Status
Not open for further replies.

nebrhahe53

Very helpful member
Joined
Jun 13, 2014
Messages
1,017
Reason
PALS
Diagnosis
06/2014
Country
US
State
Tx
City
Austin
With the new Medicare rules it seems as if Medicare will be almost worthless when it comes to extending any quality of life for ALS patients.
Do I understand correctly that we will no longer be able to get any help with devices that give us some freedom like power wheelchairs or assistive devices for being able to be on the internet and communicate with others? How much would these devices cost to purchase ourselves?
Are there any places that sell used equipment that might be affordable?
What type of equipment for speech and mobility is best?
 
Status
Not open for further replies.
Back
Top