COVID 19:Do you think you are safe? And Why? What do you do to keep yourself safe from this virus?

Hi my lovely Flaymers. Hope you are all well? How do you feel about this Covid 19 virus? Do you think it will affect us more than others because of our Immune system?
Look after yourself and keep the immune system up! xx

Does anyone else have different psoriasis on different parts of their body? My foot spots are different to my leg spots which are different to those on my face.

Im unable of taking my meds the one I mentioned in my previous post! I keep getting stomachache after consuming it and nauseous throughout the day! I felt the more i have stomachache the more my P increased ! What i did is wrong stopping the med?

Has anyone tried med called
Tine - fcon my doctor recommended them all that I know about them is that they’re made out of natural ing and manufactured in india? Did anyone try it?

What is the impact of psoriasis and Corona virus?

Today my doc recommended I start using biologics inj ... he said not to take pills for I not married yet! So what do you guys think?? I don’t know!

I had a fall in April last year while on school camp. I did some serious damage to my leg requiring major surgery with a long recovery period. Lots of physiotherapy to go and have had a constant flare since the fall. 299 days off work.

Hello all, Been a while , I am still having problems with my epidermis, keep fighting,been 6 mnth, I got urology appointment soon, Taken what left of my antibiotics as it does help a little, not good for P though,itchy etc , :)Hope all is well ?:)

Starting my phototherapy course today. Hopefully can get a bit better for me soon

Hello how's everybody doing looking for friends with psoriasis in Texas

How to deal with ear P, its been 2-3 months since I developed ear pso and its horrible!!!! How to manage it????

Today a 5 y/o girl came to me after staring for a while at my elbow P and then she said ur bleeding why is that did u fall on it? I looked at her and smiled then said no that’s my skin it’s normal to have it! Does it hurt she asked? I almost cried..

Has any one used methotrexate tablets for psoriasis and what was the outcome

Today is a better day. Yesterday it seemed all my conditions converged on me and it was horrible pain day. I read alot of the posts and it did help somewhat to know that there are others that know how frustrating it is to feel this way. Thank you all

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.

Hi my lovely Flaymers. Hope you are all well? Hearing about a possible dating site on Flaym makes things very interesting :) We all deserve someone who understand what we are going through right? Happy Wonderful Year to you all! xxx

I wonder if anyone else is in a similar position to me.
Psoriasis only started last May when I was 73. I wonder why it suddenly started at that age. Now various treatments are having little effect

I am new to all of this. I was diagnosed with psoriasis in May and psoriatic arthritis about October. My bloodwork has been off the charts. my rheumy has said she will send me to a Hematologist. I am a bit freaked. Has this happened to anyone ?

So i hear there will be a dating app for people with P called Psoriasis Singles, dated to launch 10/01/2020. what do you think about it? I have a hopeful view for it.