Jocelyn’s Journey is an annual fundraising event aimed at funding research to find a cure for Rett Syndrome, a debilitating neurological disorder. Jocelyn’s Journey funds are donated to the Rett Syndrome Research Trust a 501(c)(3) charity who has funded recent break throughs in gene therapy which has reversed the effects of the disorder.

About Jocelyn

On February 9th, 2010, 21 month old Jocelyn Jones was diagnosed with Rett Syndrome, a neurological disorder that strikes at random and affects almost exclusively girls. Rett Syndrome can be described as symptoms of autism, cerebral palsy, Parkinson’s, epilepsy, and anxiety... all in one little girl

There is Hope!

In 2007, Dr. Bird dramatically reversed symptoms in a Rett mouse model using gene therapy. A cure is in Jocelyn's future, as scientists have continuously described, "Rett is positioned to be the first reversible neurological disorder". The scientists at the Rett Syndrome Research Trust are pioneering new treatments that may one day cure thousands of little girls all over the world.

2018 Gala

Since 2011 Jocelyn's Journey has raised over $540,000 for the Rett Syndrome Research Trust. This years Gala will be held at the Town of Apple Valley Conference Center on October 20th.

Join Us

This years Gala will be on Saturday, October 20th. Join us for a fantastic evening of fundraising.

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Donate

Support the Rett Syndrome Research Trust with the donation of goods or services for raffle at the 2018 Jocelyn's Journey Gala.

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Volunteer

Give the greatest gift, your time and expertise. Learn more about supporting Jocelyn's Journey.

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