This blog is for people who have Multiple Sclerosis or who have family and friends with MS. I have good days and bad days, just like all us. I’ve learned a lot since my diagnosis in 2001 and I keep updated on the latest news.
I want to show others with Multiple Sclerosis (and their loved ones) that despite hardships life can be fun.
I want to keep you updated with the latest advances in medical technology and research.
I want to help the newly diagnosed find their path through this disease; with information, support, and resources. What you do with that is your choice.
I want to raise awareness for people who know nothing about MS; 1 in 750 people in the US are diagnosed. That’s not a small number.
I will share my life – the ups and downs- to make this Mission Statement a reality.