Cystic Fibrosis Foundation - Click here for homepage
 | Stay Informed  |  Volunteer  |  Clinical Trials
ABOUT CYSTIC FIBROSIS ABOUT THE CYSTIC FIBROSIS FOUNDATION LIVING WITH CYSTIC FIBROSIS TREATMENTS RESEARCH OVERVIEW GET INVOLVED!
In This Section
Message from the President
Foundation Leadership
Annual Report & Financial Statements
Publications & Videos
Press Room
News & Events
2008 News Archive
2007 News Archive
2006 News Archive
2005 News Archive
2004 News Archive
About 65 Roses
Locations
Governance & Policies
Milestones Campaign
Employment Opportunities
Contact Us
Quick Links
Find A Chapter
Great Strides
Become a Corporate Partner
Volunteer
Employment Opportunities
Become an Advocate
Find A Clinical Trial
Care Center Network
Drug Development Pipeline
CF Services Pharmacy
Make a Donation
Find a Chapter
Get Connected

 Watch NIH Director Dr. Francis Collins sing a song he wrote for the CF community at the 2009 North American CF Conference.
 Watch NIH Director Dr. Francis 
 Collins sing a song he wrote for
 the CF community at the 2009
 North American CF Conference.

Join us on YouTube at http://www.youtube.com/CysticFibrosisUSA Join us on YouTube





Join us on Facebook at www.facebook.com/CysticFibrosisFoundation Join us on Facebook





Follow us at twitter.com/CF_Foundation Follow us on Twitter
Display a Printer Friendly Version This Page

New Law Ensures Health Coverage for College Students with CF

October 14, 2008

A new statute that helps young adults in college keep their health insurance during a medical leave of absence was enacted on October 9th.

The legislation, known as Michelle’s Law, will help young adults with cystic fibrosis who must take a medical leave of absence from college keep their health coverage at a time when they need it most. The Cystic Fibrosis Foundation supported this legislation and applauds its enactment.

Under the new law, college students who are still covered under their parents’ insurance plans will be able to keep their coverage, even if they are forced to leave school for a short time due to their health.  Michelle’s Law helps young people with CF to continue their education without fear of losing their health coverage due to requirements stating that they must be fully enrolled in school to participate in the insurance plan.

Join the Foundation in its efforts to support legislation that protects the rights of people with CF. Sign up to become an Advocate.

Make a donation to the Cystic Fibrosis Foundation.
Sign up to get the latest news and information.
It's Time to Take GREAT STRIDES! Your steps TODAY will help find a cure for cystic fibrosis. Register for a walk near you!
Help discover and develop potential new treatments for CF by enrolling in a clinical trial. Click to learn more.
Cystic Fibrosis Services Pharmacy
Shop for gifts and -- at the same time -- support the mission of the CF Foundation.
The Cystic Fibrosis Foundation is an accredited charity of the Better Business Bureau.   The Cystic Fibrosis Foundation has a 4-star rating from Charity Navigator, America's largest independent evaluator of charities.