From the category archives:

Alzheimer’s Care West Palm Beach

By: Kerry L. Luksic

” Count your blessings.” “It could always be worse.” These were a few of my mom’s auto-replies in dealing with all complaints while I was growing up. For my mother, Bobbie Lonergan, seeing the bright side of life was part of who she was and she made a point to instill her core value of positive thinking in me and my 12 siblings. As a mother of 13 children, she knew that whining and complaining didn’t solve anything. In our home, she focused on teaching us to be strong, to fix our own problems, and to take charge of life with a “glass-half-full” attitude. Mom lived this way into her early 70′s, bringing her positive energy to everyone she touched, until everything changed. She was diagnosed with Alzheimer’s disease.
My mother isn’t alone. Today, she shares company with 5.4 million other Americans. With projections of 16 million affected in 2030 and 30 million by 2050, the Alzheimer’s epidemic is poised to explode. But Alzheimer’s doesn’t just impact the individual; it’s a family disease, with 15 million people caring for a loved one with this illness. While these numbers grab your attention, they don’t convey the emotional heartache of the disease. Here’s just one of the millions of emotional Alzheimer’s stories. Mine.
Seven years ago I was living life in a hormone-fueled, emotional roller coaster. Pregnant with my third child and trying to accept my mother’s diagnosis with Alzheimer’s, left me feeling like I was constantly on the verge of tears. As her daughter, it was hard to witness Mom’s everyday struggles-trying to find the right word to complete her sentence, find her purse, or recall if she ate breakfast. with Alzheimer’s, our roles as mother and daughter were reversing. But it was difficult to know where to intervene as she clung to her fading independence.
When I gave birth to my daughter, Morgan, in May 2005, Mom came to the hospital and her eyes glistened with tears as I placed her 31st grandchild in her arms. “Hello, sweet angel, I’m your Grandma,” she whispered as she tenderly kissed Morgan on her forehead.

Time stood still. Mom was engrossed with every delicate feature if my newborn as if she had fallen in love for the first time. Staring at my mother, I couldn’t help but think of the circle of life. My daughter was just beginning her life, one which she would build memories, while my mother’s memories were slowly disappearing. Yet at this moment, I also realized Alzheimer’s had stolen many pieces of Mom, but it hadn’t claimed the one thing that defined her-maternal love.
It has been a long road since Mom’s diagnosis. She has steadily progressed to advanced-stage Alzheimer’s in which she requires 24/7 care. But through this journey, I learned to channel Mom’s positive energy and join the fight against Alzheimer’s. All I needed to do was follow her lifelong example. As I grew up, Mom was an advocate for the poor, the hungry, and the unborn. For nearly thirty years, she took action in all of her personal causes.
Today I advocate for my mother, for the millions living with Alzheimer’s disease and their families. The projected economic burden of Alzheimer’s disease on our country is a ticking time bomb that needs to be disarmed. The time for action is now! Alzheimer’s and other dementias currently cost Americans $200 billion. By 2050, the out-of-pocket costs to families will grow more than 400 percent and overall spending will reach $1 trillion. But nothing can quantify the emotional impact. There isn’t a dollar value to measure what it’s like when your loved one no longer knows you name.
With the progressions of my mother’s illness, pieces of her continue to fade away, but those missing pieces live on in me and my siblings. Mom’s wisdom, love and core values are deeply rooted within us and will be passed down to our children. No matter what lies ahead, Mom will remain forever as the loving heart and soul of our entire family. Alzheimer’s cannot take that away, the circle of life continues.
Kerry Luksic is a writer and Alzheimer’s advocate. She is the author of the recently published memoir,
Life Lessons from a Baker’s Dozen: 1 Mother, 13 Children and their Journey to Peace with Alzheimer’s.

