Nothing goes further than word of mouth. Ring up or send e-mails to your friends and fellow MSers asking them to visit www.ActiveMSers.org. Post information about ActiveMSers on multiple sclerosis forums and message boards. Tell your neurologists and nurses about the organization. Fill in your local National Multiple Sclerosis Society (NMSS) chapter.
ActiveMSers has prepared a basic informative flyer that you can pass out at MS events. Give a stack to your local NMSS chapter and ask them to hand them out. Or request your MS clinic (or neurologist) to place flyers in the waiting room next to all those Rebif, Copaxone, Avonex and Betaseron brochures. Heck, plaster telephone poles with them, paste them on your forehead—I don’t care as long as the word gets out. And ensure what you do is legal, of course.
