EP is a community where members connect through shared life experiences-- like MS--and so much more. You are not defined by any one thing, so be your true self and find others just like you at
Experience Project.
Joined: Sep 10, 2008 Posts: 4 Location: California
Posted: Thu Sep 11, 2008 11:15 am Post subject: Hi from California
I love this website!
My uncle has secondary-progressive MS. He was being treated with chemotherapy with Mitazantrone, but had to stop the treatments because they were damaging his heart. I joined the website to help him stay informed about new treatments for SPMS.
Joined: May 04, 2006 Posts: 3371 Location: Mid-Michigan
Posted: Sat Sep 13, 2008 12:25 pm Post subject:
Welcome to the site Bovellido and your uncle is lucky to have your interest in his welfare to his advantage.
There are a lot of people in the same boat that your uncle is in. Obviously having MS is not a good thing and having SPMS/PPMS seems much more hopeless than RRMS. I think with research you will find that the situation isn't as hopeless for SPMS/PPMS as it it might seem at first glance.
Bob _________________ Wife diagnosed with MS in Feb. 2006 and is a participant in the Tovaxin IIb clinical trial.
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 You cannot vote in polls in this forum
Forum FAQ
Search
Usergroups
Profile
Log in to check your private messages
Log in
