing to do for my moms fibro
My NP has Lupus . She keeps hers in remission with diet. A food sensitivity test is the best way to know what foods to avoid to stop your body from an inflammatory response like Lupus
@@bayliesbookshelf Dani Williamson book Wild and Well. Get a copy for your mom
I also have lupus vasculitis, rheumatoid arthritis, and fibroymalgia and had three different kinds of cancer starting at age 21. And it's rough, but it will become your normal
I'm so glad you finally have answers!! Praying that once you get through the 3 weeks of dietary stuff that it'll be easy sailing.
I'm obsessed with this adorable couple!!! The way they support each h other and respect and love is other is just unbelievably heart warming!!!!!
Ellie, I have had years of struggling with the same types of symptoms. I hope this works for you!I am going to see a Rheumatologist. Thank you for sharing!
Hey Ellie, I have family with the same diagnosis and also with dietary restrictions including for myself and wow yes, it IS difficult but once you make the change in your diet and find new things to eat it becomes easier and you start to miss those bowls of ice cream less and less! Don’t take this as a punishment!! Eating different foods BETTER foods is a win in so many ways!!
So sorry to hear Ellie. I've suffered from this for over 15 years. Chin up, the adjustment will get easier with time
We love you Ellie! ❤ Your in our thoughts and prayers always!!❤
Hi Ellie! I have psoriasis it is also an autoimmune condition! It was very hard for me and sometimes still is to change my diet and eat other things that my family is not use to eating. I also cried at the beginning because I didn’t know how to balance everything. I also struggled because I have a sweet tooth, but for my body it’s a big no. You are strong Ellie and with the help of God and Jered you will come through. ❤
I also have an autoimmune disorder. I was diagnosed in 1999, with Churgg-Strauss Syndrome. It was hard in the beginning, but since I know when I’m getting sick and what to do, to be proactive, is a great help. I have a great rheumatologist and pcp. I feel we are team against my illness.
I am glad you are getting help Ellie.❤
You're not lying about how difficult managing food is Ellie, planning 3 meals a day & snacks everyday is exhausting. Especially with kids when they most times don't wanna eat what you make lol. I'm praying for you guys through this journey and hope it makes you feel 100 times better ❤️
Jared you are a great support system for Ellie!!!
It’s so awesome you have a Dr willing to help you.I have Hashimoto’s and just recently found out I have Turners mosaic as well at the age of 47 and many dr it shouldn’t have taken so long to get properly diagnosed.
Ellie so glad you have answers this will be hard yet hopefully helpful. Please share what you eat and more along with this journey I believe this information can help many people! Thanks for being vulnerable
I have so many health issues too. After years I finally did a food blood panel and can’t eat Hardly anything. But looking forward to feeling better. Prayers you will too
Prayers for you Ellie! 🙏🏻 I couldn’t even imagine!
My spouse has had sjogrens for years and has never been told to change their diet. She uses restasis for dry eye. Dry mouth drops and chewing gum for dry mouth. She also needs to take a nap most days. I hope the diet works for you. It sounds like hard work-one day at a time! So glad Jared is doing it, too. He is such a huge support and so caring.
You finally have a diagnosis! That's ultimately your first step to feeling better. Since you were unknowingly eating many of the foods you were sensitive, removing them from your diet will be a big step to being more healthy and feeling better.
I can't imagine how low and vulnerable of a state you have to be in to state outloud how hard it is to live. I pray you find healing, soon. The mind is powerful and I hope and pray you guys feel well soon. 🙏
Food is habitual. When I went vegan the first three weeks were really the hardest to develop new habits in our meal plans and snacks. It does become normal with time and before you know it it's second nature. I'm excited to see the new creative meals you come up with, and how you feel.
I am so happy you finally have a diagnosis! It will be difficult but I know you realize that it could be a lot worse! You got this Ellie!
I was diagnosed with my first autoimmune disease in 1998. Rheumatoid arthritis was first, then came Sjogren's, then can psoriasis. I also have Raynaud's. You will live with this for the rest of your life. I am so sorry, Ellie. You are young and have a young family. Once you figure out what is right for you to eat, and how much exercise you need, changes will become a way of life. Hang in there Ellie, you are not alone. There are many of us that fight autoimmune diseases. Sending hugs.
I’m glad you have answers! I’m am praying daily that your dad is getting answers too ❤
I’m so happy you finally have an answer. You and Jared make the best team! ❤️
Good luck. Prayers and love for Ellie.
Hi Ellie, you can replace your peanut butter balls with cut up dates, almond butter or sunflower seed butter rolled in cacao powder. They're delicious. Watch oatmeal...many ppl are allergic. If you are, just used crushed chex cereal instead of oatmeal for any recipes
So good you will get a chance at health now! Will you please take us along all your dietary changes, what you eat, how you feel etc.
I am praying for both of you . Jared you are so sweet and supportive of Ellie. Follow you are blessed with a nice husband.
I also have sjogrens syndrome. When I was diagnosed, I was told there's nothing they can do about it and I just have to drink more water. It was extremely frustrating so I'm excited to see how all these changes help you ❤
Oh boy! Really, you need a second opinion and a support system!
