From Carrie's posting yesterday...
Today is National LAM
Awareness Day. I found out I had Lymphangioleiomyomatosis, or LAM back in 2006
and my life hasn't been the same since. LAM affects women in the prime of their
lives robbing them of the ability to breathe and and move throughout life without
complication. There is no cure. LAM is extremely rare, therefore those of us
stricken with the disease do most of the fundraising and awareness campaigns
ourselves with the help of our families, friends and other patients. For more
information on LAM and how you can make a difference please visit
thelamfoundation.org or visit me next Saturday, June 7th at "Chairs for
Charity" at The Wade Creek House". All proceeds benefit The LAM
Foundation.
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