Symptoms of Lupus

topic posted Thu, May 19, 2005 - 7:57 AM by  Scrat
Achy joints (arthralgia) 95%
Fever more than 100 degrees F (38 degrees C) 90%
Arthritis (swollen joints) 90%
Prolonged or extreme fatigue 81%
Skin Rashes 74%
Anemia 71%
Kidney Involvement 50%
Pain in the chest on deep breathing (pleurisy) 45%
Butterfly-shaped rash across the cheeks and nose 42%
Sun or light sensitivity (photosensitivity) 30%
Hair loss 27%
Abnormal blood clotting problems 20%
Raynaud's phenomenon
(fingers turning white
and/or blue in the cold) 17%
Seizures 15%
Mouth or nose ulcers 12%
posted by:
Scrat
  • Re: Symptoms of Lupus

    Mon, November 27, 2006 - 7:07 PM
    Hello, I just joined and have a few questions...I have fibromyagia...as a matter of fact I moderate a Fibro tribe here, and I'm fairly certain I have lupus as well...I understand the two often travel together and I have at least 8 of the symptoms listed below. The problem is the last two doctors I've visited said they can't positivaly say I have it one way or the other..why...what are we, they...I ...whatever, doing wrong. I have also been diagnosed with CFS...I have had the two for 8 years...since my pregnancy. I also seem to get every cold, flu and bug that comes down the pike if i'm not extra careful. ... any advice anyone could give I would be grateful for and thanks in advance.
    • Re: Symptoms of Lupus

      Wed, November 29, 2006 - 7:50 AM
      There are several tests for lupus, the most common and reliable is the Anti-Nuclear Antibodies (ANA) test. The titer represents how likely it is that you have lupus or another autoimmune disease. The titer will fluctuate based on how active the disease is and other factors like what medications you are taking, what other conditions are present, etc. There are a lot of factors that make this test only 97% accurate in people who have lupus. Most people with lupus spend years doing just what you're doing, going from doctor to doctor and getting test after test before getting the actual diagnosis. Get your test results from the doctor and ask them to go through them line by line and explain what everything means. If the doctor is not experienced in treating autoimmune diseases, they probably will not be able to do this and you should see a doctor who is experienced. For help in interpreting test results yourself, go to www.lupus.org/education/b...abtests.html

      If you have sufficient symptomatic evidence, they can treat you for lupus without a definitive lab test. The most important thing you can do is take care of yourself. Listen to your body and do what it tells you. If your body is telling you to rest, DO IT! See my post about herbal and homeopathic remedies that can support you while you're looking for answers. I'm almost in complete remission using this regimen. Find what works for you and LIVE, LIVE, LIVE your life!!

      Namaste,
      Raven
      • Re: Symptoms of Lupus

        Fri, June 29, 2007 - 12:37 AM
        Aha, so it is possible for one to have both fibromyalgia AND lupus at the same time.

        I just realized with 99% certainty that I've got lupus (though I've not had a test--I just have had many of the symptoms--not sure of which variety, exactly, mine comes with delightfully peculiar and gross blister like welts appearing out of nowhere and quickly getting infected, though I've devised some pretty good natural remedies for nipping them in the bud over the years, as long as I can catch 'em when they're still pretty fresh.

        In any case, I don't have any insurance and did the whole drug thing years ago with the fibro and HATED the results, so I'm sticking with the natural approach as much as possible and am determined to lick this thing now that I know what it is.
        • Re: Symptoms of Lupus

          Thu, July 5, 2007 - 5:08 PM
          It is Definately possible to have Lupus and ANY other autoimmune or syndrome. I met a woman online when I ran a chat group that had SLE, FMS, Scleraderma, and MS... then she got cancer. She is an amazing woman though.

          I have Lupus, FMS, Osteoarthritis, hypoglycemia, yadda yadda yadda... lol

          **warning... gross factor*** for years I would get cystic boils that would get pus, infection and bleed.. and take forever to heal. My wonderful Rheumy/internist/immunologist (yeah, the dude's smart lol) was the only one to tell me that it's a side effect of lupus.

