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

Celiac Treatment: What Should I Expect In The 1st Year?


sandyg

Recommended Posts

sandyg Newbie

Hi Everyone,

I was diagnosed with celiac last month. . . I was seeing a cardiologist for some recurrent chest pressure that I was having. He did a thorough cardiac work-up and ruled out heart disease. However, I do have iron deficiency anemia. So, he referred me to a GI doc. I ended up having an EGD and fully expected to have some kind of ulcer, but no. . . instead they found "total villous atrophy"and "chronic gastritis". Then blood test were done, which also confirmed celiac. I am still in shock since there isn't any known celiac in my family, but the diagnosis makes sense given my history of type I diabetes, thyroid disease, and anemia.

Unfortunately the GI doctor who did my EGD doesn't seem all that interested in my follow-up care. He more or less did my EGD as a favor to my cardiologist. So, I would love to hear from all of you folks as far as what your first year after diagnosis entailed. I have embraced the diet, but it has been a hard adjustment since I don't have any obvious symptoms related to gluten. . . I am more interested in hearing about the timing of antibody testing, done density scans, and if any of you had a follow-up EGD to document healing. I do have an appt with another GI, but I would love to know your experiences prior to meeting anyone else new.

Thanks in advance for your help!

Sandy


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

You should have a base line blood test done for your levels of stuff like iron, ferritin, folate, calcium. Then a retest of these after 6 months will tell you if you are absorbing properly again. Some doctors may suggest a reendo after 6 months to a year to check if your villi are healing, I myself would only do this if I was still having problems but that call is totally yours. If blood tests were postive at diagnosis than a recheck at 6 months and a year can let you know if your still glutening yourself, if your body doesn't tell you. Be sure to check your scripts and OTC drugs for gluten also.

aikiducky Apprentice

What ravenwoodglass said... except I wouldn't have a repeat endoscopy before at least a year into the diet. Adults can take up to two years to heal on a gluten free diet, so an endo in six months might just depress you.

Pauliina

cruelshoes Enthusiast

I would also add to what the other posters said that you should have a DEXA scan to check for osteoporosis. This is extremely common in newly diagnosed celiacs, due to the malabsorption. This would give you a baseline now, an then could be checked again in a year to see if you are building bone mass.

Here is what the Open Original Shared Link about repeat testing of antibodies:

New celiacs should receive follow-up testing twice in the first year after their diagnosis. The first appointment should occur three to six months after the diagnosis, and the second should occur after 1 year on the gluten-free diet. After that, a celiac should receive follow-up testing on a yearly basis.

Also, the University of Chicago does not reccommend a repeat endoscopy. I had one a 6 months post gluten-free, and there was improvement, but not as much as I would have hoped. THe doctor said that it was normal, and it can take years to fully recover.

happygirl Collaborator

Check out the book listed in my signature----that will make a world of difference for you!

sandyg Newbie

Thanks to those who replied, but now I have another question. . . <_< A woman that I work, who also has celiac, is telling me that I will need a colonoscopy as part of the initial work-up. Is she pulling my leg???? I'm only 33 and don't have any GI symptoms. I hope not!

Sandy

loco-ladi Contributor

I am self diag'd so can't answer that question but I also wanted to mention to also check hand creams and lotions as well as toothpaste anything that has the smallest chance of getting into your digestive tract can harm you.


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



Celiac.com Sponsor (A8-M):



gfp Enthusiast

It is hard if you have no external symptoms to know just how well you are adjusting to the diet.

Many of us started off thinking we were 100% gluten-free then later found the gotchas.

Also although you think you have no symptoms doesn't mean you don't have ... we as humans are very adaptive and we get used to coping and our bodies used to handling toxins. Think of a non smoker smoking 40 cigarettes a day or a non drinker drinking what a regular heavy drinker drinks. Even though these people handle the toxins better and don't feel they have external symptoms if they quit altogether they often suddenly find they have "symptoms" they never believed they had. Many of us have found if we go REALLY strictly gluten-free (prepare all your own food from scratch) that our reactions when we slip are more severe.

Plenty of us here put symptoms down to "getting older" or "everyone has that" etc. and these can be really diverse. I am much more sensitive to traditional "allergies" (IgE) when I have been glutened. I get hay fever etc. , migraines and numerous other niggles. I doubt these will be the same for you but there is a good chance things you have accepted as normal or getting older etc. are in fact partly linked to celiac and that you can use these as metrics.

On being gluten-free vs on being gluten-free -lite .. if you share a kitchen you are undoutedly getting small amounts.... if you eat out in all but a handful of places the same problem. Sometimes these amounts are just enough to give some symptoms and not others... I seem to get neurological symptoms before others for instance.

