Psoriasis can cause fatigue in many ways. If you are affected by physical, social, and emotional fatigue because of your psoriasis, this is a space to share your experience with the community.
What causes your fatigue?
What helps with your fatigue?
We want to hear it all.
I have some patches on my scalp where i can feel
rough patches. My left knee has been very painful twice in the last month and I’m extremely tired when I wake up in the morning-I think I might be dealing with psoriatic arthritis. What should I do.
Hi @CommunityMemberba8c14, thanks for reaching out. I would definitely recommend you keep a journal of your symptoms and make an appointment with your doctor. They most likely would recommend you see a rheumatologist. I am sending you over an article that I hope can help. Jill, team member
Get tested for HLA-B27 (Easy blood test). HLA B27 is a gene associated with psoriasis and weakly associated with peripheral psoriatic arthritis. In the presence of spondylitis-associated with psoriasis, 60-70% of these cases are HLA-B27 positive" You can still be negative for it but it's one helpful blood test.
I am 47 years old, and was diagnosed with Psoriasis when I was 4, after several terrible bouts of stress-induced hives, the swelling settled down, the redness stayed, and started developing plaques. Over the years, it only got worse, but all my (many, many) doctors did was to prescribe topical hydrocortisone, some very smelly tar and or steroid treatments in creams, ointments, soaps, and shampoos. Only in the last 5 years, or so, after I joined a Facebook group for sufferers, did I finally begin amassing real and detailed information about my disease. This has been a time of learning for me, not only about the skin condition aspect of Psoriasis, but also because I find it is so much worse when I am under stress. I'm learning about myself so that I can set and maintain healthy boundaries in all areas of my life. This has changed everything. I work 4 days a week, instead of the 6 I used to. I do not ever work extra shifts or extra hours, and made sure that I entered my most recent job strictly as a disability hire, so that I am protected from being forced into any more work than I can handle. And yes, Autoimmune disorders do qualify as disabilities. I use my 1st of 3 days off to rest, and nothing but rest. Im sleeping, or relaxing, sometimes light stretching and easy yoga poses. Nothing strenuous. I turn the ringer off and the music on and just take that time to recharge. Both of these things have gone a long way toward changing how I manage my fatigue. Further, because I am no longer overdoing it on the job, I feel well enough to take much better care of my home, pets, and myself on a daily basis. This, in turn, makes me feel accomplished, which raises my self-esteem, promotes healthy dopamine production, which helps with the depression we so often face as another comorbidity of PsO. Fatigue and depression play off each other, so helping one, helps both. Ive learned, as a skills coach, that the 3 things nearly every patient deals with are:
1. Positive Self Image,
2. Perspective, and
Managing these three things has helped me in my own life to create a lifestyle, a routine, and an attitude that promote a healthy, happy way to live. Yes, I still get tired, but instead of beating myself up and feeling like Im lazy or useless, I now remind myself to change that perspective to: I have a disability and every single day I am up and living a strong and healthy life anyway, so if I need a nap or a "me day" in order to maintain, thats just what I'll do. I remind myself of all the positive moves Ive made and how far Ive come, and I remember the boundaries Ive set to ensure I dont take on too much, or become overwhelmed. All of these steps have allowed me to learn better time management, take excellent care of myself, and combat fatigue where it starts-- with me.