About MPDCI
It all began with an idea for a summer camp to help kids with Cystic Fibrosis feel normal. That was in 1972 with a long weekend and a handful of kids. Over the years that grew to over 100 kids and 100 staff for a whole week every summer. The summer camp evolved into a Family Retreat which allows for the person with CF and their caregivers a chance for summer fun. As times have changed, so has MPDCI. While we used to only focus on one thing, we are now diversified in many things. That is why we are able offer many avenues of support. Check out the rest of our website to learn more about them. MPDCI is committed to people with CF and want to help as many as we can.
MPDCI is governed by a volunteer board of directors and supported by a large membership. The board is made up of dedicated individuals who are willing to serve a two year term. The board meets monthly. Visitors are always welcome to attend the meetings. They are encouraged to take part in discussions. On any given night the board might discuss anything from transplant issues to planning an outing.
Come join us! MPDCI Board Meeting are held on the 2nd Wednesday every month from 7 to 9 p.m.