Hello, I'm Mitch, otherwise known as Enjoying The Ride. I've spent a lot of time at MSWorld, and have just joined TIMS. I was directed here by my interest in the CCSVI posts.
I am PPMS, diagnosed 8 years ago. I am currently in a wheelchair full time. About a year ago my problems spread to my arms and hands. I've been on a lot of different treatments. I participated in the Rituxan trial for PPMS, and it actually stopped my progression for 2 years. Unfortunately, it simply stopped working after a while, and now I'm progressing again.
I went on disability from my engineering job in May of this year. I spend a lot of time on my blog, www.enjoyingtheride.com. Please check it out if you have some time to kill.
I like what I see here so far. I look forward to becoming an active member.
Hello
- EnjoyingTheRide
- Family Member
- Posts: 75
- Joined: Thu Nov 12, 2009 3:00 pm
- Location: Maine
- Contact:
Hello
Mitch
Please visit my blog at www.enjoyingtheride.com
Please visit my blog at www.enjoyingtheride.com
Hey Mitch!
Welcome. I have seen you around already, been to your blog (which I think is terrific!) and I am so glad you are here. I missed your introduction earlier.
I look forward to seeing you around some more!
Beth
Welcome. I have seen you around already, been to your blog (which I think is terrific!) and I am so glad you are here. I missed your introduction earlier.
I look forward to seeing you around some more!
Beth
dx 4/09 * Stanford appointment 11/09/09 * One stent left, low jugular 11/10/09!<br />One year from treatment, I have my life back. Placebo schmebo.