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I'm Off to Jail! MDA Camp 2012 - PLEASE HELP!!!


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For the 3rd consecutive year, we are helping send kids who live with Muscular Dystrophy to Summer Camp! These kids are incredible, and are born with a disease that not only limits their life, but gradually diminishes their ability to walk.


Last year's camp, together with our match of your generosity, we donated $3,200, and sent 4 kids to MDA Camp!


(Our members donated $1,600, and Adam's and our team members matched that donation. Expenses are $800 per child for the camp that changes the life of each and every kid, FOREVER!)


We are doing the same this year, only this year, we increased our goal from $1,600 to $2,000. If we make our goal, we will send 5 kids to camp for $4,000!!


Imagine being a kid, and as you grow up, instead of becoming more capable, you become less...and less....and eventually need a wheel chair to get around. This tugs at my heart, and we are blessed to help these young people for a 3rd straight year.


Here is a video about the Summer Camp 2011:


[ame=http://www.youtube.com/watch?v=wa7qqiJxiMQ]2011 Muscular Dystrophy Video - YouTube[/ame]



If your heart is called to donate, we are matching every dollar donated 100%. Even $5 helps, and adds up! Your $10 means $20 goes to help one of these great kids!


DONATE HERE:Muscular Dystrophy Association: 2012 Boulder Lock Up


More on the MDA is available on their website: Welcome to MDA | Muscular Dystrophy Association


Thank you for your donation, and again, every $1 you donate is a $2 donation with our match.








MDA is the nonprofit health agency dedicated to curing muscular dystrophy, ALS and related diseases by funding worldwide research. The Association also provides comprehensive health care and support services, advocacy and education.


MDA combats neuromuscular diseases through programs of worldwide research, comprehensive medical and support services, and far-reaching professional and public health education. With national headquarters in Tucson, MDA has more than 200 offices across the country, sponsors some 200 hospital-affiliated clinics and supports more than 330 research projects around the world.


MDA supports more research on neuromuscular diseases than any other private-sector organization in the world. MDA scientists are in the forefront of gene therapy research and have uncovered the genetic defects responsible for several forms of muscular dystrophy, Charcot-Marie-Tooth disease, a form of amyotrophic lateral sclerosis (ALS, or Lou Gehrig's disease), childhood spinal muscular atrophy and several other neuromuscular conditions.


The Association's comprehensive services program includes diagnostic and follow-up medical consultations, flu shots, support groups, MDA summer camps for youngsters, a medical equipment program, assistance with equipment repairs and resource referral.

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Thank you very much! We are ahead of schedule big time this year, and I bet we exceed the goal, and help these deserving, kind, and challenged young people with Muscular Dystrophy more than ever in 2012! :rockon:

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Remember: your donations are TAX DEDUCTABLE!! And think of the kids you'll help. If you have healthy happy kids, grandkids, brothers, sisters, nieces or nephews, then take a look at what these kids with MD are facing. Open your hearts and GIVE!

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