MPDCI is a 501.c.3 non-profit Michigan Charity dedicated to providing direct and indirect services to enhance the lives of people with cystic fibrosis, their families, and the communities that support them.

Meet David Florshinger

A few reflections from David's mom . . .

In the days after David's CF diagnosis at the age of 5, if you had told me I would be figuring out things for him to go to college, I wouldn't have believed you. Yet here we are 13 years later. He has graduated from high school and has started college at MSU this past fall.

New content & expanded role for MPDCI

Thu, 12/09/2010 - 15:50 — Jeff Pinard

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

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

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