#autoimmune warrior

[thelupuslady]

Needed my own reminder for my stubborn ass.

#autoimmune #lupus #lupus warrior #spoonie #fibromyalgia #lupus advocate #lupus fighter #strong #chronically ill #pots syndrome

[my-brain-is-soup]

#brain fog #foggy brain #chronic pain #spoonie #chronic illness #chronic illness memes #autoimmune disorders #spoonie life #spoonie memes #spoonie strong #chronic inflammation #spoonie stuff #chronic fatigue #fibromyalgia #chronically ill #fibromyalgia warrior #fibro #fibromyalgiasucks

[spookysalem13]

Just a fellow spoonie 🥄 here to share a relatable hilarious 😄 video.

Being chronically ill, you have to learn to find the humor in your diseases. For me, it's a major way I get by day to day.

This made me smile, I hope it can make you smile as well.

#chronic pain #chronically ill #spoonie #spoonie warrior #autoimmunedisease #autoimmune #sjogrens #celiac #rheumatoid arthritis #osteoarthritis #spine problems #hypermobility #hypermobile ehlers danlos #ehlers danlos syndrome #ehlers danlos zebra #chronic fatigue #chronic nausea #chronic migraines #rare disease #im a survivor #dark humor #haha #lol #spoonie humor #fibromyalgia #fibropain #flare up #relatable #relatability

[chronicsickness]

I don’t think people understand the grieving you go through when you become chronically ill. The realization that you’ll never feel healthy again. That you’ll have this struggle and this pain for the rest of your life. That your body won’t ever be or feel the same that it used to. Sometimes I just sit and I cry and I grieve because I miss healthy me. I miss her so much.

#chronic pain #chronically ill #autoimmune disease #systemic lupus erythematosus #lupus #lupus warrior #fibromyalgia #fibrostrong #ibs #inflammatory arthritis #endometriosis #bppv #invisible illness #illness and disability #postural orthostatic tachycardia syndrome #chronically sick #i'm sad #depression #grief #grieving

[skoofie]

Its been a while but I just wanna say I love your chronic pain photo! Can i request more content? Anything you want! Your representation is so yummy <3

I’ll never pass up a chance to project <3

TLDR he got the sun is a deadly laser disease

Throws my funky DM SLE combo at him for the bit

#linked universe #lu legend #chronic pain #gives him my funky autoimmune disease wombo combo #sle and dermatomyositis #ask #ski art #oh oh the cold hands is raynauds #my hobbies include freezing ppl #Lu warriors #this isn’t a serious post dw #also ty! #its funny you say this cus im in the middle of a MONSTER flare #ty for the chance to give my blorbo my same crusty dusty skin

[kindajd]

#multiple sclerosis #ms #em #esclerose múltipla #multiple sclerosis warrior #autoimmune disease #chronic disease #chronic illness #chronically ill #chronic fatigue #chronic pain #chronic disability #actually disabled #disability #multiplesclerosis #disabled #invisible illness #TN #trigeminal neuralgia #iconic #invisible disability #disabilities #multiple sclerosis awareness #disability awareness

[blastedking]

[10/64] Universe: Law Of Fire IV - Remnants of Gods

Emphasis on "try"

#Ralathor #Warrior #Angus McFife #Angus McFife XIII #Hootsman #NA10 #Gloryhammer #Gloryhammerfanart #UniverseLawOfFire #ULFIV #ownstuff #tedonitis update: found out the anti inflammatory meds i took triggered my autoimmune issue and made the inflammation worse 👍 #now off them and it's getting better finally - so I'm soft back for now

[indyviree]

god, how i hate having lupus. everyone thinks im fucking helpless, and they underestimate me. and it fucking sucks because normally they're right. on certain days i physically can't participate in my hobbies bec i'm in horrible pain. because of it, people just think im lazy and disgusting. i can never win. i can't do anything right, i don't know why i thought i ever could.

#lupus #lupus warrior #systemic lupus erythematosus #autoimmune #autoimmine disease #chronic illness #chronic pain #chronically ill #joint pain #chronic fatigue #disability #arthritis #living with lupus

[cairocreations]

Back at it with more old man Yaoi!

Haven’t drawn these two in a while and decided they deserve my attention once again

I feel like these two just have a really unique dynamic! Their both sickly little queers and I think they probably bonded over that as warriors but we’re never anything more then casual friends.

Then when Brokenstar came to power they started spending a lot more heavy moments together- Runningnose found out that he just- focuses better with Nightpelt around. So Nightpelt helps out in the den however he can. And during this time they get really close and catch feelings- but decide not to act on them till ‘This is all over’

When it is all over though- Nightpelt is made Nightstar, and the two of them agree that a relationship couldn’t work between the two of them. Theirs just so much to do, and they’ve got a clan of vulnerable cats counting on them! The last thing they need is their relationship tearing the clan apart!

So they both agree to just try and do their jobs and settle into a quiet life of pining and stolen cuddles in medicine den watching the sunrise.

That’s how I think they gayed in the cannon storyline anyway- thanks to the power of AU I can do whatever the hell I want with them!

Bonus!!!

