Feeling alone with psoriasis?

The home light therapy going well only a few bits of white psoriosis patches on my legs money well spent

I am feeling kind of bumped because my psoriasis was getting so much better but I am under so much stress now that its been worse :/ any tips?

Hi I’m new to this group last year I under went uvb light treatment and given a load of creams which helped but just resently had another flare up and I think it might be due to my washing power so my question is what wash power/liquid do you use

Hi everybody!! Used to be here regularly a year or so ago. There has been a lot of stress my life. Trying to find balance right now. Had the worst flare up yet and cant seem to get ahold of it. Going to try cbd but need educated on it. Please help

Hello everyone
I’ve joined this social site because I’m feeling pretty miserable and anxious about my guttate psoriasis it’s neck to feet basically big bright red spots everywhere
Feel partners/friends dont understand😔

Hey Y’all,
I’m new here and struggle with plaque Psoriasis on my scalp, neck, and stomach as well as inverse Psoriasis on both my upper and lower extremities. The inverse has spread rapidly and is immensely painful. Any tips?

Has anyone here ever donated blood ? Is it ok for someone who doesn’t have P to receive blood from a person who has it ?

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.

Does anyone have the skin breaking down on there fingers. I am not sure if it is P or something else. I have P on my right calf but the only other is that skiing on my fingers crack and split.

Hey guys, has anyone something when it smells? I habe 4 different types of P one of them is Inversa and when im sweat and its wet there it start to smell. When i dont take a shower for 24 hour its realy bad. Sometime i cant shower because the other p

Stress really affects my psoriasis really bad. I have sores on the front of my head and they hurt a lot.

Hi every one it be a long time that I have been on here,I just can’t pull myself together have a bad time with my P it has gone out of control and don’t seem to be getting any better,don’t matter what I use to put on my P nothing is working

Hello,It's my first time here!I recently started drinking celery juice when I wake up, I usually wait around 30 minutes to eat after I drink it. I got this from medical medium and I was wondering if anyone else has used it and if it worked for them.

I’m trying with everything that’s in me to make living with P easier, it’s just not and it might never be. I’m just so itchy and there’s flaky skin everywhere and my clothes have blood stains all over.

Using Tar shampoo for scalp and use it for soaking and showering... getting some sun.. started to clear... my Dermatologist told me to do this... don’t like the smell... but it works.. I eat sweet potatoes and take vitamin D.

Is it normal to feel bone pain exactly under the Pso place?
Like i have pso on my elbows and knees and suddenly i started feeling pain exactly under them and the pain is felt in bone and recurrent very often!

At the hospital waiting to see a dermatology wish me luck

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?

To be honest sometimes I think it would be easier for people with P to date other people with P. Some people without P will never understand and it’s just so much harder to date when you have P. 23 and never been in the dating game

Hey fam!!! How is everyone? Hope all of you are doing fine with no flaring!
Latest update~> I am down with tonsillitis... and guess who got aggregated and started showing up with flaring, itchiness and pain?? Yessss my amazing Pso my bestieeee❤️