Anyone using? How is it?
PDcare laser: Anyone using? How is it... - Cure Parkinson's
PDcare laser
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recently started. So far it’s been relaxing and calming. I’m expecting gradual effects but noted these right away.
Hi, yes, I know that the treatment I'm using (SYMBYX PDcare) is not for everyone. Like everything (PD included), one size doesn't fit all, I will also have medication in that bracket (2018 (60) I suffered a stroke due to meds. Over the years, we have spent thousands in a 2yr period. I paid €4,550 on physio alone for the pain and cramps, we also have a box full of many gadgets, creams, etc, etc. If truth be known, most of us have that box!
So, as Audrey says, time is against us, and yes, I'll fight this PD, toe to toe. If this is buying me time,I'm taking it.
I was with a large group of friends (20+), the shortest testimonial, I asked who remembered me over a year ago, all hands up, am I changed for the better, all hands remained up. I'd wish this for all my fellow travellers, but with PD, it's never going to happen
Gavin, Audrey, yes, you must give it time. Progress with tech needs to happen, and look at how DBS has helped thousands
My wonderful mother is so happy, I can say no more.