Caregiver You Are Not Alone: Joy’s Story

Bath Time in Dementia Land

Being a dementia caregiver means choosing one’s battles. One that people often struggle with is getting the person in care to shower or bathe. They will refuse day after day, sometimes for weeks. Odor becomes a problem and we become concerned about the effect on their health.

Why does someone suddenly avoid feeling clean? There can be many reasons when the dementia brain is involved:

Fear of the bathroom. It’s often very white and sounds echo. There are usually mirrors in there.

If dementia has taken them back in time and they believe they are in their 40’s, seeing a 70 or 80 year old looking at them when the enter the room can be frightening.

Water suddenly hitting their sensitive skin can hurt. And because it’s clear, they can’t see it. So, there we are insisting they enter a scary place, naked, where their body is pummeled by an unseen source.

They may have body issues and not want to be seen naked. Or, they may not remember how to remove their clothes.

So, what does a caregiver do?

Suggest, don’t insist that it’s bath time.

If the answer is no, let go and try again later.

Cover the mirrors and lower the lighting.

Make sure the room is warm.

If they refuse to remove their clothing, leave it on. Soap and water go through fabric. They can wash through the cloth. It won’t be perfect but it will be an improvement and maybe next time it won’t be so difficult for either of you.

And one more thing, when you have an opportunity to get in the shower, make the most of it. Enjoy the warmth and comfort, you have earned it.

www.bobbicarducci.com www.RodgerThat.show bcarducci@comcast.net

I look forward to hearing from you.

Caregiver You Are Not Alone – Ellen’s Story

Get The Hell Off My Mountain

Caregivers find themselves on the receiving end of a great deal of advice. Far too often it comes from someone who is not now, and never has been, a caregiver for someone with a long-term, devastating, brain disease. They don’t live with the unpredictable changes in cognitive ability. They don’t see the aggression and downright spitefulness that some with dementia can manifest at any moment.

When they visit, the person in care is on their best behavior. It’s exhausting and short lived and will end as soon as the guests leave.

Knowing what we know, living with what he live, uninvited advice is not what we need. Help is what we require. Ellen’s story reminds people of this. I hope it inspires some to step up. If not, I encourage you to respond that the only right path at this time is yours and when their time comes to care for someone, they can choose their own way up the mountain.

www.bobbicarducci.com www.RodgerThat.com