Lupus Without Inflammation Showing Up In Blood Tests?
Oct 28, 2013
Is it possible to have Lupus without inflammation showing up in blood tests?
and ANA is high, he said 60 what ever that means. 1:60 I guess.
Oct 28, 2013
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Lupus :: Lupus And Vasculitis Tests Clear-MRI To Rule Out IBC-explanations Needed
I've had odd symptoms for many stinging pains, muscle twitching rashes, pancreatitis that is chronic but clear via scans.
Well, almost 3 weeks ago, a large red mark appeared on left breast. I've been going back and forth to doctor as I've wanted to rule out inflammatory breast cancer-it presents with redness etc but no lesions, hard to diagnose. Today when I went back, the doctor felt nodes under my armpit, confirmed during ultrasound, but said they looked benign and small. He said actually it could pop up from autoimmune. He did admit it was odd. It was on the same side as affected breast and not the other. I'm going to get an MRI of my breast as IBC doesn't show on mammogram or ultrasound often.
I've had swollen nodes in the past. I noticed a few times on my jaw line.
I haven't been diagnosed with lupus, tests many years ago were totally clear as were vasculitits tests. But curious if anyone has had nodes on one part of the body pop up. Im praying its not IBC. I'd much rather it be something else. IBC is the most aggressive form of BC and spreads in a matter of weeks, so grasping for other explanations
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To give a little bit of information on my background, I have suffered from back and chest acne since I was at high school. I also got it on one cheek on my face which has left scars. My chest and face cleared up by the time I had finished high school but my back acne was still severe and until this day it is still really bad. ( I am now 21). Obviously over the years I have been seeing a dermatologist who has given me many forms of medication and creams. NOTHING WORKED. I have also recently been on Roaccutane. HOWEVER... I have had problems with my cervix and bleeding and never got on with the implant that I had to go on whilst taking Roaccutane because I wasn't allowed on the pill as it cause my cervix to produce abnormal cells and bleed. I therefore was sent for tests and scans and it was then that the hospital sent over a letter to my doctor who said they suspected I have PCOS because of the cysts on my ovaries. The doctor however did not read this until after I suggested to him that as the Roaccutane did not work, maybe there is something causing my acne that we are missing, and it was then that he finally discovered the letter about them suspecting I have PCOS. (Roaccutane apparently does not work with PCOS).
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Really disheartening now and just want to know but can't carry on for much longer and really don't want to keep eating Gluten when I know I feel good when I don't. Any advise?
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