National MS Society Public Policy Conference 2023

I was invited to attend the National MS Society’s Public Policy Conference in Washington, D.C. at the beginning of March. We kicked it off on Monday afternoon. There were about 200 people there, many decked out in orange apparel- people living with MS, people whose loved ones have MS, MS medical personal and MS SocietyContinue reading “National MS Society Public Policy Conference 2023”

Christmas In July

The best thing happened today! I scored a video game that my kid has wanted for awhile with a great deal from an early Amazon Prime Day deal. One of my favorite responses when someone asks me where I got something, is to tell them about the deal I scored on it. I’m not sittingContinue reading “Christmas In July”

With MS, There Is Always A Cost

If you or someone you know lives with MS, you probably don’t need me to point out that Multiple Sclerosis is a very expensive disease to have. According to the National MS Society, medications, particularly DMT’s, also known as Disease Modifying Therapies, which are used to try to slow your disease progression down are billedContinue reading “With MS, There Is Always A Cost”

MSfit Travel Log- Packing Edition

At almost 40, I traveled all by myself, for the first time ever, in my life. I love to travel! I just usually travel with family or friends. I was invited by the National MS Society to attend their Newly Engage MS Activist Workshop, in person, and in Washington D.C.! (Separate post on that later!)Continue reading “MSfit Travel Log- Packing Edition”