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Unblinded trials with subjective outcome measures: I found quite a few unblinded trials which seemed to show that talk therapy benefited those diagnosed with SSD. If talk therapy really relieved the symptoms of SSD, this would indeed be evidence that the symptoms have psychological causes. However, while these trials did have control groups, the control groups received ‘treatment as usual,’ which amounts to no treatment at all. The patients knew which group they were in, and the experimental group received a treatment while the control group did not. We know that any group of patients who are given therapy of any type will report improvement; this is known as the therapy effect, similar to the placebo effect.

Furthermore, these trials had subjective rather than objective outcome measures. In the trials I looked at the outcome measure was a survey. This is not ideal because people who have received a treatment often feel that they ‘should’ feel better; they almost feel obligated to say that they have improved. Combined with the lack of blinding, this amounts to a very poor study design. It reminds me of the deluge of poorly-designed clinical trials which for years seemed to show (wrongly) that ME/CFS could be treated with counseling and exercise.

Unblinded trials with subjective outcome measures: I found quite a few unblinded trials which seemed to show that talk therapy benefited those diagnosed with SSD. If talk therapy really relieved the symptoms of SSD, this would indeed be evidence that the symptoms have psychological causes. However, while these trials did have control groups, the control groups received ‘treatment as usual,’ which amounts to no treatment at all. The patients knew which group they were in, and the experimental group received a treatment while the control group did not. We know that any group of patients who are given therapy of any type will report improvement; this is known as the therapy effect, similar to the placebo effect. Furthermore, these trials had subjective rather than objective outcome measures. In the trials I looked at the outcome measure was a survey. This is not ideal because people who have received a treatment often feel that they ‘should’ feel better; they almost feel obligated to say that they have improved. Combined with the lack of blinding, this amounts to a very poor study design. It reminds me of the deluge of poorly-designed clinical trials which for years seemed to show (wrongly) that ME/CFS could be treated with counseling and exercise.

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Extract from:
Somatic symptom disorder: Why your doctor doesn't believe you're really sick

mecfs.substack.com/p/somatic-sy...

#chronicillness #Spoonie #hiddenillness #invisibleillness

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The absence of any physical explanation for symptoms is taken as ‘evidence’ for somatic symptom disorder. This ignores the fact that most patients do not receive a thorough set of tests and referrals to specialists to rule out physical causes. It doesn’t take into account that some patients present in ways doctors find confusing or unexpected due to cultural differences, leading to missed diagnosis. It doesn’t take into account rare diseases which are often missed. It doesn’t take into account common but medically neglected diseases, such as ME/CFS, which are also often missed. (Even a common and medically recognized disease, endometriosis, typically takes 5-10 years to be diagnosed; patients spend years being told there is nothing wrong with them.) And it fails to acknowledge that medical science is not finished; there are still some medical conditions that science doesn’t understand and can’t explain.

The absence of any physical explanation for symptoms is taken as ‘evidence’ for somatic symptom disorder. This ignores the fact that most patients do not receive a thorough set of tests and referrals to specialists to rule out physical causes. It doesn’t take into account that some patients present in ways doctors find confusing or unexpected due to cultural differences, leading to missed diagnosis. It doesn’t take into account rare diseases which are often missed. It doesn’t take into account common but medically neglected diseases, such as ME/CFS, which are also often missed. (Even a common and medically recognized disease, endometriosis, typically takes 5-10 years to be diagnosed; patients spend years being told there is nothing wrong with them.) And it fails to acknowledge that medical science is not finished; there are still some medical conditions that science doesn’t understand and can’t explain.

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Extract from:
Somatic symptom disorder: Why your doctor doesn't believe you're really sick

mecfs.substack.com/p/somatic-sy...

