A Canadian.
I am from B.C.and I would love more inform... - PSP Association
I am from B.C.and I would love more information.
Will mail you all I have on Tuesday!!
Check out : Cure PSP , PSP information and the handbook.
You can download a full range of information from the PSPA website at pspeur.org
Hi Linda from B.C! I am from Washington State! Just wondering - are you looking for more PSP information or more information regarding the folk trying to get a Candadian site?
Hi dlera,
I think its great that we will have a Canadian site! I have information about PSP having been diagnosed over a year ago but I want to see what is available.
Lynda
Hi,
I have been reading info from this site since my mom has been diagnosed last Oct. It has been very helpful and encouraging. We live in Vancouver, BC and it would be great if we have a Canadian site and even a support group in the Lower Mainland in the future.
Thank you everyone for all your support.
Maryam
Thanks for answering! I live in Rossland and it is nice to know you! I have lived in Vancouver,
Hi everyone , my brother J.J. was diagnosed with P.S.P. 4 years ago at the age of 56 but probably had it for 2 or 3 years prior to diagnosis . He lives at home with my 86 year old mother .We are lucky in that we have a large family so we all take turns to look after him . I find this forum such a comfort and so helpful, as we have no support group where we live in southern Ireland .. It has taken me so long to pluck up the courage to write this . Just want to say I get such strength knowing we are not alone ...... Aine