There have been many ups and downs in this journey. I was diagnosed with my first psoriatic flare at age 8, after I had chicken pox, mumps and then strep throat that became Scarlet fever.

I'm in so much pain with my legs that I feel such a failure. I don’t want this to affect my life and I just want to find some support to help me and others through...

I had psoriasis for 30 years, it was concentrated on my joints until about 10 years ago when I developed spots all over my body.

About ten years with psoriasis arthritis. Could not walk anymore almost. Coursed by long during stress.

I have had problems with the skin and associated arthritis since 1977; My GP has started me on B12 injections and D3 medications.

I've had psoriasis for 3-4 years it's full body. It came on with stress; I've tried the creams and sprays, not much of an affect on condition.

I’m getting tired of talking about my symptoms with my family; my lovely wife I know grows tired of it. I was diagnosed in 2016 when I was 54.

I just want to share my story, ‘living with psoriasis’. I am a student at the age of 23.

I am 38 and in the summer of 2018 I was diagnosed with scalp psoriasis for the first time in my life. I have no family history of psoriasis or any other skin disorders.

I was diagnosed with psoriasis when I was 5-years old after I got my ears pierced. I found out that my father had it as well and I inherited it through him.