Praying you get relief! 💜
Ellie I have coeliac and lupus and I am still struggling but so glad you have some answers. ❤❤❤❤
I’m very excited to watch you both go through this journey! I, too, have an autoimmune disorder and experience bloating/anxiety/difficulty swallowing while taking medication for it. Please share the foods you eat!!
My husband has the same exact issues. He can't eat foods with nightshades in them (potatoes, peppers,tomatoes) he can't have wheat, he can't have dairy...it was so hard at first....but I found recipes, and substitutes, and I changed my diet to help it be easier for him...now he feels wonderful all the time, his mood is better. It will get easier...I promise, and it's all worth it in the end. You'll still crave your old food once in a great while...but it's easy to find substitutes.
Soo glad Ellie has Jared. Going through medical stuff alone is super hard!
So glad you guys have each other!! ❤
Ellie! I'm so glad that you finally have answers girl! I have been following your medical journey because our symptoms are so similar.
I will keep you in my prayers that this will be an easier transition for you & that you will see the results that you are expecting. 🙏🏼❤🤞🏻
Would it be possible to get your doctor's info. I have been chronically ill since 2012. I have received many diagnoses, but I still have unexplained symptoms that includes a lot of what you have been feeling. Most of my drs say that they feel I have to have an autoimmune disease. I have had bloodwork done, I've seen a couple of different Rheumatologist's & no one can find anything, but I know we are missing something. There are days that I can't even get out of bed. My body is full of inflammation which causes my pain to be worse. Anyways, if you are able to share his contact info please do. I'm in Las Vegas, but very willing to travel to your area. Heck its much closer then UCLA & The Mayo clinic in Arizona where I have specialists that I travel to. Thanks in advance if you are able to share & thanks for sharing the update. ❤
I too would love to get the drs name & location. God bless you ❤
It's very difficult; because of family history and dealing with auto immune and health issues myself, I did actually guess that might be her issue! Hoping things ease up soon!
So sorry about your diagnosis. I have lupus. But Jared you are the best husband for being there with Ellie. God bless you both and family
Hi! I know this sounds hard but I did the same thing and within 6 months my auto immune disorder is in remission AND I got pregnant. Something I never thought I could do. You WILL feel so much better. Just find what works for you!
So glad you finally got the answers you were looking for!
Who is it that you are seeing now? I have been trying to get answers for years, I have around 13 different doctors/specialists and I feel like I am constantly spinning my wheels. It is so frustrating! Ellie I am so happy that you finally have those answers.
i too have an autoimmune disease so i get it sending a prayer and hug your amazing i now get an injection every four weeks which helps it is sad but all we’ll be ok another great video
I have had to do the autoimmune protocol diet and its misery. You can get to the point when its under control and you are feeling much better. You can do it!
The person I am really concerned about at this point in time is JARED I can see the pain, in this man's eyes and yet it seems as though his health issues can go to the back burner!
I have never once, ever seen Jared be anything but 100% supportive and loving and it is my strong opinion right now he needs that from Ellie!
As a person who has suffered from an autoimmune disease for over 35 years I empathize with Ellie, it can be and is devastating to deal with a constant life-sucking illness, STILL, Jared is suffering right now I can see it in his eyes....and in his soul, he has even broken down and cried which is NOT like Jared, I pray to Jesus that Ellie will see how much Jared is in need right now and gives to him the love, support, and care he has always given to her!
your relationship is so beautiful thanks for letting us have insights into your lives ❤
Something that has really helped me with my inflammation is ginger/turmeric shots. I have trouble digesting food with my hashimotos. I take FRESH ginger & turmeric root & blend them up in my ninja with an orange, some water (i use coconut water) and fresh ground pepper, which helps with the absorption of the curcumen in the turmeric. Then i strain it because especially the turmeric has a lot of pulp. But you don’t have to strain it. I do this every night & literally i can feel my bloating go down.
I FEEL FOR YOU BOTH!!! Praying this is the beginning for answers & help in your health journey.
You guys can do it! Once you get past the 3 weeks like Dr Axe said it does get easier. When you start to feel better it will motivate you to keep going. Diet is a huge factor in health and like Dr said it’s what you (we ) can control. Praying you feel better sooner than later so you can enjoy the benefits of everything!
My godmother has shograns and she lives an absolute full and healthy life!!! Im so glad you finally have a diagnosis ellie!!! This is going to change your life for the better!!!
Ellie! I am so sorry. I have a ton of unexplained symptoms of things, but I don't know what causes it. I have never had one overarching diagnosis, but food seems to play a major factor. I also have gotten extreme vertigo as well. I am struggling to figure out where I can find answers. Please continue to share, because I hope it can help me figure out what to do next too.
Just remember Ellie, one of the number 1 roots of all diseases is inflammation. Once you figure out what foods cause it, it will get better. It will.
Exactly!!
I am struggling no answer tired all the time, fatigue, sleepy , muscle aches, don’t know what to do since start 2021 till now.
Seed oils, grains!
I agree restricting food is a MAJOR change in lifestyle which I also had to do for a 1 dreaded yr. We're with you guys.. Hope you feel better soon!!
I’m happy for you Ellie you now have the answer for you to get back to perfect health. I understand that you have a lot to process but with Jared by your side and doing the diet with you will make all the difference.
Love you guys ❤❤❤❤❤❤