GET INVOLVED AND DELIVER A MIRACLE
TO A CHILD IN NEED

Rhizomelic Chondrodysplasia Punctata (RCDP)

RCDP is a rare and lethal form of dwarfism affecting less than 100 children worldwide.
Join our fight in raising awareness and consider supporting a clinical trial that may help save their lives.

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A DIFFERENCE!

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A Little About JUDE
“Brave Little Warrior”

Jude Sullivan Peters has a very rare genetic disorder called Rhizomelic Chondrodysplasia Punctata (RCDP for short). He is one of less than 60 in the world. His chances for survival at birth were slim to none. His parents, Sully & Hannah Peters, have fought so hard for their baby boy, whom we affectionately call the “Brave Little Warrior.” He sees dozens of specialists, as well as occupational, physical, and speech therapists; he is defying odds every single day. Sully and Hannah travel to Delaware every few months for him to see his main medical team at Alfred I. duPont Hospital. His story is one of hope and faith in adversity. It has brought light and love to thousands of people all over the world! His facebook page is: www.facebook.com/prayingforjudesullivanpeters . He is now 2 years old, and, miraculously, we have been told there is new treatment that has the potential to save his life; but it lacks funding and national awareness. His mama has written a blog about Jude, and people from around the world follow his journey: https://hannahkatelynpeters.wordpress.com/.

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LATEST EVENTS View all »

  • 12 Nov 2016
  • 05:30PM

Black Tie Fundraiser

Nelson Manor, 15250 Hus McGinnis Rd., Huntersville, NC

Please come and help us raise support for Jude and his rhizo brothers and sisters! This event will be a…

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LATEST NEWS View all »

Baby Jude Turns 2!

Jude Peters was not expected to live past 2 weeks — but he celebrated his 2nd birthday on Sunday. Peters...
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