Click here to watch Lucy's story:

My name is Megan and my family and I are determined to give our daughter, Lucy, the best possible quality of life. Lucy was born with a rare genetic disease called CTNNB1 Syndrome. This affects her ability to do almost everything. She may never walk, speak, or do any of the things you and I take for granted. But we have hope for change!

I am in connection with the CTNNB1 Foundation which is spearheading a groundbreaking cure for this disease. It is called Gene Therapy, and it could greatly impact Lucy's future.

For her first birthday, we want to raise $100,000 to give to the CTNNB1 Foundation so that Lucy, and others like her, may have the opportunity to receive this life-changing treatment.

Other children's Gene Therapy success stories:

https://www.youtube.com/watch?v=Z9bonhfufrM

https://www.youtube.com/watch?v=pmHlcOM_PBA

Please SHARE and donate if you can.

Thank you. From the bottom of our hearts,

Lucy's Tribe