I will pick up some nopales from my nearby store tomorrow. Will report :)...
Hey there. I joined a couple years back but never really started browsing until now. I am glad to be here and look forward to making new friends who understand UC! In my research, I have stumbled...
bananagirl, i'm new to the forum, but I feel for you. I'm really glad to hear that the drugs they put you on has kept you going. I hope you don't have to get the surgery, even if the idea of living...
In my experience (I've been on and off prednisone each time I have flared up since getting diagnosed, roughly 4 years ago, and at a rate of about 2-3 flareups a year, that makes a decent number of...
I'm happy to hear you found something to seems to have so wholly cured you. I might try this very soon, myself. I know a lot of people are skeptics about these things, and many people find that the...
Hey scum, I hope your Remicade helps out. i don't take it personally, and I hear a lot of really mixed things about it - but hopefully it's a solution for you. I've been on pred for most of the...
Good to know, thanks. I know my Doc recommended I eat an avocado a day. I'm also not sure which nut butters are bad for me. I feel like I've eaten peanut butter around the time of flareups - but...
Hi everyone, I've browsed this forum a lot, and just recently decided to start posting here. I'm a 21 y.o. male, diagnosed with UC about 4 years ago. Since I developed UC, I've had a lot of trouble...
I wish you luck. Never been on it myself, though a year ago the doctor insisted I had to, or else. Big scary. Hopefully all goes well for you and you don't have any side effects....