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Follow 👉 @chronicpaincastle for more content💓🌼🥰
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#spoonieproblems#fibrofighter#fibromyalgiaawareness#invisibleillnessawareness#fibromyalgiawarrior#potssyndrome#rawarrior#chronicallyfabulous#neuropathy#cfsme#psoriaticarthritis#spooniewarrior#chroniclymedisease#meawareness#spooniemom#chronicbackpain#chronicillnessblogger#chronicpainsurvivor#chronicillnessmemes#fibrowarriors#spoonielove#spoonieblogger#chronicillnesscommunity#fibroawareness#costochondritis
3 years agoillswithskills
Until your late thirties they didn't and when they do you're at palliative care🙌❤️
3 years agollhampton64
Learning that you were never lazy or out of shape you were just chronically ill
3 years agogrowling.silverwolf
When I was 17 I regularly had bad headaches, I could feel it's INside my skull but the doc looked for bumps or bruises on my scalp. He didn't find anything and first said 'Seems like you don't drink enough water', but me and my mum advocated for me and he sent us to a radiologist for a CT of my head. Long story short: nothing found and I was sent home with no explanation or solution. It always was the same spot, punctual, not the whole head or areas. Later found out by myself I have light migraine attacks and back then had a high bloodpressure, unmedicated and unchecked.
3 years agolyraedits18
I was diagnosed with arthritis in every joint in my body when I was 16, I thought I could get better with the medication. No medication has helped, I'm 18 now and stuck in a wheelchair because it's so bad, it's spread to my chest as well. I feel like I'm dying and honestly sometimes feel like enviting it.
3 years agoaftersk444l
been progressively bleeding out more and more from a place i shouldn’t be since last november and random episodes of extreme abdominal pressure and sharp extreme pain, did the fibre supplements and didn’t work, not celiac or allergic to anything, bloodwork always perfect, colonoscopy found nothing b it perfectly healthy tissue fully intact, dual section ultrasound was perfect, sometimes the bloating is so severe i look 4mos pregnant, once went to the A&E when it was so bad i thought my appendix burst and waited 7hrs to be told to take paracetamol ……… HELP💀💀
3 years agoa.nic.l
What do I tell her? It gets worse? You're in more pain now than you've ever been? I can't do that to her... she deserves so much more
3 years agoekinemre7
Dudeeee the amount of .. it just happens ya know … i received to ‘calm me down’ ..
3 years agochristalyn.okeefe
i was diagnosed with eds and pots my dad still says i’m making it up and my mom still calls me a hypochondriac
3 years agojanet_mcgann_
I’m just now finding answers for pain I’ve had my whole life. I cherish the years before it got worse. But it is what it so I’ll tell little me to live life to the fullest
3 years agoriordan_stilinski
Yesterday after years of specialists and doctors. I was told that it's most likely physical symptoms from my horrible anxiety. I feel even more helpless because I've been fighting with my anxiety for my entire life. I'm so defeated now. There's nothing I can physically do to stop the pain and discomfort other than fix myself
3 years agobloom1ngrose
i was always sick as a child, it got much worse after I was about 13 and how nobody even questioned a chronic illness until I was 19 I'll never know. Still have absolutely fuck all clue what's wrong and Dr's dont seem interested, I just keep getting passed from specialty to specialty lol. hope it does get better soon but i hate thinking that I'd have to tell my younger self that it only gets so, so much worse 😭
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