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I have just suffered my fourth miscarriage resulting from anticardiolipin antibodies. The first two my antibodies lay undetected. My third was treated by asprin but my pregnancy did not go far enough to start on heparin. I then had a beutiful baby girl following combined treatment of asprin and heparin. I have just had my fourth miscarriage and dont understand how it can work once but not again? Does anyone have any advice.

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Submitted by Kim (not verified) on Thu, 2011-05-12 14:07.

At that time there was no information on anticardiolipin or antiphospholipin. Luckily, the physician who treated me was fresh out of residency and had just learned about this antibody. 2 years ago I was diagnosed with thyroid cancer. I have since had a total thyroidectomy and 2 parathyroids removed. Could the blood clotting disorder have anything to do with the development of this cancer? I don’t have any history of radiation exposure. Although I am a critical care nurse, I have always used a neck shield during special procedures when there was exposure to radiation. I don’t like the idea of having cancer in my body – and although the doctors say that it did not spread – I still wonder how it came about. I appreciate anything you have to offer.
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Submitted by fire pits cast iron (not verified) on Thu, 2011-05-12 12:29.

Anti-cardiolipin antibodies are antibodies often directed against cardiolipin and found in several diseases including syphilis, antiphospholipid syndrome, livedoid vasculitis, vertebrobasilar insufficiency, Behçet's syndrome, idiopathic spontaneous abortion, and systemic lupus erythematosus. They are a form of anti-mitochondrial antibody. In SLE, The anti-DNA antibodies and anti-cardiolipin act independently. In rheumatoid arthritis systemic sclerosis (scleroderma) these antibodies may tie two conditions together.

Submitted by Elvis (not verified) on Wed, 2009-09-16 13:21.

Give please. Depend not on another, but lean instead on thyself...True happiness is born of self-reliance.
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Submitted by Anonymous (not verified) on Sun, 2006-03-19 00:15.

Have you looked at the Lupus uk site? I think that there is some detailed information at that site. Take a look at it if you have the time, I found it useful. Thanks for your comments, sometimes it feels as if I am the only one with this disease. Let me know how you get on with that.

Lisa

Submitted by Anonymous (not verified) on Sun, 2006-03-19 00:19.

Here is another Lupus site with a question and answer section. I think it is worth a look too.

http://www.lupus.org/education/faq.html

Lisa