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David's Law

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  • Jun 30th, 2010
    Someone from Loxahatchee, FL signed.
  • Jun 30th, 2010
    Someone from Renton, WA writes:
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    I fully agree with this. Health should always be a priority!
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  • Jun 30th, 2010
    Someone from Selinsgrove, PA signed.
  • Jun 29th, 2010
    Someone from Los Gatos, CA signed.
  • Jun 29th, 2010
    Someone from Santa Rosa, CA signed.
  • Jun 29th, 2010
    Someone from Chickamauga, GA writes:
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    I have Cystic Fibrosis and while I am way past school age, I know how important it is for students to get their enzymes.
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  • Jun 29th, 2010
    Someone from Wooster, OH writes:
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    My son with Cystic Fibrosis will be going to school in a couple of years and this will definitely help if he can take his enzymes in his own classroom right before eating instead of having to go to the nurses office. He needs all the time he can get to eat, because he needs to eat a lot of food. He needs extra calories all the time because of the poor weight gain that most people with Cystic Fibrosis have.
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  • Jun 29th, 2010
    Someone from Malaga, NJ writes:
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    My grandson who is only 3 yrs right now will one day be in school. Who knows what will be going on in 2 years with the cuts and if the school where he will attend doesn't have a nurse then how will he get these vital enzymes? Here's a question for you, would you rather a student with Cystic Fibrosis take his/her enaymes or miss school?
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  • Jun 28th, 2010
    Someone from Newark, OH signed.
  • Jun 28th, 2010
    Someone from Vonore, TN signed.
  • Jun 28th, 2010
    Someone from Morehead, KY signed.
  • Jun 28th, 2010
    Someone from Dallas, TX signed.
  • Jun 28th, 2010
    Someone from Renton, WA writes:
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    As someone who grew up with CF and constantly having to go to the Nurses office to take medication it would have been far easier to not have to waste time doing that and thus missing out on getting into the lunch line quickly and thus being able to enjoy my recess fully. And as every kid will tell you, recess is EVERYTHING when you are in grade school.
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  • Jun 28th, 2010
    Someone from Napa, CA writes:
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    Our two children had numerous problems taking their enzymes while at school. This law would have helped them feel more normal in a world that is sometimes cruel to children with cystic fibrosis.
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  • Jun 28th, 2010
    Someone from Oakland, CA writes:
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    This crucial for all students who have cystic fibrosis! Our family knows! Marion Rojas
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  • Jun 28th, 2010
    Someone from Kingsport, TN signed.
  • Jun 28th, 2010
    Someone from Sweetwater, TN signed.
  • Jun 28th, 2010
    Someone from Boca Raton, FL signed.
  • Jun 28th, 2010
    Someone from Procious, WV signed.
  • Jun 28th, 2010
    Someone from Newark, OH signed.
  • Jun 28th, 2010
    Someone from Jonesboro, GA signed.
  • Jun 28th, 2010
    Someone from Clinton, MT signed.
  • Jun 28th, 2010
    Someone from Springfield, OH signed.
  • Jun 28th, 2010
    Someone from Frisco, TX signed.
  • Jun 28th, 2010
    Someone from Birmingham, AL signed.
  • Jun 28th, 2010
    Someone from Tellico Plains, TN signed.
  • Jun 28th, 2010
    Someone from Hamilton, OH signed.
  • Jun 28th, 2010
    Someone from Morehead, KY signed.
  • Jun 28th, 2010
    Someone from White Pine, TN writes:
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    I have 2 children with CF and this is a very serious problem. I fought with our school for over 2 years and I am still not happy with the results. I believe in this law whole heartedly! I also believe they go through enough without having to deal w/ this issue at school. They need as much "uninterruption" as possible!
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  • Jun 28th, 2010
    Someone from New Tazewell, TN writes:
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    CF children have enough struggle just trying to get through life as normal as they can on a daily basis. I know I lost my daughter last year to this disease at 25.
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  • Jun 27th, 2010
    Someone from Maynardville, TN signed.
  • Jun 27th, 2010
    Someone from Little Elm, TX signed.
  • Jun 27th, 2010
    Someone from Plano, TX writes:
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    My three year old son has CF and I fully agree with this law being passed. Without enzyme pills before each meal, this can be critical to patients and their ability to keep weight on them in order to fight off infections related to CF.
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  • Jun 27th, 2010
    Someone from Amelia Court House, VA signed.
  • Jun 27th, 2010
    Someone from Anderson, SC signed.
  • Jun 27th, 2010
    Someone from Bridgeton, NJ signed.
  • Jun 27th, 2010
    Someone from Austin, TX signed.
  • Jun 27th, 2010
    Someone from Plano, TX writes:
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    David, this is a great thing. My nephew has CF, I do not want him to be treated any differently that other children. I do not want him to miss out on lunch, school activies, etc......Let me know what I can do to help! God Bless You!
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  • Jun 27th, 2010
    Someone from Southgate, MI writes:
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    I believe this would be best for these children. My son has CF and it would make him feel much more independant and allow him to not feel different when he has to leave to take medications. I believe if they know what they are doing, and understand they can't give their meds to others it would be for their benefit to do it themselves.
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  • Jun 27th, 2010
    Someone from Mountain Home, AR signed.