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Hannah's Hope for Giant Axonal Neuropathy

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Uploaded by on Jun 1, 2008

This is one family's fight for a cure for Giant Axonal Neuropathy.

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Nonprofits & Activism

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Standard YouTube License

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All Comments (16)

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  • Good luck to wee Hannah, what a cutie she is....

  • Please vote for Hannah!

    Peace & Love,

    Tim & Kate

  • I am so sorry -- my twins have Niemann Pick Type C and it's progressive like this disease. Join the Global Genes Project team to we can team up and all have a voice.

  • We are praying that the Pepsi Refresh Funding will go to Hannah's Hope! We have rallied people on Twitter and Facebook and thru our emails.

    God Bless You!

  • Hey.. My name i Kyle. I Live in the ACT Canberra. I Have axonal Neuropathy!. Not (GAN) this breaks my heart to see this.. im 22 years of age and going strong. Nothing brings me down. Call me if you have any breakthroughs! i would love to help the research. 0432373495

  • my mom knows you guys. my school told me they would fun raise and help you guys

  • Quit arguing and support Hannah!! I also have Neuropathy. It is a terrible Disease and one that many people have not even heard of. Yes prayer is ok, but it will do nothing unless you have support. Support Hannah!! we all need a cure!!!

  • lowering carbs helped me- it's almost gone~

  • Freedom of speech baby freedom of speech!

  • This is not a random comment to a random family... I know this family. Do you? How do you know that they don't believe that prayers can help them? Mind your own business and take your comments to someone who cares. I would be willing to bet that your comments are much more offensive than an offer from me for support... whether that support is in the form of thoughts and prayers, is no business of yours.

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