Visit www.KerryLuksic.com

{ 0 comments }

Obama administration presents national plan to fight Alzheimer’s disease

HHS Secretary Sebelius outlines research funding, tools for health care providers, awareness campaign and new website

Health and Human Services Secretary Kathleen Sebelius today released an ambitious national plan to fight Alzheimer’s disease. The plan was called for in the National Alzheimer’s Project Act (NAPA), which President Obama signed into law in January 2011. The National Plan to Address Alzheimer’s Disease sets forth five goals, including the development of effective prevention and treatment approaches for Alzheimer’s disease and related dementias by 2025.

In February 2012, the administration announced that it would take immediate action to implement parts of the plan, including making additional funding available in fiscal year 2012 to support research, provider education and public awareness. Today, the Secretary announced additional specific actions, including the funding of two major clinical trials, jumpstarted by the National Institutes of Health’s (NIH) infusion of additional FY 2012 funds directed at Alzheimer’s disease; the development of new high-quality, up-to-date training and information for our nation’s clinicians; and a new public education campaign and website to help families and caregivers find the services and support they need.

To help accelerate this urgent work, the President’s proposed FY 2013 budget provides a $100 million increase for efforts to combat Alzheimer’s disease. These funds will support additional research ($80 million), improve public awareness of the disease ($4.2 million), support provider education programs ($4.0 million), invest in caregiver support ($10.5 million), and improve data collection ($1.3 million).

“These actions are the cornerstones of an historic effort to fight Alzheimer’s disease,” Secretary Sebelius said. “This is a national plan—not a federal one, because reducing the burden of Alzheimer’s will require the active engagement of both the public and private sectors.”

The plan, presented today at the Alzheimer’s Research Summit 2012: Path to Treatment and Prevention, was developed with input from experts in aging and Alzheimer’s disease issues and calls for a comprehensive, collaborative approach across federal, state, private and non-profit organizations. More than 3,600 people or organizations submitted comments on the draft plan.

As many as 5.1 million Americans have Alzheimer’s disease and that number is likely to double in the coming years. At the same time, millions of American families struggle with the physical, emotional and financial costs of caring for a loved one with Alzheimer’s disease.

The initiatives announced today include:

    • Research – The funding of new research projects by the NIH will focus on key areas in which emerging technologies and new approaches in clinical testing now allow for a more comprehensive assessment of the disease. This research holds considerable promise for developing new and targeted approaches to prevention and treatment. Specifically, two major clinical trials are being funded. One is a $7.9 million effort to test an insulin nasal spray for treating Alzheimer’s disease. A second study, toward which NIH is contributing $16 million, is the first prevention trial in people at the highest risk for the disease.
    • Tools for Clinicians – The Health Resources and Services Administration has awarded $2 million in funding through its geriatric education centers to provide high-quality training for doctors, nurses, and other health care providers on recognizing the signs and symptoms of Alzheimer’s disease and how to manage the disease.
    • Easier access to information to support caregivers–HHS’ new website, www.alzheimers.gov, offers resources and support to those facing Alzheimer’s disease and their friends and family. The site is a gateway to reliable, comprehensive information from federal, state, and private organizations on a range of topics. Visitors to the site will find plain language information and tools to identify local resources that can help with the challenges of daily living, emotional needs, and financial issues related to dementia. Video interviews with real family caregivers explain why information is key to successful caregiving, in their own words.
    • Awareness campaign – The first new television advertisement encouraging caregivers to seek information at the new website was debuted. This media campaign will be launched this summer, reaching family members and patients in need of information on Alzheimer’s disease.

 

Today’s announcement demonstrates the Obama administration’s continued commitment to taking action in the fight against Alzheimer’s disease.

In 2013, the National Family Caregiver Support Program will continue to provide essential services to family caregivers, including those helping loved ones with Alzheimer’s disease. This program will enable family caregivers to receive essential respite services, providing them a short break from caregiving duties, along with other essential services, such as counseling, education and support groups.

For more information on the national plan to address Alzheimer’s disease, visit: www.alzheimers.gov.

{ 0 comments }