What is palliative care? Q&A with Dr. Lee Burnside

Lee Burnside, MD, MBA, is a geriatrician and palliative care physician in the Division of Geriatrics at the University of Washington. He works in palliative and hospice care and is a member of the UW Memory Brain and Wellness Center. He has had a longtime interest in caring for and improving the lives of persons with dementia and their family, friends and community. He has … Continue reading What is palliative care? Q&A with Dr. Lee Burnside

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

Alzheimer’s, dementia & the healing power of music

*Editor’s note, the 2020 Discovery Alzheimer’s Regional Conference has been rescheduled to June 25, 2020. Please see note below article.  Cheryl Hodge, BFA, is an author and award-winning performer. Her first professional gig was when she was 16 years old. She spent time touring the US and Europe, taught in the vocal department for eight years at Berklee College of Music in Boston and headed … Continue reading Alzheimer’s, dementia & the healing power of music

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

Taking care of each other: Mac & Kathryn

Mac and Kathryn are a couple based out of Spokane. Kathryn is living with dementia and Mac is her full-time caregiver. The following is the story of their journey together with dementia. Mac met his wife Kathryn in Seattle on Dec. 8, 2006. Kathryn answered a Craigslist ad Mac had placed, looking for friendship. The pair quickly became friends. “I found a great friend, and … Continue reading Taking care of each other: Mac & Kathryn