#fibro life

[disabledopossum]

#fibro life #fibro things #fibro #fibromyalgia #disabled #chronically ill

[crps-chronicpain-ptsd]

Chronic pain problems •

#crps #fibromyalgia #chronicpain #spoonie #ptsd #living with pain #crpsproblems #chronic illness #crps warrior #crps fighter #complex regional pain syndrome #fibro life #bipolar #anxiety #depression

[poppy5991]

Fibromyalgia is so bizarre because there is a ton of active stuff I can do without a flare up:

Rock climbing, tennis, walking around a city all day

But then it rains and the temperature slightly changes, and my body just goes…you’re done. You’re done. Lie on the floor and suffer. We can’t handle this.

Me and my friend with lupus when the weather makes us flare simultaneously:

#also certain types of cleaning or long drives #mess me up #fibro life #chronic pain #fibromyalgia

[eclectic-ways]

People always change manners once they know that they become your weakness. And if you are facing a narcissist, rest assured, you will be exploited inside out.

Do your body and soul a favor and end it asap. There is no buts about it.

#bpd life #bpd stuff #bpd #living with borderline #living with fibro #chronic illness warrior #fibro life #borderline problems #relationship #narcissim #surviving narcissism #spoonie witch #spoonie warrior #chronic fatigue #fibrolife #witchyvibes

[fuji09]

Today has been a bad pain day and I really hope when I wake up tomorrow morning the pain will be at least tolerable.

#fuji rants #bad pain day #fibro life

[rockinichigo]

Curious if anyone in the fibro community has this same-ish symptom especially during the cold months.

Ok so best way I can describe it is like a particular section of my thigh feels sore. It hurts to touch, it hurts to move and fabric friction isnt a very nice feeling. If I am not moving then I dont really feel any pain unless I adjust or touch it.

Anyone else get it?

#fibromyalgia #fibropain #fibro tag #fibro life #fibro flare

[shesmorethanfibro]

May 12th, National Fibromyalgia Awareness Day. 🦋⠀

I was 13 when my journey with fibromyalgia began. This year it will make it 8 years since. I remember hearing from doctors, “you’re young, you shouldn’t be in pain” well, that didn’t stop it from happening anyway right? Fibromyalgia affects more than 3 million people in the US alone per year. I was cheerleading with fibromyalgia. I was going to dances with fibromyalgia. I was going to school with fibromyalgia, going to the mall, laughing, smiling, all in pain and feeling so much every single day. And there are days where I can’t even get out of bed. Or I cry when i walk a little too much. Or i get a sharp pain that has me hunching over in the middle of a store. Or when my insomnia and my chronic fatigue are both bad at the same time and i hallucinate. Just because people with fibromyalgia smile, doesn’t mean that we are not in pain. That doesn’t mean that we don’t deserve to have a cure. ⠀

I had different ideas for this post. A little positive. But I don’t have that in me. Because I am just so mad at the world. I’ve been having a really hard time with this recently. Even after 8 years for me, acceptance is hard to find. Because we do not deserve this. I don’t want to be in pain anymore. I don’t want to feel exhausted all the time. I don’t want to also have insomnia. I don’t want to deal with the symptoms my body likes to randomly throw at me like fibro fog or sensitivity to weather, whatever weird shoulder arm thing my body has decided to hit me with, numbness, skin sensitivity, light, noise sensitivity, flares, and so much more. I want to be able to one day say that I used to have fibromyalgia. I know we all do.

From a monologue I wrote for one of my acting classes, “And I feel like I’m never gonna be truly okay, because I am going to always be waiting to wake up from that nightmare. And I never will. I don’t deserve you. You do not deserve me. You don’t deserve to take my dreams, and my hope, my days, my laughter, my happiness, my life. But if you want to there’s not much I can really do about it to either succumb and let you…or try to survive through you and in spite of you. But that doesn’t mean it doesn’t hurt. But with that being said, I just want you to know… I am here. I am here fighting to have and keep those things everyday in spite of you. Good days and bad. You may win the battles, but I will win the war, I promise you that. And I will never give you the satisfaction to say otherwise. You may beat me down, but you will not break me. Because that is what I deserve.”

