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

[QBKT1987]

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.

[cspad37]

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.

[bczieg1988]

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

[hplazable]

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!!!

[bczieg1988]

@hplazable Yes the cure will be here soon!

[devine124]

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.

[bczieg1988]

@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.

[haycc454]

You are such an inspiration!

[sarahjohall]

Brooke, this is a friend of Clint's, Sarah Lackey-Hall. You are very inspirational and I'm so impressed with your video! You rock!

[sunshine4mama]

Beautiful....you & the video!

[bczieg1988]

@sunshine4mama you're kind, thank you!

[MrDojodojo]

Inspiring. God Bless



[bczieg1988]

@MrDojodojo Thanks

[01zx9rguy]

I have FA too. Gr8 vid!! Sarah

[briandonovan]

Hey whats up, proud to leave the 1st comment, Absolutely Awesome video.