Ways to Give
There are many ways to give to The LAM Foundation in addition to direct cash donations. We are happy to work with you to find giving opportunities that work for you and your family. Please feel free to contact our development team at:
877-CURE-LAM (287-3526)
development@thelamfoundation.org
Donate to The LAM Foundation: The LAM Foundation is the global leader in the fight against lymphangioleiomyomatosis (LAM). We are dedicated to finding safe and effective treatments, and ultimately a cure, for women living with LAM. Your gift is essential to making a difference in their lives.
All contributions directly support The LAM Foundation’s research, advocacy, and patient education initiatives. The LAM Foundation is a registered 501(c)3 non-profit organization. All contributions are tax-deductible to the fullest extent of the law.
Make a General Donation
Donate Online
By making a donation today, your gift has an immediate impact on women living with LAM around the world. We are truly grateful for your generous support.
By Phone
Call us toll-free at 1-877-CURE-LAM (1-877-287-3526).
By Mail
Please complete our donation form and mail it with your check to:
The LAM Foundation
4520 Cooper Road, Suite 300
Cincinnati, OH 45242
Support LAM Research
Francis X. McCormack Career Development Award Fund
As part of Dr. McCormack’s passion for leading, inspiring, and expanding promising LAM research, he has consistently encouraged young scientists and clinicians to study LAM. To acknowledge his investment in the future of LAM science, we named an annual LAM research award in his honor.
Support Patient and Family Travel to Conferences and Clinical Trials
Thanks to generous donors, The LAM Foundation is able to offer assistance to individuals with LAM and their families to attend educational conferences and to participate in clinical trials.
LAM Family Network (LFN) Travel Grant
The LAM Family Network (LFN) Travel Grant provides financial assistance to individuals with LAM from around the world, providing travel expenses related to attending LAMposium.
The Shellie Owens First-Time Attendee (SOFTA) Travel Award
SOFTA funds are specifically designated for patients attending the LAMposium for the first time and can also support one additional person accompanying them. Each conference year, we hope to welcome as many newly diagnosed and first-time attendees as possible.
Clinical Trial Travel Fund
Over the last 20 years women with LAM have powered LAM research by enrolling in clinical trials and studies. Their generosity and courage have improved the lives of all women with a LAM diagnosis. Help us support clinical trial participation by donating to the Clinical Trial Travel Fund.