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JUN
08
Does anyone else have one side of their body that your psoriasis is worse?
By:
/u/Kacidillaa
on
JUN
08
I know the obvious answer looks like I have more tattoos on my left leg. But they’re all years old. And my right arm is almost a full sleeve, and it has less than my left arm that has less tattoos. I’ve had psoriasis since I was 19, I’m about to be 31, and it’s always been like this. Well before I got tattoos. Currently I only use clobetasol propionate, no injections or anything since it just seems cosmetic and I’ve learned to live with my skin. submitted by /u/Kacidillaa [link] [comments]
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JUN
09
Koerner phenomenon, shoes, and psoriasis
By:
/u/WithAllMyHarts5
on
JUN
09
During a recent derm visit, a med student noticed my fissures are in the same spot in both sides of my feet mirrored. He pointed out multiple spots that were koerner phenomenon spots. I need to find shoes that work better for psoriasis. I guess my Hokas were too narrow. Any tips? Currently wearing fleece lined slippers 24-7 lol! submitted by /u/WithAllMyHarts5 [link] [comments]
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JUN
09
Carbolic Medicated Soap: An Experience
By:
/u/Future_pink719
on
JUN
09
I just began using Carbolic Medicated Soap and for the first time in YEARS my skin doesn't immediately itch after pat drying. My shins do not instantly feel an itchy tingle on the front. My skin is.... normal. This is day 1. And I am very hopeful. I applied my normal medicated creams and mild vitamin E rich oil to my target areas and it still felt scaly. But, no itch!!! Im so excited to use this stuff! submitted by /u/Future_pink719 [link] [comments]
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JUN
08
How I sent my most aggressive flare up ever back into remission.
By:
/u/Appropriate-Peak9363
on
JUN
08
Just want to share my experience, as I know everything is different and responds to different treatments but hopefully this might be helpful to at least one person! Background/Context I am 36, I was diagnosed when I was 18 and had full body psoriasis shortly after recovering from chickenpox, it was messy and I stayed indoors for 6 months without socialising, dropped out of college and spiraled into a severe depression. Eventually got referred to hospital for UVB therapy which completely cleared me up. Since then I've had minor breakouts usually around winter, I live in the UK so lack of sunlight is a trigger for me. It's usually a few small patches on my legs or elbows that I honestly just ignore cause they go away eventually. Last month I had to take antibiotics for health reasons and in addition to that I had strep throat just before. I also had some stressful weeks, all of this combined sent my body into overdrive and saw the worst breakout of guttate psoriasis in 18 years. I would
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JUN
08
I think it's making me depressed.
By:
/u/SquashRealistic5827
on
JUN
08
TW: Mentions of SH and Suicide (marked nsfw just in case) Some of you probably already know this, but psoriasis can actually lead to depression and anxiety, due to a decreased quality of life. I've had guttate psoriasis for I think around 6-7 years now (I'm 15) and I used to not really be that bothered by it. I never really minded covering my arms and legs since I never really liked wearing shorts and I preferred long sleeved tops anyway but as I've gotten older my mum keeps reminding me of how it's there. My mum used to make me come downstairs wearing a towel and take photos of my arms, back and legs and she would post it on Facebook for all of her friends to see. I don't know why but it always made me feel like a monster and it got to the point where I couldn't even look at myself in the mirror. My mum has been telling me that I need to "fix myself" and she keeps saying stuff like "what if you get a partner? They might not want you if you look like that". I actual
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JUN
09
Need help
By:
/u/WeddingFantastic7883
on
JUN
09
Psoriasis or athletes foot? I’ve had reoccurring athletes foot in and off since middle school, ( don’t have it between my toes currently)but the itching/burning dryness of the sides of my feet and heel is fairly recent. It’s only my inner right foot. submitted by /u/WeddingFantastic7883 [link] [comments]
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JUN
07
Listen up. Psoriatic Arthritis is a thing!
By:
/u/eatingganesha
on
JUN
07
I was just aghast reading a comment from someone who did not know PsA even existed. Everyone with psoriasis needs to know that PsA exists and you need to be aware of symptoms to watch out for because 30% of you WILL develop this debilitating disease. The number jumps over 50% if you have scalp or genital psoriasis. And it jumps even higher if psoriasis runs in your family. It is NOT the same as rheumatoid arthritis, though it is also an inflammatory type. PsA does to your bones what it does to your skin - it piles on extra cells and deforms the joint. It requires biologics and DMARDs, as well as major dietary changes, to manage. Failing to control this condition leads to immense pain, permanent disability, and complications like digitalis mutilans. The damage done by PsA to the joints is irreversible! It’s crucial that you notice the symptoms and get treatment so its progress can be slowed. The first symptoms for many people are vague joint pain, random joint swelling that resol
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JUN
08
Scalp
By:
/u/Maleficent-Wolf-1240
on
JUN
08
Hi everyone, I’ve suffered with psoriasis for the last 11 years (m28) I’ve learnt to live with it over my body but my scalp not so much, just curious for if anyone has any tips? Going to get my hair cut is horrible, although I’ve used the same barber for the last 7 years it’s still an uncomfortable situation. I use a coal tar shampoo throughout the week but my hair still snows heavy. Any help would be greatly appreciated. submitted by /u/Maleficent-Wolf-1240 [link] [comments]
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JUN
08
Nail Psoriasis UK- how to treat
By:
/u/Natural_Log2116
on
JUN
08
Hi all, I’m a 23M living in the UK, I’ve had nail psoriasis for around ten years now, it came out of nowhere and to be honest I still don’t know how or where it came from, I’ve visited GP in the Uk and got referred to a dermatologist who said there’s nothing they can to do treat it, I tried a pill for six month( can’t remember the name but they said a side effect may be lung damage in the future), this didn’t help, and I’ve tried the name of every tree top oil and cream under the sun and nothing has helped, Please see the attached photos showing my nails, they are very rigid and have a lot of white lines in there which isn’t ideal, and the nails grow in a very weird shape, As you all know this isn’t great for my self confidence as our nails are always visible, on the train or at work I always feel like people are looking at them, I wanted to ask whether anyone has any treatment or products that I could try? Or any other
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JUN
08
It sucks so bad
By:
/u/Stunning_Catch_7813
on
JUN
08
Hi i am 16M , well how i got to know about it? First it was said to be as dandruff lots of it but when i had it checked up it was said to be psoriasis , i feel stuck so much it is now filled on my scalp , my back , my thighs , my legs and well now my face , i was insecure as it is and now it covers my entire nose and 4-5 other spots , how will this go? the doc and online tells me to be stress free but how do I stay stress free with academic pressure , family problems and social problems like having no friends , idk what to do and how to deal submitted by /u/Stunning_Catch_7813 [link] [comments]
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