Hannah Kate, was recently diagnosed with Ataxia Telangiectasia (A-T), a rare genetic disorder that affects the nervous and immune systems. It's been an overwhelming time as we navigate medical appointments, therapies, and changes in daily routines. Karen and I are devastated.

A-T causes coordination difficulties, frequent infections, and long-term health challenges. Currently there is no cure for this disease and it comes with a shortened life expectancy, higher risk for cancer, and many other challenges.

We have been very blessed not only with a great support system of friends and family but also financially as well. I am setting up this Go-Fund-Me to kick start the Hannah Kate Foundation. Our goal will be to raise awareness, fund various research projects, and hopefully find a cure for this disease.