Help Jaxon go to the CdLS Conference!

Jaxon has a rare genetic disorder, Cornelia De Lange Syndrome (CdLS) that affects 1 in 20,000 people. You can learn about his syndrome at http://www.cdlsusa.org/

The CdLS Foundation hosts a national conference for all CdLS families every 2 years. The next conference will be June 2014 in Costa Mesa, CA. This will be Jaxons 1st year to attend. Please help us raise the money for him and his family to travel to California to meet other children like him.
  • Bryan brown 
    • $100 
    • 85 mos
  • Juana S. de Leon 
    • $20 
    • 86 mos
  • Anonymous 
    • $100 
    • 87 mos
  • Juana S. de Leon 
    • $20 
    • 87 mos
  • Torres Antonio 
    • $50 
    • 87 mos
See all

Organizer

Whitney Strickland 
Organizer
La Porte, TX
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