Blog · Complex Regional Pain Syndrome · CRPS · Invisible Illness · legacy · Life · Personal · Platform · Reflex Sympathetic Dystrophy · RSD · Truth To Power

Birthday Donations

Raising Money For a Cause I Care About:

On February 17, 2015 I was diagnosed with CRPS/RSD a rare and non-curable illness that has changed my life in so many ways. I have decided that instead of making my birthday all about me I want to make it all about finding a cure for this cruel and unpredictable illness. So please help me by donating money to RSDSA that can be found right here in my home state of Connecticut. Your donations will help more than you can ever fathom!

With Love,

Margaret Twitty

“Want to join me in supporting a good cause? I’m raising money for Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) and your contribution will make an impact, whether you donate $5 or $500. Every little bit helps. Thank you for your support. I’ve included information about Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) below.

The Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) was founded in 1984 to promote public and professional awareness of Complex Regional Pain Syndrome (CRPS), also known as Reflex Sympathetic Dystrophy (RSD).

Our mission is to provide support, education, and hope to everyone affected by the pain and disability of CRPS/RSD while we drive research to develop better treatments and a cure.

RSDSA is committed to encouraging research into the cause and cure of CRPS. Since 1992, RSDSA has funded $1,413,354 in fellowships and grants. During 2009-2010, we funded $168,376 in grants.

Please visit our website (http://www.rsds.org) for more information on RSDSA-funded research projects and our other initiatives.”

Contact Us:

RSDSA

99 Cherry St

P.O. Box 502

Milford, CT 06460

Tel: 203.877.3790

Toll Free: 877.662.7737

Fax: 203.882.8362

E-mail: info@rsds.org

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