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Friedreich's Ataxia; Brooke's journey from majority to minority

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Uploaded by on Nov 28, 2011

In 2002, I was 13 and got diagnosed with a rare neurological disorder called Friedreich's Ataxia. have done a lot of interviews in the past 10 years, since diagnosis, and they always ask me the sad question about how negative it is. I want people to see a positive side to FA, it needs a cure but our life is not pointless just because of it! Visit me at www.facebook.com/thebigseester and www.bigseester.com

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My Girl - Temptations (COVER by Jim Ziegler)

Your Hands - JJ Heller

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Uploader Comments (bczieg1988)

  • Thank you for this video. I can't wait to show it to my 11yr old with Fa. She needs to hear others speak out positively.

  • @devine124 Makes me sad to hear you daughter has FA too. I hope she knows she is not alone with this and I hope she enjoys this video.

  • Beautiful....you & the video!

  • @sunshine4mama you're kind, thank you!

  • Inspiring. God Bless

    

  • @MrDojodojo Thanks

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  • I created a You Tube account just so I could post a comment. I wanted to say that you are an inspiration. I have a cousin who has FA, but like you, she is not defined by it. You are an amazing person. They WILL find a cure. I, like so many others, was totally ignorant to even the existence of this disease before I had a family member diagnosed with it. Since then I have tried to share my awareness with others. We are always stronger in numbers. I will share this video with many. Thanks again.

  • @hplazable Yes the cure will be here soon!

  • @cspad37 I am glad it inspired you. I hope your grandchildren get inspired too!

  • thanks for the inspiration Brooke. My grandchildren Andre 16 and Ashley 13 were diagnosed last year. I too cant wait to have them see this.

  • Wonderful video - my son (22) has FA - the cure WILL come, Brooke - keep that smile shining and keep the great attitude! Blessings!

    and we'll all have free drinks someday!!On me!!!

  • You are such an inspiration!

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