The easiest shortcut is basically to go the whole hog.(not everyone can do this).. for at least 1-2 months don't eat out, remove all gluten from the kitchen completely, remove any old kitchen appliances (especially toasters) ... hopefully like many others you will find your health improves in ways you never thought possible. Once you are certain you have a handle on it you can start introducing new items one by one, the odd meal out then wait 3-4 days just to be sure... then you add that place to your SAFE list. The same for convenience foods etc. .. one by one ad them back...

Do a search on cross contamination on this board and read up... there are so many gotcha's.. and it takes practice as well.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      14

      Ibuprofen

    2. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      My only proof

    3. - Scott Adams replied to wellthatsfun's topic in Coping with Celiac Disease
      1

      still struggling with cravings

    4. - Scott Adams replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Oh my goodness medication causing pain !!!!

    5. - Scott Adams replied to Me,Sue's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Knowing what to do when feeling unwell.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,871
    • Most Online (within 30 mins)
      7,748

    GR82BNTX
    Newest Member
    GR82BNTX
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      Hi Colleen Are you supplementing B12/having injections? I have learned recently that sometimes when you start addressing a B12 deficiency, it can temporarily make your symptoms worse.  But it is important not to stop the treatment.  Regarding your problems with anxiety, again that is another symptom of a B12 deficiency.   I didn't know what anxiety was until it hit me like a train several months before gastrointestinal issues began, so I can certainly relate.   Two books which helped me hugely were At Last A Life by Paul David (there is a website you can look up) and The Depression Cure: The Six-Step Programme to Beat Depression Without Drugs by Dr Steve Llardi.  Although his book is aimed at people who have depression, following the principals he sets out was so helpful in lessening my anxiety.  Llardi suggests we need to focus on getting enough: - physical exercise - omega-3 fatty acids - natural sunlight exposure - restorative sleep - social connectedness - meaningful, engaging activity   ... and we should feel a lot better. That is not to stay you must stop taking medication for depression or anxiety if you have been prescribed it, but adopting the changes Dr Llardi sets out in the book should really help. Can I just ask two more questions:  1) you say that you are B12 deficient, did they test your iron levels too?  If not, you really ought to be checked for deficiency and, 2) did they check your thyroid function, as an overactive thyroid can be cause rapid heartbeat and a lot of coeliacs have thyroid issues? Cristiana        
    • Jmartes71
      Hello still dancing around my celiac disease and not getting medically backed up considering Ive been glutenfree since 1994.All my ailments are the core issue of my ghost disease aka celiac disease. Im angery because the "celiac specialist " basically lightly dismissed me.Im extremely angery and fighting for a new primary care physician which is hard to do in Northern Cali.So currently without and looking.Im angery that its lightly taken when its extremely serious to the one who has it.My only evidence is a brochure back in the days when I got news letters when I lived at my parents.It was published in 1998.I was diagnosed before any foods eliminated from my diet. Angery doctors don't take seriously when Im clearly speaking.I did write to the medicine of congress and have case number.
    • Scott Adams
      I totally get this. It's absolutely a grieving process, and it's okay to feel gutted about the loss of those simple joys, especially at 18. Your feelings are completely valid—it's not about being ungrateful for your amazing boyfriend, it's about mourning the life you thought you'd have. That "tortured by the smell" feeling is so real. It does get easier, I promise, but it's okay to sit in the sadness and just vent about how much it stings right now. Thanks for sharing that. Celiac.com has published a book on our site by Jean Duane PhD called Gluten-Centric Culture, which covers many of the social aspects of having celiac disease: This chapter in particular covers issues around eating with family and others - Gluten-Centric Culture: Chapter 5 - Grabbing A Bite Together:    
    • Scott Adams
      Many of us with celiac find that the fillers in medications can cause a reaction, and sometimes our bodies just process things weirdly. That "rebound muscle pain" and "burning feet" you described sounds awful and is a huge red flag. It's frustrating enough managing the diet without medication causing setbacks. So sorry you're dealing with this, but you're definitely on the right track by connecting the dots. You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      It's so tough when you're doing everything right and still get hit with it. I'm glad you're figuring out a system that works for you—the peppermint tea and rehydration powders are smart moves. It sounds like you've really learned to listen to your body, and that's half the battle. Sticking to simple, safe food at home is the best way to build yourself back up. It's great you can take the time to rest properly. Thanks for sharing what works; it's a big help to others figuring this out too. This article, and the comments below it, may be helpful:    
×
×
  • 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.