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?
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?