This is an amazing forum. So much more soul leading (can't think of a better term, psychological leading doesn't sound right) than on the other forums I go to, which are the Porphyria and Myeloproliferative forums at other addresses, not on Neuro talk). Completely different mood. We help people on the Porph forum, but it is primarily with addressing "triggers", not much about healing mood. On the Myeloproliferative forum, the same: discussion on drugs, side effects of drugs, etc., very little about mood. People with MS have a harder time, just in general, in getting physical help, so they must find a "soul" way to cope, I find. It looks to me definitely that MS people have a terrible time finding "drug" help that really works, or if it works, it just causes havoc with side effects. It seems to me that almost no help for MS in Medicine has been found and/or verified. Always a new drug coming out (heard of a new one yesterday for MS) but always side effects which are very difficult.