Brenda Avadian is an experienced family caregiver and author of nine books,
including “Finding the JOY in Alzheimer’s: Caregivers Share the JOYFUL Times,” and an award-winning speaker. She is the founder of
3, a website devoted to helping caregivers for people with dementia gain
knowledge and strength with humor.
Here she shares a few caregiving tips:
HWCG: You and your husband were caregivers to your father after he was
diagnosed with dementia. Journalist and author Gail Sheehy was a caregiver
to her husband during his long struggle against cancer and she too has
written about that experience. In her book, “Passages into Caregiving:
Turning Chaos into Confidence,” Ms. Sheehy has a list of the stages
of caregiving. The first stage is “shock and mobilization.”
What advice do you have for someone who has just become a family caregiver
and might be at this stage?
TCV: When families wait for a crisis before stepping forward, that’s
what usually occurs—SHOCK. Sheehy advises finding a doctor you can
trust. For many of us, we’re still not sure what we’re dealing
with. In shock, we’re frozen and struggle to act. Oftentimes, we
hastily make decisions (mobilize) that may not be in our best interests
or those of our loved one. During the last 20 years, I’ve learned
it’s best to first learn as much as you can about a loved one’s
health. Cancer? Dementia? Stroke? Learn what to expect by talking with
professionals, fellow caregivers, and reading resource materials.
HWCG: On your blog, you wrote about feeling overwhelmed in an article titled, “Caregiver, take it one step at a time.” Can you talk about a time when you learned this lesson as a caregiver?
TCV: It happened while I was writing a check at the grocery store. Exhausted
from round-the-clock caregiving for my father, I couldn’t even recall
the year! I mean forgetting today’s date is one thing, but the year?
It was at this time and after several other dementia-like symptoms (disorientation
and hallucinating) that my husband and I realized we were getting Alzheimer’s
trying to keep up with my father’s care. It was then we realized
we needed help.
We’re fortunate today in that caregivers have many resources along
the continuum of care, such as in-home care, adult day care, and assisted
living to give us respite so that we may recharge in order to function
HWCG: You have two
books titled, “Finding the JOY in Alzheimer’s” and the obvious
question is why is it important for family caregivers to find joy?
CV: People have asked me, “Are you kidding?” and “How
can you find JOY in Alzheimer’s?” My perspective is fairly
simple in this regard: We have a choice. We can choose to be miserable
and spiral into depression, and take those who love us down with us OR,
we can find the goodness in our day and feel uplifted by what remains.
How do you feel when you read both sides of that sentence? Does one half
bring you hopelessness while the other invites hope? My goal as a caregiver
has been to focus
not on what my loved one and I have lost but to direct my attention to what’s
left. It’s a life philosophy that makes the best of any situation.
As a result, caregivers from around the world have shared their uplifting
stories while bringing smiles to loved ones as families choose to make
the best of their situation.
What does it mean to be a family caregiver? For some people it means never taking a break and that's why the theme for November's National Family Caregiver Month is, "Caregiving Around the Clock."
No matter where you live, there is probably an engaging experience for your loved one who is living with dementia to check out. Read about everything from memory cafes to full-size model ships created to help those who are coping with the symptoms of dementia.
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