Lymphangioleiomyomatosis (LAM) Program

Stanford University Medical Center recently started a LAM Clinic that occurs monthly to focus on the unique needs of patients with LAM.  Drs. Stephen Ruoss and Roland Nador see patients in this clinic.  In addition, a LAM Support Group meets every other month at the medical center. Approximately 10-15 LAM patitents and their families attend meetings which usually include a guest speaker on topics of interest plus time to visit and ask questions.  The LAM Foundation has been instrumental in getting the word out by helping with mailings to its members. 

For more information, or to register for a meeting, please contact:
Susan Jacobs RN, MS; phone: (650) 725-8082 or