Is this treatment having good results for reducing tremors….Which is the best place to get it done…
He looks straight at me like he hates me. His wife of 24 years
I have a question; has anyone ever had twitching of a muscle for instance in your upper arm and it never goes away it may twitch less often some days and nights it may even be calm for most of a day or two but for months and months on end it has not completely given up twitching and sometimes it Twitches so hard that you can just see it really jumping out under the skin and I wonder if any of you can ever remember experiencing that with your Parkinson's?
My husband has had PD since 2014. My question is: Is it common for a person with PD to moan a lot? My husband is constantly moaning and he says he doesn't know he's doing it!! He has different types of moans. I always think he's in pain or that something else is wrong, but he says "no". It drives me nuts some days 🥴. Does anyone else have this problem???
Thank you 😊
He has trouble getting himself off the couch from laying down position and bed. Body just freezes. Is there some kind of “thing” available in any store or online maybe with a built-in handle on a heavy sturdy side-table to grab onto without tipping? (Showed him the bed bar that mom used that slides under the mattress but he did not think that would help him. )
My husband with Parkinson’s and I just moved to the South Strand area of Myrtle Beach area and are looking for recommendations for a neurologist that treats Parkinson’s Disease. Need someone that is easy to talk to and isn’t rushed for time. According to his last neurologist who happened to be an MDS as well, credentials don’t necessarily mean anything, if the doctor is a butthole that you can’t speak to openly.
My husband was diagnoised with Parkinsons in 2020. He now has pain and weekness in his arms. His doctor thinks that he might have Polymyalgia and has referred him to a rheumatologist. I'm curious if anyone else has these same symptoms?
Had DBS surgery about a year ago. Been off all meds for 8 months. Movement has improved significantly but I tire out more easily. Wondering if DBS can lead to brain burn out.
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