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Portsmouth Support Group
The Portsmouth Support Group is run by PSPA volunteer, Kristy Robinson.
The support group will meet on the third Tuesday of each month, offering a welcoming space for people living with Progressive Supranuclear Palsy (PSP) & Corticobasal Degeneration (CBD), along with their families and carers.
The group provides an opportunity to connect with others facing similar challenges, share experiences, and offer mutual support. It is an informal and friendly setting where you can chat openly, find encouragement, and build new friendships within a compassionate and understanding community.
*23 Sep 25 meeting: Please note a member of PSPA will be attending this meeting.
Venue and Accessibility
Accessibility Features
SUPPORT GROUP COORDINATOR
FAQs
Can my carer attend the meeting with me?
Yes! Support Group meetings welcome people living with PSP & CBD and also their family members, friends and carers.
MY PERSONAL GUIDE
To help you understand how PSP & CBD may impact you and your family, we have produced a handy guide to the conditions.
As well as information about the conditions, you will find details to help you get to grips with the changes in your symptoms and plan ahead.
LINK VOLUNTEER SERVICE
If you would like one-to-one support to help you come to terms with your diagnosis, or tackle a particular challenge, our Link Volunteer Service can help.
As part of the service, you will be linked with a trained PSPA Volunteer in your area who can provide support and information in-person or over the phone.
PSPA is the only UK charity dedicated to creating a better future for people living with Progressive Supranuclear Palsy (PSP) and Corticobasal Degeneration (CBD). We work to ensure the 10,000 people living with PSP or CBD receive support and care that is co-ordinated, has continuity and is compassionate. We rely entirely on voluntary donations. PSPA is a registered charity in England and Wales (1037087) and in Scotland (SC041199).
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