#art #traditonal art #warrior cats #warriors #runningnose #nightpelt #nightstar #shadowclan #medicine cat #leader #runningnight #runningnose x nightstar #in my brain runningnose has an autoimmune disease #and nightstar has asthma #and probably just gets throat infections really easy too #warriors fanart #exile from shadowclan

[autoimmunechronicles]

I know many of us can relate to feeling like a burden and even those dear get tired of being around chronically-ill people such us ourselves.

How do you cope with depressive thoughts?

#autoimmine disease #autoimmune #lupus warrior #systemic lupus erythematosus #lupusawareness #lupuslife #chronically ill #chronic pain #chronic disability #chronic fatigue #fibromyalgia #chronic illness #crohn's disease #spoonies #spoonie humor #rheumatoiddisease #rheumatoid arthritis

[sashi-ya]

Last days have been painfully exhausting in terms of emotions. And today, after being able to spit outloud all the things I've been keeping to myself I am experiencing the symptoms of a Lupus flare (this time rash and muscle pain, etc). Emotional stress is very real guys. To all of my autoimmune disease warriors BE CAREFUL with keeping all to yourself. Speak with someone or come to speak with me if you need. Unsatisfied accumulated emotional needs are fatal for our bodies. (And all healthy people too)

#lupusawareness #autoimmune #lupus warrior

[thelupuslady]

#autoimmune #lupus #lupus warrior #spoonie #fibromyalgia #lupus advocate #lupus fighter #strong #chronically ill #pots syndrome #posturaltachycardiasyndrome #postural orthostatic tachycardia syndrome #ehlers danlos awareness #ehlers danlos life #systemic lupus erythematosus

[my-brain-is-soup]

They want to remind you!!

#chronic pain #spoonie #autoimmune disorders #chronic illness #chronic illness memes #chronic inflammation #spoonie life #spoonie strong #spoonie stuff #chronic fatigue #spoonie memes #chronically ill #fibromyalgia #fibromyalgia warrior #fibro #arthritis #autoimmune #take your meds #reminder #reminder to take your meds

[spookysalem13]

Had to be taken to the Emergency room this morning by ambulance. I'm so grateful 🙏 for the amazing medics at the Snoqualmie Fire Station 💕 they took really good care of me.

The doctor & nurses at Swedish ER were able to treat my pain at least for the next four hours. So I'm comfortable for now.

My heart condition episode I went into this morning due to my pain being so high, that I'm still battling with that has had me falling into the walls, jello legged nearly collapsing on the floor is being treated at home using remedies that I am to use when this situation arises.

I've been contacting doctors and clinics all morning as the ER doctor said I desperately needed to do. And I'm beyond appreciative of my rheumatology care team for straight up telling me that I need to be in bed resting and normally they'd have the patient make the calls and do the work but they're going to handle it all for me to try and get me some help temporarily while I wait to get into a pain management clinic.

I'm really hoping fingers crossed that today's the day I start getting some help for all the pain I'm in.

Luckily I got in and out of the ER pretty fast and the doctor was amazing and heard me loud and clear when I said I was in pain. She didn't hesitate to help me like so many doctors have in the past and for that I am truly so grateful 💜

Today I will be taking it easy and waiting to hear back from my care team hopefully with some good news.

#chronically ill #chronic pain #chronic fatigue #pots syndrome #autoimmune disease warrior #autoimmune disease #rheumatoid arthritis #emergency room #grateful #taking it easy #sjogrens #celiac #celiac disease #ehlers danlos syndrome #eds zebra #hypermobility #hypermobile ehlers danlos #osteoarthritis #arthritis #chronic illness #warrior #story time #life update #life upd8 #autoimmune hepatitis #fibromyalgia #fibropain #fibro problems

[chronicsickness]

the amount of medical gaslighting that happens to people with chronic illness is so disappointing. Every single chronically ill person that I know have experienced some form of it. I feel like there should be guidelines in place before people in the medical field are able to throw someone’s mental health, age, or appearance in their face. So many people get sicker or go undiagnosed and without treatment for so long because of this. It breaks my heart looking back at the way I used to have to beg for help and leave every appoint disappointed and in tears because no one would take me seriously. My heart goes out to anyone in the midst of that. Please don’t be afraid to let them know if you think they’re wrong, please don’t be afraid to advocate for yourself. I wish I did sooner. I waited 5 years to find a good team of doctors and a diagnosis. It takes most people 6-10. It shouldn’t be like this.

#chronically ill #chronic pain #lupus warrior #lupus #inflammatory arthritis #fibromyalgia #autoimmune disease #postural orthostatic tachycardia syndrome #systemic lupus erythematosus #bppv #vent post #ibs #fibrostrong #anxiety #doctors #nurses #nursing #chronically sick #mental health #hospital #pain #invisible illness #illness mention #medical gaslighting

[hannahcrazyhawk]

#kofi #ko fi page #medical #disabilities #chronic illness #hidradenitis suppurativa #autoimmune disease #crohn's disease #sick and tired #Spoonie warrior #artist #crowd funding #support #autistic artist #neurodiverse stuff #queer #transautistic #trans writers #pride 2023