LAM or Lymphangioleiomyomatosis: The Center for LAM Research and Clinical Care is focused on
providing excellence in clinical care and offering the most up-to-date research for women with LAM.
Director, Center for LAM Research and Clinical Care
Professor of Medicine, Harvard Medical School
Interview with Dr. Henske on the BHD Foundation website
Our lab studies the pathogenesis of tuberous sclerosis complex (TSC), lymphangioleiomyomatosis (LAM) and Birt-Hogg-Dube syndrome (BHD)
The LAM Foundation urgently seeks safe and effective treatments, 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.
US advocacy and support organization provides information about tuberous sclerosis complex, research on its genetics and treatment, and support for patients and their families.
Your resource for Birt-Hogg-Dubé Syndrome research and support.
To donate on-line: visit http://give.brighamandwomens.org/
- Click on the yellow “Donate” button
- Under the Designation select “Other”
- In the Other textbox type in “Dr. Henske/LAM Research
- Or call 617-424-4321 with any questions or to make a donation gift via phone.