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. 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.
311438001
IČO
1995
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Cincinnati, OH 45242-5687 USA
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thelamfoundation.org
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TheLAMFoundation
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💜 So grateful for the amazing work The LAM Foundation is doing! Together, we can spread awareness and support vital research for LAM. Let’s fight this together! #RareDisease #LAM
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🌟 Every donation counts, especially during this matching challenge! Let's come together to support those impacted by LAM and push for a cure. Join the movement! #HopeForLAM #CommunitySupport
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Poslední diskuze

1. How can we enhance community engagement and support for newly diagnosed LAM patients through online platforms and local events?
Odpovědí: 3, Naposledy před 1 den detail
2. What are the most promising areas of research currently being explored for LAM, and how can the community contribute to advancing these efforts?
Odpovědí: 3, Naposledy před 1 den detail

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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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