Bryson was diagnosed at 8 months old with Acute Flaccid Myelitis (AFM), a rare neurological condition that shares similarities with polio in its physical effects. In 2018, the year of his diagnosis, there were only 238 cases reported in the United States.
AFM attacked Bryson’s spinal cord’s gray matter, initially paralyzing him from the neck down over a 24-hour period. Due to the rarity of the disease, there was limited research and no definitive treatment at the time—primarily, therapies and occasional Botox injections were used to manage symptoms.
On the 30th day in the hospital, a glimmer of hope appeared. Bryson moved a small red foam car with his hand, his first sign of regaining movement. Since then, through tireless effort from Bryson and his care team, Bryson has regained about 85% mobility, with hope for independent walking in the future.
Now, they face the next hurdle of total hip reconstruction in hopes of alleviating some pain and stiffness and assisting with his hip dysplasia and hopefully his walking.
Unfortunately, during this time, Andrew will have no income as he will have to provide 24/7 care for Bryson. Andrew is the sole provider for Bryson. He is expected to return to work, at best, in 6 weeks.
Any and all money will go directly to them to help with living expenses and medical bills.
