Hey everyone,
Don't forget about our Zoom Support Group meeting from 7-9pm ET this evening! Just a click away, you can join us right from the comfort of your home.
🔗 Message us for the link!- and if you're a bit late, no worries! Jump in anytime up to 8:30pm. If you need to mute or take a moment, that's absolutely okay. We're here for you and you're always welcome.
If your life has been touched by PSP, or if you know someone whose has, your presence and insights can be a beacon for many. Your experiences and stories are an invaluable asset to the community, even if you’re currently on the receiving end of support.
For those involved in healthcare, especially those aiding clients with atypical Parkinsonism (PSP, MSA, CBD, or Lewy body dementia), do consider joining us. Our forum isn’t just about support; we’re also a platform offering resources and guidance pivotal for patient care.
A highlight for tonight: We’ll explore avenues for you to champion awareness for these conditions. Your contribution, no matter how small, can ripple through the community in profound ways.
Whether you're here to share, listen, or simply be a part of our community, we can't wait to see you. Every voice, including yours, makes a difference.
Meeting every Thursday!
Laura Louizos
Executive Director, Coleen Cunningham Foundation for PSP Awareness
#PSPAwareness #SupportGroup #CommunityCounts
2 comments
I emailed you Connie
Thanks
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