Hi everyone. I posted a few months back about
Asacol HD and how it truly changed my life. I won't go into all the details, but if you want to see read my other post. I just wanted to let everyone know that this truly is my cure and it may work for you too. This is exactly what I do. I take three of the Asacol HD in the morning and three at night. I also take metamucil at night. I do not want to get anyones hopes up because I know how many times people post so called "cures". I understand that not one thing will work for everyone but I implore you if you are having flares and your treatment is not working for you just give the Asacol HD a try along with metamucil at night. I honestly have not had a flare now for over six months. The only time I did have a flare inbetween is when I had to go on antibiotics for a bad cold I had which messed me up. Then I had to go on prednisone again for a very short amount of time and have been fine ever since. [color=blue>This]. My only purpose in writing this is the hope that it helps even one person who then may tell another person. I mean its worth a shot right. Even if your skeptical please give it a shot. Like I said in my last post i went to naturalpaths, ate strict diets, ayrevedic (?) doctors, the list goes on and on. Also we all seem to know certain foods that really bother us. For me I avoid all ice cream, heavy cheeses, and thick chocolate such as brownies and cakes - if I do have any I do so VERY rarely. Cutting out those few items and sticking strictly to the meds I need to take has given me back the life I once had. Also if this works for you please post here so others can see and please tell anyone who has this disease about
your story. Also if anyone has any other questions that want to ask me or need to talk just shoot me an e-mail.
-Mac's email is listed in his profile; you can click on his name to find it.
Mac - I deleted it here (after checking to make sure your email was indeed listed) because I don't want spammers, etc, to pick up your address. I'm a little new at this moderating thing, but I believe we don't want emails listed in the postings, just in the profile where only members can find them...I meant no inconvenience to you!)
PS If this does not work for you I am very sorry and wish you luck in finding the cure that is right for you.
Post Edited By Moderator (songlady) : 7/11/2010 5:18:35 AM (GMT-6)