Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Newbie! - How Long Until I Feel Better?


Puckster

Recommended Posts

Puckster Rookie

Hello,

I just found out I have celiac disease (through enterolab) and was wondering what I can expect in terms of feeling better? How long does it take? What's your experience with getting on the gluten-free diet?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Mo92109 Apprentice

I THOUGHT I was being gluten-free for 6 months now and there is just something ELSE wrong with me, but as I manuver through this site (which has done so much for me already!) I am realizing that I am not being as careful as I need to be. I never thought about cross contamination (am not celiac disease, diagnosed intolerant) because I didn't think it was a big deal. Same with going out to eat... never asked about the dressing or just pulled the bread off my burger rather than ask for it bunless.

So, even though I have not answered your question (since I have no idea and am waiting too) - I am telling you that you really, really need to be careful. I am doing a total inventory of the products I use when I get home (yes, shampoo, detergent, etc. makes a difference, who knew?) and my fiancee can now buy his own bread and butter and make it himself.

Take care and good luck!!!

Rachel--24 Collaborator

It really depends on how careful you are (as the last post already mentioned) and how much damage was done. Everyone's healing time is different. You may find you also have other food sensitivities, which is common. Eating out is risky...there is always a chance of getting sick when you eat out...no matter how careful you try to be.

Carriefaith Enthusiast

Everyone is different, some feel better in a few weeks and others may takes several months to a few years. Personally, I didn't start to feel about 100% better until over a year on the diet.

julie5914 Contributor

I felt better almost immediately, but my symptoms came back because because I was still going out to eat and was still eating foods with "natural flavor" and "modified food starch" without contacting the manufacturer. Don't be in denial - you have to be extremely careful and it is best not to go out to eat until you have a few months of healing, and then bring those cards with you that the server can take back to the chef.

I now only go to places that know what I am talking about when I say gluten and can recommend something on their menu that is already gluten free. If people I am with insist on going somewhere else, I think from here on out I will just get a drink and enjoy their company. It's not worth it.

Guest nini

you can start to feel better within a few weeks to several months, but it may take years to be completely better. I guess I really started feeling better about 6 month into the gluten-free diet, and now 2 1/2 years later I am a lot better than I was, but still not feeling 100%. You have to be so careful to not get any gluten at all because even the tiniest molecule can set you back. Over the summer we went to the Tennessee Aquarium and ate at Chili's while we were there, I'm sure my meal was cross contaminated even though the wait staff was extremely careful. They couldn't guarantee that my meal was completely gluten-free.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,929
    • Most Online (within 30 mins)
      7,748

    Mike Rowicki
    Newest Member
    Mike Rowicki
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • lehum
      Hi and thank you very much for your detailed response! I am so glad that the protocol worked so well for you and helped you to get your health back on track. I've heard of it helping other people too. One question I have is how did you maintain your weight on this diet? I really rely on nuts and rice to keep me at a steady weight because I tend to lose weight quickly and am having a hard time envisioning how to make it work, especially when not being able to eat things like nuts and avocados. In case you have any input, woud be great to hear it! Friendly greetings.
    • Hmart
      I was not taking any medications previous to this. I was a healthy 49 yo with some mild stomach discomfort. I noticed the onset of tinnitus earlier this year and I had Covid at the end of June. My first ‘flare-up’ with these symptoms was in August and I was eating gluten like normal. I had another flare-up in September and then got an upper endo at the end of September that showed possible celiac. My blood test came a week later. While I didn’t stop eating gluten before I had the blood test, I had cut back on food and gluten both. I had a flare-up with this symptoms after one week of gluten free but wasn’t being crazy careful. Then I had another flare-up this week. I think it might have been caused by Trader Joe’s baked tofu which I didn’t realize had wheat. But I don’t know if these flare-ups are caused by gluten or if there’s something else going on. I am food journaling and tracking all symptoms. I have lost 7 pounds in the last 10 days. 
    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
    • klmgarland
    • DebJ14
      I only went on the multi vitamin AFTER a couple of year of high dose, targeted supplementation resolved most of my deficiencies.  I was on quite a cocktail of vitamins that was changed every 6 months as my deficiencies resolved.  Those that were determined to be genetic are still addressed with specific doses of those vitamins, minerals and amino acids. I have an update on my husband and his A Fib.  He ended up in the hospital in August 2025 when his A Fib would not convert.  He took the maximum dose of Flecainide allowed within a 24 hour period.  It was a nightmare experience!  They took him into the ER immediately.  They put in a line, drew blood, did an EKG and chest Xray all within minutes.  Never saw another human for 6 hours.  Never got any results, but obviously we could see he was still in A fib by watching the monitor.  They have the family sign up for text alerts at the ER desk.  So glad I did.  That is the only way we found out that he was being admitted.  About an hour after that text someone came to take him to his room on an observation floor.  We were there two hours before we saw another human being and believe it or not that was by zoom on the TV in the room.  It was admissions wanting to know his vaccine status and confirming his insurance, which we provided at the ER desk.  They said someone would be in and finally a nurse arrived.  He was told a hospitalist was in charge of his case.  Finally the NP for the hospitalist showed up and my husband literally blew his stack.  He got so angry and yelled at this poor woman, but it was exactly what he needed to convert himself to sinus rhythm while she was there.  They got an EKG machine and confirmed it.  She told him that they wanted to keep him overnight and would do an echo in the morning and they were concerned about a wound on his leg and wanted to do a doppler to make sure he did not have a DVT.  He agreed.  The echo showed everything fine, just as it was at his annual check up in June and there was no DVT.  A cardiologist finally showed up to discharge him and after reviewing his history said the A Fib was due to the Amoxicillan prescribed for his leg wound.  It both triggers A Fib and prevents the Flecainide from working.  His conversion coincided with the last dose of antibiotic getting out of his system.  So, make sure your PCP understands what antibiotics you can or cannot take if susceptible to A Fib.  This cardiologist (not his regular) wanted him on Metoprolol 25 mg and Pradaxa.  My husband told him that his cardiologist axed the idea of a beta blocker because his heart rate is already low.  Sure enough, it dropped to 42 on the Metoprolol and my husband felt horrible.  The pradaxa gave him a full body rash!  He went back to his cardiologist for follow up and his BP was fine and heart rate in the mid 50's.  He also axed the Pradaxa since my husband has low platelets, bruises easily and gets bloody noses just from Fish Oil  He suggested he take Black Cumin Seed Oil for inflammation.  He discovered that by taking the Black Seed oil, he can eat carbs and not go into A Fib, since it does such a good job of reducing inflammation.   Oh and I forgot to say the hospital bill was over $26,000.  Houston Methodist!  
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.