Welcome
The mission of Team Sam the Lion is to provide information and resources to those facing a DIPG/DMG diagnosis, to advocate on behalf of the DIPG/DMG community and to support and fund the medical professionals and researchers striving to find more effective treatments and ultimately a cure for DIPG/DMG.
We’ve made this oath to Sam and we are determined.
SUPPORT
A DIPG/DMG diagnosis is overwhelming. Available resources include a one-on-one nurse specialist to help navigate your DIPG treatment plan. Also, a team made up of the leading DIPG/DMG neuro oncologists in the country will review your case and recommend the best treatment options including clinical trials. Both are offered free of charge.
About DIPG
DIPG is a pediatric brain tumor that is highly aggressive and difficult to treat. It occurs in an area of the brainstem called the pons, which controls many of the body’s most vital functions such as breathing, blood pressure, and heart rate.
About Us
Team Sam the Lion is driven to bring increased awareness to the devastating impact that brain cancer has on our younger most vulnerable population and to support the research for better treatments and, one day, a cure for DIPG/DMG.
Family Resources
A diagnosis of DIPG can be devastating, but it is important to know that resources are available to help you and your family. Many foundations, started and run by parents of DIPG children, offer financial and family support. There are also Facebook groups and online support groups where you can connect with other families.
sAM’s Story
At the age of 19 our son and aspiring musician was diagnosed with DIPG (diffuse Intrinsic Pontine Glioma. Despite the tremendous efforts of his doctors, members of his medical team and Sam’s own courageous spirit he passed away nine months later from this very aggressive brain tumor.
Donate
You can help us make a difference by donating today.