in 2007 I was iagnosed with MS a CIS case.  I did not believe the disease modifying drugs were the answer.  then I found Ameds in Poland, Dec28th 2010 I was liberated. I was 90 % blocked on my right jugular, 60% on the left.  Two days before leaving for POLAND I was told I do not qualify to take Copaxone.  HUH.  when I returned I was asked that if I remember a second attack then I would qualify for the copaxone.  HUH.  I still have not had a second attack.  My qualities of lfe have improved since liberated.  Now I need to developemy own excersise program to bring all me dead muscles back to life.   Ms Society did nothing before what can you do now?  Do you have something that can help me now?

From sandra gondor