(NAPS)—Educating yourself about lupus could help those who are affected get treatment sooner. For many,it’s a long journey. An estimated 1.5 million Americans have a form of lupus, a chronic, severe autoimmune disease for which there is no cure. Every day, these patients must deal with their own immune systems turning against their bodies, resulting in health effects including heart attacks, strokes, seizures, organ failure and miscarriages. Yet, while many people are impacted by lupus, greater awareness of the disease is needed. Because symptoms such as fatigue, skin rashes, joint pain and hair loss mimic other conditions and appeardifferently in different people, lupus is very difficult to diagnose. Many people do not suspect they have a potentially disabling and life-threatening disease because lupus symptoms tend to come and go, and different symptoms may appear at different times during the course of the disease. Nine out of 10 people with lupus are female, and the disease develops most often between the ages of 15 and 44. African-American, Hispanic/Latino, Asian and Native American women are two to three times more likely than Caucasian women to develop lupus. More than half of people with lupus visit three or more doctors Many people do not suspect they have a life-threatening disease because the symptoms tend to comeand go. to find a cure for their symptoms, and experience symptoms for four or more years before finally being diagnosed. That was the case for Karon Beasley, who saw six different types of doctors over four years before visiting an allergist who suspected that she had an autoimmunedisease. “T was coming homefrom working out one day when the feeling of fatigue hit me. It was overwhelming—I’dfeel tired and short of breath just walking to my mailbox,” said Beasley, who suffered through a variety of misdiagnoses including anemia, thyroid disorders and PMS before it was determined that she had lupus. “IT couldn’t get answers and went in circles. A dermatologist saw arash on myface that was consistent with lupus, but told me, ‘Honey, that’s just hormones,’ and prescribed me a cream. I went to a neuropsychiatrist thinking my fatigue was depression, because you start to believe something is mentally wrong with you,” she said. Beasley, who has now lived with the disease for more than 12 years, encourages people with lupus to be their own advocate. Friends, family and doctors should also be considerate of what it is like to live with lupus. Beasley says, “Most people with lupus at some point hear: ‘But you don’t look sick.’ We face the issue of dealing with an invisible illness. You have to know you don’t feel well and recognize that you need to talk to another doctor and keep going. “Doctors’ appointments can be consuming unless you are prepared and can communicate what is going on with your body. They only know what you tell them, so write down every symptom you have, even if you think it is not related.” Beasley also advises patients to get educated about their disease through trusted organizations like the Lupus Foundation of America. To educate yourself more on lupus, visit www.lupus.org. To find out if you may beat risk for lupus, visit the Lupus Foundation of America’s symptom checklist at www.lupus.org/body.
