Before I forget.

Written by Trish Vradenburg and Special Guests

By 2020 Blog

June 7, 2017 - Virginia Biggar

This June 1, 2017 The Washington Post article by Marita Golden focuses on the shocking disproportionate impact of Alzheimer’s on communities of color, specifically African Americans. Older African Americans develop Alzheimer's at a higher rate than any other group of older Americans, and are about twice as likely as non-Hispanic whites to develop it or other forms of dementia.

May 4, 2017 - Marie Marley

Caregivers of people living with Alzheimer’s disease must make some extremely difficult decisions. One decision they may face is whether to place their loved one in a care facility of some type. Virtually no one wants to do it and few if any people want to go. This will be one of the most difficult, heart-wrenching decisions you, as an Alzheimer’s caregiver, will ever have to make.

April 18, 2017 - Jill Lesser

As many of you know, our beloved founder, Trish Vradenburg passed away yesterday. Our hearts are broken. In my grief, I wanted to reflect on her life and what she meant to me and to our community.

March 24, 2017 - Jason Resendez

The 2017 Aspen Summit on Inequality & Opportunity brought together a diverse mix of policymakers, thought leaders, social entrepreneurs, philanthropists, and practitioners to address the nation’s widening opportunity gap. Tucked between to-be-expected panels on manufacturing and hunger, was a 15 minute talk by Dr. Sarah Enos Watamura, Associate Professor of Psychology at the University of Denver and Director of the Child Health & Development Lab, on the biology of adversity.

March 15, 2017 - Haley Richman

My grandmother was diagnosed with Alzheimer’s disease when I was 4 years old. (I am now 9 years old).  I wanted to help care for her, so my mom gave me easy puzzles to solve with my Grandma. I felt like I was doing a good thing because when we worked on puzzles we were both very happy. As the years went by, I learned about different ways of helping my grandmother.

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Grandchildren
March 7, 2017 - Jason Resendez

There are over 15 million family caregivers providing care for a loved one living with Alzheimer’s disease or another form of dementia yet these stories are rarely found in the media, particularly the experiences of the black and brown folks that often struggle to access a diagnosis, treatment and care support. (Continue reading on Huffington Post)

February 28, 2017 - Jill Lesser and Stephanie Monroe

Two major advocacy campaigns are underway in February: Black History Month and Heart Health Month. While their connection to Alzheimer’s disease may not be obvious, each is vitally important. (Continue reading in Morning Consult.)

 

February 13, 2017 - Marie Marley

One night I was helping Ed, my Romanian life partner of 30 years, pay his bills. He’d been showing signs of dementia and always needed assistance with that task. Unfortunately, I put the stamp on an envelope a little askew. When Ed noticed, he lost it.

“Marie,” he hollered, putting his glass of vodka down forcefully and slamming his fist on the table. “Look what you did. It’s crooked. You r-r-ruined a perfectly good stamp!”

February 6, 2017 - Jill Lesser

In the United States, a change of administration always brings uncertainty. With new leaders entering Congress and the White House, we at WomenAgainstAlzheimer's (WA2) know we can turn that uncertainty into opportunity. Opportunity because we know finding a cure for Alzheimer’s and alleviating its burden on families can bring us together. WA2 is committed to continuing to lead a campaign to promote women’s brain health and fight against Alzheimer’s. 2017 is a critical year in our battle to stop Alzheimer’s in its tracks by 2020. 

January 27, 2017 - Michael Ellenbogen

As a person who is living with Alzheimer’s, I have very mixed feelings about how I should talk about it. I have become an outspoken advocate in the dementia arena, but I feel like I am always at odds with so many. And it is sometimes hard for me to decide what my message should be. Should it be about living life to the fullest or all doom and gloom about the horrible disease?

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