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

Diagnosed, Now Do I Worry About Other Stuff?


veryami1

Recommended Posts

veryami1 Apprentice

I was diagnosed with Celiac about a month ago via blood work only.

 

I've been reading up a lot on recovery and getting a bit concerned about healing. I have scheduled follow up blood work for about 3 months from now and the doctor will review at that point. I'm also meeting with a nutritionist next week. I'm still getting bouts of diarrhea about once a week, although overall I'm starting to feel better and my BMs are looking so  much better these days for the most part.

 

Do I need to request any follow up testing in regards to cancer, or other possible problems? I didn't get the endoscopy pre-diagnosis, and I'm not adding gluten back in at this point in order to test, but should I request one down the line to confirm I'm healing? Or is a change in the ttg or DGP enough? I'm scared I could have other problems (cancer) that no one ever caught, even if it's precancerous. I'm reading all these articles on how people with celiac might never heal.  I'm 33, I just want to take all the precautions I can.

 

Also considering giving up dairy, as I'm fearful that could be the reason behind my weekly diarrhea episodes, or it could be glutening, or just plain healing, I don't know....Is it normal to get diarrhea weekly if I'm only about a month into eating gluten-free?

 

thanks in advance!

 

Ami


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



Celiac.com Sponsor (A8-M):



NoGlutenCooties Contributor

Whoa!  Slow down and take it one step at a time!  You've only been gluten free for a month.  It takes awhile for your body to rid itself of the lingering antibodies (I read somewhere that the antibodies have a half-life of 3 to 4 months).  It also takes some time to heal, start absorbing nutrients again, and use those nutrients to start making all the repairs.  In my opinion, 3 months for follow-up bloodwork is asking a bit much.  I think the typical timeframe is 6 months. 

 

Still having symptoms only one month into gluten free is not uncommon.  In fact, often the symptoms get worse before they get better.  That said, dairy is a common culprit for continued issues.  You could try not eating dairy for a few days, then eat it, and see if there is a correlation with the diarrhea.  Also, make sure you are 100% gluten free.  Go through all of your food, supplements, etc. one more time - read every label carefully.  Stick to whole foods for the first 6 months or so - no processed crap.  And don't eat out either - not forever, just for the first 6 months or so.  Just so you know that you are 100% gluten-free and not getting any cross-contamination. 

 

If your symptoms don't go away significantly after 3 - 6 months, then you can pursue other tests for other possible ailments.  Yes, it's true that some people never really heal - but that's rare.  And you're way too early in the healing process to be worrying about that!

GottaSki Mentor

Good Morning Ami!

 

It is still very early for you.  Take these first few months to learn how to live completely gluten free - ingesting mostly whole foods and limiting even the labeled gluten free items to treats, rather than staples.

 

Removing dairy for the first 3-6 months is a good idea.  Be sure to trial it down the road as most folks are able to tolerate it after their digestive tract has healed.

 

Testing at 3, 6 and 12 months is standard protocol...then annually thereafter -- depending on how high your antibody numbers were and other factors, it can take some time to get completing within "normal/negative" ranges.

 

Hang in there :)

 

PS...no rush, but you should have a bone scan at some point...celiac can cause early osteoporosis -- the good news is bone is replaced within the body so if you eat clean and exercise consistently the new bones will be stronger...this happened with me...my last scan wasn't perfect, but was far better than the scan at diagnosis.  Of course age and length of time you had active celiac all plays into the bone issue.

 

PSS...there is absolutely no "normal" timeline that symptoms improve or disappear -- we are all different.

CaliSparrow Collaborator

Ami - I did the same thing wanting to be sure to care about my body and catch problems before they snowballed. This went on far too long and I didn't want that to happen again! Stay on this lily pad for a while. It's big. In the beginning, the learning process is steep. Healing did take place although, I was unable to realize it at first. I'm 17 months into it and it's still slow progress for me but when I look backward, I can see how far I've come (which is a good ways). Make sure you go through your kitchen with a fine toothed comb. I saw more improvement without the processed foods. I also was glutened a lot eating out in the beginning and I've put that on hold (unless I feel particularly lucky/risky). I would have saved myself loads of frustration had I done that earlier on in the process.

