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Real members of myRAteam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
A myRAteam Member asked a question 💭
Round Rock, TX
May 31, 2025
 · 
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A myRAteam Member

Sorry Linda I do not take it. We are on so many different types of treatment I hope someone will answer.

June 1, 2025
myRAteam

Unfortunately, there are no specific experiences with Simponi Aria shared in the provided search results. To get real experiences from others using this medication, you could start a new discussion topic in the myRAteam community to connect with others who may be using this treatment.

When starting any new medication, it's Show Full Answer

Unfortunately, there are no specific experiences with Simponi Aria shared in the provided search results. To get real experiences from others using this medication, you could start a new discussion topic in the myRAteam community to connect with others who may be using this treatment.

When starting any new medication, it's important to discuss potential benefits and side effects with your rheumatologist. They can provide personalized guidance based on your specific RA symptoms and medical history.

May 31, 2025
A myRAteam Member

BunsenBurner if I may ask what were the side affects? Im extremely tired.

June 8, 2025
A myRAteam Member

I am waiting for
Insurance to approve my infusions of this drug . I so hope it helps so I can start getting motivated again.
I hope it keeps getting better for
you.

June 6, 2025
A myRAteam Member

Hello @A myRAteam Member I just started the Simponi Aria infusion in April. I've only had the 1st two doses and will have my next one on June 26th. It was pretty painless as it is a very small IV needle, takes only about an hour from start to finish and except for feeling quite tired for 24 hours after the infusion I haven't had any side effects. I felt like it was really working after each dose for about a week or 2 but then felt like it hasn't helped much since after that but I'm trying to stay hopeful as it's still early on and I'm going to give it more time. Unfortunately I am currently having my worst flareup ever about 3 weeks ago and am on Prednisone again which is truly a miracle drug and a nightmare drug at the same time. Good luck to you if you choose to try it. I also take 3 pills oral Sulfasalazine twice a day every day and a once a week Methotrexate injection along with Folic Acid to try and prevent side effects.

June 5, 2025

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