The LAM Foundation

The Lam Foundation

Non Profit Organization Management, 4520 Cooper Rd, Cincinnati, Ohio, 45242, United States, 1-10 Employees

thelamfoundation.org

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Who is THE LAM FOUNDATION

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 d...

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  • 4520 Cooper Rd, Cincinnati, Ohio, 45242, United States Headquarters: 4520 Cooper Rd, Cincinnati, Ohio, 45242, United States
  • 1995 Date Founded: 1995
  • 1-10 Employees: 1-10
  • dollar-icon Revenue: $10 Million to $25 Million
  • tech-icon Active Tech Stack: See technologies
  • Susan Mha CEO:   Susan Mha

industries-icon Industry: Non Profit Organization Management

SIC SIC Code: 7389 | NAICS Code: 624190 | Show More

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The LAM Foundation Org Chart and Mapping

Susan Mha

Chief Executive Officer & Executive Director

Employees

Sally Lamb

Director of Patient Services

Julie Wogenstahl

Administrative and Data Coordinator

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Frequently Asked Questions Regarding The LAM Foundation

Answer: The LAM Foundation's headquarters are located at 4520 Cooper Rd, Cincinnati, Ohio, 45242, United States

Answer: The LAM Foundation's phone number is +15*********

Answer: The LAM Foundation's official website is https://thelamfoundation.org

Answer: The LAM Foundation's revenue is $10 Million to $25 Million

Answer: The LAM Foundation's SIC: 7389

Answer: The LAM Foundation's NAICS: 624190

Answer: The LAM Foundation has 1-10 employees

Answer: The LAM Foundation is in Non Profit Organization Management

Answer: The LAM Foundation contact info: Phone number: +15********* Website: https://thelamfoundation.org

Answer: 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. The LAM Foundation is the global leader in the fight against lymphangioleiomyomatosis (LAM). Founded in 1995 as a grass roots effort, The LAM Foundation has evolved into an organization that is described by the National Heart, Lung and Blood Institute (NHLBI) as "a model for voluntary health agencies." LAM is a rare and progressive lung disease that primarily affects women and has no known cure. Headquartered in Cincinnati, Ohio, The LAM Foundation provides support and education for women with LAM and their families, engages doctors and scientists to continue to learn more about the disease and raises funds for continued research. In May 2015, the FDA approved Rapamune as the first effective treatment for LAM, based on research and patient engagement supported by The LAM Foundation. Through the efforts of a committed Board of Directors and staff, the Foundation has raised more than $26 million in 24 years. Over 60% of this has been committed to research which further seeded an estimated $40 million in subsequent funding from federal sources to advance the field of LAM research. This research effort has produced more than 125 grant-related publications, a diagnostic biomarker that can obviate the need for lung biopsy, and a pivotal clinical trial that has identified the first treatment. In addition to its world-renowned Scientific Board, 60+ LAM Clinics have been established across the globe which focus referrals to expert regional centers and facilitate clinical trials. This distributed expertise model fosters scientific interest in LAM at academic medical centers around the country and provides care close to home.

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