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Ride for a Cure

June 17, 2022 - June 19, 2022

Ride for A Cure: Florida Motorcycle Ride Fundraiser

Grandfather Jim St. John is taking to the road on his motorcycle to raise awareness for 4H Leukodystrophy in honor of his granddaughters, Jamie and Layla.

A message from Jim about his Ride for a Cure:

Here’s your chance to finally tell me where to go! This time you will be choosing my stops for me.
All amounts of donations welcomed and appreciated.
With a minimum donation of $100, I will go anywhere you want me to within the state of Florida!
Want me to go by your childhood home and take a pic, how about your favorite beach, buy a beer at your favorite brewery (mine is Wops Hops shocking I know), take a pic with your family member or friend??? Wherever it is I will go there and do a Facebook Live spot from that location.
My goal this year is to raise $15,000, so start sending in your requests and making those donations.
100% of all funds will go directly to Yaya Foundation for 4H Leukodystrophy to support the research and development for treatments and a cure.
I will start the ride Friday June 17th and return home Sunday evening June 19th.
Please go directly Yaya Foundation to make your donations!

Details

Start:
June 17, 2022
End:
June 19, 2022
Website:
https://www.facebook.com/events/1373153866492209/?ref=newsfeed

Venue

Florida
United States

Organizer

Jim St. John
Our Ethos

We are driven by the dream that one day, every child with 4H Leukodystrophy will have the chance to live a long, healthy life.

So we fight for these children by acting as a catalyst and a connector—bringing researchers together to accelerate the pace of discovery, while connecting families with vital education resources and emotional support.

We won’t stop until we find a treatment and, ultimately, a cure.

about yaya foundation

Give Hope to a Child with 4H Leukodystrophy

Your generous donation funds critical research into life-changing treatments and a cure for 4H Leukodystrophy, as well as vital programs that connect, support and empower families affected by this rare disease. All it takes is a simple click.

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