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/.