I was diagnosed with MS in April of 2007. I connected with the Society almost right away because I had no health insurance, at the time, and wanted to find out what options might be available for someone in my situation.   

After seven years of living with multiple sclerosis I have faced more challenges than I can count.  It is so hard to balance quality of life with the down time my body so urgently needs.  I often feel very frustrated with not being in control of my own body and being perceived, by others, as my disability when I am so much more than that! 

The National MS Society has helped me in more ways than one; giving me financial assistance when I needed it most, a grant that allowed me to purchase a scooter and regain some independence and mobility and opportunities to give back through volunteering and Walk MS.

The Walk has meant a lot to me over the years. At first it was my coming to terms with my diagnosis, but over the years it has turned into an opportunity to share my story, meet others and raise money for a cause that has had such a huge impact on my life!

I know have a MS community around me and that the National MS Society will be there to help me when I need them.