Added: 4 years ago
From: stoelby
Views: 8,977
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  • @TheMrdragonfire2010 since the problem come from the gene that makes the protein, well the protein is fucked up, since this protein is responsible from moving water in and out of your cells it cause the mucus and the salty sweat

    The only cure would be to fix the gene which is really hard :P

  • Beautiful video, my daughter is 11 and has CF

  • Google: Lung Transplant Bradenton, and you'll find an inspiring story about a CFer who had a double lung transplant.

  • i have asthma and cf

  • i am lucky as i maybe stay in hospital 4weeks out of the year as i try 2 look after my self :)

  • I have to say that bringing awareness to the disease is great, but some of the stuff being said is for severe cases, my best friend has cf and she really don't take as many pills being said or have the physical therapy or the vest or anything unless she's battling a lung infection. Also great job to Alyssa's Angels, you're making a difference

  • great awareness for cf

  • thanks for your videos i have cf and i appritiate what you do for us thanks you

  • stay strong alyssa!

    keep fighting and stay strong!

    we WILL find a cure..... :D

  • Who cares if you have bad asthma, CF is much worse and harder to live with than asthma. I have CF and get very angry seeing people complain about asthma or having a cold etc.

  • keep fighting! were going to find a cure. for alyssa for my brother, for every one having to live wit this disease!

  • This is sad for me to watch, I have very bad asthma.

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