I was diagnosed Jan 06, following ttg blood tests that were way off the scale and endoscopy showing total villous atrophy. I was 33 at the time and believe the condition was active for many years before I finally got the diagnosis.
As my sister was diagnosed before me, I have always known the importance of not cheating, and the possibility of cc via utensils etc I am very strict about my diet - which is largely unprocessed - and about personal care products. I rarely eat out due to being paranoid about being glutened.
Despite all this, my follow up endoscopy at 9 months continued to show damage (although not as severe) and my antibodies continue to be raised (although nowhere near as high). I do have symptoms, but these could be attributable to dairy and the GI is going to test for that.
I am not losing weight, but that's only because I eat ridiculous amounts of food lol
I am borderline underweight despite having an underactive thyroid (which is still symptomatic).The dr is going to check to see if I have pancreatic insufficiency, which could explain my inability to absorb food properly, but he's worried about my antibodies given that I am strict with being gluten-free. I will be having a further endoscopy to check for refractory sprue.
Now it could be that I'm reacting to minute amounts of gluten by cc from DS (who's 4). But the GI was nevertheless worried about my antibodies.
I've been researching on the web, but what I'm not clear about is this: in refractory cases, do antibodies remain elevated, or is it 'just' the damage that remains?
Thanks to anyone who can shed some light on this
Susie