Former NFL running back Chris Johnson has revealed that he is living with amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative disease with no known cure. He shared the news during a televised interview on Good Morning America, where he spoke about the impact of the illness on his life and family.
Johnson, 40, said he was diagnosed in 2025 at age 39 after experiencing early symptoms that began with weakness in his right hand.
Early Symptoms and Diagnosis
According to Johnson, the first signs were subtle changes in strength and grip, which he initially did not consider serious.
He later underwent multiple medical tests before doctors confirmed he had ALS. Johnson said he was also informed that available medication might only slightly extend life expectancy, alongside guidance to prepare for the future.
His wife, Brittany, initially believed his symptoms were linked to physical strain from his NFL career, such as nerve-related issues, before the diagnosis was confirmed.
What ALS Means
ALS, also known as Lou Gehrig’s disease, is a condition that affects nerve cells in the brain and spinal cord, gradually reducing muscle control. Over time, it can impact movement, speech, swallowing, and breathing.
Johnson’s doctors described his condition as sporadic ALS, which occurs without a known family history and represents the majority of cases.
Amyotrophic Lateral Sclerosis (ALS) accounts for around 90% of all diagnosed cases, according to information referenced in the report.
Life After Diagnosis
Johnson shared that the disease has progressed rapidly over the past year. He now uses a speech-generating device controlled by eye movement to communicate.
Before losing his natural voice, recordings of his speech were made so the device could still sound like him.
He described how his physical abilities have changed significantly, including the loss of everyday movements he once took for granted.
Family Support and Personal Struggles
Johnson said his wife and four children have played a major role in helping him cope with the disease.
He emphasized that while ALS has changed his physical condition, it has not affected his identity or mindset.
Brittany Johnson spoke about the emotional impact on their family, especially the uncertainty surrounding their children’s future. She described the experience as deeply difficult but said the family remains hopeful for medical progress.
Treatment and Clinical Trial Participation
Johnson has been receiving standard ALS treatments aimed at slowing disease progression. He also participated in a clinical trial focused on reducing inflammation, alongside care from neurology specialists.
His medical team noted that he has been taking multiple therapies as part of ongoing efforts to manage symptoms and slow decline, though the disease has continued to progress.
Why He Shared His Story
Johnson said he chose to speak publicly about his diagnosis to raise awareness and potentially help others recognize symptoms earlier or support ongoing research into ALS treatments.
He added that despite the seriousness of the condition, he continues to focus on his family and the time he can still share with them.
Looking Ahead
While ALS currently has no cure, Johnson said he draws hope from ongoing research and clinical trials aimed at improving treatment options.
He described his mindset as one of persistence, saying he continues to fight the illness while supporting efforts that may one day lead to breakthroughs.
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