The Sarcoidosis Awareness Network is a nonprofit organization established to increase and expand the public awareness of sarcoidosis; enhance the quality of life of sarcoidosis survivors; develop and implement a sarcoidosis registry; and to disseminate current literature on the disease so the general public is better informed about sarcoidosis and its impact on the lives of those afflicted with the disease.

The network was founded by Linda D. Lanier, who is a sarcoidosis survivor. The concept for the network evolved from Linda's personal search for information and public inquiries about sarcoidosis.

While the current primary focus area of the Sarcoidosis Awareness Network is the Washington, DC metropolitan area, the ultimate goal is to provide information, support and increased public awareness on a national level.

For more information, contact The Sarcoidosis Awareness Network via e-mail at
info@SarcoidosisNetwork.info

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