Disneyland 1/2 Marathon – Sep 1

Cure CMD is participating in the Disneyland 1/2 Marathon on September 1, 2013
to raise awareness and funds to support CMD research.

John Lizares completes first 1/2 Marathon in 2011 to fund CMD research!

John Lizares completes first 1/2 Marathon in 2011 to fund CMD research!


Congenital Muscular Dystrophy has impacted each of our “Team Cure CMD” runners/walkers in a personal way. You can help them reach their goal by making a financial gift in their name or anonymously. Here’s how:

  1. Click on the donate button and donate in a team member’s name under Disneyland 1/2 Marathon.
  2. You can also send a check with the Cure CMD Team member’s name and the words Disneyland 1/2 Marathon to Cure CMD, PO Box 701, Olathe, Kansas, 66051.
  3. You may make a general donation, by using Donate button immediately below.

Cure CMD Team Lead: Dhyana Morris
Cure CMD Team Lead Email: dhyana13.1@gmail.com

For more information on the race, registration and pre-race dinner please contact Team Lead directly and provide Team Lead with your personal fundraising goal (minimum: $50). Cure CMD provides each team member with a Cure CMD dry wicking race T-shirt.

We would like to thank you for participating in a 2013 Cure CMD Team Event – your support drives CMD research to find treatments. Cure CMD continues to drive collaborative research funding, having funded over $1 million in the last 5 years together with several participating nonprofits, including LGMD2I Fund, Samantha J Brazzo Foundation, and Struggle Against Muscular Dystrophy. Dollars are raised go directly to fund annual research grants, scientific and medical conferences that are focused on congenital muscle disease and getting to clinical trials.

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Participants

Dhyana

Dhyana

Dhyana


I am running for everyone who has Congenital Muscular Dystrophy. Joe, Anne, and Maia have inspired me to help raise awareness for Cure CMD.



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  • Congenital Muscular Dystrophy

    A group of diseases causing muscle weakness at birth. Several defined genetic mutations cause muscles to break down faster than they can repair or grow. A child with CMD may have various neurological or physical impairments. Some children never gain the ability to walk, while others lose the ability as they grow older. Learn more...

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