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.

I have painful inverse P under my breasts and in my groin. Is it safe to use an anti-fungal under your breasts? How often? I was told not to use the cortisone under my breasts all the time. Has anyone had success with homeopathic remedies?

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.

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

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

so I am absoulutely gutted I can't go buy this uvb light therapy canopy because I've found out it only has arimed b tubes in it the lady turned horrible through a selling site and now I have been reported to them coz I agreed the sale before I asked

The most difficult part of this desease is the lack of understanding by others.

am so sad I thought I got rid of my psoriasis and as soon as I was done with the steroids it came back 10 times worse. I have it on my Palms of my hands and the bottom of my foot.

My one sister was diagnosed with a hereditary kidney disease today, Alport Syndrome, must have myself checked out as well. Where do all these rare diseases comes from. At least P prepared me for this in a way. One must just handle it best you can.

Psoriasis makes me sad sometimes

Hi. I’m new to this. Last weekend I started getting spots on my torso. As of today the only place I don’t have them is hands feet and face. I’m going to lose it. Trying creams, been give steroids and strep meds as I had strep but no symptoms.

I have given this a bit more thought of late. P isn't the worse thing any of us can have..I spent this entire time wondering if I was going blind...My eye Doctor has a prognosis for me,to never see my garden in full bloom again,not an option

Fed up loseing my hair with this dermatitis on my scalp
Jan

Not on hear no more

Is there anything I can do or use on my arms due to having thin skin? it’s to the point of mush N I bleed easily n bruise. I hve to b on steriods for rest of my life, due to a liver transplant. I can’t use regular band aids either. Help please......?

Emotional abuse affects the P. Acts like a trigger.....anyone agree

Hi e I'm still having uvb treatment atm but my face has got ten times worse. It looks terrible. I'm going on first holiday in 8 years. We are going to Torquay because I cant go abroad due to other conditions I have. Anyone tried pills or injections?

I just read about what I can eat and omg, I got really sad...

Feeling very down. I'm a plaque P girl (10 plaques). I have been to the doctor today and was told I have a guttate P (I thought it was sunburn or even bed bug bites in my denial)! I'm not sure I can cope-it all over me and its so itchy. :-(((

Hey all my Flaymers!
Sorry I've been away.
March saw a redeye flight to Spokane,WA and the passing of my mother in law.
April saw my "Big Sister" Maggie's mom pass.
June the kid and I were in a car accident.
And July saw my mom pass.