
Posted by Ann Napoletan | Filed under Advocacy and Awareness
20 Sunday Mar 2016

Posted by Ann Napoletan | Filed under Advocacy and Awareness
03 Thursday Mar 2016
Tags
alzheimers, Alzheimers advocacy, alzheimers semipostal, alzheimers stamp, help stamp out alzheimers
Calling all who loathe Alzheimer’s and want to see it stopped!!!
I received the email below this morning and felt compelled to share it. Please take two seconds to answer friend and super-advocate Lynda Everman‘s plea. She and Kathy Siggins have been lobbying for this for years and the time has come! We NEED an Alzheimer’s semipostal (fundraising) stamp… It’s easy to help – just click here and add your name. Let’s inundate the Postmaster General with an overwhelmingly powerful ask!! Thank you!! #HelpStampOutAlzheimers
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Friends –
As a caregiver for my late husband and an activist with UsAgainstAlzheimer’s, I know the toll Alzheimer’s takes on both patients and their loved ones, and the urgent need for a cure.
With enough funding for research, an end to this devastating disease is within reach. One untapped source of funding is the Postal Service’s semipostal stamp program, which allows consumers to pay a little bit extra to donate to important causes.
Earlier this month UsAgainstAlzheimer’s wrote to the Postmaster General urging her to establish a new semipostal program benefiting Alzheimer’s research, but now she needs to hear from YOU to ensure the Postal Service makes this a priority.
Add your voice: Join UsAgainstAlzheimer’s in calling for an Alzheimer’s semipostal stamp to fund the search for a cure!
Previous stamps have raised tens of millions for breast cancer research, and a new Alzheimer’s Awareness and Research stamp would be an incredible opportunity to raise awareness and support lifesaving Alzheimer’s research.
If each of us writes the Postmaster General, we can send a clear message that it’s time to create a semipostal stamp for Alzheimer’s to fund the search for a cure.
Thank you for adding your voice,
Lynda Everman
Please click below to ask the Postal Service to help fund the search for a cure with a new semipostal stamp and share the link widely on social media, encouraging friends to participate!
http://actions.usagainstalzheimers.org/p/dia/action3/common/public/?action_KEY=18465&okay=True
29 Monday Feb 2016
Posted in Advocacy and Awareness, Books, Caregivers, Guests, Helpful Resources, Inspiration
I’m very pleased to share the following guest post from Jean Lee, author of Alzheimer’s Daughter. In the words of Jean, “The more voices, the wider the reach of the choir.”
Caregivers. We are all caregivers. As humans we care for one another, or we should. Most especially, we care for those close to us.
But the logical timeline of maturation, love, and respect tipped topsy-turvy when my parents reached their eighties. They slowly began to lose their minds and act irrationally. I became concerned for their safety. I sought out medical treatment, and they were both diagnosed with Alzheimer’s disease on the same day.
Over the next decade I became the parent to my parents. I gradually, painfully made decisions they opposed in order to protect their well-being. In the process, I felt guilty taking everything away from the people who had given me everything.
As I struggled to keep the pieces of my life together––my marriage, my own family, my career and the care of my parents––I grasped for resources, but found few. I am a positive person, therefore I sought uplifting resources, but much of what I read was written with a negative undertone. I found books about the ill treatment of a caregiver by an unreasonable loved one, about adult siblings who fought, and about children who had grown up with angst toward a parent continuing through caregiving years. Even so, every time I found a kernel of truth, I felt as though I could keep going, someone else was brave enough to share this upside down world as well.
I came to the conclusion that sharing my story might help others.
Alzheimer’s Daughter details my journey caring for both parents who were diagnosed on the same day. It is written with wincing honesty about the cruel affects of the disease, but a WWII love story held together by faith and family is contained within the pages.
Over the past several months, four other authors from across the country and I have crossed paths, all of us affected in some way by Alzheimer’s disease/dementia.
The five of us have joined together to recognize those unsung heroes, caregivers. From each other we learned that all of us felt compelled to write our books, hoping to make a difference…hoping that we might make the pathway of others traveling this road a little less painful and lonely. Perhaps you will find comfort and support within our pages.
Somebody Stole My Iron by Vicki Tapia
Vicki details the daily challenges, turbulent emotions, and painful decisions involved in caring for her parents. Laced with humor and pathos, reviewers describe her book as “brave,” “honest,” “raw,” “unvarnished,” as well as a “must-read for every Alzheimer’s/dementia patient’s family.” Vicki wrote this story to offer hope to others, to reassure them that they’re not alone.
Blue Hydrangeas by Marianne Sciucco
Marianne describes herself as a writer who happens to be a nurse. This work of fiction is based upon her care for the elderly. It’s a tenderly told love story about Jack and Sara, owners of a New England bed and breakfast. Sara is stricken with Alzheimer’s and Jack becomes her caregiver.
What Flowers Remember by Shannon Wiersbitzky
Shannon writes this work of fiction through the eyes of a small-town preteen girl, Delia, whose elderly neighbor, Old Red Clancy is failing mentally. The aged gentleman has to be placed in a care facility, but Delia will not let him wither away. She devises a way for the whole community to remind Old Red how important he has been in all of their lives.
On Pluto: Inside the Mind of Alzheimer’s by Greg O’Brien
Diagnosed with early-onset Alzheimer’s, Greg O’Brien’s story isn’t about losing someone else to Alzheimer’s, it is about losing himself a sliver at a time while still fighting to live with Alzheimer’s, not die with it.
Jean Lee wrote lesson plans for 22 years as an elementary school teacher. She had no aspirations to write a book, however when both parents were diagnosed on the same day with Alzheimer’s, her journey as their caregiver poured out on paper through Alzheimer’s Daughter. After the sadness of her parents decline, life brought her a joyful topic–triplet grandchildren. She is currently working on a series of books for ages 9-12 entitled Lexi’s Triplets, written through the voice of the family mutt. You can follow Jean’s blog, Alzheimer’s Daughter, or catch up with her on Facebook or Twitter.