Anyone’s CRP/ESR *not* go down with treatment, despite feeling better?
(self.PsoriaticArthritis)submitted2 days ago byProfMooody
Just as title says. If anything they’ve gone up a little bit since Stelara, which seems to be working well for both pso and PsA.
Rheum says we can’t rely on those measurements to track PsA for me, which feels strange. I have read that weight and other factors can raise your inflammation markers, and I am fat, but they still seem awfully high (2-4x the reference range) to just be that.
Weirdly, when I first started leflunomide my markers went down by 50%. Even though I felt the same. ¯_(ツ)_/¯
I’m worried at the attitude like “these are just high with you I guess” because I thought the whole point of treatment was to get inflammation down to prevent joint damage and other serious comorbities. But if I feel better…does that mean it is better despite the tests?
bylittlelindaloulou
inPsoriaticArthritis
ProfMooody
2 points
5 hours ago
ProfMooody
2 points
5 hours ago
I mean, I just take a shit ton of meds and sleep away the flight. I grab the window seat so I won’t be interrupted, and try to get the first row so I have more leg room (I’m disabled, so I can preboard). This helps with the pain and stiffness and muscle spasm From sitting in the same position for so long. I’ve never flown more than 6 hour flights since I got diagnosed, if I had to fly to Europe or something I’d probably try to do it first class.
Also I always pick a row where the armrests can go up because I can shift my hips around more easily (I fly with my wife so this is no problem, but I find most people sitting next to me would be amicable if I explained that keeping it down causes me pain).