Anyone else with Seronegative RA and Fibromyalgia but low ESR/SED and no swelling or redness in joints??

Anyone else with Seronegative RA and Fibromyalgia but low ESR/SED and no swelling or redness in joints??

I am seronegative RA and Fibromyalgia. My SED/ESR is never "high" and I dont have any swelling or redness in any joints. My chief symptoms are fatigue and pain in my hands and feet. Does anyone else share these backwards traits?

A myRAteam Member said:

I am seronegative too. I also have fibromyalgia and osteoarthritis. Currently taking Arava and hydroxychloroquine. I take Tylenol for pain and I cannot take any anti-inflammatory medications due to GERD and Barrett's Esophagus. I also experience a lot of fatigue as you mentioned in your post. My feet have hammer toes and bunions all due to arthritis. So far I have not needed surgery to correct them. :)

posted over 2 years ago
A myRAteam Member said:

I was diagnosed as Seronegative. My RA factor and sed rate were low, but my C-reactive protien was peaking the scale. I have been on mostly all the biologics sometimes for long periods of time. The right combination of meds should help, it just getting there. I have taken methotrexate since the beginning, about 15 years and have to increase and decrease every now and them, but overall i am managing well. Hang in there.

posted over 2 years ago
A myRAteam Member said:

I found your post as I was searching for information about Seronegative RA. I am waiting for a diagnosis, but my Dr. believes it is RA. My major symptoms were swollen, stiff and painful ankles. The swelling was fairly brief and managed with Celebrex. Since then I have stiffness and some pain but virtually no warmth, no redness and no further swelling. My feet and ankles are the worst, but my fingers and wrists are sometimes affected, and on occasion my elbows. I am also plagued by fatigue. My ESR was a 24, with up to 30 being normal at my lab. I would be interested to see how you are doing now, since this post is a couple of years old. It was helpful to find someone who has similar symptoms to me!

posted 9 months ago
A myRAteam Member said:

Thank you!! So nice to find someone with the same strange land as me 😊 Do you have swelling or just pain and fatigue?

posted over 2 years ago
A myRAteam Member said:

I also have your symptoms and although I have had RA for 16 years my joints are not really deformed. I have read though, that if one is sero-negative, that is one of the benefits. When I first got RA my hands were very swollen, but over the years that has gone down. I am taking anti-inflammatories, but no DMards, and I refuse to take prednisone because of the side effects.

posted over 2 years ago
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