I am about 5 years in with reasonably mild symptoms and not progressing much.
My PD doctor seems to suggest that this research has ceased a bit recently. She says Mt Sinai did some inconclusive research a short while ago and then lost interest?
All the research reports seem to go back a year or so, although there does seem to be a private company working on pd at MSK with the mysterious name Blackrock?
I just discovered that 25 years ago, my wife harvested her placenta stem cells from our son's birth and we have been paying for storage ever since.
I wonder if his stem cells should be relevantly similar to mine, - and if this could be of any use to me or would I Have (according to the news reports) to travel to Lund to stand any chance of using it?