I had no idea this forum existed until today.

I have had revimmune at JH back in March ad I can both physically and clinically say it was the single best decision in my life.

It's covered by insurance and Rush hospital is officially doing it in Chi town as well.

I need to have 10 posts to be able to post a link. If you want to go to my site you need to go to chris had ms com but make it all one word and add the appropriate periods.

My wife kept a very detailed blog about the whole experience complete with blood counts and pics. She did great!

I am getting better and better everyday. It is absolutely friggin amazing!

Keri you go GF!

If you got questions....well fire away! When I have 10 posts I will put the post up proper.

Welcome to NeuroTalk, Chris and Thanks you for the info. I will look at your site and I hope your improvemnts continue..

I am happy that you have had such great results with that treatment. so many of us here have gone from one treatment to the next and back again. its all very frustrating, and well, we see so often, that what fits perfectly for one ...*stares at ViseeU holding her betaseron*** isnt so great for another. Beta was a disaster for me. I had to switch to a new treatment, and I am not happy with it.

You are very brave to do that treatment. that type of stuff scares the PJs off of me.

I am going to peek at your web site.

Well, Chris, I looked at the videos you provided, on your site and am amazed at your improvements..

Keep coming back to report to us as you continue to improve and just to join in and have some fun, here.

WooHoo!!!

Chris, welcome and I am so happy for you!!! this is something I would consider rather than all the other stuff out there. Thanks so much for keeping a virtual documentary of your experience.

I am newly diagnosed and did not do well on Betaseron. I am evaluating my options.

Glad you found this forum!

Chris - Thanks for finding us and sharing your journey. I can relate to everything you went through before your treatments. Very exciting results!

Chris,
I'm glad you found your way to NeuroTalk. Welcome! Thanks so much for sharing with us your experiences. I just spent awhile looking at your site. Great site! You're very brave and we're so proud of you. I wish you continued improvement.

Welcome to NT, Chris, and congrats on the great results. I'm going to check out your website, but with this ancient webtv, videos are out. It's really exciting hearing of a successful outcome for a change being we've all tried pretty much everything with questionable results. When you were having your treatments, were there any patients with SPMS? I hope, I hope!! We're always left out!

Wishes for continued improvement to you and please keep us up-to-date!

Take care.........

They are starting SPMS at JH in the fall. Call them and send them your records. They will do anyone who qualifies.

These people are all real, and all real good.

Wow! Thanks for the info, Chris. You were right there! Have a good weekend!