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NJ Marathon Festival at the Shore 2012

Turner Syndrome Foundation  is an Official Charity and Beneficiary of

the NJ Marathon Festival at the Shore on May 5 - 6, 2012.

Join the Turner Syndrome Foundation, Inc. in our mission to raise funds and awareness of TS by participating in one of our events or simply by making a donation.  TEAM TSF registrants will need to meet fundraising minimums, and TSF will pay your entry fee! You will receive a TEAM TSF t-shirt, wristband, and invitation to a pasta party the night before.

  • Full Marathon (26.2 miles)    $500 commitment
  • Half Marathon (13.1 miles )  $350 commitment
  • Half Marathon Relay (leg distance TBD) $350 commitment per person for a two member team
  • Saturday events $25 commitment

Let's get you started:

  1. Chose event and complete marathon registration form one per person. Full  Half  Half Relay  Saturday ** Register once online. Print the forms for ALL of the events you would like to participate. Complete forms and fax to 1-800-594-3862.
  2. Create your fundraising page for this event. Click here
  3. Email link of your personal fundraising page to everyone you know.
  4. Begin training.
  5. Like us on Facebook.
  6. Shop for Team TSF gear shop

Email a coach at to answer all of your training & fundraising questions.  

Need help registering? Contact TSF directly at 800-594-4585.

Go to NJ official website for any other details, but remember to support TSF, you must register with TSF.


Please note, your personal page will be public information, protected by your username and password created at the time of registry.  TSF has the right to remove any images, links or information deemed inappropriate to the mission of the foundation.  Guests under 18 must have parental consent prior to utilizing My Personal Page.  All users assume their own risks.

The opinions, interests, and activities expressed on this page are strictly those of the page author. Individuals who maintain personal pages assume responsibility and liability for the content of their documents. The contents of this page have not been reviewed or approved by Turner Syndrome Foundation.

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