They all finished with excellent times, and Federico Villa came in first!  What a great prelude for the London Paralympics in 2012!  Villa is the first young ataxian who’ll participate in the Paralympics!

Unfortunately, there was once a time when the disabled stayed home watching the hours pass by….but today we get to see them achieve great personal successes forged out of hard training and tenacity!  These athletes are an example to us all.

Interview with Federico

Federico Villa “The marathon let us compete with other athletes and meet other young people with ataxia.  One of them was Luca Garofalo, who completed his first marathon in 2 hours and 40 minutes.

It was a tough marathon!!!  When my bike went down the streets paved with the typical cobblestones, the shaking and the vibrations ran through my whole body and kept me from seeing.  Those of us with ataxia have trouble focusing.  My eyes were vibrating so hard that my vision was blurred.  So I let another athlete move in front of me so I could orient myself behind him.  I used him to keep me from slamming into things.  Then I got to feeling safer and I crossed the finish line in first place with a time of 1 hour 50 minutes and 40 seconds!  I’m satisfied.”

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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