#Psychologicalisation #chronicillness #ChronicPain #hiddenillness #invisibleillness

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Image of a person stuck inside a huge box
	
I have long Covid. Don’t call my chronic disease a ‘journey’: I would sooner call the experience a bad trip 
Like an estimated 20 million Americans, I have an incurable post-acute infection syndrome that goes by the name of long Covid. Some people refer to the long Covid experience as a “journey.” I wish they would stop. I’m pinned down by it, stuck with it. I feel like I’m getting nowhere. Sugarcoating my bitter pill, a chronic disease, by calling it a “journey” might sweeten it for you, but not for me.
Read more here>>

Image of a person stuck inside a huge box I have long Covid. Don’t call my chronic disease a ‘journey’: I would sooner call the experience a bad trip Like an estimated 20 million Americans, I have an incurable post-acute infection syndrome that goes by the name of long Covid. Some people refer to the long Covid experience as a “journey.” I wish they would stop. I’m pinned down by it, stuck with it. I feel like I’m getting nowhere. Sugarcoating my bitter pill, a chronic disease, by calling it a “journey” might sweeten it for you, but not for me. Read more here>>

"I have long Covid. Don’t call my chronic disease a ‘journey’: I would sooner call the experience a bad trip"

Screenshot from February 2026 AMMES newsletter

www.statnews.com/2025/11/25/c...

#chronicillness #LongCovid #hiddenillness #invisibleillness
#Spoonies #Spoonie #ChronicallyIll #MEcfs

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K. Johnstone
4d
Making sense of ME/CFS

"You'd get better if you just...." is bullying and we don't deserve it.

People with ME, Long Covid, and other chronic diseases are bombarded with messages that our illness can be treated 'holistically,' using a 'mind-body' approach. We just need to 'calm our nervous systems'. We need to 'reprogram our nervous systems'.

The treatment you're supposed to do, the one magic trick that will 'cure' you, keeps changing. Yoga. Breathwork. Mindfulness. No, a different kind of mindfulness. Massage. Positive thinking. No, a different kind of positive thinking.

It's exhausting. But more than that, it belittles us. It dismisses us. The people who insist on saying "You'd get better if you just did this one particular type of therapy," see themselves as compassionate, but they are bullies.

K. Johnstone 4d Making sense of ME/CFS "You'd get better if you just...." is bullying and we don't deserve it. People with ME, Long Covid, and other chronic diseases are bombarded with messages that our illness can be treated 'holistically,' using a 'mind-body' approach. We just need to 'calm our nervous systems'. We need to 'reprogram our nervous systems'. The treatment you're supposed to do, the one magic trick that will 'cure' you, keeps changing. Yoga. Breathwork. Mindfulness. No, a different kind of mindfulness. Massage. Positive thinking. No, a different kind of positive thinking. It's exhausting. But more than that, it belittles us. It dismisses us. The people who insist on saying "You'd get better if you just did this one particular type of therapy," see themselves as compassionate, but they are bullies.

Short blog post by K. Johnstone @kjohnstone.bsky.social :

"'You'd get better if you just....' is bullying and we don't deserve it."

substack.com/@mecfs/note/...

#MEcfs #chronicillness #hiddenillness #invisibleillness #ChronicIllnesses #LongCovid #ChronicPain

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Photo of Toni Bernhard J.D.
Toni Bernhard J.D.
Turning Straw Into Gold
Chronic Illness
How Invisible Chronic Illness Adds an Extra Burden to Life
Personal Perspective: Most people are uneducated about chronic pain and illness.
Updated November 29, 2025

Photo of Toni Bernhard J.D. Toni Bernhard J.D. Turning Straw Into Gold Chronic Illness How Invisible Chronic Illness Adds an Extra Burden to Life Personal Perspective: Most people are uneducated about chronic pain and illness. Updated November 29, 2025

How Invisible Chronic Illness Adds an Extra Burden to Life

www.psychologytoday.com/us/blog/turn...

