Congenital Adrenal Hyperplasia

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2008 No Sweat Run for a Cure
May. 6th, 2008   12:10pm
Hi Everybody

The 2008 No-Sweat Run for a Cure has started.


It is so easy to participate this year with the online feature. I had "Team Brayden" set up within minutes and emails sent out to family shortly after.

CARES has been soo helpful to my family. This "run" is the least I can do to give a little back.

Have YOU signed up yet? :)

It cost me nothing but a few minutes of my time.

A cut and paste direct from the website is below for you to preview.
..................... .................. ................

No-Sweat Run for a Cure is an annual event that makes it easy to support the work of CARES Foundation. Last year, $89,000 was raised. These contributions were used to fund CAH research, provide educational materials to families diagnosed with CAH, and subsidize travel costs for financially needy families seeking specialized medical care. This year, we hope to raise over $150,000 to accomplish even more.
As Congenital Adrenal Hyperplasia (CAH) is a relatively rare genetic disorder, CARES Foundation relies on the generosity of individuals, corporations and foundations to help fund its efforts. Your contribution can help save lives.

Event Location:

Your favorite sofa or lounge chair

Event Schedule:

No-Sweat "Run" 5/1/2008 1:00 am - 10/3/2008 1:00 am
Fees:

Standard: No Fees
General Registration

Braydensmom




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