The LAM Foundation
Non-profit Organizations • 
Blue Ash, Ohio, United States • 11-20 Employees
Company overview
| Headquarters | 4520 Cooper Rd, Suite 300, Cincinnati, Ohio 45242, US |
| Phone number | +15137776889 |
| Website | |
| NAICS | 813 |
| Keywords | International, Pulmonary, Lung, Rare Lung Disease |
| Founded | 1995 |
| Employees | 11-20 |
| Socials |
Key Contacts at The LAM Foundation
Daniel Dilling
Member, Board Of Directors
Patti Tuomey
Executive Director
Cindy Beasley
Director Of Education And Advocacy
The LAM Foundation Email Formats
The LAM Foundation uses 2 email formats. The most common is {first initial}{last name} (e.g., jdoe@thelamfoundation.org), used 75% of the time.
| Format | Example | Percentage |
|---|---|---|
{first initial}{last name} | jdoe@thelamfoundation.org | 75% |
{first name}{last name} | johndoe@thelamfoundation.org | 25% |
About 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 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.
The LAM Foundation revenue & valuation
| Annual revenue | $31,600,000 |
| Revenue per employee | $1,971,000 |
| Estimated valuation?This valuation is estimated based on industry average for the Non-profit Organizations industry and current estimated revenues | $100,900,000 |
| Total funding | No funding |
Employees by Management Level
Total employees: 11-20
Seniority
Employees
Funding Data
The LAM Foundation has never raised funding before.
The LAM Foundation Tech Stack
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