There may be days when the MS flares up and I am not at my best physically. This doesn’t stop me from being an advocate and voicing my support of agencies working with people with MS or are doing research to help end it.
With the help of the National MS Society I have contacted my representative to voice my support to fund three agencies, Congressionally Directed Medical Research Programs (CDMRP), the National Institutes of Health (NIH), and the Lifespan Respite Care Program, that are fighting the war against MS.
You can do the same by going here.
To follow up on more MS Advocacy, folloe the MS Activist Blog.
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