Julia’s family feels the same way we
do!
Julia was born just a few weeks after
our daughter, Tillery. At the age of 2 ½, she was diagnosed with a DIPG (diffuse
intrinsic pontine glioma) brain tumor. Julia’s tumor was aggressive and she
only lived a few months after diagnosis, which is common with DIPG tumors.
Julia’s family
created the Julia Barbara Foundation in her honor to raise awareness of brain
tumor signs and symptoms and to raise funding for DIPG research. A big
initiative they have taken on is creating a National DIPG Awareness Day. Julia
passed away on May 17, 2016 and there are 2 other DIPG kiddos who have passed
away on that same date. The families are working together to make this a
national day of awareness.
In addition to
raising awareness, Julia’s family is working with other DIPG families on a bill
to ask for more medical research consideration be given to pediatric high-risk
cancers, the ones with little hope at diagnosis. Julia’s family would love for
you to reach out to your US Representative to co-sponsor H.Res.69, the DIPG Resolution. If you
are willing to help, send us your email address and we will send you a letter
that you can send on to your representative.
The Julia Barbara Foundation is holding
a 5k this weekend in Knoxville. For more information, visit https://runsignup.com/Race/TN/Knoxville/ZombiesLikeBrains8kandZombieWalkforDIPGAwareness.
#JuliaBarbaraFoundation #tilleryisloved
#TILfoundation #alexsmillionmile #GoGold2017
To support childhood cancer research in honor of
kids like Julia, make a donation to our team (TIL Foundation) with Alex’s
Lemonade Stand Foundation. https://www.alexslemonade.org/mypage/1314958
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