Just Started Simponi Aria for My Ankylosing Spondylitis - Any Tips or Experiences to Share?
Hey everyone, I just started Simponi Aria infusions for my ankylosing spondylitis. The infusions are quite intense; I have to stay at the infusion center for a few hours each time. I'm hoping this will help with the pain and stiffness I've been dealing with. Has anyone else had experience with this medication? I'm curious about the side effects and how others have managed them. Also, any tips on making the infusion process easier would be appreciated. Thanks!
Just Started Simponi Aria for My Ankylosing Spondylitis - Any Tips or Experiences to Share?
Hey everyone, I just started Simponi Aria infusions for my ankylosing spondylitis. The infusions are quite intense; I have to stay at the infusion center for a few hours each time. I'm hoping this will help with the pain and stiffness I've been dealing with. Has anyone else had experience with this medication? I'm curious about the side effects and how others have managed them. Also, any tips on making the infusion process easier would be appreciated. Thanks!
Comments (10)
I can't believe it's 2023 and we're still giving infusions. Why can't they make this into a pill? It's just a pain to go to the infusion center. Plus I always feel sore for a day after.
I was on Simponi Aria for a year, and I really liked it. I felt more motivated to work out and actually started running again. The only downside was the flu-like symptoms after some infusions. It was a small price to pay for the relief, though.
My doctor warned me about the potential side effects, especially infections. I make sure to avoid crowds and wash my hands constantly. So far, I've been lucky and haven't had any major issues. I'm thinking about getting the flu shot as well just to keep safe
So, I was talking to a nurse here and she told me that some people don’t respond well to Simponi Aria and it can take a few months to kick in. Just keep at it, I know you can make a difference.
I've been on Simponi Aria for about 6 months now. The infusions are a bit of a hassle, but the improvement in my mobility has been worth it. Just make sure to stay hydrated before and after your infusions.
I had a really bad reaction to my first infusion—it was scary. I got hives and had trouble breathing. I had to go to the ER. They gave me some Benadryl and said I could try again. I asked if they could give me a pre-medication so I could avoid this reaction in the future, but I opted out and chose Enbrel instead. No issues so far. Fingers crossed it stays that way.
Make sure to tell your doctor about any heart issues. This drug can mess with your heart if you're not careful. Don't be afraid to speak up if you have concerns. Just like the post says, if you feel any of the symptoms, get to a doctor asap. Strangely enough, I actually have felt better than I used to after taking this medication. I don't need to take as many painkillers.
Really? You’re dealing with IVs and all the side effects? Ugh. I will stick with my pills. This sounds like a hassle.
You have to watch out for those infusion reactions. I've known people who got them and it’s not fun. Make sure you have your doctor's number on speed dial just in case.
You're going to love this medication. Simponi Aria has been a game-changer for my rheumatoid arthritis. I have seen a drastic reduction in pain and swelling.
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