What others with UC think about Low Dose Naltrexone (LDN) as a colitis medication. It’s a super “not so common” medication for UC, but there most definitely are some UC’ers who swear by it as far as treating the UC symptoms.
Intro: 47 year old male living in upstate NY. Diagnosed with UC about 3 years ago. Have been in remission for close to two years now. Some more about Me: Always researching the latest meds, probiotics and diet for maintaining my remission. Symptoms: No symptoms. In remission for 21 months!! Fighting My Way to Remission […]
Meet Amanda: Where to start… well, my name is Amanda. I live in Toronto, Ontario, Canada with my partner, my 2 cats and my 2 sugar gliders. Currently I work as a receptionist for a really great Travel Company, although I hope to be a Wedding Planner in the next few years. Some more about […]
If you are unsure of how diet may/may not play a role in UC, or if you want to simply learn more about some current research that is taking place, I’d highly recommend you watch the two videos that are on the links
Intro: Hi, I’m Yael and I’m 19 years old, diagnosed with UC in February 2013 after a year of heavy blood loss. I received 2 blood transfusions. I was put on oral prednisone.It didn’t work. I was then hospitalized for a week, while they tried IV Prednisone- also to no avail. From then on it’s […]
Christiana is in search of remission just like so many other UC’ers. She’s been through prednisone steroids, Lialda, and now her doctor is suggesting Humira to help with the UC symptoms. At 20 years old and a few years since her diagnosis, she’s looking for some outside help from other UC’ers.
I was in remission for the better part of 7 months. By remission I mean going to the bathroom once a day with a solid poo. I got lazy on my diet and my frequency increased and then eventually started seeing blood as well. I still considered it a mini-flare as my frequency never got […]
Hey there UC’ers, I came across two studies earlier today, and I think they might be of interest to you as well. Since I’ve been following IBD in the science world, and specifically ulcerative colitis, there has certainly been some changes in how the scientific world approaches our disease. It wasn’t long ago, let’s just […]
Intro: This is Bob, 60 years old from Baraboo, Wisconsin, I was first aware of my Ulcerated Colitis in 1995 for years I was treated with 500mg sulfasalazine. Flare ups have happened every two or three years. I now have a flare up for the last two years that won’t quit. Some more about Bob: […]
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.