This is the part you can see

When people don’t understand that psoriatic arthritis (PsA) is much of the time, a disability. However, people cannot see your stiffness, pain, or psychological well-being. They think you may be able to suck it up and push through it all. They don’t realize I am so fatigued I really don’t have any more energy to maybe even push myself out of the bed. Along with PsA, I have Palmoplantar pustulosis (PPP).

People can see PPP, but do not see the rest of the story. So, I just figure that my friends and loved ones are the ones who count the most. The rest, I always hope they’ll understand, and realize if they don’t, I just have to move on to protect my mental well-being.

Do you have a story about living with psoriatic arthritis to share too?

By providing your email address, you are agreeing to our privacy policy.

This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The Psoriatic-Arthritis.com team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

Join the conversation

Please read our rules before commenting.

Community Poll

When it comes to living with multiple health conditions, I've found my: