We want to develop the PSPA Support Group ... - PSP Association

PSP Association

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We want to develop the PSPA Support Group network accross the UK and are keen to hear from people who would interested in running a group.

PSPA_CameronW profile image
11 Replies

The aim is to have local groups that meet regularly which not only provide support, but also give opportunities for individuals to get involved in a wide range of activities that will make a difference to the lives of those affected by PSP/CBD at a local level. If anyone is interested please get in touch.

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PSPA_CameronW profile image
PSPA_CameronW
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11 Replies
SuzieQ profile image
SuzieQ

It would be great if a support group network could be developed and would be much appreciated by us carers. Sadly however, as you are obviously very aware, caring for someone with PSP/CBD is more than a full-time occupation and although I would love to get involved there are never enough hours in the day for me to get involved in running a group. May be one day.....................

SuzieQ

hmfsli profile image
hmfsli

Cameron, please get in touch as I would like to know more about what is required when running a group.

PSPA_CameronW profile image
PSPA_CameronW

Many thanks for your message. Can you let me have your contact details in a private message so I can call you, or give me a call on 01327 356130 and we can have a chat. Look forward to hearing from you. Cameron

AmyT profile image
AmyT

I would be interested in running a group...Im based in North Somerset. Amy T.

anniemay profile image
anniemay in reply to AmyT

Hi, did you get any response to your interest in running a group? We are in Frome, but would be prepared to travel to a support group. My husband has had PSP for 8 years, first 4 of those diagnosed as Parkinsons. Now he is still wobbling about, great appetite for food, off all medication as there is no significant difference with/without it, except no side effects! Feel we could benefit and give benefit to other sufferers!

regards, Ann

iris2 profile image
iris2

I would like more information about setting up and running a local group in Kent,please can you let me have more details. Also would like to hear from people in kent who are carers for loved omes with PSP

susangillies profile image
susangillies in reply to iris2

I have got PSP and my husband cares for me. I read with interest that you would like to set up a local group in Kent. Kent is a very big county so perhaps you can let me know where you live in Kent. I live in Beckenham. which is a couple of miles from Bromley. My email address is susan.gillies@virgin.net, in case it is easier for you to contact me in that way.

With kind regards

Sue.

PSPA_CameronW profile image
PSPA_CameronW in reply to iris2

Hi Iris. Sorry it has taken so long for me to get back to you.

Can you let me know when would be a good time to call you and let me have your number.

Many thanks

Cameron

jac001 profile image
jac001

Hi can anyone tell me if there is a support group in northern ireland.

I am interested in running a group in Medway-is there anyone else out there?

I am still hoping to hear re a Medway group.A few times it has been mentioned that someone would be in touch but I have not heard from anyone. At this rate it will be too late for me as mum is teetering on end stage.

Dianne

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