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As an ALS caregiver, what advice can you share?
As an ALS caregiver, what advice can you offer? What tips can you share on caregiving tasks that can benefit both patient and caregiver?
Do you have advice that you can suggest to a new caregiver of an ALS patient? What do you feel is the most valuable quality to possess as a caregiver?
Here is a link to a helpful site for caregivers: https://www.caregiver.org/ Do you recommend any other caregiver websites?
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