Joint pain: In the past I was diagnosed... - Hughes Syndrome A...

Hughes Syndrome APS Forum

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Joint pain

Heidi-B profile image
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In the past I was diagnosed with Rheumatoid Arthritis then told I had fibromyalgia when I switched rheumatologist. I quit going to doctors and taking meds (hydroxychloroquine, enbrel and mythelprednosolone) and started crossfit which did help until I needed spinal fusion (bounce house not crossfit) which did help somewhat. I am now wondering if the joint pain may have been related to HS/APS?

Is joint pain something that can happen with HS/APS?

Thanks

Heidi

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Heidi-B profile image
Heidi-B
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Tucson profile image
Tucson

It's probably the most common symptom along with muscle aches.

Heidi-B profile image
Heidi-B in reply to Tucson

Thank you!

Heidi-B profile image
Heidi-B

It was over 4 years ago that I stopped seeing a rheumatologist for RA and/or fibromyalgia. i never felt like the 2'nd doctor was correct with the fibromyalgia diagnosis and she said no to the diagnosis if RA. The meds made me sick to my stomach. I didn't like taking meds for conditions I may not have truly had. So I turned to Exercise and a healthy diet. Even with diet and exercise I do have pain in knees and hips.

I do get the headaches and that is not fun.

I will speak to my hematologist at my next appointment about the joint pain see If he can recommend a good rheumatologist.

Kalykrill profile image
Kalykrill

When I was diagnosed with APS after my DVT, heart attack, and PE. My joints have progressively gotten worse over the last 10 years. I was very active and had no joint issues until after I had my episode. Now my joints are getting worse. They say I have arthritis also fibro. People I have discussed with that also have APS have joint pain and muscle pains. Sometimes my hips hurt so bad I have a hard time going to sit down after walking to the recliner. Every day something hurts bad.

Heidi-B profile image
Heidi-B in reply to Kalykrill

That is exactly how my hips feel. I do find stretching and exercise does help somewhat. I do have awesome trainers who understand my limitations and give me modified movements.

Woke with hip pain this morning went to the gym for a boot camp style workout and I feel less stiff.

Tucson profile image
Tucson

I've never had a migraine but tbf you can find loads of excuses for joint pain, I know I did on the rare occasion I had it, until of course my knee disintegrated with no warning and now the second one is going, as a result I can barely stand and no longer walk. I currently have knee, back, elbow and hand pain.

ndstephens49 profile image
ndstephens49 in reply to Tucson

Hi Tucson, I had lots of jaw bone pain as initial symptom of APS. Turned out I had osteonecrosis of jaw bone secondary to ischemia caused by APS. I have also taken prednisone which, unfortunately, can also cause osteonecrosis. Some people end up needing joint replacements simply from taking prednisone. It's a 'double whammy' if you have APS and have also taken prednisone

I didn't realize, though, that joint pain was such a common symptom of APS. I learn something new here every day.

Keep fighting the good fight.

Nancy

Heidi-B profile image
Heidi-B in reply to ndstephens49

I am trying to learn as much as I can so I ask questions here. I never heard of APS until I was diagnosed in October 2016. I was just curious about the joint pain because I know how I feel on a daily basis. It's not fun.

Lure2 profile image
Lure2

I agree with APsnotFab that you should go back to a Rheumatologist and do ev a lot of bloodtests as it was a long time ago (4 years) you was properly evaluated.

Best wishes from Kerstin in Stockholm

Heidi-B profile image
Heidi-B

Thank you all for the feedback. My hematologist did a whole lot of blood work after my clot was discovered and redid blood work at my last visit. I know I do need to follow up on the joint pain so my task now is to find a good doctor. Unfortunately my experience with the last 2 rheumatologists weren't great.

Tucson profile image
Tucson

well the specialist at St Thomas' questioned the OA diagnosis last week he believes it's unlikely to be OA because of the sudden onset. Although I was told a year ago I needed an urgent knee replacement but I'm apparently too high a risk due to multiple strokes the last with an Inr of 4 so it seems they've gone back to square on in the evaluation process. All my joint pains came on suddenly and recently too.

Heidi-B profile image
Heidi-B in reply to Tucson

I know my orthopedist told me a few years back that my knees appear to be older than me by about 20 years. My husband asked what could be done about that & the doctor said replacement but it would be years until needed. That was when I was 45. So I definitely know I do have some osteo-arthritis. Always fun!!

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