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

Thursday, April 22, 2010

Health-Related Quality of Life in Children With Friedreich Ataxia

http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TBD-4YVRRSF-8&_user=10&_coverDate=05%2F31%2F2010&_rdoc=1&_fmt=high&_orig=search&_sort=d&_docanchor=&view=c&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=7987996878ea7a400f6a95366d9a47e5
Posted by Laurel Hosking at 4:07 PM
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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
View my complete profile

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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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