Does anyone know if family members have a "duty of care" over family members with MS? I know we frequently vent how others don't "get it" (living with MS, fatigue, etc.,) but do they have a LEGAL DUTY?
This is quite an awkward post. . .but in my heart I believe family members have an ethical duty but do they have a LEGAL DUTY?
I am a single, divorced, disabled woman with MS (20 years since dx, 15 years on DMD). My only "family" is a brother who lives out of state and is doing quite well for himself. He tells me "I'm lazy" "to get a job" etc.
I was just curious if family members are obligated to help? Really? Isn't this post just awful? Yikes!
Just wondering? I shouldn't feel guilty, but I'm thinking of signing my home, etc., everything over to the National Multiple Sclerosis Society in a will (as I should get a living will, etc.) as I feel if I ever need assistance (home repairs, etc.) I may have to resort to charity.
Thanks, in advance, for your input!
This is quite an awkward post. . .but in my heart I believe family members have an ethical duty but do they have a LEGAL DUTY?
I am a single, divorced, disabled woman with MS (20 years since dx, 15 years on DMD). My only "family" is a brother who lives out of state and is doing quite well for himself. He tells me "I'm lazy" "to get a job" etc.
I was just curious if family members are obligated to help? Really? Isn't this post just awful? Yikes!
Just wondering? I shouldn't feel guilty, but I'm thinking of signing my home, etc., everything over to the National Multiple Sclerosis Society in a will (as I should get a living will, etc.) as I feel if I ever need assistance (home repairs, etc.) I may have to resort to charity.
Thanks, in advance, for your input!
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