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

Three Weeks Post-Gluten--Joys And Concerns


StClair

Recommended Posts

StClair Apprentice

I am getting close to three weeks post-diagnosis and gluten-free and am seeing some positive changes, while some concerns are still fully present. On the plus side (very plus!) my migraines have improved dramatically. My digestive problems have improved as well. As long as I avoid certain intolerances, like dairy and sugar, and keep to a balanced diet (gluten-free, of course), I am free from the bloating that has been a constant companion for so many years. Constipation has popped up, but I assume I'm just temporarily adapting to my gut being less irritated/stimulated.

What has not changed, or not changed enough, is the icky fatigue and painful acid reflux. Maybe the reflux is possibly a bit better, but the fatigue has me worried and wondering if I should book a doctor appointment before the one scheduled in three weeks (post h pylori test results). Every day, usually in the afternoon, I start to feel sick with fatigue, even after a good night's sleep. If I can rest or nap, it's not too bad, but working in the afternoon, long car trips, etc, are torture. I go from plodding in the early part of the day to dragging myself forward by the afternoon.

Just wondering how common this is at this point, as I need to decide on whether to bug my awesome doctor or wait three weeks. Also, even though I'm being insanely vigilant, and rewashing everything in the kitchen before using it, I'm paranoid about cross-contamination. How can you tell if it has happened?


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



Celiac.com Sponsor (A8-M):



MycasMommy Enthusiast

Well it may be that the only way you know cross contamination in your own kitchen has happened is a blood test.  It has made my life a bajillion % more wonderful that my whole family went gluten free (inside our home) and the worry of CC is now gone. Its such a safety relief.  They still eat gluten, just when the are out and about, now.  The recovery... feeling 100% better?  It took me about 6 months to stop feeling tired and achy..and I slowly started waking up and every morning I would realize HEY I FEEL FANTASTIC... but that took months to get there. Everyone is a bit different and will take a varying amount of time to feel better BUT BUT BUT... if you do not feel good, you SHOULD bug your doctor. That is why you give him/her your MONEY! It could be that any number of your vitamins are low.. or even that there is some other thing going on. There are some things that are often co diagnosed with Celiac.  Its better to say something.  I think so anyway.

StClair Apprentice

Yes, I wondered why my doctor did not order blood tests to rule out the typical vitamin deficiencies when I was diagnosed. I especially wonder now since other symptoms are improving, but not the fatigue. Also a Dexa scan, since the last one, three years ago, showed osteopenia, and the one before that actual osteoporosis.

You are right that we should feel free to ask these questions. I can do it by message on their mychart page. It would be nice to have needed tests done before the appointment in three weeks.

Thanks for the advice and perspective!

RMJ Mentor

Could you be anemic?

nvsmom Community Regular

I'm afraid that three weeks is almost nothing in most celiac's recovery.  Your body is most likely still making autoantibodies so intestinal healing probably hasn't even started yet.  Early on, and the first three months is considered to be early in recovery, usually the main improvements are the obvious after dinner bloat and pain, and a few other symptoms like migraines.  Other symptoms like vitamin deficiencies, anemia, pain, and cognitive issues can take many months, to a couple of years, to improve.  Patience is required, but hard to muster up.

 

I myself was convinced that I must have lupus or some other AI because at 3 months gluten-free my pain was worse than ever, and my fatigue and hair loss was no better.  I couldn't believe it was still due to celiac disease even though those who had been gluten-free for a long time told me it could still be celiac disease - they were right.

 

By all means, talk to the doctor about it, but keep in mind you are still recovering and will be for many more months.  You could always make sure he checked the usual culprits: A, D, B12, K, Mg, Ca, Fe, Zn, Cu, ferritin, and check into hypothyroidism which is common among celiacs.  

 

Hang in there

StClair Apprentice

Thanks so much. That is reassuring. Sorry I have to hear it multiple times! As you said you felt at three months, what I am really afraid of is that my long, long undiagnosed celiac has caused something grave, and that my current symptoms belong to that rather than just healing the celiac damage. Hearing your experience, and others, is so helpful, thanks.

cyclinglady Grand Master

It took me six months to resolve my anemia after going gluten free (not to mention healing my vertabrae fractures related to celiac disease) and total of two years before feeling completely normal. Now, just dealing with my thyroid and other hormone issues like so many women!

Hang in there! There is a steep learning curve in avoiding gluten, so expect a few set-backs, but you can get better! I wish you well.


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



Celiac.com Sponsor (A8-M):



badcasper Explorer

try super b complex and avoid night shades.  Tomatoes give me extreme fatigue and sting pain pain  with my arthritis. I feel like I have been run over by a freight train for days. might be what your eating for lunch. The super b complex brought my energy level back up almost immediately.

StClair Apprentice

I feel much better after reading these responses. Thank you! Just today I started B-Complex. Hope it works for me like it worked for you, badcasper. Best of luck to all.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,699
    • Most Online (within 30 mins)
      7,748

    RelievedP
    Newest Member
    RelievedP
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      @Gigi2025  Thank you for your interesting post.  Some of what you say chimes with something my gastroenterologist tells me - that he has clients who travel to France and find the same as you  - they will eat normal wheat baguette there without issue, for example.  His theory was he thought it might be to do with the locally sourced wheat being different to our own in the UK? But I have to say my own experience has been quite different. I have been to France twice since my diagnosis, and have been quite ill due to what was then (pre-2019)  poor labelling and cross-contamination issues.  My TTG test following my last visit was elevated - 'proof of the pudding', as we say in the UK!  It was not just a case of eating something like, say, shellfish, that disagreed with me - gluten was clearly an issue. I've also been to Italy to visit family a couple of times since my diagnosis.  I did not want to take any chances so kept to my gluten free diet, but whilst there what I did notice is that coeliacs are very well catered for in Italy, and many brands with the same ingredients in the UK are clearly marked on the front of their packaging that they are 'senza glutine'.  In the UK, you would have to find that information in the small print - or it puts people off buying it, so I am told!  So it seems to me the Italians are very coeliac aware - in fact, all children are, I believe, screened for coeliac disease at the age of 6.  That must mean, I guess, that many Italian coeliacs are actively avoiding gluten because, presumably, if they don't, they will fall ill?        
    • deanna1ynne
      Thank you both very much. I’m pretty familiar with the various tests, and my older two girls with official dxs have even participated in research on other tests as well. I just felt overwhelmed and shocked that these recent results (which I found pretty dang conclusive after having scott clean labs just six months ago) would still be considered inconclusive. Doc said we could biopsy in another six weeks because my daughter was actually way more upset than I anticipated about the idea of eating it for years before doing another biopsy. It doesn’t hurt her, but she’s afraid of how it may be hurting her in ways she can’t feel. She’s currently eating mini wheats for breakfast, a sandwich with lunch, and a side of pasta along with every dinner, so I’m hoping we’re meeting that 10g benchmark mentioned in that second article!
    • knitty kitty
      Have you tried a genetic test to look for Celiac genes?  No gluten challenge required.  
    • knitty kitty
      Hello, @ElisaAllergiesgluten, Have you tried going on a low histamine Paleo diet like the Autoimmune Protocol diet?  A low histamine AIP diet would help your body rid itself of the extra histamine it's making in response to allergies.  Are you Celiac as well?   Since we need more thiamine when we're stressed, adding Benfotiamine, a form of Thiamine Vitamin B 1, can help the body calm down it's release of histamine.  Benfotiamine improves Sailors' asthma.  
    • knitty kitty
      Don't skimp on the gluten daily while undergoing the gluten challenge!  
×
×
  • 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.