This Is MS Multiple Sclerosis Community: Knowledge & Support

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Bob,

You're more bonkers than I thought. I can't see what you are on about.

I think you should start smoking again and getting back into your old ways of spending your evenings in sleazy lap-dancing clubs.


Ian

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OK-- I just got off the phone with Dr. Hammond and I was told that Revimmune is not very effective in people with SPMS. I am soooo finished now. I was diagnosed with RRMS and he said they are using RRMS patients. So if I had the treatment when diagnosed RRMS (2002) it would have been better?????????

I have to wait until I am peeing/shi---- on myself??? So I have a husband and 2 chidren and they suffer because I can do nothing now for them!! sorry---venting--UGH

GOD help. My mother had MS and I am worse. Been desling since I was 12 years old. Stemcell transplant??

what a f$$king joke!

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Had ms for over 19 years now.

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I think some who have had treatment, and doing well, were PPMS. I thought PPMS was worse than SPMS---I am thinking about email to send to JH...........

Shar----

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so there is 9 people with ms treated with Revimmune and they are saying that it won't be as affective with spms, how do they know that?

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Had ms for over 19 years now.

There are a lot more than 9.

Just that study had 9.

There's a couple of hundred. Still not huge numbers admittedly.

jamie how many total in this trial were spms?

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Had ms for over 19 years now.

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so there is 9 people with ms treated with Revimmune and they are saying that it won't be as affective with spms, how do they know that?
just say the trial at JH

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Had ms for over 19 years now.

9 people at JH. 1 gets better--what if I am the 1. To me EVERYONE deals with medication differently. If Revimmune takes away my immune system then all will be gone. I was told to take the pulse of Cy---difference?? I agree that 'progressive' is 'progressive.