Hello everyone 😊 I am new to this site and I have introduced my mother in law ( wheel race) to it to as unfortunately my father in law has PSP and CBD. What an amazing, reassuring and informative site it is! There is so much information and advice to be found and all given by such lovely compassionate people who are all suffering the fate of this despicable disease! It is a real comfort to our family that we are not alone. I just need more hours in the day to read and digest and hopefully help my in laws in getting the very best out of life for them. Thank you all xx
Inspirational, reassuring and heartfelt! - PSP Association
Inspirational, reassuring and heartfelt!
Welcome Both of you, and let us know if we can help with anything: finding historic posts on a particular question or whatever!
Anne G.
I know you will receive kinds words and lots of advice. Welcome to you. Jxx
You are in the right place. Everyone on here has more information and experience than most neurologists.
thanks flutterbyes you are a star what would we do without our wonderful family
Hi Wheelrace
and you are a star too.
This illness is not easy to cope with and then there is care on top. You clearly have the determination to work through this. Strength to you. It is hard, but it is totally do-able too.
Looks like you are a part of a wonderful family!
I am sure together you will make your husband's path comfortable and good.
Welcome to the site.
PSP is most definitely despicable, and it helps to know and communicate with others who are dealing with it.
You and your family will find a wealth of information here.
Take care,
Teresa