The primary aim of this Group is to provide a forum where people affected by PSP & CBD and their families, friends and carers can meet and give support to each other as well as having the opportunity to chat informally, make new friends and generally relax and enjoy a cup of tea or coffee.
We are hoping to have a visiting reflexologist (hand massages) and regular visits from other professionals such as PD Nurse Specialists and Neuro Nurses.
The Group is open to all…
Whether you are affected by PSP now, are a former carer, want to raise funds and awareness or want to lend a hand at the Group – all are welcome! In order to save costs, in future we plan to email these invites, so please ensure you let us have your email address.
To help with our planning, please email Val Cole and let her know if you will be able to attend or not.
I do hope you will be able to join us and look forward to hearing from you soon. If you require further information, please do not hesitate to contact me.
2020 Dates for your diary:
Please note, due to the Covid-19 crisis, face to face meetings are on hold for the time being.
Instead Local Group meetings have been taking place virtually via Zoom. We will keep you updated with any future meeting dates, when they have been confirmed.