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Susan Simpson's Fundraiser
A CURE FOR PLS
or at least some effective treatment options :-)
Hello family and friends,
You all have watched me live a good life, DESPITE PLS since 2000! That's 25 years, people. And the treatment options are all the same, mostly just support for symptoms of PLS. We're no closer to a cure than in 2000 when I was diagnosed. I'm fundraising for SPF again this year, because they are dedicated to PLS and HSP, another motor neuron disease. We want our donations to be front and center for PLS!
Let’s support good in the world and make a difference, by funding medical research to find cures for HSP and PLS for Spastic Paraplegia Foundation, Inc.
Love and blessings,
Susan Simpson