Hi Peilan . . . Welcome to the forum. I don't have any experience with Immuran, but I wanted to welcome you to the forum and encourage you to do whatever your body needs in terms of holding back the auto-immune attacks on your body. Like Patty said, if you have confidence in your doc, then you can be pretty sure about
this new treatment. I think they use as little meds as possible and they are cautious about
over medicating too. But, since you've stated that you've been worse recently, its a good bet you need more help in the way of meds.
There are several here who take Immuran, so I'm sure you'll get more responses and welcomes over the next couple days.
Glad you found us and I hope you make some good friends here. I have found this to be a loving supportive group and I am blessed each day by the support that I get here.
In His Grip
AlwaysRosie "We can't control the waves, but we can learn how to surf!!"
Co-Moderator - Lupus Forum
UCTD, Hashimotos, Inflammatory Bowel, Inflammatory Arthritis
Clickable Links: Lupus Resources Lupous.Org Lupus Criteria (4 of 11) Lupus Chapter Locator
Post Edited (AlwaysRosie) : 9/26/2007 2:16:55 PM (GMT-6)