There has never been a posting like this on the site, until now…
Why Not?…..
I thought it was time to start using some of the super informative talks/discussions/replies that take place everyday on the iHaveUC facebook page (www.facebook.com/ihaveuc) and turn them into a little list for some of the non FB users (or the hardcore FB junkies:) to see and read, and of course participate in if you like.
The iHaveUC FB page is something that anybody can access and read even if you are not a member of FB. So, below are some of the most engaging posts from the past several weeks that I though would be interesting. Give a look and lets see what you think!
Wishing you all a great weekend,
Adam
Headaches…..
Not fun right amigos….Do you get headaches?
Do you think they are COLITIS RELATED?Medication…
Posted by I Have UC – Ulcerative Colitis Support Group on Sunday, January 24, 2016
Our boy Thomas is having some hard times, who has some idears:
“‘s 1:30 am and I can’t seem to stay away from the…
Posted by I Have UC – Ulcerative Colitis Support Group on Friday, February 5, 2016
from Jena:
“”Has anyone else grown awfully comfortable with talking about your bowel movements and the typical ‘too…
Posted by I Have UC – Ulcerative Colitis Support Group on Sunday, December 27, 2015
Tip from a UC’er:
” Comments: Hey Adam, Love your site. Thank you for all your time and effort in creating and…
Posted by I Have UC – Ulcerative Colitis Support Group on Saturday, December 12, 2015
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.