After her husband Kris was diagnosed with Alzheimer’s, Catherine realized their future would be uncertain and unplanned. She has learned to embrace small steps and present moments, finding “windows” of light through support groups, resources like the Alzheimer’s Association, and even bi-monthly trips for treatment that bring unexpected joy.

Valerie Bill had both a mother and a mother-in-law who had dementia. Now at Fallon Tribal Health Center, she educates Northern Nevada Native communities about dementia, promoting early detection, healthy habits, and open conversations to reduce stigma.

When Bob was diagnosed with vascular dementia during the pandemic, he and his wife Amy moved to the Bay Area to be near family. Amy joined an Alzheimer’s Association® support group that has guided her through caregiving. Here, she shares how Bob’s diagnosis has changed their holiday celebrations, especially their wedding anniversary.

Before Alzheimer’s, Robyn was a natural leader and communicator. Her introverted, autistic husband Alan shares how her illness reversed their roles—and how he learned to read emotions and use unconventional tools to care for her.

After being diagnosed with Alzheimer's, Dennis found he qualified for Lecanemab. Dennis shares how he travels to Sacramento for treatment. His hope is that the funds he raises for Walk to End Alzheimer’s will help find a cure.

Tara Blessinger, a death doula, helps families navigate end-of-life care. Inspired by personal loss and her own risk of developing Alzheimer’s, she became a sponsor for Walk to End Alzheimer’s – Northern Nevada. Her message: share, feel, heal.