Experiences with

ANA test

Doctor is looking at possible Lupus but ANA test is negative. I have joint pain, muscle pain, basically pain anywhere and everywhere. I’m wondering if it could be lasting damage from the chemo or should I have fully recovered from that? I did have mild joint pain before but nothing like this.

I’ve been unwell for nearly 3 years and all the bloods tests carried have come back normal apart from the ANA test which showed slightly higher levels of inflammation & CRP test which also came back with slightly higher levels of inflammation.

I’ve been from pillar to post but recently had a positive ANA test and pretty sure after a couple of recent sunbeds I have a malar rash across my face. So I am now wondering if it’s lupus and the tick bite was a red herring.

I have an under active thyroid and have been on 150 Levothyroxine for a few years. Latest blood tests show my thyroid is where it should be. Last year my hands and feet got painful and swollen and X-rays of my hands show osteoarthritis. Doc ordered more blood tests to check,for Rheumatoid Arthritis.

My immunoglobulin level was 954 my doctor suggested Ana test and I have diagnosed with ANA week positive and AMA M2 positive with value of 18.. Positive for PBC I have been told I may suffer pbc in future presently my l GGT and alkyne phosphate level is normal..

My immunoglobulin level was 954 my doctor suggested Ana test and I have diagnosed with ANA week positive and AMA M2 positive with value of 18.. Positive for PBC I have been told I may suffer pbc in future presently my l GGT and alkyne phosphate level is normal..

Does PA cause a positive ANA test result? I had two positive results back in 2018 but the man negative in 2021 and April 2022. I had labs done last week due to some symptoms I’ve been having and my ANA came back positive.

My neuropathic specialist thought it could be lupus but ive had negative Ana test and nothing showed in my kidney biopsy that would show lupus.

Since 2020, I have now had 4 positive ANA test results, all homogenous. They were 1:640, 1:1280, greater than 1:1280, and 1:640. I have been on Naltrexone now for over a year I believe. Symptoms have a habit of coming and going, being mild at times, more severe at others.

My ANA was negative but asking biopsy was positive for interface dermatitis ???? the skin doctor said possibly cutaneous lupus. Is it possible to have it on skin only and not in the blood?

I'm having the ANA and anti - ds/DNA blood test in 2 days to see if all my symptoms are Lupus related and my concern is this:I'm currently taking Fexofenadine 180mg and flucloxacillin 500mg for extreme rashes and finger infections, I'm wondering would this reduce ANA in my bloods?

An antibody test showed Positive ANA. Went to rheumatologist and been having tests for other stuff including Raynauds testing. Raynauds came back as secondary. My rheumatologist then diagnosed Undetermined Connective Tissue Disease. He thinks it will probably progress to Lupus or similar.

doctor conducted ANA blood test which came back negative so she says I definitely don’t have Sjogrens. My symptoms have stayed, my eyes particularly worsening with pain from dry eyes, making it difficult to drive and see in general.

She tested him for antibodies, an ANA multiplex with reflex test and it came back positive. She also did another test go see which antibodies he has. The test is called Auto Immune ABS, multiplex. The only antibody that came back positive on that test was the Scl70 antibody.

Also waiting for ANA blood test to come back. He listened to my heart for like a minute and of course it sounded good and was beating fine. Like Idk anymore maybe I really am just making shit up even though I do feel real things.

Hi All This is my first post and I appreciate that you may not have the answers just looking for guidance. I was diagnosed with Optic Neuritis in February and was put on short intensive steroids in March sleep deprivation the worst! but sight hasn’t fully and won’t fully return. Ophthalmology thought

As some of you are aware I was told I had a fatty liver after a US scan last February.Since then I have had 2 ct scans,1 MRI and 1 fibroscan.Found a cyst on liver Had COVID Nov 22 This year my stools have been pale,tired,itchy skin,hairloss,spider veins.headaches and a tad forgetful diarrohea,low BP

Good morning, I am waiting for my next Rheumatologist appointment and have recently been suffering with issues , I have been on antibiotics 3 times in the last months due to high protein levels being found in my urine ,no blood present,on Reagent strip dip sticks. Once at the hospital ,then two at my

I have had an mri and my ANA (lupus) test were both normal.  thanks so much in advance for your advice and thoughts. It’s very much appreciated.

I have not been diagnosed yet and have recently been given an urgent referral to The Royal Free. I have been having flare ups for the past 10 years but they are getting more frequent and worse. My GP has sent me to A&E 3 times. Does anyone get shooting stabbing pain in their ribs and sternum? It feels