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

Ttg Iga Down! But Still Having Issues...


C-Girl

Recommended Posts

C-Girl Contributor

After much waiting, my third (3rd time a charm?) gastroenterologist finally got back to me with my labs from my last visit two weeks ago.

 

Abdominal ultrasound, normal. C-reactive protein, normal. Pancreatic enzymes, normal. Good news? tTG which was >100 in October is now down to 5! That's a huge, huge drop, so why am I still having these issues? I'm clearly sticking to the diet.

 

I'd been having big D - 10 trips or more a day - and feeling lousy. I know it wasn't gluten. I've been having sporadic episodes of D plus stomach pain and esophageal spasms over the past 5 months, since diagnosis with celiac. The last one included what felt like gallbladder pain (sharp, stabbing down from the right shoulder blade to the center of the sternum).

 

A week of barely eating at all, followed by a week of eating absolutely nothing except rice, eggs and fish, and I'm down to maybe 1 trip/day of D that follows one or two normal BMs. I'm also down to 114 lbs from 120. The only change I've made in the last few days is adding the Culturelle probiotic to my day. I'd been using a different one and I just don't think it agreed with me. In fact, it may have been making things worse.

 

Now the doctor wants to do both an endoscopy and colonoscopy to "rule out microscopic colitis" and see the level of inflammation in my stomach. It seems like a lot of pain and expense to go through to rule something out.

 

I'm fairly convinced that all of the issues stem from my trip to Italy - I got traveler's D, which persisted, and led to my celiac diagnosis after being symptom free for eons. I'm fairly confident that whatever bug I had is still there, and if I give it the right fuel it grows back and I get the symptoms again. I need to starve the little fookers out and bombard my guts with the right kinds of bacteria until it all goes back to normal!

 

I guess my question is: should I go through the misery of these procedures? Last time I had an endoscopy I was in abject agony for days with esophageal spasms.  I'm terrified to go through it again, terrified of being put under again, terrified of someone shoving things up my rear. I'll do it if the doctor can make me better, but I can't imagine what she's going to find. It'd be nice to see if my villi were growing back (total atrophy in November), but ... I don't need to know that badly. The 5 on the IgG's tells me I'm on my way.


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Congrats on getting the blood work down so well!

Have they done a stool test to look for parasites? You could just try the simple plain diet you are on for a few weeks and see if that helps. Maybe add cooked sweet potato? Give it a couple of weeks before you decide.

Edit- I just looked at your post again. It's just been since Nov? That really is fabulous on the blood work! I would say that it took my system about 1 1/2 years to get working like a normal person's. Even now, if I eat a bit differently for more than a couple of days, it will get out of whack.

C-Girl Contributor

Congrats on getting the blood work down so well!

Have they done a stool test to look for parasites? You could just try the simple plain diet you are on for a few weeks and see if that helps. Maybe add cooked sweet potato? Give it a couple of weeks before you decide.

Edit- I just looked at your post again. It's just been since Nov? That really is fabulous on the blood work! I would say that it took my system about 1 1/2 years to get working like a normal person's. Even now, if I eat a bit differently for more than a couple of days, it will get out of whack.

They did a stool test in October, found no cysts or ova. No salmonella, shigella, campy, yersinia or E. coli 0157. But there are other bacteria that can cause travelers D. Who knows, maybe if that's it I'll get immune eventually. My immune system ought to be looking for things to destroy now that it's not working on my small intestine....

IrishHeart Veteran

Now the doctor wants to do both an endoscopy and colonoscopy to "rule out microscopic colitis" and see the level of inflammation in my stomach. It seems like a lot of pain and expense to go through to rule something out.

 

 

 

I'd do it. My friend with celiac also had microscopic colitis and c.diff  it made her life hell. It is easily treatable.

Why not get to the root of the problem and resolve it so you can feel better?

You're doing a great job being gluten-free and reducing the TTG, but if something is still wrong, don;t you want to find out what it is?

nvsmom Community Regular

I agree. You might as well go for it and hopefully get more answers.  It could still be celiac disease causing it (my C did not improve until almost 10 months gluten-free) but the only way to determine if it is celiac disease is wait... and wait and wait. You might as well check out that avenue in the meantime.

 

I hope it goes better for you this time since you are regaining your health. Congrats on that 5!  Awesome!  :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,993
    • Most Online (within 30 mins)
      7,748

    Kelly C
    Newest Member
    Kelly C
    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

    • Wheatwacked
      Have faith, you will survive. I get mine from Pipingrock.com.  500 capsules of 10,000 IU for $22.  That is almost two years worth for me.  250 caps 5000 IU for $6.69 if you only take 5,000 a day.  It's like half the price of Walmart.
    • Wheatwacked
      Testing can't alone be trusted.  Else why would it take so many years of testing and retesting and misdiagnosis to finally be told, yes you have Celiac Disease. As to what to eat, I like pre 1950 style food.  Before the advent of TV dinners.  Fresh food is better for you, and cooking from scratch is cheaper.  Watch Rachel Ray's 30 Minute Meals for how to cook.  Keep in mind that she is not gluten free, but her techniques are awesome.  Just use something else instead of wheat, barley, rye. Dr Fuhrman is a ex cardiologist.  His book Eat to Live and Dr Davis' book Wheatbelly were instrumental in my survival.
    • Scott Adams
      If you have DH you will likely also want to avoid iodine, which is common in seafoods and dairy products, as it can exacerbate symptoms in some people. This article may also be helpful as it offers various ways to relieve the itch--thanks for the tip about Dupixent, and I've added it to the article:  
    • Scott Adams
      I just want to clarify that what I posted is a category of research summaries we've done over the years, and nearly each one shows that there is definitely a connection to celiac disease and migraine headaches. The latest study said: "the study did indicate some potential causal associations between celiac disease and migraine with or without aura, as well as between migraine without aura and ulcerative colitis...this study did not find evidence of a shared genetic basis..." Anyway, there is definitely a connection, and you can go through more of the articles here if you're interested: https://www.celiac.com/celiac-disease/celiac-disease-amp-related-diseases-and-disorders/migraine-headaches-and-celiac-disease/
    • SusanJ
      Two months ago, I started taking Dupixent for dermatitis herpetiformis and it has completely cleared it up. I can't believe it! I have had a terrible painful, intensely itchy rash for over a year despite going fully gluten-free. See if your doctor will prescribe Dupixent. It can be expensive but I am getting it free. When the dermatitis herpetiformis was bad I could not do anything. I just lay in bed covered in ice packs to ease the pain/itching and using way too Clobetasol. Dapsone is also very good for dermatitis herpetiformis (and it is generic). It helped me and the results were immediate but it gave me severe anemia so the Dupixent is better for me. Not sure if it works for everyone. I cannot help with the cause of your stress but from experience I am sure the severe stress is making the celiac and dermatitis herpetiformis worse. Very difficult for you with having children to care for and you being so sick. Would this man be willing to see a family therapist with you? He may be angry at you or imagine that your illness is a psychosomatic excuse not to take care of him. A therapist might help even if he won't go with you. Also do you have any family that you could move in with (with the kids) for a short time to get away? A break may be good for you both.
×
×
  • 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.