What is the life span of someone with lupus

What is the life span of someone with crest lupus?

http://wiki.answers.com/Q/What_is_the_life_span_of_someone_with_crest_lupus

There is no such thing as crest lupus. Crest disease is a different disease alltogether. It is however an autoimmune disease just like lupus.

What is now the lifespan of someone diagnosed with Lupus??

http://answers.yahoo.com/question/index?qid=20070911194224AAIUrsv

I think that alot of doctors just don’t know alot about Lupus. It’s hard to diagnose, and essentially is what you are told you have when all other diseases are ruled out in some cases. The biggest danger of Lupus is organ failure, especiall…

Related Questions Answered on Y!Answers

what is the average life span of someone with lupus?

Q: i was diagnosed 10 years ago with RA but found out 2 days ago that i tested neg for ra and positive for lupus. i am in constant pain and always tired.i am a single mom what can i expect? how long will i live?

A: I have been living with Lupus for 15 years. There is no cure (yet) but lifestyle changes are important! I ran a Lupus Support group for 3 years and it affected each individual different. There is no “average life span” of a Lupus patient. If the doctors tell you that you have a certain amount of time left don’t listen! They told me that I would not live through the night and that was in 1992. If you have joint pain and fatigue then it is “mild” opposed to organ involvement which is severe. Don’t start worrying about dying but rather just live life. None of us knows when we are leaving this earth (whether we have an illness or not) and it is only up to God when we do. Stay out of the sun, avoid stress as much as possible, try to stay away from chemicals in food and products you use on your body and learn to listen to your body. When you need to rest do it. You can live until you are 90 just like everyone else. Don’t believe in quick fixes or a magic pill because there are a lot of people out there claiming they have that one cure for you and it is basically to fill their pocket full of money. Work with a doctor that will listen to you because it is your body and surround yourself with supportive people because even though you look completely fine sometimes you won’t feel that way and it is good to have people that understand. Try and find a Lupus support group in your area. God Bless You.

Lupus sufferers pls help ?

Q: I have had a couple of ppl ask me ” Are you sure you might not have lupus ? ” Now I am wondering if what i am sick with isn’t a lupus flare up . Here are my symptoms I have a sore in my nose Get sores on my legs that don’t heal for months and look like shaving bumps or ingrown hairs . very sore joints ears and throat are sore extremely tired bruising easily having some edema here and there sometimes feel like as if my soul is very far away yet my body is here . If this does represent a lupus flare up what type of doctor do i go to get tested for Lupus ? Also how lung is the life span of a lupus patient ?

A: Unfortunately, those symptoms can be from many different things. But your regular doctor can check you for lupus. Its a simple blood test. Also one of the other things to look for is a red rash on the face, that looks like a butterfly that covers the bridge of the nose and cheeks, its very common with lupus. And the life span depends on what organ involvement you have. There are things you can do to avoid flairs if it is lupus, like avoiding the sun. Also eating right and exercise can help, the better shape you are in, the better you will feel.

lupus went from 1.4 to 1.6 so how bad is this?

Q: Doc said i had lupus in 2003 I take a lot of meds was in pain went to him and he checked me for the levels of lupus which came back as 1.6 so his nurse says. I have been on morphine for years due to another reason. How do they scale lupus and what really causes it? I can’t find on the web any grafts of progress of lupus or charting nor scales to find out just where I stand with this. Have to go to specialist yet. what is the life span of someone with lupus? I don’t get rashes and etc. Mine is joint pain and swelling

A: I have Lupus and APS and have never hear that scale other than in an INR. Either way numbers will go up and down as disease waxes and wanes. But the numbers do not necceasarily tell the whole story.You need to be followed by a rheumatologist. I certainly hope they have you on Plaquenil. Despite the symptoms of lupus and the potential side-effects of treatment, people with lupus can maintain a high quality of life overall. One key to managing lupus is to understand the disease and its impact. Learning to recognize the warning signs of a flare can help the patient take steps to ward it off or reduce its intensity. Many people with lupus experience increased fatigue, pain, a rash, fever, abdominal discomfort, headache, or dizziness just before a flare. Developing strategies to prevent flares can also be helpful, such as learning to recognize your warning signals and maintaining good communication with your doctor.It is also important for people with lupus to receive regular health care, instead of seeking help only when symptoms worsen. Results from a medical exam and laboratory work on a regular basis allows the doctor to note any changes and to identify and treat flares early. The treatment plan, which is tailored to the individual’s specific needs and circumstances, can be adjusted accordingly. If new symptoms are identified early, treatments may be more effective. Other concerns also can be addressed at regular checkups. The doctor can provide guidance about such issues as the use of sunscreens, stress reduction, and the importance of structured exercise and rest, as well as birth control and family planning. Because people with lupus can be more susceptible to infections, the doctor may recommend yearly influenza vaccinations or pneumococcal vaccinations for some patients.Women with lupus should receive regular preventive health care, such as gynecological and breast examinations. Men with lupus should have the prostate-specific antigen (PSA) test. Both men and women need to have their blood pressure and cholesterol checked on a regular basis. If a person is taking corticosteroids or antimalarial medications, an eye exam should be done at least yearly to screen for and treat eye problems.Learning to recognize the warning signs of a flare can help the patient take steps to ward it off or reduce its intensity.Staying healthy requires extra effort and care for people with lupus, so it becomes especially important to develop strategies for maintaining wellness. Wellness involves close attention to the body, mind, and spirit. One of the primary goals of wellness for people with lupus is coping with the stress of having a chronic disorder. Effective stress management varies from person to person. Some approaches that may help include exercise, relaxation techniques such as meditation, and setting priorities for spending time and energy.Developing and maintaining a good support system is also important. A support system may include family, friends, medical professionals, community organizations, and support groups. Participating in a support group can provide emotional help, boost self-esteem and morale, and help develop or improve coping skills. Warning Signs of a Flare -Increased fatigue -Pain -Rash -Fever -Abdominal discomfort -Headache -Dizziness Preventing a Flare -Learn to recognize your warning signals -Maintain good communication with your doctor Learning more about lupus may also help. Studies have shown that patients who are well-informed and participate actively in their own care experience less pain, make fewer visits to the doctor, build self-confidence, and remain more active.Tips for Working With Your Doctor -Seek a health care provider who is familiar with SLE and who will listen to and address your concerns. -Provide complete, accurate medical information. -Make a list of your questions and concerns in advance. -Be honest and share your point of view with the health care provider. -Ask for clarification or further explanation if you need it. -Talk to other members of the health care team, such as nurses, therapists, or pharmacists. -Do not hesitate to discuss sensitive subjects (for example, birth control, intimacy) with your doctor. -Discuss any treatment changes with your doctor before making them.