The Yellow Brick Road Project is a charitable foundation whose mission is to fund research to identify, understand, treat, and ultimately cure those impacted by HNRNPH2 mutations. We do this by funding initiatives to identify more individuals with HNRNPH2 mutations, connecting families impacted by HNRNPH2 in order to contribute to the understanding of the disorder, raising awareness of HNRNPH2 mutations in the general public and scientific communities, and by funding research into HNRNPH2 mutations.
"Learning that your child has a rare diagnosis is one the scariest things a parent can go through. Luckily for us, within 24 hours of getting this news we were connected with the YBRP. It was like meeting long lost family. We instantly had a tribe, and a voice, and hope." - Julee Armitage, Mom- Massachusetts, USA.
"My daughter Whitney was 17 before we got her HNRNPH2 diagnosis. Within one hour of getting the letter, we were in touch with the YBRP talking about shared experiences. It was such an emotional experience to find this wonderful group that has given us hope and so much support." - Jennifer Whiting, Mom- Florida, USA.
“The Yellow Brick Road Project is amazing, because it’s taken families from around the world and gotten them together, and for many of them this will be the first time they’re meeting each other face to face. And that experience just in terms of realizing that you’re part of something more than yourself and also being able to appreciate that someone else understands you is really profound…” - Dr. Wendy Chung
"Ainda me lembro do dia em que soubemos da existência de outras famílias HNRNPH2 e do YBRP... a sensação de encontrar pessoas que realmente nos entendem e conhecem a nossa menina quase como se ela fosse também a deles. Estávamos sozinhos e assustados e de repente sentimo-nos mais fortes e apoiados – a melhor sensação depois da tempestade e do sem fim de perguntas que nos dominavam. Saber da existência do YBRP e da sua missão deu-nos esperança. Soubemos desde aquele momento que não seríamos deixados de lado no nosso pequeno país ensolarado, afastados de todos os estudos e investigações possíveis. Somos Raros, mas somos abençoados e sentimo-nos orgulhosos porque podemos fazer parte deste incrível projeto. Não estamos mais sozinhos." - Andreia Lages Ramos, Mom-Portugal