Meet Ty & Paige

Our children, Ty and Paige live life every day affected by their GAMT diagnosis.  Even with treatment, their days are filled with challenges most people never face – hundreds of pills per day, daily trips to the nurse’s office at school, and having to stop what they’re doing three to four times per day to take medications that are less than perfect. Despite all of this, both Ty and Paige have generous hearts and inspire us with their willingness to help others.

A real treatment would be life-changing for Ty and Paige, enabling them to lead typical lives without the constant burden of their current medication regimen. This community has helped our family recognize that we are not alone, and gives us hope that one day there will be a cure.