.jpeg)
Lauren French's Fundraiser
Together We Drive Discovery
This August, help shape the future of Smith-Kingsmore Syndrome research
I’m fundraising in memory of my son, Mason, who lived with Smith-Kingsmore Syndrome (SKS), an ultra-rare genetic condition.
Mason was diagnosed at just eight months old. He faced more challenges in his four beautiful years than many will face in a lifetime, but those challenges never defined him. If you knew Mason, you remember his smile, his contagious laugh, his determination, and the joy he brought everywhere he went.
Mason should still be here. I can't change the outcome of his story, but I can make sure it isn't the end of his impact.
That's why I'm continuing to raise funds for SKS research. Families deserve more answers, better treatments, and more hope. Research is how we get there.
If Mason's story has ever touched your heart, please consider donating in his memory or sharing this fundraiser. Every donation and every share helps move our small but mighty community forward.
I can't change Mason's story, but together, we can help change the future for someone else.
Thank you for helping me continue his legacy!
For Mason. For Hope. For Every Family. 💜
