I once had a bit of psoriasis on my back shaped like France I haven't even been to France!!!!
I'm the same dean, I have been on a drug for the last 7months that has kept p under control, but now it's starting to get cold here I'm starting to flare, I'm feeling sore even where there is no lesions, and feeling the cold unbelievably, I went back to professor yesterday and she told me because I have so much inflammation in my body that's why I'm so cold all the time, I'm waiting for blood results to come back and all going well I will be starting some new exspensive drug fingers crossed...I've had to be so strong and positive my whole life with this disease but lately I've been thinking a person can only do this for so long....I'm at the stage where I'm nearly well and truly over this😪
I am lucky at this stage where I am at. My body as a lot of it for a long time now. I do not itch in most places anymore. i do remember a while back how it did itch horribly. I would just scratch and scratch and then look and see the blood pouring out. Very attractive! Also if I squat down to pick up something, the sides of my knees will crack open and the burning is like someone took a knife to it and its cracks so deep and pours blood out!!!! Horrible!!! I do not squat anymore.
I'm currently thinking about trying wild water swimming as I was thinking it would be better for my skin and I can wear a full body wet suit but then comes the challenge of taking it off without exposing my skin think I would get very funny looks if I tried to drive home wearing a wet a suit !!!! I really miss swimming but I'm not brave enough to wear a costume in public 😩
Hi Dean, my skin loves salt water pools to the point where if I spend a couple of hours swimming they almost go....but as soon as I get in chlorine my skin breaks out and I'm so itchy....I try to avoid chlorine and if I do come in contact with it I find qv body lotion relieves it and reduces inflammation.