This Is MS Multiple Sclerosis Community: Knowledge & Support

Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.
It is currently Wed May 22, 2013 11:13 am

View unanswered posts | View active topics


Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

All times are UTC - 8 hours [ DST ]



Post new topic Reply to topic  Page 1 of 1
  [ 2 posts ] 
  Print view Previous topic | Next topic 
Author Message
Lyon
 Post subject: .
PostPosted: Sun Nov 18, 2007 6:39 pm 
Offline
Family Elder

Joined: Wed May 03, 2006 3:00 pm
Posts: 6063
.


Last edited by Lyon on Fri Dec 02, 2011 10:03 pm, edited 1 time in total.

Top
 Profile  
 
HiCy
 Post subject:
PostPosted: Mon Nov 19, 2007 5:25 pm 
Offline
Family Member
User avatar

Joined: Tue Oct 30, 2007 4:00 pm
Posts: 63
Good Find! I wish I had read that in 2004 instead of 2007. It pretty much sums it up. They were very cautious during treatment when my white levels were low. Well I am two months out and I will be back in JH next month for my first three month check up. So far not a sniffle. I would have to say that my immune system is working again. We will see if the MS damage is able to heal itself. Its a waiting game at this point.

HiCy
Top
 Profile  
 
Display posts from previous:  Sort by  
Post new topic Reply to topic  Page 1 of 1
  [ 2 posts ] 

Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

All times are UTC - 8 hours [ DST ]

Who is online

Users browsing this forum: No registered users

You cannot post new topics in this forum
You cannot reply to topics in this forum
You cannot edit your posts in this forum
You cannot delete your posts in this forum

Search for:
Jump to: