juliefitz
Member
- Joined
- May 10, 2009
- Messages
- 14
- Reason
- Loved one DX
- Country
- US
- State
- NC
- City
- Greensboro
Hi all,
Well, mom's right arm (which is all she has left, other than holding her neck up) is dying fast, which leaves us scratching our heads about whats next as far as communication goes. We ordered the fancy DynaVox several months ago, and I has come in-FInally! BUT- now that she is in hospice, Medicare won't pay for it and neither will Hospice(understandably), so they won't ship it. My question is...IF my parents primary insurance doesn't pay for it either, can anyone out there talk about other non-$9,000 methods of communicating? Has anyone gotten an i-Pad? Any luck with that and any software? This form of ALS she has certainly seems to be robbing her of every last ability she has. After she loses her right arm/hand, and she cant talk at all, is what I am assuming is the locked in state. Is that correct? Is anyone out there in this stage...and can you give any advice on how to help mom? We want to do anything and everything we can to help her, but arent sure what to do. Before ALS, she and I spoke 8-10 times a day- what a difference a year can make. :-( I miss her voice. Thanks in advance, Julie
Well, mom's right arm (which is all she has left, other than holding her neck up) is dying fast, which leaves us scratching our heads about whats next as far as communication goes. We ordered the fancy DynaVox several months ago, and I has come in-FInally! BUT- now that she is in hospice, Medicare won't pay for it and neither will Hospice(understandably), so they won't ship it. My question is...IF my parents primary insurance doesn't pay for it either, can anyone out there talk about other non-$9,000 methods of communicating? Has anyone gotten an i-Pad? Any luck with that and any software? This form of ALS she has certainly seems to be robbing her of every last ability she has. After she loses her right arm/hand, and she cant talk at all, is what I am assuming is the locked in state. Is that correct? Is anyone out there in this stage...and can you give any advice on how to help mom? We want to do anything and everything we can to help her, but arent sure what to do. Before ALS, she and I spoke 8-10 times a day- what a difference a year can make. :-( I miss her voice. Thanks in advance, Julie