Life ain't what it used to be
I've had psoriasis since I was 9. The only time I was completely clear was while I was pregnant with my children (reckon I had enough on my plate without being a flake on legs!).
Getting diagnosed with psoriatic arthritis
I was diagnosed with PsA earlier this year. I've had inflammation, pain, and fatigue for years, but nobody bothered checking why. Now on methotrexate and sulfasalazine. I have the odd day here and there without much pain. And I LOVE those days. Sadly, they are few and far between.
My fingers, wrists, hands, elbows, knees, ankles, toes, and shoulders are affected. And there are days I can't do anything. I feel useless. It affected my mental health quite badly as I've gone from being an adrenaline junkie, who used to free climb, play all manner of sports, to someone who struggles going up and downstairs (down is harder than up).
Dealing with PsA fatigue
There are days I feel like giving up but... I'm no quitter. I hate this. I know I have to accept that this is my life now but I HATE IT. I used to have energy. Now I'm like a permanently exhausted pigeon. Some days even going to the bathroom exhausts me. It's no fun that's for sure.
My current treatment plan
I take a high dose of Vitamin D, B complex, omega 3, evening primrose oil, naproxen, paracetamol, turmeric, and glucosamine. I'm pretty sure I rattle when I walk from all the meds, as well as the blood pressure meds, antidepressants, and HRT. It's like having a second breakfast of tablets each day. But... I plod on. I love this site because only those who have PsA know what it's like.
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