The LAM Foundation
The LAM Foundation
Delivering facts about #LAM #RareDisease and The LAM Foundation. We're dedicated to funding research, advocacy and awareness to improve the QoL for all LAM pts. The LAM Foundation is a non-profit, voluntary health agency whose primary goal is to find an effective treatment and ultimately a cure for lymphangioleiomyomatosis (LAM) through peer-review funding of promising research.
311438001
EIN
1995
Founded
Cincinnati, OH 45242-5687 USA
Address
thelamfoundation.org
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All Gifts Matched Double your impact on Rare Disease Day with 2x match until we reach 30k or 1159 PM PT Join Our Community Wherever you are on your journey with LAM were here when you need us. Tap into our rich network of expert clinicians support groups and other exceptional resources. Your Strength. Our Support.
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