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. In partnership with the Histiocytosis Association, LAM clinics are also interested in improving the care and treatment of patients with pulmonary Langerhans cell histioctyosis and other rare lung diseases.

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.

Click here for a list of all US LAM Clinics.

Disclaimer:
The LAM Foundation attempts to verify the accuracy of information regarding LAM Clinics and health care providers prior to posting on this website. The Foundation 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. The LAM Foundation is not liable for any damages that may result from the use of this site.

Neither The LAM Foundation nor any staff member is qualified or intended to serve as a source of medical advice. All material contained or referenced on this website, including health- or medical-related materials, is for informational purposes only. Always seek the advice of a qualified health provider with any questions you may have regarding a medical condition

If you think you may have a medical emergency, call your doctor or 911 immediately.