Target demographics: Women in their child bearing years 16-90
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.
go to http://www.thelamfoundation.org/images/pdfs/milestones.pdf
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Three months ago I was confused and scared, knowing there was something wrong with my lungs, but not having any idea what. One doctor suggested it might be LAM, but it is a rare disease, and she didn't know. I looked up LAM on the internet and found all kinds of scary information, but I also found... more »
When I was diagnosed with LAM, I felt so lost and alone.. I did the online research and was filled with dread. I found one foundation dedicated to help people like me, the LAM Foundation, and I don't know where I'd be if not for them. I'm still very sick, on oxygen and in need of transplant -- but ... more »
I am Nadin and I have LAM. I think the LAM foundation is a great nonprofit because after I was diagnosed; the LAM foundation was my doctor’s point of information and also my family’s. Since it is a rare disease, many doctors have no clue about it. I have learned with experience now, to print the... more »