The Jessie Rees Foundation is dedicated to supporting children and families fighting Diffuse Intrinsic Pontine Glioma (DIPG) and other childhood cancers. Knowing the many additional struggles you may be facing while caring for your child fighting DIPG, our goal is to help to provide you with resources, information and support during this very difficult time.
Here are some things that you might find helpful at the Jessie Rees Foundation:
1) Request a JoyJar for your courageous fighter against DIPG. JoyJars are colorful and
inspirational jars filled with hospital-approved toys and games that are sent to children fighting cancer around the world (sent at no financial obligation to children fighting cancer).
2) Visit our NEGU Support Network to locate children’s hospitals, Ronald McDonald Houses and other organizations dedicated to serving children and families fighting cancer.
3) Request one of our special “I’m a NEGU Kid” t-shirts to help encourage your courageous fighter to Never Ever Give Up!
4) Visit our NEGU Kids website to find fun activities, games and printables for your courageous fighter.
5) Nominate your courageous fighter for our NEGU Kid of the week. Our NEGU kids are introduced to our facebook fans and are sent LOTS of messages of encouragement and love.
6) Meet Jessie, learn about her journey, her mission, her wish and her legacy.
Dear Parents,
I want you to know the Jessie Rees Foundation is here for YOU and your courageous child. Stacey 
and I know first-hand what it feels like to be told your child has cancer, search for treatments around the world, watch bills pile up, try to manage your other kids, keep your job going, pray for a miracle, try new foods, sit at chemo, wait for radiation to get over, attend MRI …the list goes on.
NO child or parent should have to go through what we have, but they do, so we HELP.
We hope the Jessie Rees Foundation and the NEGU Family Network can help you. Please visit us at www.families.negu.wpengine.com.
NEGU,
Erik & Stacey Rees