 To Donate go to www.connormoran.org Click on the button under Nevaeh's picture. Thank You!!!  Nevaeh needs to go to Philadelphia Children's Hospital to be evaluated and treated by specialists. She was born with a syndrome know as DiGeorge Syndrome. At 8 months old she had open heart surgery, she is now 2 and needs to see the specialists at Philadelphia Children's Hospital, they have her approved and ready to go but her Insurance company has denied this coverage and her parents need to pay $20,000 out of pocket to get her the treatment she needs. Help us send Nevaeh to Philly. Philadelphia Children's Hospital and Ronald McDonald House are taking care of the airfare and housing. We need to raise $20,000 to pay for the doctors, testing and labwork needed to give Nevaeh the treatment she needs. We can come together and donate $5 - $10 each and get her the treatment she needs to ensure she is able to live a normal and productive life. In a world where so many need help let's start with one baby from Tequesta Florida. Let's send Nevaeh to PHILLY!Check out the links below for further information: http://www.upstate.edu/uh/ent/vcf/ http://www.chop.edu/service/22q-and-you-center/about-chromosome-22q112-deletion/ There is no genetic cure for 22q11.2 deletion syndrome. Certain individual features are treatable using standard treatments. The key is to identify each of the associated features and manage each using the best available treatments. Wikipedia |
||||
