I'm brand new to this site, but unfortunately I have many years of experience with MP. And it's getting worse. I've been looking for a support group (one where you can talk with each other) but haven't found anything other than this site. I'd like to start one, ideally in the San Francisco Bay Area. Please let me know if you're interested. I'm also open to the idea of using Skype or something like it, which would remove any geographic limitations. I'm just not familiar with how best to approach that, so would welcome suggestions. This site is fine, but there's nothing like TALKING, ideally face to face, with people who suffer from a common condition. I look forward to hearing from other MP sufferers. It's a nasty condition, and my hope is that we can learn from one another how best to live with it.