I think for me it would have been to keep walking and enjoy swimming. Eating healthier would have been on the list too. Eat more fish less red meat, and less sugar.
I wish I knew that people can be really ugly and our healthcare team doesn't understand what we are experiencing. Sometimes I feel like they are learning with us. Or that we would always have pain, swelling, stiffness, and flakes and take medications. I wish someone had told me this would be a lifetime journey.
What do you wish you knew about living with PsO and PsA when you were first diagnosed? We would like to hear from you. Diane (Team Member)