less than
0
kids are living with rcdp

just
0
of you can make a difference


Fighting for an RCDP cure,
…because these children can’t wait.

With your donation, you can change the tomorrow of a child with RCDP. Giving is as simple as one dollar, one day, one moment.

Donate today

We'd love for you to meet our kids.

Miracles in Action

Will You Help?

We are grateful for our supporters, who through their donations make it possible to continue our mission of finding a cure for RCDP. Donations support RCDP research programs, and a yearly conference where families learn about RCDP and discover ways to improve the quality of life for their child. Without our supporters, these things would not be possible

Hope for Rhizo Kids

What an amazing video and story by The New York Times!



Have More Questions?


There are great families waiting to help you find the answers.

You are not alone!


Ask them here

Find out more

A Parent Friendly Description.

A Parent Friendly Description.

Written by Mary Ellis, mom to Ian Ellis and founder of Rhizokids International.

This is an explanation of RCDP that your doctor will understand.

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A Doctor Friendly Description

A Doctor Friendly Description.

Written by Dr. Nancy Braverman -McGill University.

This is an explanation of RCDP that your doctor will understand.

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Have more Questions?

A RCDP NATURAL HISTORY

RhizoKids International is sponsoring a registry of individuals with Rhizomelic Chondrodysplasia Punctata (RCDP). The purpose of this registry is to learn more about RCDP and how to predict and treat medical issues that arise as a result.

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Ohio Chapter


RhizoKids Ohio chapter was founded in 2008 by Mindy Cirner and Jeff Cirner the proud parents of Jake and Jordyn Cirner who both are affected with RCDP Type 2.
Find out more!