I mean to correct last post. Being around people with Narcissistic traits can possibly lead to developing autoimmune illnesses like psoriasis.

I was looking on the Quora page in relation to narcissists and they said being around people with these traits can lead to developing a hyper immune disease. I have psoriasis and it got worse the more time I spend with my narcissistic mother.

So update i have moved back to South Africa, not under the best of circumstances and flaring up. Think its all the stress and diet changes again. Can only keep up the good old fight, and stay positive.

Hi, does anyone feel like their perspective on life/relationships with others has changed since P?

Hello all, Well i thought the problem had gone gone up and down but okay , Cause unknown?I can only put it to my immune system thats causing the problem as i am clear of anything ,No cause found, I am taking natural meds in pill form . :)

Merry Christmas and happy holidays to all of you guys from toronto Ontario. By biking my psoriasis and being busy my psoriasis is almost clear. Still have a few spots in my elbows.

Anyone get the “regular” skin around a patch of P going a dark grey colour. The patch on my right knee has this, just went like that in the past couple of weeks. It’s not painful or itchy.

Decorated my daughters bedroom over the weekend today I'm having a day of rest as I tend to get poorly every few months n I wear out quickly half term joys lol

Hi all. I have never written a post. I have had psoriasis for over 40 years. Never had any treatment plan work for me. My new dermatologist is putting me on an injectable biologic. Kind of nervous about it.

I might move to the Netherlands 🇳🇱, Hoping that I find advanced treatments over there and lift my spirt up in a new place, my anxiety is taking a troll on me so maybe knowing new people might help me...I really don’t know..sigh

Hello! Been a while since I have been on. Hope you are all keeping well! I've recently had a flare up. I quit smoking & started with a vape about 4 wks ago. Wondering if the vape is the cause of this Flare up. Anyone experience something similar?

Hi, since last visit I have been diagnosed with Psa, severe in feet, treated with injections. The upside is I can walk but pain was so bad I gave up work. Off to Dermatologist today. Hope you are all doing well. Yayyy site is up and running again 😊

Its been a while , August in the UK hasnt been that good with weather, Skin is up and down ,Been rough for over week due to a lot sick people at work but slowly getting over it , I couldnt dodge it ,all been okay though, Hope you all are too? :)

At the risk of sounding like an alcoholic... for those whose psoriasis is affected by alcohol, has anyone found a type of alcohol that is less inflammatory?

My psoriasis has been a problem for me ever since I was a little girl. I have tried all different kinds of shampoos just for psoriasis and nothing worked. In the last few years, I have started getting it on my chest, face, and neck.

Its been a while since Ive been here. It seemed like the place had been abandonded but Ive just noticed emails from Flaym and I had loads of notifications when I opened the app. So if we spoke before, Hi again and if we never, Hi.

My flair up always come on the same spot on my body and goes away when I stop eating certain foods. I’m beginning to think I may have a liver problem. Could psoriasis, where the liver is not able to deal with toxins in the body?

Opinions on Dead Sea Salt for Psoriasis....?

Hello all,

Haven’t been on this site for quite a while. How are you all coping with your skin? It’s summer here in Canada so getting sun on my skin helps a lot. Hope you’re all doing well. 🙂

Hey guys I have a question..
so I used aloe vera gel for few days and i noticed aggregation in my pso, faster building up of skin and itching..has anyone experienced something similar or am i the only one?!!? And should i stop using it?