Should mouth guard work to stop biting tongue and/o r cheek in sleep?
Getting $500 guard from dentist Monday.
Will Insurance reimburse if PD doc writes Rx?
Dentist doesn't think so
I'm interested in trying but can find no current references on its therapeutic benefit for exercising? There is no local PD PT team in my area and I thought this could be a good alternative. The PD Warrior program looks interesting but is rather pricey.
Ok I don’t post much but read all I can. My symptoms are progressing it seems at an accelerated pace in the last couple years.
This past week has been tough to just get out of bed. I have no energy or motivation but always have been able to push through. Not Sunday. I woke, showered, ate breakfast and hit a wall. I ached all over could hardly move. Went back to bed and stayed all day. Woke Monday and back to normal. Is this a new thing to look forward to???
Thx for reading.
read the "how to" about it here. ---> https://myhealthteams.freshdesk.com/support/sol...-
The toes were numb and tingling for a couple of months before the swelling started. They are not sensitive to touch but sometimes they feel like they are going to burst and then they really hurt. My neurologist thinks i may have nerve damage but I can’t get a test to find out until December.
Like slapping someone's hand away and being just cantankerous, argumentative, and flat refusal of aid?
I only see lists that are pre-picked, but I'm missing it, if there's a search bar.
I discovered research that smell reduces in nearly 85% of people before diagnosis. Yet that isn't used or tested for. Smell can be reduced for other reasons. But my smell seems normal. It's unclear yet if I have PD or maybe vacscular PD or maybe something else (I've had drugs for lymphoma). Is the lack of reduced smell a good sign that maybe I don't have regular PD?
What does that mean for a diagnosis? I may have PD or Vascular PD or Essential. Doctor's aren't sure yet. Will get first DapScan results tomorrow.
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