Joined January 2019
755 Photos and videos
Yes to this! There's a mistaken belief that you've got a low pain threshold, that #opiods are making you feel the pain more, that it can't possibly be that bad b/c you're a woman, that you look okay. When I say my pain is agonising, I mean it. #chronicpain #chronicillness
“Because the body’s nerves are constantly firing they never get a rest, so when they get triggered by “smaller” things, they will hurt more than a “regular” person.” Please Don't Confuse #ChronicPain With Low Pain Tolerance buff.ly/GOw4yWr #intractablepain #chronicillness
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If only... 🤣🤣🤣 I didn't have much to start with. I have less since chronic illness & weight loss 😯 instagram.com/p/DZpQvsfDGW3 #wtf #chronicillness #spoonie #funny #lol
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This is a major flaw in the system. If someone is medically diagnosed with a lifelong /or deteriorating condition a vast amount of money is wasted in a programme of reassessments. There needs to be a shift to acceptance of lifelong being just that and if someone is identified at needing the highest level of support then that being confirmed forever. The stress of unnecessary reassessment also complicates people's lives - the fear of losing the needed support etc Disabled people with lifelong conditions facing ‘unnecessary’ Pip reassessments ‘Pointless’ reviews are wasting public money and ‘significantly harming’ the mental health of claimants, charity says theguardian.com/politics/202…
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Are you a carer? You can get help and support if you're responsible for looking after someone who has a disability, is getting old or has become ill. Learn more about what a carer is, your rights as a carer and the support available ⤵️ citizensadvice.org.uk/family… #CarersWeek
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While others can learn & empathise, only the person living it can truly know what it's like. It's more than just the illness/pain/disability, it's the whole experience that can affect all areas of life. That person is the expert of their own experience but they're often ignored.
"Disabled people are experts in our own lives – listen to us." Associate Professor Bernadette Jones speaks out about the system's failure to adequately respond to the crisis in Disability Rights and Healthcare. newsroom.co.nz/2026/06/09/di…
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InvisiblyMe retweeted
"#Pain is a deep, dark pit that co-exists with the poisonous snakes of severe #depression, #anxiety, and yet more pain. There can always be more pain, and there can always be different kinds of pain": buff.ly/Fqebe2V #ChronicPain #ChronicIllness #NEisVoid #MondayBlogs
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You’re not failing at #life if you’re finding things difficult. 💜 Struggling means that you are trying, despite the challenges you face. instagram.com/p/DZXqKNJjKk0/ #tuesdaythoughts #quotes #quote #chronicillness #chronicpain #mentalhealth #inspiration #motivation #blogger
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InvisiblyMe retweeted
The DWP is secretly testing sweeping new rules – described as a “recipe for disaster” – on disability benefit assessments, which will reduce the influence of healthcare professionals and hand greater responsibility to civil servants. disabilitynewsservice.com/dw…
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A rainy #weekend is a good excuse for a little spring cleaning, something that seems to have become a never-ending task for me since living w/#chronicillness & #chronicpain. 🌻 7 Things To Spring Clean In Your Life 🌻 invisiblyme.com/7things-spri… #blog #blogger #lifestyle
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InvisiblyMe retweeted
"From a clinical perspective, a #doctor might dismiss the #pain, as “#men do not ‘really’ get #ChronicIllness or #fibromyalgia”. Within a societal narrative, men r often expected to b “strong & stoic” — pain is..suppressed voluntarily, yet reluctantly.": buff.ly/6cJoqbU
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We're launching a nationwide conversation to understand what matters to Disabled people today. We want it to inform our strategy and how we campaign for years to come! Have your say👇 Survey surveymonkey.com/r/DRUKstrat… Easy Read surveymonkey.com/r/surveyeas… BSL surveymonkey.com/r/strategyB…
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Replying to @HColumns
All comments returned Understanding The Let Them Theory: Why It’s Changing Lives We live in a world where a sense of control is often lacking, yet we still desire that sense. But two simple words can set us free: Let them unwantedlife.me/understandin…
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It makes it all the harder when PIP questions aren't relevant to your personal situation, abilities or requirements. There's no grey areas allowed in answers either. It's like trying to explain the problems when you aren't allowed to use words.
I worked for the NHS for over 20 years in disability rehabilitation, before my disability wasn't accomodated by my employer during the pandemic. PIP has been the most dehumanising, humiliating experience of my life. It degrades me. I wish non PIP claimants understood that.
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Seems the #heatwave is already on the way out but it has been a welcome change, albeit challenging w/ #chronicillness 😎☀️🌻 instagram.com/p/DY6847MjCl3/ #chronicpain #uk #summer #milkshake @ShakeawayLand #Health #disability #invisibleillness #spoonie #ostomy #stoma #blog #blogger
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They should do it for those with chronic, long-term conditions that aren't going to or are unlikely to improve, too. Claimants can be asked every 2yrs if anything has changed, but w/o another application/ review unless there's improvement.
❗️People with terminal or lifelong conditions and disabilities shouldn’t have to keep proving they’re ill just to get support. We're standing with @mariecurieuk to call on the UK government to change this, so people don't have to go through repeated stress and uncertainty.
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InvisiblyMe retweeted
‼️Ends Tomorrow! ‼️ Have a #Disability, #chronicillness #chronicpain or are a #carer? Please consider submitting your thoughts on the Timms PIP review👇 gov.uk/government/calls-for-… #Health #UK #England #politics #benefits #labour #government #news #Health #healthcare #disabled
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