US LAM Clinics and Research Network
The LAM Foundation is always seeking ways to improve the care and treatment for all women with LAM. As such, LAM Clinics are strategically located in hospitals or medical centers across the United States where there are clinicians and researchers who have an interest in LAM and who value research in rare diseases. In order to become a LAM Foundation approved LAM Clinic, an application must be submitted and reviewed by the Foundation’s LAM Clinic Committee before being accepted into the network.
LAM clinic care teams are also interested in improving the care and
treatment of patients with other rare lung diseases, and are often referred to
as LAM & Rare Lung Disease Clinics. Rare lung conditions of interest
include: pulmonary Langerhans cell histiocytosis, pulmonary aveolar
proteinosis, sarcoidosis, Sjogren’s syndrome, Alpha-1 antitrypsin deficiency,
and pulmonary fibrosis, among others.
LAM Clinic participation is voluntary and while The LAM Foundation makes every effort to update its information and monitor the application process, it does not guarantee, and is not responsible for the accuracy of information or the quality of medical care received at any institution, clinic, or by a medical provider listed on our website.
For information about joining the LAM Clinic Network, please contact:
Nishant Gupta, MD
Assistant Professor of Medicine, Director - Interstitial Lung Diseases Center, Divisions of Pulmonary Critical Care and Sleep Medicine
The University of Cincinnati, 231 Albert Sabin Way, ML 0564, Cincinnati, OH 45267-0564
Tel: 513.558.4831 Fax: 513.558.4858 Email: GUPTANS@UCMAIL.UC.EDU
or
Laura Bowers
Clinical Program Coordinator, The LAM Foundation
Click here for a list of all US LAM Clinics.