#PSORIASIS

[moved-to-piersgender]

i hope everyone with acne, eczema, vitiligo, psoriasis, dermatitis, dermatillomania, and skin conditions have a good day today

[positivelyqueer]

Hi people with chronic dandruff, psoriasis, eczema or any other skin conditions which cause dryness and flaking. I hope you’re having nice, low pain or pain free days. Know that you don’t have to access treatment you don’t want or that doesn’t benefit you for the sake of other people’s comfort. You are amazing.

[unfilteredrealities]

Hey Google , how to not beat yourself up for being chronically ill and how to still be compassionate with yourself when it’s very hard to do so? 😭

[chronicillnesshumor]

[3liza]

hit me with your eczema advice. it's on my hands and it kills. I'm pretty sure it's eczema and not psoriasis but I'm not 100% certain it's one thing or another, it's just painful peeling that is either a surface allergy or responding to some other trigger idk. what is your advice for treating the symptoms. I'm going to ask for a dermatology referral. don't worry about what I've already tried, just pile on the advice, if something I'm already doing helps you I want to know

[thechronicpaingame]

[caintooth]

shout out to my fellow bitches with skin conditions in impossible to hide places! my psoriasis forms around my eyebrows and beneath my nostrils. doesn’t stop me from being cool and sexy

[neuropathyfordpines]

Hey if you have big noticeable rashes/hives due to eczema, psoriasis, or even allergies, or for any reason at all: I love you. You deserve to exist in public. You don't have to cover up to make other people more comfortable.

[fleshwizard]

science doodles done at the lab during reunions

tertiary lymphoid structures

flow cytometry

leucocytes (back of the sketchbook)

neuroendocrine carcinoma

psoriasis

cellular leiomyoma

[remuslupinslittleslut]

So ive just been diagnosed with arthritis at TWEMTY FOUR from my 💞psoriasis💞

CUE: me writing Remus Lupin my chronically ill KING with psoriasis/arthritis from now on

I know ive read him with arthritis before, but here comes the skin issues too babay

[unfilteredrealities]

Struggling with Psoriasis since I am 2 years old is a different kind of hell I do not wish upon anyone not even to my enemies.

Each goddamn year when winter season hits my body decides to go BRRR in Flare.

Each summer my body partially decides ok let’s be sort of ok and let’s heal but not completely so she can’t wear short pants in summer due to deep rooted shame.

I got bullied in school being called a “contagious Monster” due to my Autoimmune Disorder.

I have trauma still from that to the point I can’t wear short pants because I’m too ashamed and scared that people would not want to be around me anymore.

I see people stare at my legs whenever I wear flowy pants in summer that when a gust of wind blows it reveals my legs and they will stare.

Im chronic in pain and agony and fatigued due to my body constantly fighting against itself against its own skin. Its 24/7 growing too much skin as if it feels pressured to change my whole skin layer not every 7 years but faster 😭

Be kind to people who have skin issues they can’t control.

Be nicer. Don’t be an ass.

[chronicillnesshumor]

As shirts/mugs on my Etsy store [ https://www.etsy.com/shop/ChronicIllnessTees?ref=dashboard-header ] or pins, stickers, magnets on RB [ https://www.redbubble.com/shop/ap/167203459 ]

[savavsa]

Being chronically ill feels like you popped out of the womb as a well loved stuffed animal and every week you have to sew yourself up with double thread and hope and pray

[stargirlie-sharon]

ok i should put this out there so people who are following me/my mutuals are aware, or even people who are just passing by and don't know me

i'm chronically ill, diagnosed with psoriasis, an auto-immune skin condition (which i really hate a lot). it's been getting rough for me and honestly my mental state isn't the greatest rn

i'm experiencing a flare up rn. and my skin hates itself so it just decides "hey, i'm gonna fuck up this person's appearance and make them insecure for as long as they have this condition" or something, and usually when my skin clears up, it's still most likely going to come back

so um while you're here, would you mind giving me a few words of encouragement? i kind of need it rn.

and if you know anyone with any chronic conditions, disabilities, invisible illnesses, or anything of the sort, just be there for them and give them support, it might mean the world to them

thank you for reading <3

[aceofstars0]

[thechronicpaingame]

Today I learned about achenbach syndrome! Ive always had this weird thing with my hands where I get this like spiky pain and it hurts to touch the skin and later on it's bruised (on the inside of my fingers). So when it happened today I decided to have a Google and voila! It's nothing exciting, I just find it so interesting when I find something that's like, oh yeah it's definitely that haha. Medical stuff is my specialist interest and I think always will be haha.