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Kruz and Paizlee Davenport

Finding a cure for Schimke Immuno Osseus Dysplasia (SIOD)

Our Mission:

Jessica Davenport with daughter Paizlee

Our Purpose:

Providing a place of hope for SIOD families

Are you a parent looking for answers? A physician needing some more information? Find answers and the support you need.
We have created a special "Next Steps Guide" to help walk you through life with SIOD.
The Davenport family

Meet Our Founders

We are the Davenport family! As you can see, we have the two of the cutest kids on the planet with the sweetest personalities. Kruz & Paizlee rarely meet a stranger, but their life is different from others. On June 30th, 2016, our son was diagnosed with a rare genetic and “incurable” disease called, Schimke Immuno Osseous Dysplasia (SIOD).

From the time he was nine months old, we spent two years and went through at least ten specialists to help us put together the puzzle. Later, we genetically tested our daughter out of precaution since it’s a recessive mutation, even though she presented no clinical symptom at that time. On August 24th, 2016, we received a call explaining she also had SIOD. Our world turned upside down. Our children were the first siblings in the United States, making this a 1 in 80 million chance.

Meet Kruz and Paizlee

Kruz and Paizlee Davenport
Kruz Davenport
Kruz and Paizlee Davenport
Paizlee Davenport

Kruz was diagnosed with SIOD just days before his third birthday. He received an allogeneic stem cell transplant at Stanford by Dr. Alice Bertaina and had a kidney transplant in 2019.

Paizlee was a year and a half old when she was diagnosed with SIOD. She was only tested because her brother was diagnosed. Her diagnosis made she and her brother a 1 in 80 million chance and the first siblings in the United States.

Thank you to our partners and teams involved in the research to find a cure

Stanford Medicine
Lucille Packard Foundation for Children's Health
Lucille Packard Foundation for Children's Health
SIOD Research Lab
SIOD Research Lab
SIOD Research Lab

We provide life-saving research funding to allow children diagnosed with Schimke Immuno-osseous Dysplasia to have a treatment plan and a chance at a longer life. Dr. Lewis and his team have began unraveling the mystery of how SMARCAL1 protein deficiency leads to the clinical features of SIOD.

Accelerating new therapies and treatments for SIOD patients

Our Vision:

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