- Joined
- Aug 26, 2011
- Messages
- 6
My name is Heather. I was diagnosed with Chrohns in 2006 after years of living with a-typical symtoms which made it difficult to diagnose. After three colonoscopies and a small intestinal x-ray it was ruled "UC/Chrohns" as my ulcers mainly effect 15 cm into my colon currently.....I have been on an array of different medications: Canasta, hydrocort enemas, Lialda, Asacol, Prednisone and now Azathioprine....and stool softener/Vitamin D suppements.
My symtoms (mucus, blood, chronic constipation) have been around for years and so I learned to "Normalize" them a bit so when finally diagnosed I just didn't want to believe it.....well, after a few rounds of prednisone and in/out of remission I FINALLY realize I need support of people who can understand what it is like to live with this disease.
My symtoms (mucus, blood, chronic constipation) have been around for years and so I learned to "Normalize" them a bit so when finally diagnosed I just didn't want to believe it.....well, after a few rounds of prednisone and in/out of remission I FINALLY realize I need support of people who can understand what it is like to live with this disease.