Meet Our Partners

NoahBRAVE is proud to partner with the following organizations to support families and fund research

Arms Wide Open Childhood Cancer Foundation’s mission is to fund less toxic therapies for children with cancer so they can have a better quality of life as they battle the disease and to give children battling cancer and their families hope during the most difficult days of their lives.


https://www.awoccf.org/ 

Ansley is a 7 year old goofy girl who loves to have the time of her life! On 5/12/20, her world got flipped upside down. She was diagnosed with a rare cancerous brain tumor called DIPG. This page is for updates and to create awareness for our baby girl!


https://www.facebook.com/ArmyforAnsley/

Diagnosed with DIPG in September of 2023, AJ Congdon remained sweet, affectionate, and funny throughout his entire illness. He’d love to show you silly dog videos, play a card game, or proudly tell you about his last touchdown at a football game. AJ’s energy and zest for life continue to inspire everyone who knew him.

In the fight for a DIPG/DMG cure, we help patients and families by funding game-changing research and providing navigation throughout their journey.

https://chadtough.org

On August 5, 2021, a month to the day after his baby sister Lucy was born, Eli was diagnosed with Diffuse Intrinsic Pontine Glioma (DIPG) and we were given the worst news any parent could ever receive. Our world was turned upside down and for the next year we focused every effort on our family and making memories together. Just after his 7th birthday, and a year after his diagnosis, Eli was taken from us by DIPG.


After brainstorming ideas to honor his memory, we decided one way to keep his fun-loving spirit alive is to help other families battling pediatric cancer! 


Join us by donating and/or fundraising to bring joy to kids battling cancer like Eli, the happiest, bravest boy!


https://www.classy.org/campaign/eli-the-brave/c462126

Our Mission:


To help families, create awareness, and fund research in the fight against DIPG Pediatric Brain Cancer while honoring our son, Grayson Lawrence Stumpf, Forever 12.


https://www.livegraysway.org/

The M Family Foundation is a non-profit organization that raises awareness for, and directly supports families battling ovarian and pediatric cancers in Florida.



https://mfamilyfoundation.org

Our Mission:


  • Honor & remember Maddie by sharing her legacy of kindness.
  • Pay it forward as a token of thanks to the amazing community that rallied behind us during Maddie's battle.
  • Create something magical because we believe that sometimes the most beautiful things can come from the darkest places.


https://www.magicformaddie.com/

In honor of Mikey Goodwin


Son, Brother, Friend, Athlete.... Mikey was taken too young by Diffuse Intrinsic Pontine Glioma (DIPG) a deadly brain cancer with no cure.


We raise money to fund research, provide assistance to warriors battling this deadly cancer and to CRUSH DIPG.


https://www.instagram.com/mikeystrongfoundation/

Experienced nurses are here to personally help families make informed decisions and do what is best for their loved ones.


Designed by families who have faced a DIPG/DMG diagnosis, this is the unique FREE resource they wish had existed during their own fight.


Serving DIPG/DMG patients being treated in the United States.


https://chadtough.org/my-dipg-navigator/


The SantiagoStrong Foundation is a non-profit organization dedicated to support families and their children in the fight against Diffuse Intrinsic Pontine Glioma (DIPG). Our goal is to spread awareness and raise funds to provide assistance to those currently battling DIPG. 


Through fundraising events and through the community's support, the SantiagoStrong Foundation will be able to achieve its goal. No family should have to go through this alone



https://www.santiagostrong.org/

Our Mission is to fund cutting edge research and clinical trials that will lead to a cure for DIPG/DMG, while also advocating for those children battling and their families. We want to see these children fulfill their potential and dreams so that the statement, “When I’m Better” is a reality.


We envision a world where a child battling DIPG/DMG can enjoy their life, fulfill their potential and bring their dreams to fruition when they state, “When I’m Better, I am going to….”


https://whenimbetter.org/


Sunnie Strong

SunnieStrong is a 5013c non-profit foundation that focuses on providing grief support to families that have lost a child to pediatric brain cancer. SunnieStrong will also continue to provide financial support to DIPG research so that one day a cure can be found. 


https://sunniestrong.org


Neev Kolte and Brave Ronil

We support kids impacted by DIPG/DMG pediatric brain cancer. Our mission includes helping sponsor novel cutting-edge research, and clinical trials anywhere in the USA, advocacy at all levels of government, raising childhood cancer awareness in the community, access to care, data use, and integration. Assisting patients and those who provide services to patients or their family members in California.


https://neevronil.org


Forever Sarah Foundation

Our mission is to raise funds for research and provide families with support and resources while facing pediatric brain cancer.

https://foreversarah.org


Memories and Magical Moments

At Memories and Magical Moments, we believe in creating cherished memories for children with DIPG and their families. We provide unforgettable Disney experiences, assist with travel and medical expenses, and offer emotional support to help lighten their burdens during this difficult journey.

https://memoriesandmagicalmoments.org



The Ayla Foundation

Our mission is to raise awareness and fund cutting-edge clinical research for pediatric brain cancer; focusing on cancer’s biggest bully, DIPG.

https://www.aylasarmy.com




En Pointe for Ava

Our goal at En Pointe for Ava is to provide advocacy and financial support for children with life-threatening brain cancer who need to travel for treatment. Obstacles to treatment, like travel expenses and housing, shouldn't be a concern for families when the only thing parents should be worrying about is loving and caring for their child.

https://enpointeforava.org




Mary Strong and Marc Jr Foundation

The mission of The Marc Jr Foundation is


  • To fund research toward finding a cure for DIPG.
  • To offer educational and financial assistance to families facing a DIPG.
  • To build awareness today for tomorrow’s cure.


We are a largely volunteer based organization that helps families and hospitals around the country and because of the unique services offered by the Marc Jr Foundation, services we can offer from other foundations due to our unique partnerships with them, and our commitment to the DIPG community, our services are becoming more in demand each day. We are hoping, with your help, to continue these services for families who so desperately need them.


https://marcjr.org

Emily's Light

We’re here to support other young adults, who, like Emily, have been diagnosed with terminal brain cancer. Generally, we support adults between the ages of 18-35, but we assess gifts on a case-by-case basis—which means you may be eligible for a gift even if you don’t meet these exact criteria.

https://www.emilyslightfoundation.org