	Registration is $25 until 1/15 $35 (1/16 - 2/10) $40 (DAY OF REGISTRATION)
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ABOUT CUPID'S UNDIE RUN

Cupid's Undie Run is a 1.5 mile run in your bedroom-best on Valentine's weekend. No, we're not crazy, we're just crazy serious about raising money for The Children's Tumor Foundation.

Festivities start at noon on February 11, 2012 in six cities nationwide (DC, NYC, Atlanta, Seattle, Denver and Cincinnati), then we strip down for the Undie Run at 2pm, have our fun and come back for post-race festivities and awards. Registration is now open and is going to sell out quick, so act fast! (register here)

You can fundraise as an individual or join a team, and the prizes are better than ever this year! Custom undies, embroidered bathrobes, Kindles, romantic getaways... tons of cool stuff for doing your good deed and fundraising for such a great cause. With facebook and twitter, fundraising is easier than ever!

ALL Fundraisers will be entered for our
Prize Give Away! 2 GIANT VT Teddy Bears!

Help us make this amazing day worthwhile! Sign up and get started fundraising today. Your effort means a lot and February is just around the corner. Get ready to run for the kids... but let's just hope they aren't watching!

WHY ARE WE DOING THIS?

The Children's Tumor Foundation is the world's largest non-government organization dedicated to ending Neurofibromatosis (NF) through research. NF is a genetic disorder that causes tumors to grow on nerves throughout the body, causing blindness, deafness, learning disabilities and severe chronic pain. Currently, there is no cure for NF and there are frighteningly few treatment options. The Children's Tumor Foundation is a Charity Navigator 4-Star charity that prides itself on efficiency, spending 82.4% of its revenue on program expenses and less than 8% on administrative costs.

NF affects roughly 1:3,000 births in the U.S. and is in desperate need of new discovery, which is why 100% of funds raised through Cupid's Undie Run go directly to the Children's Tumor Foundation.

The Foundation's mission is to advance peer-reviewed research to develop treatments and cures for NF; support persons with NF and their families by making thorough and accurate information readily available; to assist in developing clinical centers and best practices to improve access to quality healthcare for those who live with NF; and expand public awareness of NF to improve diagnoses, increase understanding of the challenges that NF presents, and encourage support for NF research.