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Take off the Cape: The Dual Role of Care Partner and Loved One Can Be Too Much, Even for a Superhero

By Eric Worley | 0 comments
Take off the Cape: The Dual Role of Care Partner and Loved One Can Be Too Much, Even for a Superhero

When you’re travelling on an airplane, there’s a small part of the safety instructions that’s easy to overlook. The sentence is very specific, but its general meaning can be applied to numerous scenarios. It’s a procedural step that one might think is common sense, until the situation arises and it’s easily forgotten:

“Secure your own mask before assisting others.” 

Simple enough, but do you know the true meaning of this statement?

You can’t properly help someone else if you can’t help yourself. You need to put your own oxygen mask on before you can assist those around you who are less capable of helping themselves. It’s not selfish. Consider this:
 

  • You shouldn’t feel guilty about making sure your own needs are met so you’re better able to help meet the needs of others.

  • It’s demanding enough to be a relative of someone with Alzheimer’s disease or dementia, but the added responsibility of acting as caregiver as well can be too much for some.

  • You need time to recover and rest or your judgment may be compromised.


“For better or for worse, in sickness and in health, through good times and bad, until death do us part.” 

Some variation of these words is spoken at most weddings. And though it’s often unspoken in other relationships, it most often applies to our connections with all our loved ones.

It basically means “no matter what.”

It’s something loved ones hold onto during times of turmoil—especially when it comes to acting as a caregiver for someone with ADRD. You want to be by their side every minute to make sure they’re receiving the proper care. The only thing that makes sense to you is to put their needs above all else.

But there’s nothing wrong with admitting that you can’t do it all.

Very few people can, so asking for help is not only expected, it’s preferred. That doesn’t mean you can’t still be involved in care planning and providing important information.

Keep in mind that with a paradigm shift toward person-centered care, facilities are looking to learn as much as possible about each resident. Sometimes that resident can’t express likes or dislikes, so having a family member around to relay that information is vital to proper care planning. Plus, being a familiar face in a new setting can help lessen the transfer trauma for your loved one. 

Remember: Secure your own mask before assisting others. Those closest to you will be forever thankful.
 

More Resources

Compassion Fatigue [article]
The Comfort Garden With Laurie Barkin [podcast on vicarious trauma in caregivers]

 

Read about dementia care training on our Knowledge Base page and gain access to our free eBook, Communication Tips for Serving Individuals With Dementia.

Dementia Care Specialists (DCS) is the premier dementia training and consulting company. With nearly 60 years of cumulative experience in dementia care training, DCS provides state-of-the-art dementia products, training, and program consultation.

Posted August 2012. Updated November 2015.
 
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