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APR
26
my life is ruined
By:
/u/Usual_Swordfish_7484
on
APR
26
i have pustural psoriasis. I’m 51 almost and diabetic type 2 . There is no empathy out there . i’m suffering badly with pain on my hands and feet for two years . I can’t stomach the meds for the condition and even the newer type i can’t stomach I do take other medications which i think are interacting . I got diagnosed March 2025 finally with this condition . I suffering it since feb 2023 after a second degree burn on a trip to an island under foot of. my left first 3 toes . My life has been getting progressively worse as i can’t seem to get on top of this condition and being violently sick on at least three meds this year has been awful . Seeing my fourth dermatologist atm prior to her i had seen a specialist podiatrist who didn’t even pick up that it’s a psoriasis i had on my toes like she’s a specialist 🙄. i have seen GP’S i have seen so many people who have basically not helped much … i am parenting a child alone. also i
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APR
25
So what is happening
By:
/u/HeyBesties-
on
APR
25
My psorsis is changing shapes and colors weirdly , the first photo is today and the other photo was from March and I have no idea why the shapes and stuff changed so weirdly I’ve been on all sorts of medicine but hasn’t gone away because I got strep throat twice ! submitted by /u/HeyBesties- [link] [comments]
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APR
26
Psoriasis on both feet
By:
/u/Tocayo21
on
APR
26
I've had psoriasis on both feet for five years. Many people say it's fungal. I've bought ointments, but they don't work. How can I get rid of it? submitted by /u/Tocayo21 [link] [comments]
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APR
26
Results?
By:
/u/Busy_Try_4461
on
APR
26
Hello! I’ve been using VTAMA for 5 days now and see a slight difference! I’m wondering for anyone who’s used it when you saw major changes submitted by /u/Busy_Try_4461 [link] [comments]
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APR
25
Suggest some itch relief tips please
By:
/u/Open_Quote_460
on
APR
25
What do you do for itch/burn during severe flare ? submitted by /u/Open_Quote_460 [link] [comments]
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APR
25
Penile steroid withdrawal, advice?
By:
/u/Rude-Percentage9646
on
APR
25
Hey everyone, I wasnt going to mention that my psoriasis was located on multiple parts of my penis, especially the glans. (But I thought someone could relate) For many many years I have relied on Trimovate (medium potent steroid cream, about as strong as you can get for that part of the body). Without this cream I basically have no sex life. Symptoms of not using include, fiery red skin, peeling flakey plaque like skin, and in the worst cases (that have been many) full split in multiple parts of penis skin with bleeding. The reason I want to come off this cream is because of multiple symptoms that include, thinning skin (some patches of penis has paper thin skin because of years of application) dark spots on penis (no doubt have been caused by thin fragile skin) and finally over reliance on this cream and not allowing my skin to fight for itself to repair itself. I have commited to some time away from sex and sexual activities in persut of allowing my skin to not become so reliant on t
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APR
25
Looking for platonic psoriasis friends
By:
/u/Sweet-Roe3846
on
APR
25
I realized on of my main stressors is that I don’t have anyone in my life who truly understands what it feels like to live with this chronic disease and I’m hoping to change that. It’s important to find people who know what you’re going through and understand the struggles of being itchy at night. Even if nothing come from this I hope whoever reads this knows they aren’t alone and I hope you have flakeless day 💗 submitted by /u/Sweet-Roe3846 [link] [comments]
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APR
26
Trial with 3 creams
By:
/u/Ordinary-Speech-4166
on
APR
26
It was always such a hassle putting in creams when I was younger and i don’t even know if they worked. Anyway, it has progressed over the years and am ready to give these a solid shot and stay consistent with them. The PSA is a whole other story. One goes on my forehead and the other two each get one side of the body for comparison. Anyone have good/bad luck with any of these? The VTAMA came from a “special” pharmacy and I know my insurance was not having it, but it was cheap enough to give it a good honest try. So any experiences good or bad? submitted by /u/Ordinary-Speech-4166 [link] [comments]
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APR
25
can shaving cause psoriasis to spread?
By:
/u/Mammoth-Climate-1443
on
APR
25
Usually i only trim "down there" with an electric razor, so not skin smooth, but 1 or 2 weeks ago i tried shaving clean with a razor. Now, ive been noticing itching where i shaved and also a quite large and slightly red area and i think my psoriasis may have spread. Is this just a coincidence or could the shaving have caused the spread? ( i only shaved once before it happened ) Thanks in advance submitted by /u/Mammoth-Climate-1443 [link] [comments]
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APR
25
Skyrizi Co pay assistance
By:
/u/mdman211
on
APR
25
Just got pre-approval from my insurance company to go on skyrizi. Was pretty hyped but after speaking through my pharmacy, the medicine costs $22k, and my Cigna choice fund oa plus insurance covers 14k. The manufacturer's copay assistance only covers an additional $4k, leaving me with an out of pocket costs of $4k. Anyone with additional insights here? At this point I don't think I will be able to afford this at all. It appears I have to go back to the doctor to review other alternative medications. submitted by /u/mdman211 [link] [comments]
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