A little background info: I was raised by two inspiring people who’s hearts are always in the right place. They instilled in me my biggest values: love, loyalty, a respect and awe for the natural world, and to question everything. Since my diagnosis every one of these values has been tested in inexplicable ways, and […]
Right after you are diagnosed with ulcerative colitis, it FOR SURE is an awful time. With doctor appointments nearly every day, and medications needing to be picked up from the store and countless visits to the bathroom each day…it’s not a fun time. But like other parts of UC, the diagnosis period is part of the process to getting things under control and the stories below detail first hand experiences of what it is like.
Hello everyone my name is Eli, I am 19 years old and got diagnosed with mild Ulcerative Colitis on August 1st of this year. I am just wondering how long a flare can last because for me it seems like an eternity, going on more than 1 month while figuring out a right diet and […]
I was diagnosed with Ulcerative proctitis during my 2nd colonoscopy 3 weeks ago and my biopsy results confirmed Pan-Ulcerative Colitis. What are my symptoms right now…diarrhea, bloody mucous, severe cramping, rapid weight loss, loss of appetite, fever’s, and loss of body fluids, joint pain in knees and hips, headaches, fatigue.
We’d recently moved so it was a challenge to find a GI doc and even though I explained about the bleeding and tissue/mucus discharge, it was explained away as hemorrhoids and IBS. Well. That all changed quickly at the colonoscopy. I currently have eight inches of UC proctitis that has been flaring for three months.
Intro: Lacey was diagnosed the same week as her 18th birthday at Children’s Hospital of Pittsburgh. She’s determined to keep living the life she wants, without UC stopping her. Some more about Lacey: I am a ballet dancer training to become a professional. This past summer I spent 5 weeks dancing in Nashville, TN and […]
Diagnosed in December 2013, after 6 months of bleeding. Other than being tired all the time and bleeding, I really didn’t have other symptoms. Feeling so much better today because of what I’ve read on your website.
Lori was recently diagnosed with UC and she want to make sure the disease doesn’t become the focus of her life. Find out some ideas on how to explain the disease to others when you are finding yourself in the constant spin of explaining UC all day long.