We can fund a full-time postdoc researcher, supporting ongoing Smith-Kingsmore syndrome research

1. This past January, Braxton was diagnosed with a rare disease called Smith-Kingsmore Syndrome. After years of neurologist and neurosurgeon appointments, we were relieved to get some answers to why Braxton has major developmental delays and medical issues. As we move forward with a future of so much unknown for our boy, we want to do whatever we can to ensure Braxton thrives and lives his best life, despite the challenges this syndrome brings. We are excited to partner with the SKS foundation to help fund research on this very rare disease.
2. Join me in supporting real change. Let’s support good in the world and make a difference. Help us accelerate personalized, precision treatments for people diagnosed with Smith-Kingsmore Syndrome

Just a small donation will go a long way to helping me meet my goal for Smith-Kingsmore Syndrome Foundation