Hey UC’ers and followers of the website. My name’s Adam, and I have UC. I was diagnosed back in October of 2008, and I run this website. If you are brand new to this website today: “Thanks for joining us! We’re happy to have you here. This place is all about ulcerative colitis, which you’ve probably already figured out.”
We recently ran a survey about “Joint Pains and UC”. Well…..it was a big success in terms of “voter turnout”. By that I mean, holly molly, 99 people filled out the survey which is pretty incredible. I was out of town last weekend and when I came back late Sunday night I was shocked at how many people filled out the questions. With that said, I want to thank everyone who participated in the survey. I promise to have the results posted on the site in the near future, but I have ALOT of copy and pasting to do for each person’s response. But I’m sure everyone will find great value in reading the responses.
There’s Five new UC stories coming up on this website. They are stories that were submitted by UC’ers like you in the Colitis Venting Area.
- Autumn wrote: “Rough Times”
- Ian (6 Years of UC) “The New Drug” about a drug in trials right now
- UC Doctor “Urgency is So Frustrating” that’s right an actual doctor wrote that story
- Jesse’s story: “7 Factors I think Lead to UC”
- Heather who was diagnosed March 2010, she’s a nurse in Las Vegas!!!! “My Skin Problems with UC”
I’d like to take just a quick moment and thank everyone who participates in the iHaveUC site! I really think its amazing that so many people from around the world have been able to come together here and learn from others who are also living with this disease we all share.
A Picture of Me Last Weekend and a Personal Update:
Because I interact daily with people from all over the world who are often extremely sick with active UC symptoms, I’m always being reminded of how difficult our disease can be. If you are reading this from the bathroom, or if you are lying down in bed with painful cramping feelings right now, I understand what that’s like. I remember those days, weeks, months, and even years of living like that too.
But for those who are feeling colitis at its worse, you must keep your head up, the hard times will pass. Things can and will get better. I’m living proof of just that. Just 3 years ago I was in the middle of extremely severe symptoms that never would end. Back then it was bleeding all day, cramping, and absolute hell. But I gained control of it, and learned how to live a normal life again.
Last weekend I went on a hunting trip with a friend of mine named Milenko who’s from Croatia. Joining us was Milenko’s friend Saba who is from Bosnia. We didn’t get any wild boar, but it was a great weekend, and I’ve now got a friend from a new country. Getting away from the computer, cell phone and TV for 4 days is a real treat. I’d encourage others to do the same when the time is right for you.
Talk to you soon,
If you haven’t signed up already, I’d encourage you to get on the FREE newsletter – click here
So I like UC’ers. That’s been going on since 2009 I’d say.
I started site and the eNewsletter(you can join that below) shortly after being diagnosed with ulcerative colitis in October of 2008 with severe pancolitis (when my whole colon was inflamed).
For me, it was a very rough start with severe symptoms. Getting bounced from medication to medication was not easy or too helpful. But, I did meet another UC’er, changes several parts of my diet, and of course the rest is history.
Leave a comment, ask a question, take advantage of our past experiences here, use the search boxes, they are your friends to0:)
Remember while using the site that:
UC symptoms and flare ups don’t last forever and no two people are the same.
You cool with that? good!
now get on our newsletter so we don’t forget about you.