What are our rights legally? How do we manage financially? Where can I go for support groups? I have so many questions and I don't know where to turn to find the answers. I was wondering what your stories were for when you or your loved one was first diagnosed with MS. Where did you turn? Do you have any tips for caregivers? For people that are newly diagnosed? Please, any information at all would be useful. Thank you so much.
Accelerated Cure Project publication for newly diagnosed:
http://www.bostoncure.org/downloads/bcp ... tsnext.pdf
U.S. National MS Society page on living with MS:
Canadian MS Society page for newly diagnosed:
UK MS Society page for newly diagnosed:
Daily news updates on MS:
Some more documents, interviews, book reviews
Other documents (not ours) and pointers to other MS organizations
Feel free to contact me if you have questions, I'm happy to help out.
You can see what we have to offer at
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