michiganpulmonarydiseasecommunity

Just an FYI - The Cystic Fibrosis Support Network of Michigan has a couple of fundraisers that we are asking you to consider supporting. 
The first fundraiser is a lottery with a 1st prize of $250, a 2nd prize of $150, and a 3rd prize of $100. 
The second fundraiser involves a night out at the theater and an auction.
 

I want to thank CFSN for all of the wonderful packages that you send in the mail to my daughter Madison Valles.

Madison was in the hospital for two weeks at Spectrum and gained weight last Thanksgiving. She was ‘spoiled’ at the hospital.

She now does her vest two times daily for 30 minutes; has three treatments through the nebulizer twice daily; and of course, her enzymes with meals and snacks. Madison needs to go into the hospital again to have some more polyps removed. Other than that, she is doing well.

There are big changes coming for MPDCI we're excited at the things to come.  Though the group is HQ'ed out of Michigan, this site will be expanded to be an active resource for many Cystic Fibrosis Families.
It will take a bit of time, but expect to see an expansion of the site over the next 6 months.  If you'd like, register and sign up for our Quarterly Bulletin to see what we're doing in the community. 

Pulmonary Disease in the News is a page for summaries and references to news articles and stories.  For now, you will find links to interesting articles that you can read yourself.  In the future, this page will also include links to full summaries and other writings. (updated: 6-18-2011)

Research

May 2012 Letter from the President