With years of experience in pediatric oncology, our nurses will directly help you better understand the diagnosis and treatment options, connect you to the proper resources you need, and support you any time throughout your family’s entire DIPG/DMG journey.
Get support from nurses who understand DIPG/DMG and the journey families face.
Our dedicated DIPG/DMG navigators are here to help (available in the United States only). Some of the ways we can help include:
How the My DIPG Navigator program works
We know you are overwhelmed. We want to make it as simple as possible for you to get the help you need, when you need it, at any time throughout your DIPG/DMG journey.
Provide basic contact information so one of our navigators can connect with you.
One of our navigators will reach out to you to learn how we can help.
Your navigator will connect you to experts that specialize in DIPG/DMG, as well as other helpful resources.
Your navigator will help educate, connect, and support you throughout your family’s DIPG/DMG journey.
About DIPG (diffuse intrinsic pontine glioma) and DMG (diffuse midline glioma).
Regardless of your diagnosis, we want to help make sure you have all the information you need.
Learn the basic facts about DIPG/DMG tumors.
Expert advice on first steps after a DIPG/DMG diagnosis.
From diagnosis to treatment to managing side effects, we are here to help.
Many organizations want to help meet your needs, including financial, travel, and emotional support.
No family should ever have to find their own way through a DIPG/DMG diagnosis. We know because we have already taken the journey.
This navigation program stems from the vision of DIPG hero Jace Ward, who was passionate about ensuring all patients had quick access to the most current information about best practices and treatment options.