thechronicpaingame
The Chronic Pain Game
2K posts
A day in the life of blog, written by someone with Polyarteritis Nodosa, Fibromyalgia, Adrenal Insufficiency, Stills Disease & more. 34 years of experience. Giving a safe place and platform for others to communicate and seek advice/help in dealing with these and similar conditions. My name is Rosie & I'm very friendly. If I follow you it'll be from my main account 'whiskeyoverwine'.
Last active 2 hours ago
Don't wanna be here? Send us removal request.
thechronicpaingame 22 days ago
Text
https://www.jci.org/articles/view/144201
Link to the study for all interested 馃グ if you have a little Google though there's plenty of places that explain the study in layman's terms if needed.
Has everyone seen the latest fibromyalgia research? We're almost at the final conclusion of the "is this autoimmune" saga! Very interesting, very good news all round. But also, with all of this present why it hasn't been labelled sooner is beyond me.
Tumblr media
199 notes View notes
thechronicpaingame 27 days ago
Text
Has everyone seen the latest fibromyalgia research? We're almost at the final conclusion of the "is this autoimmune" saga! Very interesting, very good news all round. But also, with all of this present why it hasn't been labelled sooner is beyond me.
Tumblr media
199 notes View notes
thechronicpaingame 2 months ago
Text
Woke up absolutely raging today. Checked the calendar and what do you know, it's the start of my PMDD week. A benefit to living alone is I can hunker down in these weeks and just not talk to other humans.
5 notes View notes
thechronicpaingame 2 months ago
Text
So sorry to my US friends, specifically my disabled US friends who aren't eligible to emigrate with news of Trump's win. My trans friends, my black friends, my gay friends and honestly just women in general. I am so heartbroken for so many people today. I don't ever really talk politics on here (just because it's not a political blog) but I think I should firmly acknowledge my position in these times. This is forever a safe space for everyone.
I think people in the UK feel shocked, but also I think it's entirely naive to believe we're not headed in the same direction.
Just fucking sucks huh.
28 notes View notes
thechronicpaingame 3 months ago
Text
Tumblr media
Ta daaaaa. I still think it's more likely cEDS but they didn't think it was worth sending me for genetics (馃檮) but it answers some questions for sure.
Now just have to deal with the added grief (again) that things are not going to get better. I don't know why I have so much trouble with accepting how my life is but honestly I really struggle in that regard. I think I just wanna be able to work and buy a little house for me and my dog but even that is not a reality in my world. I dunno. Ranting.
16 notes View notes
thechronicpaingame 3 months ago
Text
I did this again a few days ago and it sucked again. I will never learn 馃槀 super high fever this time round (was hallucinating in the night), mostly back to normal besides still having a slight fever. I'd rather a few days of this than full blown flu or covid tho!
Had my flu & covid vaccine yesterday afternoon and man are they hitting me hard this year. I think it's mostly the flu jab as I'm usually super and hit and miss with how it affects me. Covid I've always done okay with. Fever, aches, headache, crippling nausea, the whole 9 yards this year.
32 notes View notes
thechronicpaingame 3 months ago
Text
Gastroparesis said a big fuck you to me tonight and I am in so much pain. Usually I have a lot of discomfort but little pain but tonight is wild.
6 notes View notes
thechronicpaingame 4 months ago
Text
me when the disability disables me: oh what the fuck? this sucks. what the hell man!
97K notes View notes
thechronicpaingame 4 months ago
Text
I am open to every and all gastroparesis tips, and help and everything btw!
Tumblr media
Hate to say I told you so to all the doctors but, I TOLD YOU SO (I don't really hate to say it I LOVE to say it, I absolutely relish in saying it) 馃槞
11 notes View notes
thechronicpaingame 4 months ago
Text
Tumblr media
Hate to say I told you so to all the doctors but, I TOLD YOU SO (I don't really hate to say it I LOVE to say it, I absolutely relish in saying it) 馃槞
11 notes View notes
thechronicpaingame 4 months ago
Text
I got zero answers for this by the way. Couldn't tell me what it was, said maybe it was overall a viral infection, not even any blood tests done. And people wonder why I never seek medical attention generally 馃檮
TW : EMETOPHOBIA
Seeing my GP tomorrow about my blood sick incident 馃槀 the main thing I want an answer to is what exactly did I throw up?! I will not bless you all with the photo, but this was something rubbery in texture, COVERED in blood and bile. Not food. The two people I've showed it to have both said "what the fuck is that" and my sentiments exactly. A piece of stomach tissue? A growth of some kind? I wish I'd kept it so they could've tested it 馃槀
9 notes View notes
thechronicpaingame 4 months ago
Text
TW : EMETOPHOBIA
Seeing my GP tomorrow about my blood sick incident 馃槀 the main thing I want an answer to is what exactly did I throw up?! I will not bless you all with the photo, but this was something rubbery in texture, COVERED in blood and bile. Not food. The two people I've showed it to have both said "what the fuck is that" and my sentiments exactly. A piece of stomach tissue? A growth of some kind? I wish I'd kept it so they could've tested it 馃槀
9 notes View notes
thechronicpaingame 4 months ago
Text
Friends, how are we treating our PMDD? I just spoke to my GP and he's said the best option is the coil but like, things I'm reading online say the opposite.
6 notes View notes
thechronicpaingame 4 months ago
Text
Just your casual Friday morning vomiting blood 馃檭 it looked like there was a piece of tissue in there (from somewhere) but besides the nausea and being tired I'm okay so just keeping an eye on things because I refuse to go to a&e to wait 10 hours and be sent home.
4 notes View notes
thechronicpaingame 5 months ago
Text
Back at it again with the pregabalin. Turns out, it was helping! 馃槀 I honestly thought it wasn't having any effect but I have seen the light on how much worse things can be.
6 notes View notes
thechronicpaingame 5 months ago
Text
After years of struggling I finally had my gastric emptying scan yesterday. Now we wait to see if what I think is gonna be found, is. Or maybe I am just losing my damn mind.
17 notes View notes
thechronicpaingame 5 months ago
Text
Okay maybe the pregabalin was helping? This knee pain is out of control. Nothing is touching it. The only way I can describe it for myself is like one of my polyarteritis flare-ups but confined to my knee. I don't know what to do with myself. Tramadol, paracetamol, ibuprofen, freeze spray. Nothing is lowering the level or intensity of the very deep ache.
6 notes View notes