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What a negative video. My husbands health has changed dramatically since he adopted a gluten free diet following his diagnosis some 30 years ago. it is very easy for him to eat gluten free, and he rarely has a slip up, which generally doesn't' result in many symptoms.

9:23 came for the science, stayed for the ART!!

I have IBS, scleroderma, and celiac disease. It's really hard when you do diligence to avoid gluten. People don't understand how horrible it really is. NO breaking bread and going to bbqs or events. No eating out, no parties nothing but stay home and eat safely.

What’s the update on Nexvax2?

Does rice and corn have gluten?

How can I get tested? What doctors look for this? Tell me how I can find a doctor? I live in Southern California.

Is there a support group? Does it affect the eye sight?

If there was a treatment that allowed me to eat out and not worry about cross contamination i would be happy. Just the endless worry and seeing crumbs everywhere drives me crazy. Not to mention the eateries that refuse to serve you with Coeliac 😢

Celiac disease is not celiacs

😮😢😊😎🐓😘❤🕊✌🏻✝️🙏😏

I have a ten years old daughter with celiac disease. I am so proud for how strong she is. She was diagnosed when she was six years old. Going to parties, to a friend's house to play, to any type of trip or vacation needs a lot of work. Appart from gluten lactose is not an option as well for her. Also because she has been through all this she cant eat so many fruit and vegetables. I try make best to cook as good as possible for her but she won't be a child forever. Soon she will be a teenager wanting to hang out with friends.....

I have all the symptoms of celiac I have dq8 , my test where all negative but I did notice gliadin going halfway almost at 19

I was misdiagnosed with celiac disease in the end of 2021. I cried out of happiness in may 2023 when the doctor said, forget about celiac disease. You don't have it. Now in june 2024 I still haven't got any diagnose and I am taking Doxycycline to treat tropical sprue which is what I suspected early on. Noone listened to my travel history. The antibiotics is just taken as a last resort and the diagnosis is not sure. If I dont have tropical sprue, I dont know what to do anymore. All I want i a diagnosis. As strange as it may sound, I rather have celiac than not knowing what I have with all that follows with that, like not knowing how to cure my villous atrophy.

It’s hard to imagine as an Italian, to give up pizza, pasta and bread. 🥖 But good thing, you were able to catch this auto immune disease early. Some patients are misdiagnosed and took them years before they got a confirmatory result.

It's B complex deficiency!!!! I had CD. I had literally every B complex deficiency in the book and in severe form (with the sole exception of the butterfly rash, absent almost certainly because my photophobia was so bad I never went outside during the day)' ataxia was one of the worst. I could not walk across flat unbroken pavement without continually tripping over my own feet! I started taking B complex. 100mg/day did nothing. My urine was still clear like water. I upped the dose 100 MG/day until my urine turned yellow again, held it at that dose for a few days, reduced it 100mg/day and it stayed yellow kept it there, if it turned clear went back up and so on. Within two weeks all about B complex deficiencies started to improve rapidly and by the end of the third week when my urine finally turned yellow at 2000 MG/day all deficiency symptoms had totally disappeared. In fact all the areas that had been problems were now working far better than ever before. I was not only back to normal function but considerably better. Celiac ataxia is due to being vitamin deficiency which can be corrected in very short order by vitamin supplementation without having to wait for the intestinal lining to recover! I had been 20% below normal lien healthy weight but had only recovered a small part of that before my vitamin deficiencies were gone. In addition I strongly suspect that the vitamin supplementation (I also supplemented all of the vitamins for which I had deficiency symptoms) enabled everything including the lining of my intestine to recover much more quickly than normal. (Total elimination of all processed foods probably had a great deal to do with that because it is the only way that you can reliably exclude all gluten) Doctors should stop listening to all of the garbage spewed by pharmaceutical representatives and start thinking VITAMINS! It's not "the most expensive urine in the world", it dear God is one of the most effective therapies in the world!

My son needs help dealing with celiac disease.

Eliminating Bread and Pasta was the best decision i made, my overall health and well-being greatly improved, no more fatigue and stomach upsets ....😊

Hahaha youre too tall to have Celiac disease 😂

Jesus is Lord

Currently going through tests after trying the low fodmap for IBS. Have the gene so i now have to take the 4-6 week gluten challenge.

What is interesting is that all my skin problems and weight problems lear up when I'm off dairy as well as gluten. I don't have celiac genes. We will someday have a good test- No one should ever have to take poison to get a proper test. I can't imagine I lived for years in so much pain. Thank God for Gluten Free RN and Peter Osborne. I highly suspect Essential Tremor and Parkinsons are gluten and dairy related. Look how many people Dr Terry Wahls has helped who have MS.

Its NOT just gluten!! Its gliaden, which is left in the wheat. Read Dr William Davis book called. Wheat BELLY and Wheat Belly total health 😢😢😢

czcams.com/video/WYSV27ueCGg/video.htmlsi=PV55ctX1YkF3kCs4

The various book clubs can mistake you for somebody , and if you can't walk on water , guess what kids .....

