|Our mission||The LAM Foundation urgently seeks safe and effective treatments and ultimately a cure for 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.|
|Ways to help|
Development or Fundraising
Fundraising and development opportunities include organizing special events, organizing quick fundraisers, joining The Foundation’s online fundraising efforts, soliciting major gifts, and recruiting other volunteers.
Communications or Public Relations
We can use your help in producing and distributing news releases, creating posters and flyers, and developing positive relationships with the media in your community.
Hold an educational event about LAM and The LAM Foundation in your home, school, church or other social outlet.
Make calls, write letters and send e-mails to your legislators when there are critical issues that affect healthcare, research and rare diseases. Your voice makes a difference.
|How you help||Volunteers help in many ways including educational events about LAM, fundraising (organizing special events, quick events, or online), communications and PR (producing and distributing news releases, creating posters and flyers, and developing positive relationships with the media in your community), advocacy, and more.|
|About us||The LAM Foundation is a non-profit, voluntary health agency whose primary goal is to find an effective treatment and ultimately a cure for lymphangioleiomyomatosis (LAM) through peer-review funding of promising research.|