Help FA in SA

This Blog was created for people interested in Friedreich Ataxia in South Australia. It provides a relaxing place to share and communicate what is going on, as well as links to FA groups and information from around the world. FAinSA is a non medical site for patients, families and friends of FA. All comments are a purely personal nature and do not replace advice from trained medical professionals

Tuesday, March 16, 2010

interesting news for babelFAmily

http://www.babelfamily.org/en/latestataxianews/721-genetics-telethon-italy-funds-discovery-of-the-cause-of-a-new-form-of-ataxia

http://www.babelfamily.org/en/latestataxianews/720-we-can-fight-friedreichs-with-research

Posted by Laurel Hosking at 10:55 AM
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About FAinSA

Laurel Hosking
Gawler, South Australia, Australia
HI!. My son was diagnosed with FA in 2007. Since then I became aware how little is known about FA in South Australia. Early 2008 I chose to change this. This Blog was created to unite those with FA or touched by FA in South Australia
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  • Help Friedreich Ataxia in South Australia
  • FA Babel Family ( Scientific Research and Fundraising)
  • FA Parents Group
  • FARA (USA)
  • FARA(A)
  • Friedreich Ataxia Network inc
  • International Network of Ataxia Friends

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