Life Experiences for LAM
On Thursday, November 15, 2018, Andrea Slattery, Board Chair of The LAM Foundation, and her husband Quint will host “Life Experiences for LAM”, a dinner and live auction to benefit The LAM Foundation. This event, in the beautiful setting of the Merion Golf Club, will celebrate The LAM Foundation’s progress in its search for safe and effective treatments, and ultimately a cure, for lymphangioleiomyomatosis (LAM). Please see below to purchase tickets or sponsor this event.
Lymphangioleiomyomatosis (LAM) is a rare, progressive lung disease that strikes women in the prime of their lives, usually during their childbearing years. To learn more about LAM, CLICK HERE.
The LAM Foundation is a 501(c)3 non-profit organization with a mission “To urgently seek safe and effective treatments, and ultimately a cure, for lymphangioleiomyomatosis (LAM) through advocacy and the funding of promising research.” Achieving this mission is only possible with the generous support of individuals, families, and organizations that help raise funds to benefit the foundation.
We hope you will consider supporting The LAM Foundation by attending or participating as a sponsor of this very special night. If you have any questions or want to learn more about The LAM Foundation, please contact Katie Jensen, Development Director, at firstname.lastname@example.org or (513) 777-6889.
Thank you to all of the generous sponsors who help make this event possible. For information on how you can become a sponsor, CLICK HERE.