Hi! My name is Sarah and I'm a long-time follower of your blog but a first-time commenter. I'm a college student who works with special needs kids. I also follow more than 200 blogs, and I'm sending a very special message to all the blogs I follow: YOU have the chance to be part of a miracle!
If you are a member of Facebook or know someone who is, please take the chance to do something incredible!
Chase Community Giving is awarding $1 million to 5 charities! The Gwendolyn Strong Foundation is working to find a cure for Spinal Muscular Atrophy - and they could use the money!
Fast Facts: - SMA is the #1 genetic killer of infants under the age of 2 - 50% of those diagnosed will not live to see their 2nd birthday - kids with SMA lose the ability to sit, stand, walk, talk, eat, swallow, and breathe - 1 in 40 people is a carrier - the National Institute of Health says that SMA is the #1 CURABLE disease if given research funding - right now there is NO cure and NO treatment - right now SMA is a DEATH SENTENCE
Want to change that? Vote for the Gwendolyn Strong Foundation on the Chase Community Giving app on Facebook! You have five votes to tell the world that you want a CURE for SMA!
Tell your friends and blog contacts - let them know they could be part of a MIRACLE - be part of a CURE - and give these kids a FUTURE!
5 comments:
what a cute little sidekick you have. I miss him so much.
You're so good at seeing the little bits of magic in our lives! Thanks for pointing them out... they're instant happiness when you notice them.
k, April, I just have to say, He is SOOO cute!!!!!
Hi! My name is Sarah and I'm a long-time follower of your blog but a first-time commenter. I'm a college student who works with special needs kids. I also follow more than 200 blogs, and I'm sending a very special message to all the blogs I follow: YOU have the chance to be part of a miracle!
If you are a member of Facebook or know someone who is, please take the chance to do something incredible!
Chase Community Giving is awarding $1 million to 5 charities! The Gwendolyn Strong Foundation is working to find a cure for Spinal Muscular Atrophy - and they could use the money!
Fast Facts:
- SMA is the #1 genetic killer of infants under the age of 2
- 50% of those diagnosed will not live to see their 2nd birthday
- kids with SMA lose the ability to sit, stand, walk, talk, eat, swallow, and breathe
- 1 in 40 people is a carrier
- the National Institute of Health says that SMA is the #1 CURABLE disease if given research funding
- right now there is NO cure and NO treatment
- right now SMA is a DEATH SENTENCE
Want to change that? Vote for the Gwendolyn Strong Foundation on the Chase Community Giving app on Facebook! You have five votes to tell the world that you want a CURE for SMA!
Tell your friends and blog contacts - let them know they could be part of a MIRACLE - be part of a CURE - and give these kids a FUTURE!
Thank you!
We are surrounded by so much magic that we take for granted. It's a good thing that we have kids to remind us.
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