The moringa oleifera tree is now considered by many as a miracle tree for its medicinal benefits. The trees leaves are typically utilized to make moringa extract which includes anti-inflammatory components. Moringa also carries anti-toxins, anti-oxidants, vitamins, nutrients, and amino acids to develop one's wellbeing and immune system. With these perks, the World Health Organization, the European Union and other none government offices in the world appreciate moringa. To combat malnutrition, countries like the Philippines and Africa cultivate moringa trees to be utilized as components for drugs and cosmetic products, and also as products from bulk production and wholesale of its oil and powder form.

One of the most imperative functions of moringa is the truth that it inhibits the COX-2 enzyme which is accountable for swelling and pains in the body. In this case, lupus and the battle in opposition to it comes into the situation. In a nutshell, Lupus erythematossus is an illness with unknown reason which leads to the inflammatory conditions of several parts of the body counting the kidneys, joints, and the skin. Another truth about lupus is that it can influence anybody without thought to their age and sexes, and you can anticipate that things are not going to be pleasant. In addition, the pain of the production of the COX-2 enzyme particularly throughout the constant flare ups could be hard to bear. No one really understands what causes these flare-ups and many sufferers of lupus are continuously on the guard of how to stay away from them. This states that sufferers need to keep away from sunlight and eat foods rich in omega 3. The way of life of the lupus sufferer can be very costly because of all the drugs they need to take to inhibit the disease. Moringa being a cheaper form of alternative medicine and a source of nutrition, aids the sufferers to decrease their bills.

As it contains natural anti-inflammatory properties it is thought to be to be safer to use on the long term than the NSAIDs which can be addicting or can cause some unwanted unwanted side effects. There are lots of side effects to anti lupus drugs can do to a person. For example, it can affect the kidneys, the circulation, the digestive system and many more parts of the body. Apart from being less toxic, taking in moringa is also more effective. Now moringa is made in many forms and to name a few there are moringa leaves and powders which can be acquired in bulk over the Web.

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Source: http://www.sooperarticles.com/health-fitness-articles/anti-aging-articles/moringa-oleifera-substitute-remedy-lupus-356594.html


symptoms for lupus flare up

9 thoughts on “Symptoms For Lupus Flare Up

  1. Ern

    Is lupus always diagnosed during a flare?
    My understanding is that when someone has lupus they go through periods of remission and flares. My question is- is it possible to diagnose lupus (using the blood tests commonly used) during a symptom free remission or is blood work only atypical during a flare?

    1. Linda R

      Some markers will be present, flare or not. This would included a speckled antinuclear antibody and a few other autoantibodies, but the levels may vary.

      Things like sed rate and complement would vary widely between remission and flare.

  2. betsy_51783

    Does anyone have discoid lupus and is pregnant?What are your symptoms? How do you deal with them?
    I am about 9 weeks pregnant and I cannot take my medication to help prevent the rash. Every day about 2 hours after I wake up I get a flare up on my hands, arms, legs, ankels, neck and chest and they seeming to get worse. Is this normal? I can’t get into my dermatologist for 2 weeks and none of my other doctors will touch the lupus issue. HELP!

    1. Linda R

      Call the dermatologist back and be very firm about getting in earlier. If they gatekeepers still refuse, ask to have the doctor call you that day. If that does not work, call your rheumatologist.

      Personally, I would look for another dermatologist ASAP. Lupus patients need to be able to see their doctors within a reasonable time when there is a problem Two weeks is not reasonable. It is most likely the receptionist who is the obstacle. Asking the doctor to call you should by pass him or her. Don’t bother telling her your whole story. You can also fax the doctor explaining your symptoms clearly and asking him or her to call you ASAP. You can also call after hours and get the doctor’s service and leave a message with them if you think your other approaches are not getting through to the doctor.

      You might also call your ob/gyn and ask if over the counter cortison cream is permissible during pregnancy. Throughout your pregnancy the doctors who treat your lupus and your obstretician should be working hand in hand. You will be the one who has to make that happen.

  3. Taylor L

    What does lupus do to the different organs of the body, and what would the symptoms include.?
    One of the characters in a story I am writing is dieing of lupus in the early 1940’s. Her character is suppose to have had flares of the disease for years and years, but the disease is becoming more and more serious until a point where she is so weak she can barely walk. Is that far-fetched?

    1. Linda R

      I attended a funeral for a member of my lupus support group. She was 36 and died of a stroke. She had antiphospholipid antibody syndrome that often occurs with lupus.

      Half of us will have kidney disease. There is a woman with lupus in my apartment complex whose kidneys have totally failed. The doctors have stated that she would most likely not survive a transplant. She is on dialysis 3 times a week. The lupus nephritis will ultimately kill her.

      I know a man whose wife died from lupus when it attacked her liver.

      A young woman I know died of lupus kidney disease while waiting for her third transplant.

      I nearly died from lupus in 2003. I had bone marrow failure, pancytopenic anemia, pericarditis (very common in lupus), pleurisy and pleural effusions (also very common), and beginning renal failure.

      As recently as 20 years ago, a diagnosis of lupus was considered a death sentence.

      The meds we take to try and control the lupus have some nasty side effects. I know two lupus patients who have had avascular necrosis of the hips from high doses of steroids. Both women have had both hips replaced. One was only 22 at the time. Many of the immunosuppressive drugs we take for the more serious cases predispose us to cancer because they suppress tumor necrosis factor.

      90-95% of lupus patients have joint pain and inflammation. At my worst, I could not even stand to shower.

      PS My lupus is well controlled now through a combination of medications, regular medical monitoring, and a very proactive approach to managing the disease.

      PPS I think your character is dying not dieing. And her character is “supposed” not “suppose” to have had flares. You might want to consider having someone proof read your story before you submit it anywhere.

  4. Jeanie B

    Is it possible for the Lupus rash to be more prominent on the nose and less noticeable on the cheeks.?
    I have several of the Lupus symptoms, however, the rash is more noticeable on my nose. I don’t normally run a fever. My temperature usually runs below the normal 98.6–averaging about 96.5 to 97.5. The days that I feel really run down are the days when my temp jumps up, and then it is about 99.9. Can someone please give me a little more information on Lupus SLE?

  5. momzpeachy

    need some help understanding MS? How often are the flare ups and how does it get diagnosed?
    I had an MRI done early February due to neck and arm pain. That was of the brain and showed no lesions. Since that MRI ..I had a major flare of pain all over and all kinds of symptoms that go along with MS. My vision got blurry and nlood pressure raised. I was a real mess. I was told by the neurologist that since that MRI was negative there is no chance I have MS. I had those symptoms for a few weeks and now I am better. It’s really weird how it all went away. Except for the vision part…I still have blurry and distorted vision. Flourescent light drives me nuts!

    I am quite concerned as to whether the neurologist could be wrong. I was also told it could possibly be lupus but all the blood work came back negative.

    I’m wondering if some of you might be able to help me and guide me in a direction. I am seeing a rheumatologist tomorrow but not sure that’s the right doctor to see. What other tests need to be done and who orders them?

  6. Cap10

    What are the symptoms and avalible treatments for Lupus?
    Any information, links to information, experience or suggests are welcome. They are for a close friend of mine who was recently diagnose with Lupus and is understandably a little frightened.

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