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Member Since 19 Jul 2008
Offline Last Active Dec 07 2008 10:40 AM

Topics I've Started

What Can The Autoimmune Thing Do To Us?

04 December 2008 - 02:36 PM

I know Celiac disease is an "auto-immune" disease, but why? What's up with that? Does that mean I can have a hard time with infections or getting over colds too? I don't know what the auto-immune dangers are.

Casien? Is This Even More Trouble?

11 November 2008 - 03:37 PM

I've been gluten free for three months after my biopsy diagnosis, but still can't touch milk, soy or corn products. Any of them. I read that casien may be the culprit with me. Geeze! How bad can this get, anyway? I thought celiac was bad enough. Anyone know about the casien thing??? Help!!!

Healing Now..but Why Do Non-gluten Foods Make Me React?!

11 November 2008 - 03:33 PM

I'm in the in the initial healing process, and I know it's supposed to be hard. Been diagnosed by endoscopy biopsy. Eating non- gluten of course, bit still have WAY too much trouble reacting to many non-gluten foods. Such as fruit or anything sour...any starchy veggies...milk products. And can I please ever make a non-gluten baked good that I don't react to??? Seems like anything too complicated or diverse sets me off even if the individual ingrediants usualy don't. What up with all this?? I'm so confused!!!

I Need A Really Good Website That Lists Good Foods And Bad Foods And The Common Non Glu...

23 October 2008 - 01:59 AM

I'm on fish and vegetables and buckwheat only right now. I can't even do rice ar any grains at all. No starches. No fruit. Almost no fats ( common dietician says) Lactose intolerant, of course. Absolutely no strong flavors of any kind. But then I'm just beginning the healing process and am grateful just to out of the IV clinic finally!
I really wish I could find a good web site that doesn't just say don't eat wheat, barley, or rye. Geeze! Wish it were that simple! And what are these "night shades"? I'm so limilted right now and keep making mistakes like when I tried eggs. Bad 4 me! Potatoes, beans...I never know what to do, so I'm just sticking with what I know right now. Fish and non starchy veggies and buckwheat. Starving here!!! AAUUGGHH!!!

Does Anyone Else Get That Annoying Buzz In The Head During Reactions?

09 September 2008 - 11:56 AM

I've just stared my healing process, so I still get reactions lots of times unexpectedly for various reasons. The first thing I'll always get when I start a reaction is a buzz or hiss in the head. If it's a bad reaction this hiss can be very loud! Does anyone else get this? Also it's the last thing to go away..lasting often into the second day ( a bit less then) and sometimes even slightly into the third day. It's so annoying! I really feel sorry for people that have tinitus all the time!

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