Posts Tagged ‘relief’

Project Lifesaver

Friday, May 14th, 2010

Project Lifesaver Locates Your Loved One

Project Lifesaver is a network of first responders who combine the power of simple, effective tracking technologies with proven search and rescue techniques to find your loved one safely and quickly, should they wander. The first responders are located in most police departments.

Don’t let another day go by without enrolling your family member diagnosed with Alzheimer’s or a related dementia, especially if you are concerned that they may wander or drive unaccompanied by another person.  For a limited time, up to 1,800 families may enroll in the Family Stipends program at no cost, thanks to a grant from the U.S. Bureau of Justice Assistance.

Follow us on Twitter @AlzheimersInfo

Protect your family member who wanders or shouldn’t drive: To enroll in Project Lifesaver, click on the link below.

http://tiny.cc/zg9fb

Call to Action

Monday, April 13th, 2009

CALL TO ACTION

 

I received this information today in the Alzheimer’s Association’s ENewsletter.  Please join all caregivers to make a difference in the lives of those who are battling this difficult disease.

 

 

Advocate Impact: Forum 2009 

Last month, over 600 advocates from around the country marched on Capitol Hill to demand that our lawmakers make Alzheimer’s a national priority.

During meetings with advocates, members of Congress made the following commitments:

*       188 indicated support to end the two-year waiting period for Medicare;

*       181 indicated support for a $250 million increase in Alzheimer research funding; and

*       83 indicated support the creation of an Alzheimer’s Solutions Project Office.

*       65 members indicated support for all 3 issues!

You can catch a glimpse of the action at: http://www.alz.org/forum

We have great momentum and now is the time to “seal the deal”. Read on…

What Can I Do Now?

Ask your members to co-sponsor the End the Medicare Two-year Wait Bill!
People under age 65 with dementia who lose their jobs are likely to lose job-related health insurance. Many become uninsured and uninsurable. Just when they need coverage the most, federal law requires them to wait two years to become eligible for Medicare. Because of this wait, families face soaring out-of-pocket costs for health care or completely forego care. http://alz.kintera.org/endthewait 

Email your members of Congress now. Ask them to co-sponsor the Ending the Medicare Disability Waiting Period Act of 2009 (S.700 / H.R.1708).

Go to:

For more information on how you can impact the lives of those with Alzheimer’s contact www.alzcaregroup.com or 317-218-5113

Daily Journals For Caregivers

Friday, January 2nd, 2009

I recently received a call from a daughter caring for her dad with Alzheimer’s.  Her challenge was communicating with the family physician about Dad’s care.  It seemed that each time Dad went to the doctor, he was able to answer the questions perfectly therefore the doctor didn’t think there was cause for concern.  What the doctor didn’t know however was that five minutes after leaving the office, Dad couldn’t remember that he’d even been to the doctor that day.  Care at home was becoming increasingly more difficult because the family was not able to get him to take a bath, his meds, or (at times) eat. 

            One of the best tools that families can utilities when preparing for any kind of visit to a physician is a daily journal.  In this journal, a care giver can keep track of all the important information that the physician will need to know.

            My family encountered this same situation when my grandfather began having challenges due to Alzheimer’s.  Providing the doctor a clear picture of what was occurring daily made it easier for him to prescribe medication and advise my grandfather.  When it came time to give up the keys to his truck, he did so willingly because the doctor advised it.  Had that bit of information come from his family he would have fought us.

 

The Alzheimer’s Association recommends the following list:

 

·        Any medications taken that day.  List any over the counter, prescribed, or herbal   remedies.

 

                                    -Medication name

                                    -Dosage

                                    -Time of day taken

 

·        Changes in:

 

                                    -Behavior

                                    -Memory

                                    -Personality

                                    -Activities of daily living (such as bathing, eating, dressing, etc.)

                                                How much assistance does the person with AD need to

                                                complete these tasks?

 

·        Activities the person with AD enjoyed that day and how much assistance was needed to complete these events.

 

·        Caregiving strategies that worked and those that did not. 

 

            Caregivers should also remember to note when they themselves are feeling overwhelmed in certain situations.  Asking for help in these situations should never be considered a failure and is encouraged in order to maintain the caregiver’s own health and well-being.

 

www.alzcaregroup.com

 

www.behomelivelife.com

Good People Taking Care of Good People

Thursday, November 6th, 2008

Good People Taking Care of Good People Means Good Business

 

“I’m only 42.  She’s only 67.  I thought Alzheimer’s was an old person’s disease.  My mother is driving me crazy…and I don’t want to say that out loud.  It’s not her fault.  For so many years, she’s been my rock, my role model, my confidant.  But not anymore.  I’m her rock, and my father’s, and my sister’s, and my brother’s, too.  And my kids are so busy in high school.  My husband, God bless him, tries so hard to keep us sane.  Some weeks it’s a zoo around here.  I really don’t know how we’re maintaining.  We just keep plugging away, but can anyone really survive doing this for very long? …”

 

This was the first few minutes of a very long phone call I received at 9 pm the other night. She needed to vent and I needed to provide some “just right” answers.