I eliminated dairy and eventually as it became more evident, other things that bothered me. Sometimes I react to grains, sometimes I don't. That target keeps moving and so I keep it limited.

I too was frightened by what I read in the beginning. It was overwhelming.

Hang in there!

nvsmom Community Regular

:) Don't you wish healing would be instantaneous like every seems to think it should be?  ;)

 

There are a few things you could check. Like Lisa said, a bone density scan can be helpful for some if their disease affected their bones. Nutrient testing can help you pi-point what areas will need some help until you are better. Calcium, magnesium, iron, ferritin, B12, D, A, zinc, copper, and.... I think I'm forgetting something, anyway, those can all be checked. Hypothyroidism is more common among celiac than the general population so if you have any symptoms of hypothyroidism at all, you should be tested. TSH, free T4 and free T3, and TPO Ab are a good place to start.

 

About 50% of celiacs are lactose intolerant at diagnosis.  Once healed, many celiacs regain that ability to eat dairy - the norm seems to be about 6 months.

 

Give yourself time. Healing takes a while and backsliding is quite common in the first 6 months. I can honestly say that some of my symptoms became quite bad again at 3 months gluten-free, but it really did start to sort itself out after that first 6 months.  As for bathroom issues, my C did not improve at all until I was gluten-free for well over 6 months. Waiting isn't fun, but sometimes that's all we need to do.

 

All that being said, if you suspect a more sinister health problem has cropped up, based on symptoms and not just stats for untreated celiacs, by all means get it looked into as soon as possible. If there are no symptoms, try not to worry as your health is on the upswing now.  :)

 

Hang in there.

LDJofDenver Apprentice

Whoa!  Slow down and take it one step at a time!  You've only been gluten free for a month.  It takes awhile for your body to rid itself of the lingering antibodies (I read somewhere that the antibodies have a half-life of 3 to 4 months).  It also takes some time to heal, start absorbing nutrients again, and use those nutrients to start making all the repairs.  In my opinion, 3 months for follow-up bloodwork is asking a bit much.  I think the typical timeframe is 6 months. 

 

Still having symptoms only one month into gluten free is not uncommon.  In fact, often the symptoms get worse before they get better.  That said, dairy is a common culprit for continued issues.  You could try not eating dairy for a few days, then eat it, and see if there is a correlation with the diarrhea.  Also, make sure you are 100% gluten free.  Go through all of your food, supplements, etc. one more time - read every label carefully.  Stick to whole foods for the first 6 months or so - no processed crap.  And don't eat out either - not forever, just for the first 6 months or so.  Just so you know that you are 100% gluten-free and not getting any cross-contamination. 

 

If your symptoms don't go away significantly after 3 - 6 months, then you can pursue other tests for other possible ailments.  Yes, it's true that some people never really heal - but that's rare.  And you're way too early in the healing process to be worrying about that!

You may be able to have the endoscopy without adding gluten back, especially since you've only been gluten free for a month (my endoscopy was a couple months after going gluten-free and still showed extreme damage and confirmed celiac disease) - contact a G.I. doctor and see what they have to say about it.  Also, given all the vitamin deficiencies we celiacs suffer from, probably worth an appointment with an endocrinologist -- I had to be on prescription level Vitamin D for almost 2 years.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to Ginger38's topic in Related Issues & Disorders
      15

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - Tazfromoz replied to Ginger38's topic in Related Issues & Disorders
      15

      Shingles - Could It Be Related to Gluten/ Celiac

    3. - hjayne19 posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Celiac Screening

    4. - yellowstone posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Cold/flu or gluten poisoning?

