Hi all,
I just got out of the hospital yesterday after a colonoscopy mishap and the woman discharging me told me about this disease. She is 62, very Irish, and was just diagnosed 2 years ago with it and as i was talking to her, she just kinda looked at me like I was telling her story. I'm 52 and have had issues for too many years to even remember. After a lot of discussion and Q&A, she said i had classic symptoms.
My father spent years rubbing his stomach complaining of belly aches and how the doctors could never find anything wrong with him. I've had horrible visions over the last bunch of years remembering that because i've been doing the exact same thing. I've dreaded having to live a life of absolute misery.
My younger brother had a bowel resection because of diverticulitis when he was only 17.
Over the last 5 years I've been diagnosed with GERD, IBS, diverticulitis and Barrette's. My last 2 endoscopes have found polyps and I've been taking protonix twice a day to try to control the acid and thats not including all the chewable antiacids and alkaseltzer in between. Diarreha has become the norm for i couldn't tell you how many years.
I just had a colonoscopy and they found 2 polys and unfortunately, one of them was biopsied and 6 days later began to hemmorage. I just got out of a 6 day stay at the hospital after they spent 3 days trying to stop the bleeding.
However, none of these tests did a darn thing for the intensity of pain I've been experiencing over the last year in my abdomen. It's so bad now I can't eat and I just got back from my PCP with a script for hyoscyamin to alleviate some of the pain so I can eat.
I never heard of Celiac Disease until this woman told me about it yesterday and how since she's been on a gluten free diet for the last 2 years it's changed her life like night versus day.
I told my doctor about it and just went for the blood test for it today and I am also going to my GI doctor Wednesday and discuss a biopsy with him.
With polyps removed from my esophagas last year and getting the results of precancerious and major polyps in my colon today, I felt certain the intense pain in my guts was cancer eating me alive and I just broke down.
I have a glimmer of hope after talking to my doctor today that, according to him, most polyps are precancerious and I shouldn't jump to conclusions and give the Celiac tests a run for their money.
I think you all can understand my apprehension that after years of suffering, I surely thought I was doomed.
Thank God for the nurse that signed me out of the hospital and her encouragement. I feel like I have a chance. She printed out all this literature and information on Celiac and turned me on to this forum.
I'm sure noone wants any disease but if I have a choice between the lesser of evils, celiac or cancer....well...you know which way I want to go...and to imagine a life without all the reflux and burning and pain..
I'm not sure if this woman is active on this forum but if you are.."THANK YOU" for some hope.
Al
