6 Ways to Help a Dementia Caregiver Through COVID-19

For individuals and families facing dementia, the need to observe social distancing is critically important to their health and safety. But social distancing should not lead to social isolation. No one should face these uncertain times alone.  The Alzheimer’s Association Washington State Chapter is encouraging the community to lend a helping hand. Below are six things people can do to help dementia caregivers and their … Continue reading 6 Ways to Help a Dementia Caregiver Through COVID-19

COVID-19: Resources for You

Last updated: March 26, 2020 at 11:30 a.m. PDT Based on guidance from local public health agencies, our staff in Washington State and North Idaho are currently working remotely. During this time, the Alzheimer’s Association is available to you 24/7 for around-the-clock care and support: •  24/7 Helpline: Through this free service, specialists and masters-level clinicians offer confidential support and information to people living with … Continue reading COVID-19: Resources for You

2020 Alzheimer’s Disease Facts and Figures

The 2020 Alzheimer’s Disease Facts and Figures report was released March 11 and contains the most up-to-date data on Alzheimer’s prevalence and mortality, caregiving and the costs of health care for people living with the disease. Below are key takeaways from the report, including data for Washington State and Idaho. This year’s special report, “On the Front Lines: Primary Care Physicians and Alzheimer’s Care in … Continue reading 2020 Alzheimer’s Disease Facts and Figures

Janet Callahan: The Longest Day Coordinator

Janet Callahan lives in Edmonds, Wash. with her husband and son, “The Nicks,” (also known as Nick and son Nicholas) and their two chubby cats. In January 2020, Janet joined the Alzheimer’s Association Washington State Chapter as The Longest Day Coordinator. Janet came to the Alzheimer’s Association through “total serendipity.” While attending a Journey Dementia Family Caregiver Conference in November with her father, she happened … Continue reading Janet Callahan: The Longest Day Coordinator

Dementia Reimagined: Q&A with Tia Powell, MD

Tia Powell, MD holds the Trachtenberg chair in Bioethics at Albert Einstein College of Medicine, where she is Professor of Epidemiology and Psychiatry. She directs the Montefiore Einstein Center for Bioethics and the Certificate and Masters Programs in Bioethics. She is recognized for her bioethics scholarship related to dementia, LGBT issues, end-of-life care and health policy. Read her full bio here. You are an expert … Continue reading Dementia Reimagined: Q&A with Tia Powell, MD

My Advocacy Story: Todd Larson

By Todd Larson (Pictured above on the left) 1980 was a very memorable year for me. That year, I finally mustered the courage to ask out a work friend who would become my future wife, Sandy. I asked Sandy out in a way that she would talk about for years to come. It was just after my birthday. When Sandy asked me about my birthday, … Continue reading My Advocacy Story: Todd Larson

Year in Review: Impact Report FY19

The Alzheimer’s Association Washington State Chapter is pleased to present to you — our loyal supporters — the Impact Report for Fiscal Year 2019. We are grateful for the many ways your support enhances the lives of people in our community affected by Alzheimer’s disease and other dementias. Below are key highlights of all we accomplished together in the past year. Thank you again for … Continue reading Year in Review: Impact Report FY19

My Advocacy Story: Seema Abbasi, MD

By Seema Abassi, MD (speaking in photo above) My father was a retired air force officer. He was in excellent health until one day, when he was 80 years old, he suffered a heart attack and needed an emergency bypass surgery. The surgery was a success, but after his discharge from the hospital, we noticed significant memory changes and thence began his seven-year journey with … Continue reading My Advocacy Story: Seema Abbasi, MD

My Advocacy Story: Dee Anne De Angelo

Above: Dee Anne and her mother, Rose Dee Anne De Angelo is an Air Force veteran raising two teenagers in Wenatchee, WA. In addition to raising her kids, Dee Anne is the founder of a group that supports women veterans, and was the sole caregiver for her mother with Alzheimer’s disease who recently passed away. This is her Alzheimer’s advocacy story.  Dee Anne’s father was … Continue reading My Advocacy Story: Dee Anne De Angelo

Quarterly report: documenting my wife’s journey

By Bill Fulton (pictured above with his wife Deryn) Bill Fulton is a caregiver in Snohomish, WA for his wife Deryn (DJ) who was diagnosed with Alzheimer’s in 2015. Bill keeps a quarterly report of his wife’s journey with dementia to document her changes over time. “I’m afraid.” That was all she said. It was 2009, and we were skiing very steep and deep powder … Continue reading Quarterly report: documenting my wife’s journey