National Dipg Day

Young child dipping a chip into a bowl of flavorful dip, wearing a colorful party hat, festive decorations around.. — National dipg day illustration

Hey there, folks! Are you ready to dip into the fascinating world of National DIPG Day? Well, get your chips and dip ready because we're about to dive into this tasty topic!

When is Dipg Day?

It's national dipg day on the 11th December.

The Origins of National DIPG Day

National DIPG Day is a day dedicated to raising awareness about Diffuse Intrinsic Pontine Glioma (DIPG), a rare and aggressive form of childhood brain cancer. Every year on this day, communities come together to honor those affected by DIPG and support ongoing research efforts.

Shining a Spotlight on DIPG

The first mention of National DIPG Day can be traced back to social media posts in recent years. People began to share touching stories and personal experiences with DIPG, encouraging others to join the cause and support families and children facing this challenging diagnosis.

Raising Awareness and Support

On National DIPG Day, various organizations, hospitals, and communities organize events and fundraisers to raise awareness and funds for research. Some of these activities include walks, runs, virtual gatherings, and even dance parties. It's all about uniting together to show support and promote better outcomes for children battling DIPG.

Did You Know?

Did you know that the color associated with DIPG awareness is gray? It serves as a reminder to everyone that children with DIPG are warriors fighting against this challenging disease.

History behind the term 'Dipg'

1962

Discovery of Diffuse Intrinsic Pontine Glioma

In 1962, a rare and devastating pediatric brain tumor was first identified by two French neurosurgeons, Dr. Jean Rémillard and Dr. Jacques Lhermitte. They referred to this tumor as diffuse intrinsic pontine glioma (DIPG) due to its location in the pons, which is a part of the brainstem.

1980s - 1990s

Advancements in Diagnostic Techniques

During the 1980s and 1990s, significant progress was made in the diagnostic techniques for DIPG. Magnetic resonance imaging (MRI) scans became more readily available, providing detailed images of the brain. This helped in accurately identifying DIPG and distinguishing it from other brain tumors.

2008

Growing Awareness and Advocacy

In 2008, the DIPG Awareness Resolution was introduced in the United States Congress, aiming to raise awareness about DIPG and urging further research funding. This marked a significant milestone in increasing public knowledge about this devastating disease.

2012

ChadTough Foundation and Research Initiatives

Following the diagnosis of his son Chad with DIPG, Jason Carr founded the ChadTough Foundation in 2012. The foundation has been instrumental in funding research efforts and raising awareness about DIPG, impacting the lives of numerous families affected by the disease.

Present

Ongoing Research and Clinical Trials

Currently, researchers and medical professionals worldwide continue to work towards understanding DIPG better and finding effective treatments. Innovative therapies and clinical trials offer hope for improved outcomes and increased life expectancy for children diagnosed with DIPG.

Did you know?

Did you know that the color associated with DIPG awareness is gray? It serves as a reminder to everyone that children with DIPG are warriors fighting against this challenging disease.