Reposted from an email I sent to my family and friends.
Hi everyone!
OMG, I've never set out to try to write an internet forward before, but I wanted to tell you all about an article that appeared in the LA Times today, Sunday, August 25th, 2002 on the front page, and I hope you'll want to share their story with others and help out. The headline was "Hard Choices in a Genetic Calamity" and it was written by Charles Ornstein. Its about three children, Ciara, Hunter, and Tommy Bennett, who have a rare genetic disorder, Sanfillipo Syndrome. The disease is slowly killing them and their insurance company, Kaiser, is refusing to pay for a cord blood transplant, which is the only treatment that might save them. Kaiser's comment about the situation was "If we are going to hold costs down...some people are going to die." This comment made me feel sick! The article then went on to say that there is something you and I can do.
Their family has set up a foundation, The Bennett Children Foundation, to try to fundraise the $1.4 million dollars needed to save their children. Please, please, please, go to http://www.helpachild.net and read their story. Then click on the "contribute" button on the top of the screen and send whatever you can. The contributions are through paypal, so you can use your credit card. All the donations are tax deductable. I gave them what I could afford, and I hope you will too, but if not, at least forward this email to everyone you know who might help out. This is a case where people really can make a difference, and every little bit counts.
-Kris (Nightingale)
nightingale8472@yahoo.com
Hi everyone!
OMG, I've never set out to try to write an internet forward before, but I wanted to tell you all about an article that appeared in the LA Times today, Sunday, August 25th, 2002 on the front page, and I hope you'll want to share their story with others and help out. The headline was "Hard Choices in a Genetic Calamity" and it was written by Charles Ornstein. Its about three children, Ciara, Hunter, and Tommy Bennett, who have a rare genetic disorder, Sanfillipo Syndrome. The disease is slowly killing them and their insurance company, Kaiser, is refusing to pay for a cord blood transplant, which is the only treatment that might save them. Kaiser's comment about the situation was "If we are going to hold costs down...some people are going to die." This comment made me feel sick! The article then went on to say that there is something you and I can do.
Their family has set up a foundation, The Bennett Children Foundation, to try to fundraise the $1.4 million dollars needed to save their children. Please, please, please, go to http://www.helpachild.net and read their story. Then click on the "contribute" button on the top of the screen and send whatever you can. The contributions are through paypal, so you can use your credit card. All the donations are tax deductable. I gave them what I could afford, and I hope you will too, but if not, at least forward this email to everyone you know who might help out. This is a case where people really can make a difference, and every little bit counts.
-Kris (Nightingale)
nightingale8472@yahoo.com