I started Simponi ronight, hope it woks a well as Humira use to work...bent and swollen fingers crossed.
My wife was getting her hair cut today and a nurse with PsA was seated next to her. The nurse preceded to tell my wife about the "horrible" choices I was making with biologics. She claimed Humira wrecked her life and caused her to get P and working hard to rid her body of the Humira toxins. Before she came home she bought me the nurses prescribed cure all...fish oil and glucosamine & chondroitin.
I thanked my wife and told her I will take the pills, every little bit helps, but it won't due anything for the P and it won't stop my body from attacking my joints.
Tonight, sorry...PIMF. Sounded like Scooby Doo there for a minute.
Sometimes free advice is worth exactly that- nothing. I try to tell myself people care when I receive such helpful advise but it is hard. Sometimes I just want to tell them to shut it!
I agree Michael. I got really tired of the free advice from everyone five years ago when I was first hit with PsA. I've had every suggestion including tart cherry, yoga and a Mexican Curandero (witch doctor). Most of the advice came from those with no skin in the game.
I now thank people, then go about my own business.
Good luck with the Simponi. How long does it take to see a result?
Frances
Best wishes on the Simponi! I used it for about a year and it helped me quite a bit (much better than Humira).
Advice like that is sooooo annoying! UGH.
Marietta, why did you stop the Simponi?
It just stopped working for me after a year :(
Jorline said:
Marietta, why did you stop the Simponi?