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    <title>LupusMCTD ™ : The Official Site

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    Aside from living with chronic pain, how would you like to be living with a disease that attacks your own cells and organs?
    Things like your skin, heart, lungs, brain, joints and kidneys?
    How would you like to be living with a disease in which your own body has turned on you ? That would be lupus.
    You’ve probably heard of it, but do you know, exactly what Lupus is? Or a MCTD? (Mixed Connective Tissue Disorder) Join us and read our day to day life.
    Fibromyalgia: Oddly enough, people with fibromyalgia tend not to have the "half moons" at the base of their fingernails, with the exception of the thumbs.
    Another indicator with fingernails is if they have brittle, vertical ridges.
    Raynaud Patients: Order drinks with " no ice". Let cold drinks sit on the counter and come to room temperature before drinking.
    Use oven mitts or regular mittens to take items in or out of the freezer.
    Make Your Own Rice Socks (mini heating pads)
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    Disclaimer: Information contained in these www.LupusMCTD.com™ 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.

    www.LupusMCTD.com, founded as a non-profit, charitable organization in 2005, is 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. The 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". www.LupusMCTD.com 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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