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.

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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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Does anyone else dread Routine Blood Tests scared that they are going to detect some "Blood Cancer"? I've been looking up Leukemia and Lymphoma symptoms all morning. I'm getting a CBC for Fertility treatments.

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Less Blood For Tests - Thickness Of The Blood And The Small Veins

Weekly blood removal was ordered by my hematologist.  Being needle phobic I knew it wasn't going to be fun.  Since being misdiagnosed since 2007 my iron levels were greatly increased.  After going for my first blood removal, I was concerned since after trying both arms, they were unable to get the 500 ml due to the thickness of the blood and the small veins,  I believe they were only able to get 50 ml  Has anyone else experienced this?  Or does anyone have any recommendations on how to get more blood out? 

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Interstitial Cystitis :: Inflammation Causing Blood On Toilet Paper After Urination?

Can IC inflammation cause blood on toilet paper after urination? Couple years ago my doctor thinks I may have IC. Couple times a year I do get bladder infections. Right now I'm on Cipro for a bladder infection and I'm on my 10th day of antibiotics when I saw blood on the toilet paper. My bladder symptoms however seems better now that I'm on antibiotics.

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Infertility :: Pelvic Inflammatory Disease - Blood Work Normal But Inflammation

From 4 yrs i have been suffering from severe pelvic pain with lots of inflammation in both hips. all blood works come normal but mri does show inflammation. Doctors cannot find what it is, can it be my ovaries or fallopian tubes inflammation or infection which is causing this, plz somebody help. I want to get pregnant but my pain in pelvis which is that worse that I limp many time is not allowing me.

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Blood Tests :: Vitamin B12 Levels

Had a blood test for this the other week and got my results back. It's says 200 but next to it says (180-900). Is mine low and need medical attention.

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Polymyalgia Rheumatica :: How Often For Blood Work / Tests?

Other than feeling ill/flare, is it recommended to have blood tests at any regular times?  I`m under my doctor, which I prefer...can't "work" with my Rheumy...but struggling with fatigue to get under 11mg....wonder if I should have  blood tests more often....probably had one a year ago.  Have had PMR 4 years now...(started on 15mg).

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Polycystic Ovary Syndrome :: With Normal Blood Tests ?

I have recently been told by the doctor that I may have PCOS. However I have a few questions around my recent blood test results and therefore was wondering if anyone could help answer some of my questions.

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).

Anyway... this leads me on to my question. I have had the blood tests which was meant to be on the 21st day of my cycle but I have come on my period late and therefore was wondering if this will affect the results? My results came back normal. I haven't had my 3rd day cycle blood tests yet though however. Can your tests still be normal if you have PCOS?

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Coeliac Disease :: Negative Blood Tests - Gluten Free Diet Helps

Basically I am 25 years old and as i've grown up I've noticed more and more that I was getting stomach cramps and bloating more and more often. It is very sporadic and I couldn't really say exactly what was causing it but I just thought it was normal. This was until the last 12 months when I started to think a bit more about it. I do a lot of exercise and play a lot of football. I was finding that I would get some form of cramp during a football game. Usually quite mild but sometimes worse. I also like to run and when training for a half marathon found that after a certain distance I would get pains. Almost every time after about 30-40 minutes running. It would normally be worse when running in the evenings. I started thinking about it and tried taking several things out of my diet. I am 95% certain I have a lactose intolerance as since cutting that out around 6 months ago I have seen an improvement. But I would still get pains.

This all resulted in me going Gluten Free and I finally experienced what it feels like to have a normal stomach. I was relaxed and could do whatever I wanted without any fear. So I decided for my own health I should get tested for celiacs disease and after 7 weeks of eating gluten again had the blood tests. Today I had the results and they have come back negative. I feel so deflated and just angry. What do I do now? I just feel like going back to Gluten Free and living like that self diagnosed. The weird thing I find with my disorder is it seems to be worse when i'm up and about. If me and my fiancee have gone out around town and have lunch it is often worse when walking around afterwards. I don't always get blinding pains either. It is often just severe constipation or stomach cramps just making me feel uncomfortable.

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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Can anyone tell me is this anything to worry about or not?

Veins are being showed on my stomach .. I am very fit 22 year old , i work out /etc.

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I'm anemic and have been since I was a kid. My chest is tight most of the time. I'm not taking any meds regularly. But around 18 hours ago, I took a Brufen 400mg for a nasty headache I had. It's still there, btw.

It's 4 in the morning here so I can't go to a doctor right now. If you can give me an idea what it could be or even what kind of doctor to go to in the morning, I would appreciate it.

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