you know the only answer to the cure is!
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I was a caregiver for my mom. She died 15 years ago
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I’m a part time care giver to my mom who has this. The medical community has totally failed these people. No help at all.
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Caregiver here for my mom with dementia. Recently she was hospitalized for 7 days & I was kicked out after triage, but could hear them asking her “Do you have a history of x? Do you take meds for x?” I made it clear she has dementia. Healthcare workers need better training.
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If I hand the triage nurse a list of current meds, history & current conditions, why are they asking my mother any of these things? I talked on the phone with my mom hours daily & hear nurses asking her questions she doesn’t know the answer to! Educate the medical community!
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I am one of those caregivers for my mother. It is emotionally exhausting.
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I was a caregiver to my husband, who died 2 years ago. It was a mental, physical and spiritual exhaustion I was not prepared for, let alone the isolation. Caregivers deserve so much more support.
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I helped my mom care for my daddy before he passed away last year from Alzheimer’s/dementia. All you’ve said is true as I can empathize. The bereavement of his loss is unbearable. The trauma as his caregiver is unexplainably painful. None of those emotions will ever go away.

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Rather than a retweet I think those of us going bankrupt while trying to fund dementia care for a loved one would prefer MEDICARE COVER DEMENTIA CARE.
#AlzheimersInAmerica What other disease at this scale is NOT covered by Medicare?Thanks. Twitter will use this to make your timeline better. UndoUndo
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My late father had dementia and it was horrible to deal with, for him and I. Rest his soul.
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