Tuesday, March 6, 2012

Highlights from MS Public Policy Conference

Day One of the conference sped by so very quickly. Read about the opening afternoon sessions in my post - Washington from the Inside: The Political Climate and Multiple Sclerosis. Day Two is not yet complete, but you can catch up on a very important issue, the Lifespan Respite Care Act, in today's post - Family Caregivers, MS Research, and MS Champions. In just a few minutes, I'll head back down to the Ballroom to kick back and enjoy the comedy stylings of Brett Leake, a standup comic turned sit-down comic who lives with muscular dystrophy. My interviews with two inspiring MS activists will be posted tomorrow while we are all headed to The Hill.

2 comments:

  1. thanks for doing this Lisa...for all of us who can't but wish we could. YOU are an MS rockstar!!!

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  2. Love your blog! You are an inspiration to me!~hugs~
    Olivia

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