I find it so hard to even see myself dealing with one more day with fibromyalgia. But I’ve made 8 years. And no matter how hard it gets, I can say that I’m surviving it. And that’s something fibro will never take from us. That we are survivors, we are WARRIORS. And by raising awareness, we can get actual helping medication, we can get a cure. Because we deserve that. So I’m asking you guys to stand up, and wear purple, share, like, comment, whatever because we with fibromyalgia and chronic illnesses do not deserve this. And maybe if we all raise awareness for it that we won’t have to deal with this forever. Cause I know for a fact us warriors are SO strong. But that doesn’t mean that strong people don’t get tired. So let’s all please raise awareness so that we can come up from this nightmare one day. Thank you. 💜

#fibromyalgia #fibro #fibrowarrior #fibrofighter #fibrosucks #fibro sucks #fuck fibro #fibro life #fibropain #fibro problems #fibroawareness #fibrostrong #fibro tag #fibro things #fibro fog #chronic illness #chronic pain #chronicpainwarrior #chronic fatigue #chronically ill #chronic problems #invisibleillness #spoonie #fatigue #fibrolife #fibro flare

[achybutcurious]

So it's carnival and we get a five day holiday from work, from Saturday to Wednesday

So I'm at mom's, hanging out with the dog, spent the whole day yesterday smooching with bf

I'm having a laid bac, nice time, you know

Inspite of all the relaxation, I have just been overwhelmed with pain

#fibro life #fibromyalgia #fibro problems #fibro

[sidprescot]

i cleaned the house today but at what cost

#my body is like bitch??? what the fuck???? #fibro life #rj.txt #dl

[justsomerandomgay]

something that isn’t talked about enough with chronic illness is knowing that going to your appointments and doing your exercises and all that will help but being in too much pain or too fatigued to go, so your just stuck in this constant cycle of knowing what you need to do to get better but not being able to do it because your sick

#chronic illness #chronically ill #chronic pain #cripple posting #cripple punk #cripplepunk #crip punk #cripple shit #functional neurological disorder #queer cripple #fibro problems #fibromyalgia #crippunk #cripple life #cripple problems

[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

[disabledopossum]

I absolutely do not.

#fibro #fibro life #fibromyalgia #fibro things #meme #depression #chronic fatigue #chronic pain #chronic illness

[fallenstarcat]

i think people underestimate the power of sitting. sitting down has saved my life. i sit in the shower, i sit to cook, i sit to get dressed, i sit and now i can do those things more and enjoy doing them now because i’m not in unbearable pain from standing!

#seriously #i recommend sitting down to all my friends #disability #disabled #actually disabled #physically disabled #fibromyalgia #fibro #chronically ill #mobility impaired #disabled life #spoonie #spoonie things #cripplepunk #chronic pain

[chronicallyuniconic]

Painscrolling

When you're in too much pain to sleep and can't do anything else except lie there, so you scroll aimlessly, hoping it all goes away

#chronic fatigue #chronic illness #chronic migraine #chronic pain #chronically ill #fibro #fibromyalgia #mental health #myalgic encephalomyelitis #chronic life #out of spoons #cripple punk #chronic fatigue syndrome #no spoons #chronic pain syndrome #joint pain #painrelief #doomscrolling #pain flare #me/cfs #me cfs #Myalgic Encephalitis #fibrosucks #nerve pain #fibrowarrior #fibro problems #chronically tired #chronically disabled #chronically sick #chronically online

[cistematicchaos]

I need some of you to stop thinking that being visibly disabled comes with some kind of inherent privilege. I need some of you to stop thinking people are less ableist to us because they can easily tell we’re disabled. I need some of you to stop using us as a prop in your discussions about other disabilities, saying shit like “You’d never say or do X to a visibly disabled person so why-.”

I need some of you to stop telling physically disabled people that they’re the most privileged in disabled spaces. I need some of you to stop coming into discussions specifically about physical disabilities and the ableism directed towards physically disabled people and then claiming we’re excluding you because you’re not currently being centered.��

We are all disabled, all part of the same community. But that doesn’t mean you can’t be ableist towards other disabled people and I’m seeing a lot of you do it and it’s exhausting. So, take a minute, step back and think about it and stop. 

#Disability education #ableism #physical disabilities #cripple life #fibro #chronic pain #chronic illness #actually neurodivergent #neurodiversity #mental illness #mental disabilities #actually disabled #actually mentally ill #spoonie #physically disabled #mentally disabled #chaos is speaking #invisible disabilities #There's numerous flipsides to this as well #ngl i already have one in my drafts lol #but this one's been driving me crazy so here we go

[thesecretlifeofmecfs]

#chronic illness #spoonie #but you dont look sick #spoonie life #chronic illness life #fibromyalgia #fibro tag #fibrowarrior #mecfs #cfsme #myalgic encephalomyelitis #chronic fatigue syndrome #ehlers danlos awareness #ehlers danlos syndrome