    5. - Churro replied to Churro's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      17

      Celiac disease symptoms

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,076
    • Most Online (within 30 mins)
      7,748

    Monica L
    Newest Member
    Monica L
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • cristiana
      Thank you for your thoughtful contribution, @Tazfromoz. I live in the UK and the National Health Service funds free vaccines for people deemed to be at heightened risk.  I was pleasantly surprised to discover that as a coeliac in my 50s I was eligible for this vaccine, and didn't think twice when it was offered to me.  Soon after diagnosis I suffered mystery symptoms of burning nerve pain, following two separate dermatomes, and one GP said he felt that I had contracted shingles without the rash aka zoster sine herpete.  Of course, without the rash, it's a difficult diagnosis to prove, but looking back I think he was completely spot on.  It was miserable and lasted about a year, which I gather is quite typical. For UK coeliacs reading this, it is worth having a conversation with your GP if you haven't been vaccinated against shingles yet, if you are immunosuppressed or over 50. I have just googled this quickly - it is a helpful summary which I unashamedly took from AI, short for time as I am this morning!   My apologies. In the UK, coeliac patients aren't automatically eligible for the shingles jab unless they're severely immunosuppressed or over the general age for vaccination (currently 50+) but Coeliac UK recommends discussing the vaccine with a GP due to potential splenic dysfunction, which can increase risk, even if not routine for all coeliacs. Eligibility hinges on specific criteria like weakened immunity (chemo, certain meds) or age, with the non-live Shingrix vaccine offered in two doses to those deemed high-risk, often starting from age 18 for the immunocompromised.
    • Tazfromoz
      My understanding, and ex I erience is that we coeliacs are likely to suffer more extreme reactions from viruses. Eg we are more likely to be hospitalised with influenza. So, sadly, your shingles may be worse because you are coeliac. So sorry you had to go through this. My mother endured shingles multiple times. She was undiagnosed with coeliac disease until she was 65. Me at 45. I've had the new long lasting vaccine. It knocked me around badly, but worth it to avoid shingles.
    • hjayne19
      Hi all,  Looking for some advice. I started having some symptoms this past summer like night sweats and waking at 4 am and felt quite achy in my joints. I was training heavily for cycling for a few weeks prior to the onset of these symptoms starting. I have had low Ferratin for about 4 years (started at 6) and usually sits around 24 give or take. I was doing some research and questioned either or not I might have celiac disease (since I didn’t have any gastric symptoms really). My family doctor ran blood screening for celiac. And my results came back: Tissue Transglutaminase Ab IgA HI 66.6 U/mL Immunoglobulin IgA 1.73 g/ My doctor then diagnosed me with celiac and I have now been gluten free for 3 months. In this time I no longer get night sweats my joint pain is gone and I’m still having trouble sleeping but could very much be from anxiety. I was since referred to an endoscopy clinic to get a colonoscopy and they said I should be getting a biopsy done to confirm celiac. In this case I have to return to eating gluten for 4-6 weeks before the procedure. Just wanted some advice on this. I seem to be getting different answers from my family physician and from the GI doctor for a diagnosis.    Thanks,  
    • yellowstone
      Cold/flu or gluten poisoning? Hello. I've had another similar episode. I find it very difficult to differentiate between the symptoms of a cold or flu and those caused by gluten poisoning. In fact, I don't know if my current worsening is due to having eaten something that disagreed with me or if the cold I have has caused my body, which is hypersensitive, to produce symptoms similar to those of gluten poisoning.        
    • Churro
      I'm no longer dealing with constipation. I got my liver test last month and it was in normal range. Two years ago I did have a vitamin D deficiency but I'm know taking vitamin D3 pills. Last month I got my vitamin D checked and it was in normal range. I don't believe I've had my choline checked. However, I do drink almond milk eat Greek yogurt on a daily basis. 
×
×
  • 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.