Strong like Téa ❤️ Fighting Alagille Together

Hi, my name is Michelle and I’m raising awareness and funds for Alagille Syndrome, a rare genetic condition that affects the liver, heart, and other parts of the body.

My daughter Téa was diagnosed at just 6 weeks old. Doctors discovered mild scarring on her liver, and at a very young age, she also suffered with painful xanthomas (skin lesions caused by her condition).

Despite the challenges, Téa is truly a fighter. Today, she’s thriving—she loves dancing, traveling, and embracing life with her fun, spunky personality. Her journey inspires us every day.

Because Alagille Syndrome is so rare, research and resources are limited. Your donation will help:

💛 Fund research for better treatments and a cure

💛 Support families facing this rare disease

💛 Spread awareness so more children like Téa can have brighter futures

No gift is too small—every dollar brings us closer to hope. If you’re unable to donate, please consider sharing Téa’s story to help spread awareness.

From the bottom of our hearts, thank you for supporting Téa and the Alagille community.

Love the Music Family