Why do so many people suffer from Systemic Lupus yet doctors / insurance companies dont consider it serious? - best lupus doctors
I was diagnosed with systemic lupus erythematosus at 18 years, I am now 23 years old, but it's a constant struggle for me to cope with this disease. I am continually humbled by the people and the doctors and I am always proove to them that I am ill and I have a real problem. Lupus took my skills for me, is sometimes so painful that I would be dead. The situation is grave and it is my reality, but the doctors act like its a walk in the park why lukiemia cancer (cousin of lupus) or other diseases of the blood taken seriously, and treat lupus when their offer is not great? I'm tired of being treated like second class person, humiliated, because changing the companies discriminated against the ignorance of my life, painful disease. Lupus is the real hard life change, I believe, the responsibility is something for everyone to know what it is. It is surprising that, if u ask someone at random, what is lupus, do not know very well, but know someone who has. Come on people watch the network. Inform yourself!
Tuesday, January 12, 2010
Best Lupus Doctors Why Do So Many People Suffer From Systemic Lupus Yet Doctors / Insurance Companies Dont Consider It Serious?
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4 comments:
I feel the same! .. I am immune deficiency syndrome chronic fatigue syndrome and fibromyalgia ... "But you look fine !"... duh! .. I have 6 years in bed, life is not much better with the exhaustion and pain 24 / 7 (to morphine, sleeping pills, hormones, etc.) ...
I think some people try to help or be nice, but I do not know what to say .. some are critical, if not emaciated, ill (jaundice, or bleeding), then great, everyone is tired and stressed out, etc.
The only thing they really know how it is, are housewives, dr. 'S or family or friends (if any!) .. We see every day, and how you ... However, if you have the same illness, or have been, in fact, suffering, it is difficult for naive or ignorant, to be compassionate, or feel nothing ... not in a position .. when it comes to PR, so it seems to them more .. But again, they are also human beings, and even armed with the facts, it is as ... You know .. and you know who to call if you have to say after they minimizedor .. devalued is hard, hard reality, and very unfortunate for us and for all other disabled people, people are not only educated and do not know how to help or respond to ... I'm so sorry ... It is less painful, after 16 years of business, but it depends on who wins .. Yesterday was a neurologist ... Creep!
pink rainbow
Now it seems that you want to understand the world you and they do not. I know that lupus is a serious illness and a major problem for his life. You should try to educate people to change the world. There are no good treatments known to doctors feel very bad. There are a lot of ignorance. Therefore set to work educating people. Meanwhile, forgive them their ignorance and do not let the problems of the world in their stress.
And take yoga. This is the best treatment.
Read my page and certificates.
I'll tell you what they are buying.
News Now, there are good and bad here. When I was diagnosed with SLE 30 + years, my doc said I could die within a few weeks. Now consider that most doctors and insurance companies as a terminal chronic lupus. This does not mean, however, are an easy disease to live. Looks like you need a really good rheumatologist, you can manage your missiles and taking control. More about taking Plaquenil, an antimalarial drug, has done wonders for me. Prednisone beats that make you psychotic and destroys the muscles and bones. Also told me that my rheumatologist SLE tends to improve over time as they get older. It is true that for me. ) I was very sick (kidney infection when I was diagnosed at age 19. It flares up and down lot about ten years and my SLE in remission, a. Here, boy, and demand good treatment for "What's wrong!
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