About The LAM Foundation
The LAM Foundation urgently seeks an effective treatment and ultimately a cure for lymphangioleiomyomatosis (LAM) through advocacy and the funding of promising research.  We are dedicated to serving the scientific, medical and patient communities by offering information, resources and a worldwide network of hope and support.  For more information on The LAM Foundation, visit http://www.thelamfoundation.org.  To view LAM videos on YouTube, click here.

About The Midwest Friends of The LAM Foundation
The Midwest Friends of The LAM Foundation, formed in late 2007, is comprised of individuals that share hope for friends and loved ones diagnosed with LAM.  The group is committed to raising both funds and awareness for LAM.

The Midwest Friends of The LAM Foundation Board Members
Kori Aldrich
Julie Boczkowski
Meg Chalmers
Carla Galvanoni
Jenna Hnilo
Peggy Lanigan
Chris Lentz
Laura Lentz
Michelle Lezotte
Katrina Martin
Andrew Romanosky
Kim Romanosky
Jody Rowley
Holly Schofield
Jim Schofield
Jennifer Seuring
Joy Walton
Jennifer Wangerow
Meghan Wierzbicki
Tory Wierzbicki