Support Group
Hi,
This is my first time posting. This may seem like a silly question, but I'm looking for some support and I don't know if it is best to reach out to my local ALZ caregivers support group or the support group in my Dad's state. Which would provide me with better support and resources? Does it even matter?
Also, I don't really know much many hours my Dad might need with the home care providers. I'm looking at agencies and private people. Do I need to be concerned about insurance issues with private people?
There is so much to navigate...
Many thanks, LP
Comments
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Welcome to posting. Please, if you do not get a response within a couple of days, post also on another board. This one does not get much traffic.
Nothing wrong with trying groups in both places if that is possible, with most groups it is a "come when you can" scenario.
It is usually wise to have an additional liability policy, not expensive, contact your father's insurance agent.
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I would definitely start out with a local, face to face in-person group. I just did my first one ever and it was fabulous. You then could add a remote support group in his area to help with resources.
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Commonly Used Abbreviations
DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
EO = Early Onset
FTD = Frontotemporal Dementia
VD = Vascular Dementia
MC = Memory Care
AL = Assisted Living
POA = Power of Attorney
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