I saw my old doctor that diagnosed me with IBS the other day (don't go to him anymore) and he asked me how I was and I said well for the 2 years you kept telling me I had IBS it turned out to be Multiple Sclerosis - you should dig a little deeper next time and don't diagnosed because you have no other explanation. But I guess I should cut him some slack since my only symptom was C and a numb hand. I used to babysit for him so I know him well enough to say that to him. It did feel good making him feel like he sucked at patient care. Hopefull my comments will make him think a little bit.Life in MS land is still the same, getting my shots every Friday and getting sick from it Saturday - but oh well, I need to take them. Had a relapse about 3 weeks ago and had to go back on IV Steriods, but it has already cleared up. I went 8 months without a flare-up and the neuro said that was pretty good.My company has been really cool, they installed a T1 line in the house and the office network just in case I need to work from home when I don't feel well. They are doing alot of fundraising for MS too which makes me feel really cared about.I miss coming here, but since I don't have IBS I feel I have nothing to contribute. My C is still under control with the Ezekiel Bread. I spend a good amount of time on a MS Bulletin Board similar to this one. I am still new to MS so I don't contribute much there either cause I don't know that much, but I sure do read alot.Hope all is well with my "buds" - take care and I will check in from time to time.------------------DeAnn "Dee"