She has ME/CFS herself but the article is not specific to any illness

#invisibleillness #chronicillness #ChronicPain #Spoonielife
#hiddenillness #Spoonies #Spoonie #ChronicallyIll

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When I Don't Feel 'Disabled Enough' as Someone With a Chronic Illness

Elaine Rush  •  
Follow
Last updated: August 2, 2024
1.1K13

Photo of signs for restrooms

How many of you who have fibromyalgia or similar chronic illness sometimes feel like you’re judged for not being “disabled enough?”

When I Don't Feel 'Disabled Enough' as Someone With a Chronic Illness Elaine Rush • Follow Last updated: August 2, 2024 1.1K13 Photo of signs for restrooms How many of you who have fibromyalgia or similar chronic illness sometimes feel like you’re judged for not being “disabled enough?”

"When I Don't Feel 'Disabled Enough' as Someone With a Chronic Illness"

themighty.com/topic/fibrom...

"How many of you who have fibromyalgia or similar #chronicillness sometimes feel like you’re judged for not being 'disabled enough?'”

#invisibleillness #Spoonie #hiddenillness #Spoonielife

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THE LONG COVID ULTIMATE BINGO

Grid showing lots of irritating comments people with long Covid and other chronic illnesses may hear said to them

THE LONG COVID ULTIMATE BINGO Grid showing lots of irritating comments people with long Covid and other chronic illnesses may hear said to them

Many with ME/CFS and other chronic illnesses may be able to relate some if not many of these

This was posted as a comment on my FB page today, but I'm not sure who created it originally.

#LongCovid #MEcfs #chronicillness #hiddenillness #invisibleillness #ChronicIllnesses #Spoonies #Spoonie

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Disability Rebellion
@DRDisabilityReb
🛑 Blue Badge Myths – Busted ♿🚗

Disabled people are facing increasing harassment for using Blue Badges. Let’s get the facts straight.

🔴 Myth 1: “You don’t look disabled.”

✅ Fact: There is no such thing as a disabled ‘look’. Many disabilities are invisible, fluctuating, or not obvious to strangers.

🔴 Myth 2: “Blue Badges are only for wheelchair users.”

✅ Fact: Blue Badges are for people whose disabilities affect mobility, pain, fatigue, breath, balance, safety, or ability to walk distances — not just wheelchair users.

🔴 Myth 3: “If you can walk, you shouldn’t have a Blue Badge.”

✅ Fact: Being able to walk is not the same as being able to walk safely, repeatedly, or without severe pain or exhaustion.

🔴 Myth 4: “People just get Blue Badges easily.”

✅ Fact: The application process is strict, evidence-based, and often stressful. Many disabled people are wrongly rejected and have to appeal.

🔴 Myth 5: “Blue Badge misuse is widespread.”

✅ Fact: Fraud exists, but it is rare. Media outrage vastly exaggerates the issue, while ignoring the real harm caused by harassment of legitimate badge holders.

🔴 Myth 6: “Challenging people helps protect disabled parking.”

✅ Fact: Public policing harms disabled people, not fraudsters. Enforcement is the responsibility of local authorities - not strangers in car parks.

⚠️ Harassing someone over a Blue Badge is discrimination. You are not entitled to medical details. You are not entitled to judge.

📣 Disabled people don’t owe you proof.

