Before anyone was diagnosed with fibromyalgia did you have bloods done to check for any other imflamtory
Fibromyalgia dignosing: Before anyone... - Fibromyalgia Acti...
Fibromyalgia dignosing
Yes most of not all people will have this done as a matter of course
Hi. I did have bloods taken but I was experiencing severe pain on my knees so I asked GP for bloods to rule out any inflammation there and they were all clear. My knees aren’t as too bad but I do have times when I would struggle to walk but thankfully it’s not all the time x
Hi yes I did , and all came back clear although I don't understand it at all. Does anyone know why it comes back clear?
Because as far as we know Fibromyalgia isn't an autoimmune condition, like arthritis for example, so there are no inflammatory markers in our blood.
Thank you for that! I have arthritis in both my knees and bloods came back negative for inflammation. But can clearly be seen on xray. Would that just mean I wasn't inflamed on the day they took the blood tests?
My mother is the same, she has visibly swollen knees and can see it on the x-rays but her markers aren't raised enough for their liking. I'm sure other people know way more than about this though! Lots of things don't behave in predictable manners in regards to inflammation, my friend has Lupus, as does her aunt and her mother and sister, despite having very clear lupus symptoms her blood test came back negative, her doctors say she does have it and its just one of the things they use to diagnose as its often inconclusive....
there is something called seronegative arthritis that does not trigger on relevant blood tests but not sure if it does not have inflammation markers on CRP / ESR tests. Our bodies are complicated
they may also test for anomia and thyroid (more complicated discussion) and they come back clear or within bounds. Doctors come to a diagnosis and use serology like blood tests to confirm or rule things out.
With fibro we do not have biomarkers to rule it in so they are ruling things out or investigating them when they show up.
I was first diagnosed with lupus and seen by a different rheumatologist every time I went for routine check up. The last one decided that as my blood hadn't shown any indication for over a year that I hadn't got lupus but fibromyalgia and she didn't need to see me again. I was sent home with a leaflet and left to get on with things.
Oh my goodness that's terrible... how are you getting on now? Thank you for reply
Yes I did have bloods done. Results came clear, but had low vitamin D. I have been taking Vit D now for 6 years.
Yes I've recently had bloods done it was all fine but have never even been able to actually see a doctor face to face it was myself who had to actually suggest could I have fibromyalgia and was told it's very likely! Feel like I m having to self diagnose after a year and a half of pain not been given any medication either!!
Yes I did and also to look at the enzymes in the muscles as that can show similar problems.
Hi,
My blood tests brought up an HLA-B27 antigen marker that lead to my diagnosis of Ankylosing Spondylitis (AS) an inflammatory auto-immune disease at age 32. Although I have AS I was experiencing numerous other symptoms that were not expressed by other AS patients. Sixteen years later I finally got a FM diagnosis as well! No one had ever mentioned to me the existence of FM until 2 years ago, and when I looked into it I found that I have every single symptom registered around a FM diagnosis.
Conclusion: Blood test can help to diagnose an illness... but they can also ring fence you to a single condition in the minds of health professionals. Do not make the mistake I made and not push for further answers.
Hope this helps you.
You would probably have better experience today as it is now recognised that having AS or arthritis puts you at 12-15% more risk of fibro,
Hi Desquinn,
thank you for replying... can I ask where you get your information from?
Thanks,
P.
Done of our was published at our around the bsr 2019 conference as that's when I started talking about it. I think it was professor Gary MacFarlane that initially mentioned it to me about as but the studies will be available.
Would give you sources but that would have to wait until I am on pc. Generally I get info from Google searches on journals and pub med etc or interactions with medical professionals and researchers via email and or medical advisory board.
If you can please send me the sources when you have time then that would be great. Do you have AS as well as FM?P.
Not what I was looking for but this is a helpful article ankylosingspondylitis.net/f...
I do not have AS