I am a support group leader for psp aka supranuclear palsy
I am a support group leader for psp aka supranuclear palsy...would appreciate any feedback, help we can use for this disease...
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Hi @afoster80, welcome to Connect.
I'd like to hear more about your support group and your role as a leader. What kind of feedback or information are you looking for? It will help me connect you with other people familiar with this disease.
I was diagnosed on Nov 15/23
I was told no cure for the disease but I could join the trial clinic in the spring.
it hasn’t happened yet. I am Canadain and winter down in Yuma so am home now. Any ideas when the trial clinic is going to happen.