Disability Rebellion @DRDisabilityReb 🛑 Blue Badge Myths – Busted ♿🚗 Disabled people are facing increasing harassment for using Blue Badges. Let’s get the facts straight. 🔴 Myth 1: “You don’t look disabled.” ✅ Fact: There is no such thing as a disabled ‘look’. Many disabilities are invisible, fluctuating, or not obvious to strangers. 🔴 Myth 2: “Blue Badges are only for wheelchair users.” ✅ Fact: Blue Badges are for people whose disabilities affect mobility, pain, fatigue, breath, balance, safety, or ability to walk distances — not just wheelchair users. 🔴 Myth 3: “If you can walk, you shouldn’t have a Blue Badge.” ✅ Fact: Being able to walk is not the same as being able to walk safely, repeatedly, or without severe pain or exhaustion. 🔴 Myth 4: “People just get Blue Badges easily.” ✅ Fact: The application process is strict, evidence-based, and often stressful. Many disabled people are wrongly rejected and have to appeal. 🔴 Myth 5: “Blue Badge misuse is widespread.” ✅ Fact: Fraud exists, but it is rare. Media outrage vastly exaggerates the issue, while ignoring the real harm caused by harassment of legitimate badge holders. 🔴 Myth 6: “Challenging people helps protect disabled parking.” ✅ Fact: Public policing harms disabled people, not fraudsters. Enforcement is the responsibility of local authorities - not strangers in car parks. ⚠️ Harassing someone over a Blue Badge is discrimination. You are not entitled to medical details. You are not entitled to judge. 📣 Disabled people don’t owe you proof.

Blue Badge* Myths – Busted

*a blue badge is what a disabled parking badge/permit is called in the UK

x.com/DRDisability...

#Disabled #Disability #Hiddendisability #Invisibledisability #chronicillness #hiddenillness #invisibleillness #Spoonie

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Shame, (In)visibility, and Ill Feelings — Katharine Cheston
"I investigate how diagnostic labels employed in these contexts render suffering and sufferers (in)visible, and illuminate how fusing genres offers Hattrick a particular form of (controlled) visibility. Finally, I consider the implications of this analysis for our broader understanding of shame, and for our approach to literary life writing."

Shame, (In)visibility, and Ill Feelings — Katharine Cheston "I investigate how diagnostic labels employed in these contexts render suffering and sufferers (in)visible, and illuminate how fusing genres offers Hattrick a particular form of (controlled) visibility. Finally, I consider the implications of this analysis for our broader understanding of shame, and for our approach to literary life writing."

Shame, (In)visibility, and Ill Feelings by @kacheston.bsky.social

muse.jhu.edu/article/975548

Screenshot from latest Science for ME weekly update

#MEcfs #chronicillness #Fibromyalgia #hiddenillness #invisibleillness

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some disabilities look like this (figures using cane, crutch, wheelchair)
some look like this (figure with no visible disability)

some disabilities look like this (figures using cane, crutch, wheelchair) some look like this (figure with no visible disability)

On International Day of #People with #Disabilities, remember that some disabilities are #invisible

#DisabilityRights #DisabilityRightsAreHumanRights
#IDPD #IDPD2025 #Disability
#HiddenIllness #ChronicIllness #InvisibleDisability

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Medical Gaslighting
Medical Gaslighting YouTube video by Carolyn Sullins

"Medical Gaslighting"

www.youtube.com/watch?v=Kwp_...

A light-hearted 3-minute song with a serious message, with which many may sadly be able to relate

#MedicalGaslighting #chronicillness #hiddenillness
#invisibleillness #Gaslighting #ChronicallyIll #ChronicPain

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compassionatereminders Follow
I hate how people will hold you to higher standards as a disabled person than they would if you were abled. I mean literally no one will expect your average abled person to exercise every day and give up alcohol and only eat vegetables, but as soon as you got a chronic illness or a mental disorder suddenly everyone is holding you to health standards literally no one else is expected to actually meet- and if you don't do xyz, then they will insist that's why you're ill. Even though THEY aren't doing it either
Bendy Bunny

compassionatereminders Follow I hate how people will hold you to higher standards as a disabled person than they would if you were abled. I mean literally no one will expect your average abled person to exercise every day and give up alcohol and only eat vegetables, but as soon as you got a chronic illness or a mental disorder suddenly everyone is holding you to health standards literally no one else is expected to actually meet- and if you don't do xyz, then they will insist that's why you're ill. Even though THEY aren't doing it either Bendy Bunny

#chronicillness #ChronicPain #hiddenillness #invisibleillness
#ChronicIllnesses #Spoonies #ChronicIllnessMemes
#Disabled

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Alone & at Ease
Alone & at Ease YouTube video by Within A Dream

lil' snippet of a previous broadcast, #adream54321 pulled from deep #withinadream54321 #wellnessmusic #relaxationmusic #hiddenillness #nursemusician #EDnursing #breathedeeply
youtu.be/a1mEm4Lf0u4

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"Akin to the ideal victim, the ideal claimant of hidden disability must navigate a system built by (and from the perspective of) those with specific preconceived notions of what it means to be a person with a disability and to present as one."