 

This is the quality of life experienced by many of the so-called “sandwiched” generation, raising their own families and simultaneously caring for aging parents.  They are trying to be SuperMoms and SuperDaughters; SuperDads and SuperSons.  Working all day, taking care of their own children (and maybe even grandchildren), and then coming home at night to start their second job taking care of their parents.  They do so gladly and respectfully, yet with great burden.

 

And it’s not just the “busy-ness” of caregiving that is burdensome.  Caregivers of persons with Alzheimer’s disease and other dementias shoulder a particularly heavy burden of care.   The real burden is the mental stress and the anguish of watching a parent slowly lose his or her mind.  While only one person is diagnosed with the disease, dementia impacts each and every family member for a very long time.

 

These same sons and daughters are the ones calling in late to work because there’s a crisis at home, leaving at lunch time to make sure their parent and the house is safe, and occasionally leaving work early to take Mom to the doctor or to run errands.  Nearly one-fifth of all workers are caregivers.  67% of working caregivers report that they miss work because of their caregiving responsibilities.  In fact, 27% of all unscheduled absences are due to family issues.  Twenty seven percent.

 

Multiply that 27% by the number of Baby Boomers hitting the prime ages of either caring for an aging parent with dementia, or being diagnosed with dementia themselves.  The Baby Boomers were born between 1946 and 1964, making them 62 to 44 years of age.  At 62, 10% will be diagnosed with dementia. 

 

Our workforces and their families are burdened and in need of relief.  The primary caregiver for a person with dementia is generally (but not always) a daughter, 45 to 55 years of age, whose siblings live seven hours apart.  One in four of you reading this has already been impacted by dementia in your families and close associations, yet our companies may offer little beyond a referral source. 

 

How can you and your business or business organization be a catalyst for relief?

 

 

It starts by identifying your colleagues, employees, friends, relatives, and neighbors who are fading under the heavy burden of caring for an aging parent with dementia.  Often, they won’t complain, but you can see it in their eyes and hear it in their voices when you simply ask, “How’s your family?”

 

Offer flexibility in work hours and workplaces to employees who demonstrate responsibility in accessing that option.

 

Implement a decision support service, run by a professional provider network, which tailors “just in time” solutions for individual employees and their families, including

  • Individualized relief plans for the employee, his/her family, and aging relative based upon a thorough assessment
  • Training for caregivers and supervisors
  • Consultation on stress relief and healthy stress management practices
  • Training and consultation in managing the crises and complexities of the disease issues
  • Organization of community-wide partners for relief
  • Education of those partners about the struggles of families facing Alzheimer’s and related dementias

 

Activate the responsible network 24 hours a day, 7 days a week.  Family crises do not usually happen at 2 pm on a Tuesday; they happen at 9 pm on Thursdays and 3 am on Saturdays and 11 pm on Sundays.  The network is of no service if it is unavailable when needed. 

 

And here’s the really important step – the culture of the workplace must support the services, benefits, and policies that are in place in order to be fully accessible to those in need.

 

Anyway you look at it, good people taking care of good people is good business.

Written by Ellen Dunnigan

CEO Alzheimer’s Care Group/Sollievo

www.alzcaregroup.com        www.mysollievo.com

 

Seeing Grandpa with Alzheimer’s

Monday, April 7th, 2008

Recently, my family had a small family reunion. We were able to spend a long weekend together in my dad’s hometown.  Both my grandparents on my dad’s side are still living, and I am very thankful for that.  However, my grandpa has Alzheimer’s.  He is still living at home, and my grandma still takes care of him.  

It was hard at times to be around him, because I know he doesn’t know me.  He looks at me in an odd way when I refer to him as “grandpa”.  It is interesting though that he will pick my youngest cousin out of a crowd and say, “Look there’s Elizabeth!”  Why is it that he can recognize her, but not even recognize his other grandchildren? Why is it that when he sees his great grandkids playing with toys that he seems to come to life and want to interact with them?  It is all very confusing, emotional and hard on everyone.  It is hard to see your dad try and interact with his dad and not get the response that he so desperately wants.  It is hard to watch your grandmother who has so lovingly stayed by her husband’s side for almost sixty years not be recognized by her own best friendas his wife.  BUT, the point is she stayed, and she continues to care for him. He follows her around like a puppy dog, and will do anything she tells him to do. She has him make the bed in the morning  and do things to help her around the house. She has kept his life active as much as she is able. She has kept meaningful tasks for him to do throughout the day. She has been able to keep him home all this time, and has kept him safe and secure.

That is what an educated caregiver can do. Keep their family member home just a little bit longer.  She has used the resources that my company provides. She has asked the questions and has searcded for the right answers.  I am sure she can get discouraged; actually I know she does, but she has been persistant in wanting to keep her husband to stay at home as long as possible. 

There are answers for those struggling with caregiving. There is relief.