Is anyone on long term mesalamine suppositories?

Basically the title. I was given mesalamine suppositories when I was first diagnosed and they worked wonders. I just asked for another dose, and was given some, but it’s only 7 days. I was wondering has anyone been on long term suppositories cause they are the only thing I have taken since my diagnosis that has worked. Oral mesalamine failed, entyvio failed, rinvoq failed, and humira failed. I’m hoping this round of suppositories will work again, I just hate taking them but it’s better to feel I little uncomfortable for a few seconds then be in pain 24/7.