Parent Project Muscular Dystrophy: Thanks! Together, we did it!

Dear Friend,

This has been a truly humbling holiday season. We are more awed than ever by you, the amazing Duchenne community.

When Ralph and Louise Haberfeld offered a $15,000 challenge match, we had no idea that Rick and Lelia Ginder would add $30,000 to it, and we never dreamed that Marty and Geri Karlin would add another $15,000. A $60,000 matching challenge was unprecedented for PPMD, and to be honest with you, we had some concerns that we wouldn't be able to take full advantage of this terrific opportunity, especially in light of today's economy.

What were we so worried about? You came through, like you always do. You not only met this challenge—you shattered it!

Your $115,829 in online donations plus the matches have given us a total of $175,829. We are floored by your generosity. You inspire us to keep fighting for every boy with Duchenne, so that they can live longer, healthier lives.

2009 was a difficult year for me personally, as most of you know. But 2010 shows great promise. My husband Tom reached the end of his treatment and is doing well. The Care Considerations document provides vital clarity and guidance about looking after our young men.

And recently, you've all stepped up like you've never stepped up before. Thanks to your votes, and because you encouraged your friends to vote, we received $25,000 in the Chase Community Giving Program on Facebook. We're now one of 100 organizations in the running for $1 million.

You really gave from the heart this holiday season to meet the challenge from the Haberfelds, Ginders, and Karlins. It's inspiring to watch you continually reach higher. You define the word community.

Again—and I can't say it enough—thank you from the bottom of my heart and from all of us at Parent Project Muscular Dystrophy. Here's to a wonderful 2010!

	Sincerely,
	Pat Furlong Founding President and CEO Parent Project Muscular Dystrophy

Our Mission: To improve the treatment, quality of life and long-term outlook for all individuals affected by Duchenne muscular dystrophy through research, education, advocacy and compassion.