Kevzara
I am curious about other’s experience with KEVZARA. I am currently taking 11 mg of Prednisone, down from 60 mg in April 2024. I am continuing to experience pain and stiffness daily, especially in the late evening and the morning. I am also fatigued most days. I am on an anti-inflammatory diet, walk daily and do a little restorative yoga. My Rheumatologist suggests going back up to 12.5 mg but I do not think that will be helpful as it will only lengthen the time I am on a drug that appears to not be helpful. She has suggested KEVZARA and we are now waiting on approval from my insurance company. My questions are: should I wait a bit and stay at 11 mg to see if anything changes (I have been on this dose for 4 weeks) before I start KEVZARA? Is it too soon in my treatment to start a biologic? It seems as tho my autoimmune system is not responding to the Prednisone or maybe I need more patience? My doctor was vague on these questions. Thank you in advance, I really appreciate this forum!
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Reading about your success with Actemra infusions and eliminating prednisone in your life, gives me hope! Just had my second infusion on Wednesday. I started feeling better 2 weeks after the first one. Stepping down to 10 mg. tomorrow.
Actemra has helped me tremendously. It was still a rocky road to finally taper myself completely off Prednisone. Depending on how long you have been on Prednisone ... it might work faster for you.
People say Actemra doesn't help with adrenal insufficiency. I would say it might not help directly but indirectly it does ... without Actemra, I would have never been able to stay on a low enough of a Prednisone dose that would allow my adrenals to recover. I had to stay on 3 mg or less of Prednisone for more than 6 months for my cortisol level to improve. I couldn't get much less than 10 mg without Actemra. Whenever I managed to get to 7 mg ... I flared and had to increase my dose again.
Actemra doesn't suppress my adrenal function so that was a huge benefit. Plus if Actemra doesn't work it can be stopped easily. It is worth a try but no guarantees. Actemra also has some side effects and it is expensive,
I've been on Prednisone since the last week of July 2024. Started with 60 mg. for 6 weeks, due to suspected GCA. When I got to 8 mg. the beginning of December, I had a flare, that set me back to 13 mg. That's when I told my rheumatologist that I wanted to try Actemra.
I am aware of Actemra side effects, but I'm over dealing with the Prednisone side effects. I honestly think that, when I was having headaches, blood sugar spikes (>200) and chest pains over the past few months, it was the Prednisone. I'll take my chances with Actemra. I'm lucky that I have Medicare.
I want that :). My hospital is Yale and they don’t have that kind of dedication.