Russell Andrews revealed his ALS diagnosis during a CNN interview on May 16 alongside his fiancée Erica Tazel, confirming he was diagnosed in late 2025.
“I am a person living with ALS,” Andrews told Michaelson while seated beside Tazel, who CNN reported will be taking on the role of caregiver.
Andrews said initial concerns included a possible stroke, pinched nerves, and dropping cups and glasses, which led him to seek medical evaluation.
He also noted insurance loss during the strike period, followed by consultation with a primary care physician who recommended a neurological assessment within minutes, according to the Muscular Dystrophy Association.
Tazel said the early signs were subtle changes in walking and daily tasks, prompting concern before diagnosis. She said, “[There] was not a sigh of relief, but some understanding of what was happening,” adding her support for him.
The couple also referenced joining ALS Network, describing it as a supportive community assisting with care and awareness. Tazel said the experience reinforced her view of unconditional love while caring for him.
ALS destroys nerve cells in the brain and spinal cord, causing muscle weakness, slurred speech, and eventual paralysis, per Mayo Clinic. There is no cure for ALS, and the typical survival is 3–5 years, though some live decades.
Andrews described the diagnostic process as gradual, beginning with a medical referral from a primary care physician to a neurologist after early symptoms worsened over time, and culminating in confirmation in late 2025.
He said he and Tazel found support through the nonprofit ALS Network, which helped with care coordination, awareness, and access to ongoing treatment during his public announcement.
The interview marked their first joint public discussion of his condition and caregiving journey.