Years ago a gentleman suggested to me that I should start a blog about my MS experiences. I brushed it aside, thinking, why would anyone be interested in what I have to say, mostly because at that time I still believed that my MS was different from anyone else’s. 

A true statement although my emotional symptoms were very similar. A loss is a loss.

I wasn’t even sure how to begin, due to technical limitations. A son-in-law generously helped me through the mechanics of starting a blog and I was off and running. It has been over a year since I took a good look at my disease, both physically and emotionally. I had no idea the benefits I would receive from writing down everything I have experienced and sharing it with other men and women in the MS community. 

If you have never connected with my blog, I ask that you check it out and hopefully find a comment, a tip or an experience that you can relate to, thus reducing some of the loneliness and isolation that we go through from a lifelong diagnosis of Multiple Sclerosis. 

mslivinglife.com