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Rare Virus Triggers Lethal Condition That Wiped Out Father's Muscles

Aug 26, 2026 •Wellness

Jared Maynard was in the best shape of his life. The father-of-three from Ontario, Canada, trained six times a week as a physical therapist and an avid bodybuilder. He worked hard, lifted heavy weights, and felt unstoppable. Then came January 2023. A bad cold hit him. He thought he could shrug it off easily. Instead, his skin turned yellow. His mind went fuzzy. Within days, he was fighting to stay alive.

Doctors rushed him to the hospital. Tests revealed a monster hiding in his system: hemophagocytic lymphohistiocytosis, or HLH. This rare condition makes the immune system turn on the body itself. It attacked his liver and kidneys until multi-organ failure set in. Forty percent of patients with this disease die. In Maynard's case, Epstein-Barr virus triggered it. That same virus can lie dormant for decades and usually causes mononucleosis.

He went onto life support. He moved to hospice care. Two months passed before he started recovering. His muscles had wasted away completely. It took another two months just to relearn how to walk, sit, stand, speak, and breathe on his own. Maynard thought the nightmare was over. But five months later, something else happened. His peripheral vision began to vanish.

'I thought being on end-of-life care would be the last battle I had to face,' the now 34-year-old said. 'But the next one I literally couldn't see coming.'

This is not his first fight with sight. As a teen, he suffered night blindness. His eyes struggled in the dark, especially when driving. At 17, doctors told him he could not legally drive anymore. He had choroideremia. This genetic disease affects one in 50,000 Americans, roughly 6,000 people, mostly men. It stems from a mutation in the CHM gene on the X chromosome. The retina and choroid begin to degenerate slowly. For most patients like Maynard, minor changes happen first before severe vision loss takes hold.

'It started off with night blindness,' he said. 'Then my peripheral vision was eaten away until only a narrow tunnel was left.'

Doctors believed his condition would not worsen until his 50s or 60s. They were wrong. The near-death struggle with HLH sped up the decline, likely due to inflammation and cellular stress. Now, Maynard knows central vision will vanish soon as well. At 33, he could no longer see his own computer screen. An eye doctor spoke the words he dreaded: 'You're legally blind.'

'I'm only 34,' he said. 'I survived the disease that was supposed to kill me, only to find out that while I cheated death, I was blindsided in the process.'

The impact on his community and future is heavy. He lost years of potential work time. His ability to drive ended long ago due to night blindness, and now daily tasks require new adaptations. The risk here is clear: surviving a fatal illness does not guarantee safety from other devastating outcomes. In fact, the trauma can accelerate existing genetic flaws.

'I thought I had time,' he said. 'But everything declined faster than anybody expected.'

Maynard adjusts to his vision loss every day. He hopes to return to competitive bodybuilding by year's end. That goal feels impossible right now, yet he keeps pushing forward. Everything he does runs on four words: you're not done yet. That isn't a promise that everything goes back to how it was. Some things don't.

There is no cure for choroideremia, and treatments like gene therapy designed to manage progression remain strictly experimental. Some scars stay, Maynard said. He recently bought a white cane to help him navigate daily life and warn others of his vision impairment, even though he is still getting used to it.

'I was so scared of the noise it made that I barely touched it to the ground,' he admitted. Then he tripped over a bench he could not see and fell hard in the middle of a packed airport. 'I wasn't just the blind guy anymore. I was the blind guy that face-planted in front of everyone. It was humiliating.'

Yet as he adapts, he refuses to let this break him. He keeps working and uses assistive technology like screen readers for his day-to-day tasks. He is also getting a guide dog. By the end of the year, Maynard hopes to return to competitive bodybuilding.

'Everything I do now runs on four words: you're not done yet,' he stated firmly. That isn't a promise that everything goes back to how it was. Some things don't. Some scars stay. But 'done' is only when you stop trying to become the person you want to be – and I'm nowhere near that.

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