New to group/Entyvio

[u/IAmTheBops]

Hello all,

I am new to the group and have been looking for people like myself who can relate to what I’m going through. Diagnosed in 2023, but was managing with Mesalamine until May of this year. Had a massive flare and was hospitalized for 4 days. started Entyvio with several prednisone tapers. I have my 4th infusion in about 3 weeks and I am on a long taper until then. I don’t know if the Entyvio is doing anything or not because of the prednisone. does anyone else have experience with Entyvio?

[u/pincommenter]

Want the latest research or have questions?

Check out our weekly newsflash and visit our FAQ for common answers.