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

Improvement


cirrus16

Recommended Posts

cirrus16 Newbie

Hi everyone,

I had been in a fog for years - treated for depression etc - but it was really the weight loss that got my doctor searching. The biopsy last December confirmed celiac disease. I'm 57 and who knows how long I've had celiac disease. I'm still in the fog, but have noticed improvement. Now I would like to get an idea of what to expect regarding improvement. I'm sure I'm like a lot of you -- ok I'm celiac disease, I'm gluten free, but I want to have an idea about how/when recovery occurs to know I'm on the right track.

Is there a way the damage to the villi can be defined - minor, moderate, etc?? And would the degree of damage help predict recovery?

How often should blood work be done?? I assume this is a way to monitor improvement. My clinic uses ARUP Laboratories in Salt Lake City.

Last question. I believe I read something about celiac disease masking poor thyroid function. Does anyone have info about this? Should thyroid testing be done differently for us with celiac disease?

Thank you.


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



Celiac.com Sponsor (A8-M):



KaitiUSA Enthusiast

There are degrees of damage to the villi and the less damage you have the quicker you are more likely to heal. Usually they say being gluten free for 3-6 months heals the damage(for most people)

For some people it takes symptoms longer to go away though. I know it took me 3 months to feel alot better but another few months to get back to normal.

Some people it takes over a year to have symptoms go away but their damage can be gone sooner then that.

It depends on age, how good you are with the diet, etc. for how long it will take yout intestines to heal though...every person is different.

I get followup bloodwork every 6 months for celiac. It is to monitor how complient you are being with the diet.

Thyroid as well as other things are highly connected with celiac. I have graves disease(hyperthyroid) They test you the same as anyone else.

Have you noticed any difference on the diet? Are you 100% positive you are gluten free...nothing slipping through any foods or products you use that can get to your mouth easily? Good luck

Ally2005 Apprentice

In addition to what Kati said, there are four stages that reflect the amount of damage. Stage four indicates complete, total villi destruction. I had stage 3 B which meant partial to sub toal damage.. I was diagnosed two months ago. I am 42 and have had symptoms on and off for 10 years. Kati is right...healing is different for EVERYONE. You have to be patient.

Ally

tarnalberry Community Regular

I just want to reiterate the statement that healing is different for everyone. While you may see some improvement in the first few days, you may find you continue to see improvement for months. It depends on your body, how much damage their was, and how careful you are about gluten-free now. Not to mention the other things in your life like how much stress, exercise, vitamins/minerals, and family support you get.

Lesliean Apprentice

Kaiti, you are an angel on this board. You guide us all!

Cirrus16- I am on thyroid and am tested every year. I also had a bone density x-ray because so many Celiacs have not been absorbing calcium and because so many Celiacs have to give up dairy, at least for a time, because of villi damage. If you have osteopenia or ospeoperosis you will now absorb calcium at a great rate no matter what age you are. But your doctor might want to individualize a calcium supplement plan to help you (ie-Citrocil for instance, 500mg 4 times a day and don't worry about food you can be empty or full, just space the capsules out across the day).

Also B12 is often deficient so I recommend a subligual B12 supplement for a while.

Anemia is common so you might want to make sure you get enough iron if your CBC test showed low iron.

I thought my life had completely changed for the better after a week gluten-free but its been 3 months now and the positive changes just keep on coming (asthma medicine to 1/2 and throat clearing and allergies gone recently). I must have caught it early because I think its more common to get changes gradually over a year or more.

Leslie

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. - trents replied to Atl222's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Increased intraepithelial lymphocytes after 10 yrs gluten-free

    2. - cristiana replied to Atl222's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Increased intraepithelial lymphocytes after 10 yrs gluten-free

    3. 0

      Celiac Friendly Sports Camps - Academy Camps - Virtual Open House

    4. - lizzie42 posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Low iron and vitamin d

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

    • Total Members
      133,219
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • cristiana
    • trents
      Cristiana, that sounds like a great approach and I will be looking forward to the results. I am in the same boat as you. I don't experience overt symptoms with minor, cross contamination level exposures so I sometimes will indulge in those "processed on equipment that also processes wheat . . ." or items that don't specifically claim to be gluten free but do not list gluten containing grains in their ingredient list. But I always wonder if I am still experiencing sub acute inflammatory reactions. I haven't had any celiac antibody blood work done since my diagnosis almost 25 years ago so I don't really have any data to go by.   
    • cristiana
      I've been reflecting on this further. The lowest TTG I've ever managed was 4.5 (normal lab reading under 10).  Since then it has gone up to 10.   I am not happy with that.  I can only explain this by the fact that I am eating out more these days and that's where I'm being 'glutened', but such small amounts that I only occasionally react. I know some of it is also to do with eating products labelled 'may contain gluten' by mistake - which in the UK means it probably does! It stands to reason that as I am a coeliac any trace of gluten will cause a response in the gut.  My villi are healed and look healthy, but those lymphocytes are present because of the occasional trace amounts of gluten sneaking into my diet.   I am going to try not to eat out now until my next blood test in the autumn and read labels properly to avoid the may contain gluten products, and will then report back to see if it has helped!
    • lizzie42
      Hi, I posted before about my son's legs shaking after gluten. I did end up starting him on vit b and happily he actually started sleeping better and longer.  Back to my 4 year old. She had gone back to meltdowns, early wakes, and exhaustion. We tested everything again and her ferritin was lowish again (16) and vit d was low. After a couple weeks on supplements she is cheerful, sleeping better and looks better. The red rimmed eyes and dark circles are much better.   AND her Ttg was a 3!!!!!! So, we are crushing the gluten-free diet which is great. But WHY are her iron and vit d low if she's not getting any gluten????  She's on 30mg of iron per day and also a multivitamin and vit d supplement (per her dr). That helped her feel better quickly. But will she need supplements her whole life?? Or is there some other reason she's not absorbing iron? We eat very healthy with minimal processed food. Beef maybe 1x per week but plenty of other protein including eggs daily.  She also says her tummy hurts every single morning. That was before the iron (do not likely a side effect). Is that common with celiac? 
    • Scott Adams
      Celiac disease is the most likely cause, but here are articles about the other possible causes:    
×
×
  • 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.