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Our member, Betsy Howe, whose husband Dave, gave us the essay on his insightful look at his own his Alzheimer's Disease - "Living in an Evil Fog", has written the first in a series of caregiver tips for the Alzheimer's Association.She has generously allowed me to share it with you.

Alzheimer's ~ Association@
- Support, Part 1-

Dealing with dementia in a loved one
can be overwhelming at times, or most
of the time. Not only do we have our
own lives to conduct, we are trying to do
the best we can for our loved one. All
the time we are also grieving the loss we
both are undergoing. You about get used
to one level of effort and things change
and get harder.

As caregivers we are advised to reduce
stress,keep a life of our own not involved with caregiving, exercise,and eat properly. The focus of this article is reducing stress. The caregiver's key to reducing stress and keeping THEIR sanity is .... support support support ...and the most important...SUPPORT.

Many articles tell us that if we don't take care of ourselves we can, and do, become statistics ourselves. We die earlier than our non-caregiving peers, or worse yet, before the loved one we are caring for. One of the useful things I've been advised to do is make a list of all my friends, family and acquaintances. Next to each name I indicate what role they can play in reducing my stress level through support in three categories:

1. 'D' goes next to the names of those who can be counted on to 'Do'. There are and will be things we inevitably will need done or need help doing or leaning to do ourselves.
2. 'L' goes next to the names of those who can be counted on to
'Listen.' We need people we can talk to, even if we end up saying
the same things over and over. I suggest, if possible, you find one or two you can literally call 24/7.
3. 'C' goes next to the names of those who prefer to 'Continue on' as if nothing has happened. They prefer not to talk or hear about the nasty things going on in our lives and the life of our loved one. BUT they are willing to continue to be our friend. These people are essential for those times when we just want to 'get away' and pretend to be like everyone else (non-caregivers).

Think about those you know in all avenues of your life - work,
professional associations, family, friends, church. Be sure to include all people you know. You might be surprised at the number of potential support people you have. Don't forget to think about those who know/ knew your loved one. Often they will be happy to support your loved one by supporting you.

Keep your list in a notebookor on your computeror electronic planner so it's easy to find and add to. If you are extremely lucky you will have one or two people who are all three- D, Land C! Just try not to 'bum out' any one person. If they can support you in more than one category, it's easy to do. You are in this for the long haul and need 'D', 'L' and 'C' support long term.

I am finding that those of us actively involved in caregiving truly CARE for each other as well as our loved one. Sometimes helping someone else is a stress relief for me! Be open to new friendships with those you meet through various support groups, such as the Lincoln Alzheimer Association YoungOnset Support Group that meets twice a month and has activities periodically.

Don't forget the Alzheimer's Association 24/7 Helpline, 1-800-272-
3900, or as someone to 'Listen' but also provide helpful suggestions. I prefer the phone if I have immediate issues involving my loved one and want to know how to handle something that's going on right now. They have trained personnel with whom you can speak.

Even if you have a great local counselor or psychologist with whom you are working, the local professionals aren't generally available 24/7. If you are looking for something that is not so immediate, the email address is a good bet.

Betty went on to give a superb recommendation to this website. I thank her for the informative article and the advertisement for the website. I really liked her D,L,C tip, and I am working on my own list right now.

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The material included on this website contains general information intended as information only. This site is not intended to provide personal, professional, medical, or psychological advice, and should not be relied upon to govern behavior in any certain or particular circumstances. The opinions in the blogs are solely those of the owner of the website. The opinions on the message boards are not necessarily endorsed by the owner of this website, and are the opinions of those persons writing the messages. All material on this web site is for demonstration and informational purposes only.



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