          For other folks that get mouth sores/peeling inside the mouth. I know a semi-common cause is Canididia (sp??) or a yeast type of infection in the mouth. I don't get mouth ulcers, but I do get "sore".. very tender and sensitive on my tongue and the roof of my mouth. When this happens I gargle with a 50/50 solution of hydrogen peroxide and water. Just DO NOT swallow... and be prepare to spit foam for a few minutes.

          HTH
          Toni
          • Re: Symptoms of Lupus

            Wed, July 11, 2007 - 6:30 PM
            Brand new here - glad I found you all.
            I have Lupus, Sjogrens, RA, Vitiligo, etc......
            The Candida is what nails me - I look at a piece of bread and my mouth breaks out.
            I found a little tea tree oil in water works wonders - tastes like crap but it really helps.
  • Re: Symptoms of Lupus

    Fri, June 29, 2007 - 6:05 PM
    oh, yes.. so many this afternoon.
    I was first given a urine test in 1981 after my sons birth.
    i wonder if anyone knows what that was, back then.
    I wanted people to know the ANA is tricky.
    My antibodies are clumped...
    so I must be sure the order the qualitative titer,
    or it may say neg
    the q titer will show my 1:800+
    with spekled appearance.

    Also, don't be scared away by young doctors.. saying its fibro.
    there are different tests, and many times they clinically call it fibro and dismiss me.
    at a new clinic. and there is hope for both sets of symyoms.
    i am in both tribes, and love all the feedback.

    lastly, and hopefully not offending,
    I have many family with Celiac.
    finally found a dr to test after years of chest pain, etc...
    and now get vitc IVs and Vit B shots, and with a gluten/wheat free diet
    am much healthier. in studies it is frequently associated with sle and diabetes.

    Thank you all for these great trin=bes.
    They give so many suggestions and hope
    Joy
    • Re: Symptoms of Lupus

      Sat, June 30, 2007 - 3:57 PM
      Celiac disease, Chron's (if I spelled that correctly) and Diabetes also run in my family and I thought I'd escaped those yucky things. But then, I've never been a very big fan of wheat products and immediately preferred brown rice pasta, even, once I'd tried it, but have been unable to find it in Costa Rica so far. I did bring some back with me from a recent trip to the U.S.

      I have also had strong cravings in recent years for coconut and ginger--two things I absolutely love and have gotten to be some of my favorite things to consume and, oddly enough, I guess they've been helping to keep my symptoms at bay. Ginger, especially, is something I consume in one form or another just about every day, especially in tea.

      I also take MSM with glucosamine and chondroiton, which I'd tried separately, together and without the MSM but that's the magic combination for me and my arthritis is infinitely better than it was--in fact, I rarely have TMJ flares anymore and the carpal tunnel syndrome I was diagnosed with is completely gone. Seems to be, anyhow.

      However...lately I've been having more pain in my bones, especially of my right forearm and if I just rest it on a table pains shoot through it, so I don't know WHAT the hell that's about.

      Shoot, don't have time to post more now but it's been such a relief finding out what the cause of those nasty wounds has been, especially the ones in my mouth, which seem to be the hardest to treat.

      Does anyone else get blister and/or ulcer type stuff? How do you deal with it?
  • Re: Symptoms of Lupus

    Sun, July 1, 2007 - 12:10 PM
    oh, yes. i forgot to list a few symtoms as that is the title of this post
    first i had weakness after the birth of my son.
    I was afraid to drop my son and did not hold him
    then the tiredness and it was the knee pain that caused the dr in 1981 to do an old urine test and ana
    over the years, those symtoms repeated, as warnings.
    and if i did not rest for a month, i would end up with blood in urine and pain in my sides.
    that was when the mouth sores became more worse than when i was a child.
    the dr said it was classic with lupus, and face rash, and scalp bumps.
    i even get nose sores. yuk.. wat an embarrassing post.. i hope this helps anyone
    the last few years i have itchy bumps on my arms, and my tongue peels.
    all in the literature for Celiac. so the mouth sores are both deseases.
    and I found releif by taking b, Lysine and lecithin

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