Julianna Sayler Foundation

Julianna Sayler Foundation Julianna Sayler Foundation, non-profit organization,
is dedicated to raising awareness, supporting f To read Julianna's story visit: www.teamjulianna.org

The Julianna Sayler Foundation, a non-profit organization,
is dedicated to raising awareness, supporting families and empowering researchers to cure Diffuse Intrinsic Pontine Glioma brain cancer.

07/28/2025

Shark attacks are all over the news at this time of year, but according to the University of Florida, the odds of being attacked by a shark are 1 in 3,748,067. While the odds of a child getting cancer are only 1 in 260, it looks like it's up to us to break the news that shark attacks AND research investment specifically for are REALLY more rare kids' cancers.

Our sweet girl was so proud to spread awareness for pediatric brain cancer. This picture was taken 6 months after her DI...
05/18/2025

Our sweet girl was so proud to spread awareness for pediatric brain cancer. This picture was taken 6 months after her DIPG diagnosis and in 3 short months to the day we would loose her. We miss her with every breath and know each new day brings us closer to finding a cure and being reunited!

May 17, 2017~ 6 months after 8 year old Julianna’s DIPG diagnosis.

03/20/2025
Amazing work by Julianna’s Dr. Vitanza and his team!
01/10/2025

Amazing work by Julianna’s Dr. Vitanza and his team!

Encouraging success from Seattle Children’s cancer doctor and researcher Nick Vitanza dosing CAR T cell therapy directly to brain for patients with DIPG.

♥️ Happy Thanksgiving!Memories are such a treasured gift and grow more precious each year ♥️
11/29/2024

♥️ Happy Thanksgiving!
Memories are such a treasured gift and grow more precious each year ♥️

Nov. 22, 2016, was the first day we heard 4 words that would change our lives forever and steal our precious daughter . ...
11/21/2024

Nov. 22, 2016, was the first day we heard 4 words that would change our lives forever and steal our precious daughter . . .
Diffuse Intrinsic Pontine Glioma.

D day never gets easier but it does mean we are one day closer to being together forever.

Julianna, the Sayler's middle daughter, was diagnosed with a rare form of pediatric brain cancer called DIPG at 8 years old. Her family traveled the world lo...

05/17/2024

We were given only 271 days or 6,490 hours from the moment of diagnosis to the moment we said good-bye💔Some families are...
05/02/2024

We were given only 271 days or 6,490 hours from the moment of diagnosis to the moment we said good-bye💔
Some families are blessed with more time, others less.

Just the thought that you can actually count the hours you had together after diagnosis tells you how aggressive this cancer is. Nine months is the average time a parent is given after a DIPG diagnosis but some families are only given days...

Until there is more attention given to this lethal cancer the time families have left together will not change.

Awareness - Support - Action
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Go Grey in May ~ Brain Cancer AwarenessNov. 21, 2016 changed our lives forever. Our family will forever have a "before" ...
05/02/2024

Go Grey in May ~ Brain Cancer Awareness
Nov. 21, 2016 changed our lives forever. Our family will forever have a "before" and "after" DIPG Brain Cancer in our family's timeline. Cancer affects the whole family. Help us spread awareness during Brain Cancer Awareness Month!

Address

PO Box 690, College Place
College Place, WA
99324

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