The National MS Society has a variety of resources for patients, their families and caregivers. Since being diagnosed, I have spent a lot of time on their website and requested several publications. One day when I was on the site, I saw a link to their connection groups. This sparked my interest, however, I noticed the only local group was held during the day in a neighboring town.
After some discussion with the Mid America Chapter of the MS Society, I decided to become a connection group leader! My first group was last night!
I am so glad that I have found another way I can reach out to those with MS and their families!
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