Jenna Rossow's Fundraiser
We are walking to raise awareness and funds for Dup15q Alliance. Getting the word out about dup15q syndrome is a key piece of the Alliance’s mission.
Take a walk with us and support the Dup15q Alliance! If you can't make the walk, please consider a donation to the Dup15q Alliance.
We are no longer accepting donations on this campaign, but there are other ways for you to support us today!
Colleen Parsley
"We got you!Love, Colleen"
$50
Katie Adrian
"I am so proud of you and Ajax for all of the work you put in everyday! 🐞❤️"
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Emilia Worthey
"We love you and support you! 💜 Worthey Family"
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Bailee Mitchell
"Wish we could be there to walk with you. Jax is lucky to have you and your family that does so much for him 💕"
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Steve & Tessa Richards
I donated in support of this campaign.
$25
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Erin Scarcliff
I donated in support of this campaign.
$25
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Phillip Berryhill
"I choose to give because Jenna asked nicely."
$100
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JULIANNA PEARCE
"I LOVE YOU SO MUCH, AND ALL THAT YOU STAND FOR."
$100
A supporter of Jenna Rossow
I donated in support of this campaign.
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Alex Spengler
"Love ya Jenna and Jax, excited to crush this walk with you both!"
$100
A supporter of Jenna Rossow
"Thank you for explaining this diagnosis and what your life looks like with Jax. He is blessed by having you as his mom and willingness to find support"
$50
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Kimberly Conley
"Jenna, I love you and Jax. You are an amazing mother. Keep up the great work!"
$100
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Samantha Hilton
I donated in support of this campaign.
$25
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Jessica Dawson
"We love you, Jax!!"
$30
Click Here To Register for the 2022 Denver Believe Walk
My son, Jaxtyn, was diagnosed with Dup15q Syndrome around two years old when he wasn't meeting developmental milestones. This is a rare genetic syndrome, but with more genetic testing, more children are diagnosed every day.
Dup15q Syndrome is tied to many other secondary diagnoses as a result: Autism, Epilepsy, Cognitive Impairment, Apraxia, Sensory Processing Disorder, Cortical Visual Impairment and Hypotonia are just a few, which Jax deals with a few of these on a day-to-day basis. Visit dup15q.org for more information!
Gather your family and friends. Dress in blue (our signature color). Know that you're part of something bigger. By raising awareness we can help other families who may still be searching for answers. Any funds raised will go to Dup15q Alliance who empowers individuals living with dup15q syndrome and other related rare diseases to reach their full potential by advancing breakthrough research and life-changing therapeutic treatments, supporting families affected by dup15q, and promoting advocacy. .
If you can't make the walk, please consider a donation to the Dup15q Alliance.