Today 5/17 is DIPG AWARENESS DAY. These children watch their friends thrive and do the things that they SHOULD be doing. I ask of nothing more than for you to just share the information about DIPG awareness. Did you know only 4 percent of all federal cancer research funding goes towards pediatric cancer? Why are children only getting 4 percent of funding?

DIPG is not genetic! It isn’t a disease that runs in families, nor is it something that can be tested in utero or at birth. It could happen to any child at any time. By the time you start to see symptoms, it’s often too late. It’s a monster and Mia, along with countless other children didn’t deserve to die so young before reaching the many milestones they deserve in life. DIPG can’t be cured with diet, or some magic mouthwash, or by changing your home cleaning products. It can’t be cured with supplements or eating salmon until it comes out of your ears. There are things that can help with symptoms like THC and CBD, but it isn’t a cure.

Our only wish in this life is that were able to live long enough to see this monster become a thing of the past. Let’s honor these children and spread awareness. They deserve it! We will miss our Mia forever and will hold you close until we see you again. We Love U MORE!!!!!!

For more information regarding DIPG, please visit our website. Or submit your information via our contact form, and our team will reach out to assist with your needs.