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Welcome to LupusMCTD

Official Sites of www.LupusMCTD.com and www.MixedConnectiveTissueDisorders.com

Perhaps you know someone with an autoimmune disorder such as Lupus or Mixed Connective Tissue Disorder. If you don't know what it is... it's our body attacking itself on the inside. You can't see it. You can't catch it. It is not contagious. You would never wish this illness on anyone.


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Another LupusMCTD community, please visit:  http://lupusmctd.ning.com/

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Disclaimer

Disclaimer~
Information contained in these lupusmctd™ pages is not meant to be taken as an endorsement of any medical approach, procedure, or treatment of any kind. If you have symptoms, seek immediate professional medical attention. The topics here are presented solely as potential options to be discussed with your medical professional. If you think you may have a medical emergency, call your doctor or 911 immediately.

The LupusMCTD Foundation founded in 2005 as a peer-to-peer endeavor run entirely by volunteers -- patients who are dedicated to providing information and support to people interested in Lupus and Mixed Connective Tissue Disorders.

LupusMCTD Foundation is financially supported solely by individuals who have personally experienced or witnessed through the site what giving can do to make awareness more available to the unknown conditions that are often hidden and called "Invisable Illnesses".

LupusMCTD Foundation does not accept corporate contributions from any industry. None of the people involved in this effort receive a salary or other compensation. The Foundation's mission is to provide information for patients, practitioners and the general public about this important, most often overlooked illnesses.



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