Friedreich's Ataxia; Brooke's journey from majority to minority
Uploader Comments (bczieg1988)
All Comments (15)
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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.
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@hplazable Yes the cure will be here soon!
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@cspad37 I am glad it inspired you. I hope your grandchildren get inspired too!
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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.
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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!!!
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You are such an inspiration!
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 2 months ago
@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.
bczieg1988 2 months ago
Beautiful....you & the video!
sunshine4mama 2 months ago
@sunshine4mama you're kind, thank you!
bczieg1988 2 months ago
Inspiring. God Bless
MrDojodojo 2 months ago
@MrDojodojo Thanks
bczieg1988 2 months ago