We always wanted to be parents. We both wanted babies as soon as we got married. We didn’t expect it to take 3 years, countless medical procedures, losses, and the gift of modern science to have one. But it did. Jack is our miracle.
Jack was born in August of 2017, perfectly healthy. When he was around 6 months old, we noticed he wasn’t meeting some milestones. Devin was worried but everyone, including doctors, told us he was just fine. He might be delayed but he would develop in his own time. We started Jack with physical therapy anyway and began working with a pediatric neurologist to determine the cause of his delays.
Everything changed on April 6, 2022. After years of therapy, evaluations, and testing we were told that Jack has an extremely rare genetic disorder called SPG50. The doctors told us that SPG50 is degenerative, both physically and mentally. The doctors explained that spasticity starts in children’s legs, slowly taking away their ability to walk. The spasticity then takes away their ability to use their hands, and ultimately, their mental capacity.
Our world stopped turning at that moment. The bottom fell out from beneath us. Hearing that for our sweet little boy was pain like we’ve never experienced before. Our hearts were broken.
On our darkest day, we were also given a ray of hope. Doctors told us that a father in Canada, Terry Pirovolakis, had spent 4 years working to develop a gene therapy to treat his son who also has SPG50. Just weeks prior, his little boy Michael had received the first dose.
It was incredibly hard to process, but in the midst of the devastation and fear and sadness, there was hope. We could save Jack.
And that’s why we started Jack’s Corner. We need your help to cure Jack and other children with SPG50.