By Caregiving.com — 2020
As a non-caregiver, you don’t have to know every detail of a caregiver’s life to understand that their needs often go unmet. Here are some simple actions you can take to help a caregiver.
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It’s the rare person who doesn’t need help coping with the stress, fatigue, and frustrations that chronic fatigue syndrome can bring. As a caregiver, you’ll need to learn all you can about chronic fatigue support.
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Expert advice on finding the right words, listening well, and getting specific about offers of help.
When it comes to providing emotional support, skip the platitudes. What matters is being honest and human.
How to keep it in check by tolerating ambivalence, maintaining balance and staying realistic.
Caring for a loved one with dementia, such as Alzheimer’s disease, can be a difficult task. Often this task falls to a family member, and as the disease progresses, the care needs become greater, requiring more hours of the caregiver’s time.
My mom’s Alzheimer’s diagnosis and decline were a painful and lonely journey, one that coincided with an otherwise unbearably hectic time. My two children were still in diapers.
As caregivers, we need to be more than problem solvers. We need to be portals to a larger possibility.
Last week was the one-year anniversary of the beginning of my husband’s health crisis. As I gaze at the permanent handicap placard and at him sleeping, once again, on the couch, I’ve been reflecting on what I’ve learned this past year.
When someone you love falls ill, gets in an accident or receives a scary health diagnosis, it’s never easy. In fact, it may be the hardest thing you’ll ever have to face. Unfortunately, it’s also inevitable that we’ll all deal with this kind of situation in life.
No one can prepare us for the experience of providing care for a seriously ill family member or friend. When sickness strikes someone close to us, there may be a sense of chaos, urgency, and confusion.