Got it back.

I am hearing challenged and lost the captions early so this was of no value.

What test did he do? My bloodwork looks negative.

Pediatric celiac psychologist. Never knew that was even a thing but I know from my own experience that it's necessary.

The topic speaks to me...

U need to repair the damage... Options include: Zinc carnosine, Cabbage juice , Probiotics & fermented foods, vit D3. Stopping gluten alone wont heal years of damage.

If I may offer a suggestion that this video certainly does not, lol.. 1.) Try cutting out dairy too. Vegan cheeses and milk can be good. Oh especially cow’s milk! Leave that alone, even organic. If you don’t have an allergy, nut milks are better (but not really oat milk bcus that can irritate some CeD issues). 2.) In addition, fasting and juicing greens, citrus and tarts (cherries, strawberries, Acai, blue/blackberries) 3.) You MAY have issues due to diet or the CeD attacking other parts of your body. This can cause connected issues such as: Candida/Yeast Slowed Gut Bile H. Pylori bacteria in the stomach Liver necrosis Lymphadenitis Lack of K2, Selenium, D3, Iron and Zinc Lack of Micronutrients: Magnesium, Calcium and Potassium Try cutting out dairy, doing a juice fast and replenishing these vitamins for at least 2 weeks and see how you fare. Best Wishes to All. ❤

It makes me feel so different

In my Opinion, whats working for me, It has to literally be White Rice(Instant) Sourkraut, and Wisconsin Provolone Cheese...for 3 to 6 Months. Absolutely no Gluten, or Gluten free products. No Veggies, No Tomatoes, No Potatoes, No Chips, candy Bars, Juice, Soda, no sweets, as the Instestinal Villi needs to regrow, and become un-inflamed as it as become Atrophic and Flattened.

26:24

Im 65! Finally! I inow this is it! Been suffering 25 years! My Neice is carrier her boy has it! Bingo! My gut is destroy

Thank you to both Valerie’s for all of your hard work, and willingness to share your knowledge and experience!

Urdu please

I HATE IT. ITS RUINED MY LIFE

Take a plan of action re. Improving your gut. I view it as an opportunity to make and taste new foods. Eat whole foods and not processed a nd packaged stuff. Research high anti oxidant foods which will help improve the condition. It may require more than avoiding gluten. Start with adding b vitamin supplements to raise the mood. While it isn't easy, it is way easier now than it was 18 years ago when it was seen as rare. People here have really bad attitudes. Your health can turn around, but it would require researching your particular issues and seeing a naturopathic doctor.

Its not this emotional for me. Am I even Celiac?? Stopped eating gluten on my own before getting tested not I'm too afraid of the symptoms to go back.

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so you didnt have to add any zantham gum, tapioca or anything and it still rose? Also, the recipe you did is 1/4 of what the normal recipe is? So we should use 3 x more than you used for the real recipe

thank you all for actually doing something for us!! i was diagnosed about 15 years ago and damn, I really want soup dumplings and a croissant!

Maybe I don't have it so badly but I just exclude gravy, soy sauce pasta breads and cakes etc that have gluten. I don't worry about minor contamination. I have cheese cake and just don't eat the base. Popped a Nexium last night and gobbled some pizza. I don't do that often to be fair. The diet calmed my dietary system and I am slowly losing a bit of weight thankfully. I take a few vitamins, avoid gluten and when I indulge I protect myself with the antiacid. Am I missing something?

This video needs to call out the FDA who still think it’s acceptable to not label gluten in food AND PRESCRIPTION MEDICINES. And for not requiring any testing or proof for companies using the “gluten free” label, still allowing small amounts of gluten to be present anyway, not requiring labeling cross-contamination, and failing to act and recall when companies are caught blatantly lying with this label. Yes, it is hard being celiac. But the US FDA makes it thousands of times harder than it should be.

just diagnosed this morning, im 28 and have had issues for my whole life. luckily, because i have endometriosis, i went gluten free years ago.

I was born with celiac disease.. But four years ago I was always sick.. Fainting... Everything.. Since then.. i'm eating gluten free and I feel so much better. It's a daily struggle but you also get used to it.. 😅

I have been diagnosed nearly 20 years I hadn’t realised the on going problems I have are coeliac related! I thought being gluten free fixed it all. Thyroid issues. Brain fog. Cramps. Tiredness ( so bad ) Emotional issues. Thanks for posting this. My respect ❤

I tried introducing purity oats here in Canada 7 months ago . Around that time I triggered my DH and have been flaring since. I can’t say for sure that it was the Oats but this is only the 2nd major DH I have had in 8 years since my Celiac diagnosis. I assume that minor contaminations which of course happens routinely is not enough to cause this severe of a flare. I either ate something with a good amount of gluten or my body reacted to the Oats. Perhaps a study on Oats with people who have DH would help to shed some light. The good thing about DH is that it can’t be confused for something else. It’s very conclusive and easy to biopsy.

Beautiful lady