Guest guest Posted May 16, 2005 Report Share Posted May 16, 2005 Hi there, I have coeliac disease which was diagnosed in 1988; this is an autimmune disease. I am 59 and have had CP sysmptoms since my first attack at the age of 5! In childhood and early adulthood, my symptoms were occasional week-long attacks of VERY severe abdominal pain. There were no other symptoms and I was fine for 50 weeks of every year! Nothing was diagnosed. Malabsorption began in my 30's. I certainly did see improvements, especially in those dreadful malabsorption symptoms, when I went on the gluten-free diet (required for coeliacs) in 1988 but I was never completely cured and bad abdominal pains returned with increasing severity and frequency around 1999. Finally, in 2003, chronic pancreatitis, thought to be hereditary, was diagnosed folowing CT scan. In 1965 my mother died of an acute attack of pancreatitis after several years of CP and unsuccessful surgery in 1959. At my last visit to the clinic a couple of weeks ago, it was suggested that I MIGHT have autoimmune pancreatitis rather than classic HP, and that I could have inherited a tendency to autoimmune diseases from my mother rather than having inherited straight CP. Anyway, this is only a possibility and blood tests are being done. I might not know the results for some time as I don't have another clinic appointment for about three months. I think I'll try to get the results sent through to my GP in the meantime. I know very little about autoimmune pancreatitis but the suggestions I've seen indicate that calcifications and inflammation of the duodenum are rare with it. I have both! Probably mine will turn out to be classic HP after all. The pattern of my CP, starting in childhood, with malabsorption beginning later, does fit in with HP. It's now a waiting game. Regards, Fliss (UK) Quote Link to comment Share on other sites More sharing options...
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