today I had good session with my consultant, things haven't decreased too much, not much change in 12 months. He asked if I had heard about this, I explained I signed up yesterday, I'm pleased to know he also will be involved, I think this a very positive & exciting step forward.....
It is your right,especially as we are from all over the country,weve been asked and our neuros are involved. As I said it a few hours with a neuro,longest most of us have spent under there noses,and they do all seem fired up about this study.Its a fantasticopportunity for us to do something positive and perhaps will be a way forward to future engagement
heres hoping x
Good for Scotland. 40 centers around the country. Sounds promising!
I think it is the best thing...you would have thought someone would have thought of this sooner??? Set up a world wide data base so when they diagnosed someone with PD they could have them fill out a survey.....
Thanks . It's wonderful news. I just hope that the USA gets involved quickly.
PEMF mat therapy update
Update on B1 effect for St8farm
Mannitol and dizziness?
Back again with another question about spouse's DBS results
Doing better without Carbidopa/Levodopa...??
