Hi there! Thanks for letting me in. I am Danish living in Køge some 50 km south of Copenhagen, married, 2 adult children, 3 Grand children. I am 65 years old. I was diagnosed PD May 2014 and re diagnosed April 2017 Atypical PD PSP (Proggressive Supranoclear Parese) It is my hope to make contact to others with the same diagnosis; PD PSP, in order to find out the best possible way of living whith it, I have tried the Danish and the Swedish PD Facebook fora, however, without any results.
Welcome to the forum. How have you been getting on since your diagnosis?
This is a great place to ask any questions and find support from people who understand.
Joanne - Digital team.
I was almost completing a post to Mr Skibeka, wellcoming him in his own language when, in a instant it was replaced by cookie info, now I am very , well upset is a understatement as It took some time to gather the words I needed, and then more usefull Danish words which are hard to spell never mind form them into sentances, so im going now as if I go on Ill make mistakes Im so angry
Not been on the forum for a while I took my wife to see a different consultant last Friday and he says she has PSP. This is after being diagnosed in October 2013. Progressive being the operative word. He said to keep taking Sinemet as it helps and to face problems as they arise and that he will continue to see her.
All the Best to you all Billy