September 23, 2012 at 10:20 pm | edit
Good evening everyone how are you all doing hope that everyone is having a great week we are working on a law called Davids law helping patients with cystic fibrosis and some with MS as well please take a look at the law 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 nurse’s 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 student’s 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 Doctor’s note, should be able to carry and administer their own medication. If the student demonstrates understanding and compliance 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 David’s Law will become law as soon as possible.
If you have any questions or want to help the cause, please contact David Wagner’s Cystic Fibrosis Hotline at 612-282-1211 please support this new hopeful law at http://www.petition2congresss.com/2418
Helping people lose weight is one of my greatest passions. I get to see the smiles, hear the screams of joy, and watch as timid and quiet people become SUPER DIVAS & ALPHA DOGS as they regain their healthier, thinner bodies back. I love what I do each day…it’s such a blessing! I am a product of our product as well, so I know it works!
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I am Janet, a Scentsy consultant and you can find my website here. janetjackson.scentsy.us Please take some time to check out our products. Scentsy has the perfect gift for any occasion and even some everyday home product items like shower gel, lotions, perfume, laundry scent enhancers and so much more! Thanks for your patronage! 🙂
if you can,plz load some pictures of your scentsy! or a scentsy catolog!
place to buy awareness gear:
awesomew site.. beautiful puzzle rings…
If you have a girl, or if you love bows please check out ‘Lil Muffinheads!! facebook.com/LilMuffinheadsTM I hand make bows and Hand paint beautiful bow holders!!
Body cooling vest and other cooling products for next Summer. The world’s favorite lightweight cool vest is the Arctic Heat cooling vest and it is available from Arctic Heat USA. http://www.ArcticHeatUSA.com
As a special offer for MS Huggers we are offering a 15% discount on all orders over $100, valid until 31 Dec, 2012. The discount code is mshuggers which is entered during checkout at http://www.CoolDownUSA.com
Heres my new blog for my blogging about my disability.
and here are my Bryce render site, My crafty blog and my writings.
Please come and browse and I hope you enjoy.
http://terrysthoughtsandthreads.wordpress.com is my new blog where I update my health status. Family and friends who want to know how I’m doing can read there. Others who share my diagnoses of multiple sclerosis, clinical depression and malignant melanoma are also welcome to read and comment.
https://www.facebook.com/#!/bowsn.bling.1 I MAKE RHINESTONE SHIRTS AND OTHER THINGS! I HAVE LOTS OF DESIGNS TO CHOOSE FROM AS WELL AS CUSTOM DESIGNS! TAKE A LOOK! JUST UPLOADED SOME DESIGNS FOR MS AS WELL! SO CUTE….GO LOOK!
Chicago Rare Disease Foundation is dedicated to helping save children one gene at a time at http://www.chicagordf.org
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