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!

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

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❤️

The weather is so bad over here it makes the skin sticky not to mention the humidity unbearable!
P.s: Pso started showing up on my face..and somehow I’m accepting it with a smile on my face thinking of it as a gift from god telling me im different!

Today I was made fun of and criticized cause of my psoriasis...I feel like crying my eyes out! I know I should be stronger and not let anything put me down..but im only human in the end..

I have some concerns about something i hope someone answers me, if by accident i apply Pso ointment on a place the doesnt have pso will i get pso in that place? Cuz im noticing this unless im superstitious or crazy

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?

Hi

So my derma prescribed dipro...ointment for me to use everyday twice, in the morning i apply it normally and at night i apply it then wrap my Pso with plastic food wrap and go to sleep until next day for 2 weeks

Im not healing!! I don’t know what to do😭😭😭😭

Im trying to raise an awareness!
Isn’t weird that not many people know about pso and they think it’s 😷 contagious ! Im sick of trying to explain that pso isn’t contagious 😭😭🤯😡

How do you scrub your body?

Hello..
I had my pso 4-5 years ago, but what happened with me is that I didn’t know I had it until last year..4-5years ago i went to a dermatologist who is my friends mother back then she knew what I had but she didnt want to scare me->