Hello all,
I am an Occupational therapy student at a university in Ontario. I have taken an interest in helping people who have ALS and their caregivers. I friend of mine has a husband who was diagnosed 5 years ago and has stressed that there is not a lot of caregiver support in the area we live in. I was hoping to create a support group for caregivers and their families of people who have ALS. If I can do a good job I will give the protocol to the society or try to implement it myself (when I graduate). I was hoping that some of you guys could give me some insight as to what topics you feel should be addressed in such a group. Anything you feel is important is great feedback.
Thank you so much for reading this. I would really like to help out as much as I can and I feel that this might be a good way to start
Thanks again
TMG
I am an Occupational therapy student at a university in Ontario. I have taken an interest in helping people who have ALS and their caregivers. I friend of mine has a husband who was diagnosed 5 years ago and has stressed that there is not a lot of caregiver support in the area we live in. I was hoping to create a support group for caregivers and their families of people who have ALS. If I can do a good job I will give the protocol to the society or try to implement it myself (when I graduate). I was hoping that some of you guys could give me some insight as to what topics you feel should be addressed in such a group. Anything you feel is important is great feedback.
Thank you so much for reading this. I would really like to help out as much as I can and I feel that this might be a good way to start
Thanks again
TMG
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