Ride Ataxia Tampa Bay - April 13, 2010
• 50 miles, pretty flat, scenic.  10 and 25 mile options.
• In partnership with the Outback Steakhouse Pro Am.
• Detailed info and online registration at: http://rideataxia.org/tampabay
Ride Ataxia Nor Cal - May 15-16, 2010
• 100 miles in 2 days with over 7,000 feet of climbing.  Folsom, CA to Grass Valley, CA and back.  10 and 25 mile options.
• Detailed info, route maps, and online registration at: http://rideataxia.org/norcal
Ride Ataxia Philadelphia - Mid October, 2010
• 50 miles with about 4,000 feet of climbing.  10 and 25 mile options.
• Partnered with the Children's Hospital of Philadelphia.
• Event website (update in progress): http://rideataxia.org/philly
Ride Ataxia So Cal - December 4-5, 2010
• 100 miles in 2 days along the beaches from LA to San Diego.  10 and 25 mile options.
• Detailed info in the late summer
Dallas - March, 2011
• More Info soon.
• Gonna be huge!
So keep an eye out for more information.  I would like to consolidate to one mailing list so if you would like to keep receiving updates please join the FARA mailing list.  Enter your email address and you will be given several options for updates including Ride Ataxia.

See you on the road!


Kyle Bryant
Ride Ataxia, Founder/Program Director
Friedreich's Ataxia Research Alliance (FARA)
This email address is being protected from spambots. You need JavaScript enabled to view it.
(916) 203-3238
curefa.org | rideataxia.org

The legacy of Marie Schlau: literature to help cure Friedreich's Ataxia

If you feel like reading an unputdownable novel while collaborating with a just and solidary cause, "The Legacy of Marie Schlau" is your book! 100% of all funds raised will be dedicated to medical research to find a cure for Friedreich's Ataxia, a neurodegenerative disease that affects mostly young people, shortening their life expectancy and confining them to a wheelchair.

The life of Marie Schlau, a German Jewish girl born in 1833 hides great unsolved mysteries: accidents, disappearances, enigmas, unknown diagnoses, disturbing murders, love, tenderness, greed, lies, death ... alternatively a different story unfolds every time and takes us closer to the present. Thus, there are two parallel stories unravelling, each in a different age and place, which surprisingly converge in a revelatory chapter.

Paperback and Kindle versions for "The legacy of Marie Schlau" available for sale at Amazon now!



Research projects currently being financed by BabelFAmily

Currently, BabelFAmily is financing two promising research projects aimed at finding a cure for Friedreich's Ataxia. Whenever you make a donation to us or purchase a copy of "The legacy of Marie Schlau", this is where all funds raised will be devoted to:

1) Gene Therapy for Friedreich's Ataxia research project:


The project is the result of an initiative of Spanish people affected by this rare disease who are grouped in GENEFA in collaboration with the Spanish Federation of Ataxias and the BabelFAmily. The Friedreich’s Ataxia Research Alliance (FARA), one of the main patients’ associations in the United States now joins the endeavour.

2) Frataxin delivery research project:

The associations of patients and families Babel Family and the Asociación Granadina de la Ataxia de Friedreich (ASOGAF) channel 80,000 euros of their donations (50% from each organisation) into a new 18-month project at the Institute for Research in Biomedicine (IRB Barcelona). The project specifically aims to complete a step necessary in order to move towards a future frataxin replacement therapy for the brain, where the reduction of this protein causes the most damage in patients with Friedreich’s Ataxia.

The study is headed by Ernest Giralt, head of the Peptides and Proteins Lab, who has many years of experience and is a recognised expert in peptide chemistry and new systems of through which to delivery drugs to the brain, such as peptide shuttles—molecules that have the capacity to carry the drug across the barrier that surrounds and protects the brain. Since the lab started its relation with these patients’ associations in 2013*, it has been developing another two projects into Friedrich’s Ataxia.



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