Isabella Santos Foundation

Description

• When she was just two years old, her parents learned that Isabella Santos had a rare pediatric cancer called Neuroblastoma. This terrible disease has a survival rate of just 40%. For five years adorable Isabella fought bravely, but on June 28th, 2012at just 7 years old, she surrendered. Isabella's parents did everything right, and yet, they ran out of options to save their little girl because pediatric cancer research is tragically unfunded. Isabellas parents established The Isabella Santos Foundation to honor their daughter and to carry on her mission of finding a cure for Neuroblastoma. Isabella had three wishes: Beat Cancer, Grow Hair, Live My Dreams. This disease cut her dreams short. With your help, we can fund the cure to ensure other children battling pediatric cancer have the time to realize their dreams.New drugs and therapies that can make dramatic advancements towards a cure are on the horizon. That cure did not arrive in time for Isabella, but our Foundation wants to help ensure other families do not have to endure this horrific loss. Nearly 80% of funds raised by The Isabella Santos Foundation support Neuroblastoma research, such as Memorial Sloan Kettering Cancer Center and Helen DeVos Childrens Hospital. We also support the Ronald McDonald House of Charlotte, the Make-A-Wish Foundation of Central and Western North Carolina, Levine Children's Hospital, and other local children's charities that benefited Isabella throughout her battle.Over the past several years, ISF has DONATED over 1 million dollars in Isabella's honor.
• 

  Headquarters:526 Briar Patch Ter , Waxhaw, North Carolina, United States

  More
• 

  Phone Number: +1 704-361-3074

• 

  Website: https://www.isabellasantosfoundation.com

• 

  Employees:21

• 

  Revenue:$10 - 50M

• 

  Legal Name:Isabella Santos Foundation

• Isabella Santos Foundation's Social Media

  
• Is this data correct?

• |  NAICS Code: 813319  |

  Show More