| FAQ/Help |
| Calendar |
| Search |
| Today's Posts |
12-03-2011, 06:55 AM
|
#4 | |||
|
||||
|
Grand Magnate
|
We have to be our own best advocates, always informed and educated. I like my neuro and PCP but feel "It's my body and we work as a team", in the end no one now what and hos as much as really concerned and involved us. They get really busy and don't have all the answers.
Had a wheelchair repair guy here who in the end wasn't really helpful. In the end I ended up problem solving as It's me who can't walk and is so dependent on my chair and do know it and this life very intimately.
__________________
Kicker PPMS, DXed 2002 Queen of Maryland Wise Elder no matter what my count is. |
|||
|
 Reply With Quote
|
| "Thanks for this!" says: | SallyC (12-03-2011) |
|
|
Similar Threads
|
||||
| Thread | Forum | |||
| ERUOPE only..."Real Life Real PD Survey" (European Parkinson's Disease Association) | Parkinson's Disease | |||
| How It Works About Us Contact Info Share real results with real patients for real dis | Multiple Sclerosis | |||
| Not a "power pin" problem, but a power adapter problem. | Computers and Technology | |||
Threaded Mode