Rules for the Care and Treatment of Caregivers

by Jeff Lester on Tue, 2005-02-01 17:00
Jeff Lester and family: wife Lisa, infant daughter Emily, and daughter Kelsey
Lisa, Emily, Jeff and Kelsey Lester

As a person with ALS who has been fighting this disease for over 11 years now (seven of those on a vent), I realized early on that if I were to have a somewhat normal life, I would have to depend on my incredible wife, Lisa, to achieve it. This meant that I would have to follow some rules about the way that I treated her, my primary caregiver.

It’s essential and appropriate that caregivers and care receivers have some ground rules about their behavior toward one another.

The only rules I would give to caregivers are: Keep the relationship the same as it was before ALS entered the equation (don’t make it an adult/child relationship). And don’t abuse the power you’ve been given as the other person becomes dependent on you.

Lisa’s and my close intimate relationship only partially prepared us for the changes that occurred as I became dependent on her for my most basic needs. Therefore, this transition could be even more difficult for two people who don’t start out with an intimate relationship. These changes are very difficult for both parties, especially if the person who is becoming dependent starts neglecting his or her role in the relationship. That is why the following rules are for the people with ALS:

1. Don't take advantage

When I have to ask for something, I try to ask myself, "Is this something I would have done myself or am I using my condition and others’ empathy to get something extra?" For instance, we shouldn’t demand a gourmet meal when Spaghetti-Os were OK before, or insist on watching what we want on television (I have had to develop an appreciation for Lisa’s soap operas since I’m around all the time now). If we violate this rule, I feel it’s entirely appropriate for our caregivers to call us on it.

2. End pity parties

Those of us with ALS are alone responsible for our happiness. I don’t mean that we shouldn’t express our true feelings of frustration or pain about our situation, but we shouldn’t wallow in it. If we do, it’s right for our caregivers to point it out.

3. Be useful

No matter the limitations, there always are ways that people with ALS can be useful and contributing members of our households and world. It’s up to us to find out what those ways are, even if it’s just listening to those around us and being supportive. Contributing is vitally important because it allows us to see that our lives still have meaning. This participation is much easier to achieve today because of advances in computer technology.

4. Take care of yourself

As much as possible, people with ALS need to stay involved in planning for our needs, whether it’s the need for a lift, wheelchair, adapted van, special diet, constipation aids, PEG tube — or whatever. Also we must keep in mind easing our caregivers’ burdens whenever possible. We should keep knowledgeable about the best way our needs can be met, and when possible we should be the leader in our care decisions. It is entirely unacceptable to take a passive, or even worse, a resistant role in care decisions and then complain when something is not done to our liking.

It’s inevitable that problems are going to arise between caregivers and care receivers. It’s helpful for both to write down their needs and talk together when they’re calm. I think the most important thing that my wife and I do is to make sure my care doesn’t interfere with our normal spousal relationship. We absolutely don’t let disagreements over my care have any impact on our marriage. Care and marriage are best dealt with as two totally separate relationships.

I feel strongly that those of us with ALS have responsibility for our own care and actions, even though our lives may depend entirely on the efforts of our caregivers.

May God bless our caregivers for all they do for us!

Jeff Lester ("ragingbear") founded and hosts the weekly "Living with ALS" chat on the MDA Web site www.mda.org/chat/calendar.html. In 2004, he became a co-editor of the "Will Hubben ALS Research Digest" (www.als.net/).

Besides working to help others cope with ALS, he keeps busy writing, doing genealogy, helping in his family’s printing business, and being a husband as well as dad for his two daughters (born since his ALS diagnosis), Kelsey, 9, and Emily, 2, and expected third daughter, Jordan, due April 24. Says Jeff, "I am a true believer that you can LIVE with ALS."

Freelance
Your rating: None Average: 5 (1 vote)
MDA cannot respond to questions asked in the comments field. For help with questions, contact your local MDA office or clinic or email publications@mdausa.org. See comment policy

Advertisements

myMuscleTeam