Pearl
Active member
- Joined
- Aug 20, 2006
- Messages
- 77
- Reason
- Friend was DX
- Country
- US
- State
- Georgia
- City
- Atlanta
Hi, I'm a friend of a CALs. As the disease progresses, my friend's husband (the PALS) finds himself now at home (on disability). He gets fatigued very easily and has been spending most of his time in his chair watching tv. Well...that's getting a little boring for him. I know that this transition will be difficult, but can anyone share their experience of how they dealt with the change from work to home and limited activity?
Does anyone have suggesions for what he CAN do? May I ask how some of you fill your days? Or what has become important to you?
Thanks for any insight.
Does anyone have suggesions for what he CAN do? May I ask how some of you fill your days? Or what has become important to you?
Thanks for any insight.