Not a good week. My inverse P has now spread from my bum and johnson to my groin, uncomfortable. And the next dermatologist appointment is in February.

Hi i been havibg flare up really bad night trouble sleeping and i dont take my hydroxyzine anymore makes me moody i am trying claratain pill it helps the doctor said there nothing i can take on daily basis for my trigger points for night itchying bad

2 weeks into vitamin D analogue cream applied daily. Arms are looking so much calmer, torso slower to respond but getting better. Redness, sting, both feeling much more positive. Hurray for science and synthetic vitamins! 👌

Hi everyone I thought id check in and say whats happening. Basically ive had a small flare up but im seeing a demoltoligist on my birthday to discuss another treatment.

Hey al sorry life has kept me quite busy since the move and new job ect , P is on and off still and pustular P has been behaving and hasn't flared once so i am over the moon, just trying to find what is ok and is not except for stress ;)

I think the most difficult thing I've had to deal with since getting psoriasis is my declining love life. My relationship wasn't exactly a romance novel but it was pretty good. Now, I have literally nothing but myself. I'm still surviving but barely.

My psoriasis is clearing up on my face and on my hands after having used a lot of steroid creams. I’m not a fan of these creams, because the skin get so thin and sensitive, but when you’re desperate enough you do it, at least I do. -> comment

Hi guys, I was recently diagnosed of Scalp and Guttate Psoriasis. Everything is new and overwhelming. I feel very conscious and very frustrated on what is happening. Any tips for newly diagnosed people? Im currently using steroids for management.

Getting on with a daily application on vitamin D analogue cream to bring my guttate flare down. One week in and it's feeling much better! For those who've never tried it, is non steroidal. For me, a good option!

Hey everyone so I had a bad experience today at the supermarket decided to wear shorts and the manager saw my psoriasis on my legs and made a face of disgust :( then was rude to me afterwards I felt so humiliated :( lost my confidence to wear shorts

A new facial cream...

Crunchy face still! Bad on visible places that you cannot hide,percievering and not going to that dark place yet,sucks though,what does every one do when nothing works? I just live and deal and try not to get down

3 days in to using coconut oil on my inverse P. So sore and reddest yet. Had to use steroid to calm it down as walking was challenging! Does it calm down at all?

How many of my fellow Flaymers have changed their diet to see results in their P?

No break 7 hr day ,3 hrs mandatory,so no choice,but man did my behind hurt sitting that long,thought I was getting better,done this training last 10 years so nothing new to learn,it hurts to sit and it suxs,just venting

I am considering having a Lasik done on my eyes. Has anyone had this surgery done and does it affect your psoriasis?

Does anybody have advice on psoriasis between the bum cheeks? Painful. Have been told to use steroid ointment, silkis and epaderm but find all the ointments grease stain my clothes which is getting expensive!!

if anyone wants to add me on the well known social site please do so..my name on there is lisalou and I'm wanting to have meetups n get to know some of you? I've moved to harworth inbetween doncaster and Nottinghamshire lets connect

Happy Wednesday everyone hope your feeling good.

Recent flare up getting worse... Off to the GP I go later this week! Hoping to find some options that I can add in to my daily routine to stop my guttate turning into plaque... I knew that prolonged sore throat would not be my friend!