is there anyone on here going to the group meeting in Shropshire on 26th March.
Ive never been to a meeting before. We are not local to Shropshire, but being from West Bromwich, near Birmingham this is the closest meet up to us. I’m somewhat apprehensive. As don’t what to expect, but I am keen to be able to speak to others who are going through the same. My husband was diagnosed with PSP after 4 years of symptoms s.
Rosaleen
Hi Pinkcamelia, I suggest you phone the PSP Association Helpline and ask them to put you intouch with the organiser so you can get more information.
Thank you
Hello Pink C. Great idea to go to meeting. I am 6-7 yrs into PSP, aged 83, male, no longer driving, and liviNg in MAVERN. used to go to Droitwich for meetings, but Covid collapsed it. its good to have local contacts, an I'm happy to chat. Will give you my number if yu wish to follow up? What age and stage of PSP are you at? I can also emaail you my 7pages of notes, iinfo, and suggestions, if you send me your personal e-address. Best wishes Tim Willcocks
It’s my husband who has PSP. Diagnosed Nov 21. Has had symptoms from early 2017.. Our son has offered to take us to the meeting. I’m just worried, it might be too much for him.
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New to this.. mum has CBD
