FAQ/Help |
Calendar |
Search |
Today's Posts |
|
Caregivers Support A place for people who are a caregiver to another to find help and support. |
|
Thread Tools | Display Modes |
01-14-2010, 05:00 PM | #1 | |||
|
||||
Senior Member
|
http://www.ehow.com/how_5800334_cope-aging-parents.html
I was reading this article on how caregivers can help their family member with a disability or an aging parent. It got me to thinking? What can we "the person in need" being doing now, along the way, to make our caregivers' life easier, more fullfilling, etc.???? I know, I often wonder, how my husband and children feel about my MS. And what I could do to reassure them or help them. Or what DOES your family member in need already do for you that helps you out SO MUCH!? We have some WONDERFUL caregivers here at NT. Do any of you have any ideas???? Thank you!
__________________
~ Friend2U . . HANG IN THERE! If I had to sum up FRIENDSHIP in one word, it would be COMFORT. ~Adabella Radici MS/dx2006 BETASERON (Quit May 2011) COPAXONE (Began June 2011) |
|||
Reply With Quote |
|
|
Similar Threads | ||||
Thread | Forum | |||
Calling BMW.... | Survivors of Suicide | |||
Calling Chasmo | Parkinson's Disease | |||
Calling in Sick | Peripheral Neuropathy | |||
calling all pals | ALS | |||
Calling Everyone Calling Everyone | Reflex Sympathetic Dystrophy (RSD and CRPS) |