Jeanne9, hello my name is Terri 👋 yes, if one has the correct mental person on their side, has many Hands to reach out to, like a Village, if done Right ✅️ 😀 and that doesn't happen all that often. But in 2019 is when I began with A Doctor for Study Drugs for Ps, PsA, & all its commodities, & for those 6 years, I never had been PAID not 1 🔴 cent, it was great & treated was like a Queen ...one of the best thing i ever done toward postive change

I believe the way most of us found Out what is wrong with Us ,was to get a Rheumatologist, or dermatologist, or go to YOUR PCP... This would be your BEST first line of Defense. Good Luck

I had a phenomenal Dermatologist who was always asking about any joint pain. The minute I said yes she sent me to the Rhuematologist and they worked together on my treatment plan. I am so lucky to have gotten such great care and feel Bad that others don’t Get that same level of care. Then the blood work and elimination of other options as there is no test for PSA. But my elevated CRP was what confirmed it. Started on Otezla and it was then I realized how much pain I had been in. Good care exists. I wish that for all!

Who you asking? do you THINK I may have some Intel on The Treatment or Rx's 🤔 that you have received & maybe some Skills that have Helped You in your journey that you had traveled. That could really be beneficial to All Members here a MyPsoriasisTeam. Thanks 🤓 a

Have you have any treatments yet