david s law

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Children with Cystic Fibrosis are required to take supplemental pancreatic enzymes before meals. These enzymes allow the student to digest food properly. Currently, the law states, each student must go to the nurseís office, each day. The nurse than administers the medication to the student. This is a time consuming process, which takes forces the student to leave class early or miss part of the lunch hour. This inhibits the studentís ability to either learn or have adequate time to finish lunch. This is also becoming problematic, due to budget cuts in the schools. Some schools are eliminating full-time nurses, which would make it impossible for students to take their medication each day.

Some schools have passed laws that allow students to carry medication such as over over-the-counter pain relief medications. The main impetus for the current restrictions is to insure the safety of the students by keeping controlled substances (such as prescription medications) out of the hallways and classrooms of the school.

However, the danger of someone taking un-prescribed pancreatic enzymes is negligible.

We believe students who have Cystic Fibrosis and require pancreatic enzymes before meals, with a Doctorís note, should be able to carry and administer their own medication. If the student demonstrates understanding and compliance with the prescribed dosage, before the school nurse, the student should be free to carry and administer the medication.

If you agree, please sign this petition and contact your lawmakers both state and federal, so Davidís Law will become law as soon as possible.

If you have any questions or want to help the cause, please contact David Wagnerís Cystic Fibrosis Hotline at 612-282-1211

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This needs to become a law . CF children know what medication they need far better than any school nurse. And their learning is being impeded by having to leave class early and they usually miss too much time due to hospitalizations and dr appointments. Or they miss par t of their lunch time which is medically impairing them because food intake is mandatory because CF children have a very hard time keeping weight on because of their illness.
We need this law passed pronto.