We've got a range of #SupportNetworks meetings regularly via Zoom.
Meetings include:
28 October @11am Newly Diagnosed Group
29 October @2pm Hertfordshire Local Group
6 November @11am London Regional Group
10 November @2pm Lincolnshire and Suffolk Regional Group
12 November @2pm Cambridgeshire Regional Group
23 November @2pm Oxfordshire and Berkshire Regional Group
23 November @2pm Leicestershire Regional Group
If you need support, no matter what stage of your #PSP or CBD journey, find out more about our support networks at pspassociation.org.uk/infor... or by contacting our Helpline at helpline@pspassociation.org.uk and 0300 0110 122.
Written by
HelenPSPA
Administrator
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You don't need to ask questions or share information, you can just attend and listen if you prefer.
We do offer Q&A sessions with healthcare professionals too but we don't have a date for the next one yet. I'll post on here when we do - as they are good to listen into also.
My wife was finally diagnosed in March this year after 2 years of symptoms. She can not walk unaided and is rapidly losing her speech. We seem to be going down hill rapidly. Does that put us in the newly diagnosed category? If so myself, Sally and her carer would like to join the zoom call.
Yes that would put you in the Newly Diagnosed Group. To join the meeting, please email our Helpline on helpline@pspassociation.org.uk and they will send the invitation information across.
Hi Helen, I attended a Zoom meeting for Kent area on 7th October & I thought another one was scheduled for the beginning of November. It was a great meeting which my husband ( he has PSP) & I really thought was worthwhile, as we met another couple very similar to ourselves. Can you tell me if another meeting is planned.
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