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i was dxd in 2001, since 2005 my life became agonizing painful ms
i've tried it all abc drugs,ldn, abx and a few other things. some minor improvements over the last couple years but pain is still aweful.
i have no use of my legs, my left arm and hand and since dec my right arm and hand are slowly losing their strength and pain is starting to settle there as well as the rest ...

Hello,

I'm a pretty infrequent poster, but avid reader on this forum. This revimmune treatment seems to be very promising to say the least. I was diagnosed in 2005 but had symptoms going back to 2000. Currently asymptomatic with the exception of some tingling in my legs after exercise. Would someone with no disability be allowed into this trial? It would be great to stop progression before any real damage has been done.

ps. Best ...

This is a very interesting technique.


I did a bit of research for those interested the link to read the full text and the is below.

Here is the link

http://rapidshare.com/files/94168957/1388.pdf.html

Cheers

Sandon

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I want to agree with everyone who said the team at JH is incredible. I phoned Carrie Trecker, got phoned back by one of the doctors on the team, who spent more time reviewing my status/symptoms than my neurologist has in total over two years. His careful detail made me feel very positive about the treatment and I'm waiting for a cancellation on their schedule to fly out to JH for an full appointment.

I ...

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Is there anyone that would like to share their experience with Drs Brodsky & Kerr's high dose cyclophosphamide treatment for multiple sclerosis?

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