I'm not sure if this post is allowed or not. I apologize if I've broken a group rule and/or offended anyone.
I just wanted to let everyone know that as one of my daughters (Serena who will turn 5 years old July 21) disabilities is Hydrocephalus. Currently there is no cure & the treatments used, such as shunts, have a lot of dangers & problems.
In September of this year will be the 6th annual Hydrocephalus Association's walk in St. Louis. Serena and I were able to attend the 2nd annual walk but subsequent years Serena was hospitalized. Last year we almost made it but the day before the walk ended up with bad pneumonia & was in hospital for 2 weeks. Also last year we managed to raise $315 to help funding for research of cures. This year we would like to try & triple what we raised. Serena & I have set a high goal to try to raise $1000 for research. If anyone would like to help us with our goal or join our team (even if just as a virtual walker or for encouragement) please visit:
https://www.kintera.org/faf/search/searchTeamPart.asp?ievent=1025931&lis=1&kntae1025931=788C49C76BE84FFFBACEF4A2FE55DA24&supId=361560861&team=5119170
There you can join Team Serena and/or make donations by credit/debit card. If you don't have credit/debit card but would like to make a donation by check/money order/cash or have questions than please feel free to email me at: smile512002@yahoo.com
Or you can call me at: (314)983-8211
Thank you all so much. And feel free to pass this information on to as many people as possible.
Thank you again.
Erin & Serena Bross
Sent via BlackBerry by AT&T
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