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Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

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chrishasms
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PostPosted: Sun Mar 02, 2008 10:55 pm 
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Lyon
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chrishasms
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Lyon
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Jamie
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PostPosted: Mon Mar 03, 2008 6:09 pm 
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Thank you, so much.

What you are doing is a beautiful thing.

The internet truly is mankind's greatest achievement. If it wasn't for the medium and more specifically the content, people like you, then we would be going through even more hell right now.

The internet is the the cure for isolation and ignorance.

We travel to Baltimore tomorrow, it's a shame our paths don't cross both Mel and I have remarked we'd like to shake you hand (or at least wave at you in your isolation ward!).

Take care old chap, I hope this is everything you are hoping for and more.
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chrishasms
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MaggieMae
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PostPosted: Tue Mar 04, 2008 7:45 am 
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Chris,

I just watched your videos. Thank you for sharing. I think the videos will prove to be very important, especially after your treatment and everyone can see how you are improving.

I feel you have made the right choice to try Revimmune. I was shocked and saddened to see what MS is doing to you. Words could never explain (as the video does). My husband has had MS for over 30 years and I have witnessed a lot of changes over time, but you are so young to be suffering so much.

Three cheers to you for being brave, for not just letting MS happen to you, for sharing so that we can all learn from your experiences, and for helping others.
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chrishasms
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Sharon
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PostPosted: Tue Mar 04, 2008 2:50 pm 
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Chris -

You are an inspiration to so many.

Good luck and God Bless!

Sharon
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Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

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