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LAM Foundation
June 14, 2010

The LAM Foundation was established to spur interest and raise funds for medical reasearch to fund a cure for Lymphangioleiomyomatosis. I am so thankful that they began this process 15 years ago! I was diagnosed a year ago and they have been a credible, reliable source of information to me. They are doing a wonderful job of educating the medical community and raising awareness of this rare lung disease.

The Great!

I've personally experienced the results of this organization in...

I've received information critical to my health condition through the foundation. I've been given information on how to contact other women with this rare disease so we can share coping mechanisms and heartfelt stories.

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The kinds of staff and volunteers that I met were...

...so friendly and hard working! They always have a smile on their faces even when they're working so hard for all of us.

If this organization had 10 million bucks, it could...

...find a cure to this rare, progressive disease that kills mothers, sisters, aunts, and daughters in the prime of their lives.

How frequently have you been involved with the organization?

About every week

When was your last experience with this nonprofit?

2010

MY ROLE:
Client Served & It helped me learn about LAM after my diagnosis.