“Parkinson’s is a relentless companion, but it doesn’t have to define us. And maybe, just maybe, it’s possible to rewrite this story. To find ways to be interesting, engaging and fun again - even with a tremor in my step and a running commentary in my head.”
Great piece #pdcommunity

My Dad had DBS in 2021. He was unable to do a lot of things on his own from zipping up his coat to eating. He got his life back.

I am not ready for the S word to be in the forecast.

For my YOPD people in the US, has anyone been approved for the pump yet?

My parents are visiting right now, and I have felt the need to explain everything. Like my big toe has stiffened up and I can’t put my weight on it as I limp around the kitchen. Usually I am saying these things to my dogs….

For me my it’s my left foot. I do stretches and hope my C/L kicks in soon.

Thank you for sharing. I am 46.