#MEcfs #invisibleillness #hiddenillness #spoonie

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Video

view from the beach at #HarissonLake from #adream54321 #withinadream54321 #serenity #peaceofmind #hiddenillness

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But you don't look sick?! 


My illness is commonly referred to as an invisible illness. Did you know that 96% of people with a chronic illness have an invisible condition, and that 74% of disabled individuals do not use visible mobility aids like wheelchairs? Please don't judge my health based on my appearance. 

CHRONICALLY RISING

But you don't look sick?! My illness is commonly referred to as an invisible illness. Did you know that 96% of people with a chronic illness have an invisible condition, and that 74% of disabled individuals do not use visible mobility aids like wheelchairs? Please don't judge my health based on my appearance. CHRONICALLY RISING

#chronicillness #invisibleillness #hiddenillness #Spoonie #spoonies

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Table 2. Never-WordsforPatientsWithInvisibleIllnesses– Liza Di LeoThomas,MD Di Leo Thomas, L Never-WordPhrase Alternative Explanation “But you look fine.” “At least you don’t look sick.” “Great news! All your tests are negative!” “You can’t believe everything you see online. Let’s not diagnose you based on a TikTok influencer.” “At least you’re not bedbound, wheelchair bound, don’t have cancer, et cetera, et cetera, et cetera….” “Wedon’t knowmuchaboutthisillness. There’s nothing I can do for you.” “It must be frustrating to feel so awful.” “The goodnewsiswehaveruledout (A, B, C) by doing these tests. But I believe there is something wrong, and I will work with you to figure it out.” “Thank you for taking such an interest in your illness and advocating for yourself. Let’s talk about what you saw online.” “It sounds like you are suffering with this quite a bit. Can you explain how it has affected your quality of life?” “I realize the research on Long COVID is slow to come, andIcan’t imagine how frustrating that is for you. Let’s see whatwecandorightnowtotreat someofyoursymptomsandimprove your quality of life.” Telling patients they look fine may make themfeel like you are doubting their illness, even if you are not. Somepatients maynotfeel like it is great newsthat test after test is negative whentheyknowsomethingis absolutely wrong with them. Online communities have become ahuge source of support for patients with LongCOVIDandotherinvisible illnesses. Hearing someone else describe the same symptomscanbe incredibly validating. Avoid dismissing these sources outright. Avoid starting with “at least,”which can sound dismissive or invalidating. Instead, explore how the illness impacts the patient’s life. Even without definitive treatments, providers can offer symptom managementandhope. Acknowledging the patient’s frustration while focusing on what can bedoneisempowering.

Table 2. Never-WordsforPatientsWithInvisibleIllnesses– Liza Di LeoThomas,MD Di Leo Thomas, L Never-WordPhrase Alternative Explanation “But you look fine.” “At least you don’t look sick.” “Great news! All your tests are negative!” “You can’t believe everything you see online. Let’s not diagnose you based on a TikTok influencer.” “At least you’re not bedbound, wheelchair bound, don’t have cancer, et cetera, et cetera, et cetera….” “Wedon’t knowmuchaboutthisillness. There’s nothing I can do for you.” “It must be frustrating to feel so awful.” “The goodnewsiswehaveruledout (A, B, C) by doing these tests. But I believe there is something wrong, and I will work with you to figure it out.” “Thank you for taking such an interest in your illness and advocating for yourself. Let’s talk about what you saw online.” “It sounds like you are suffering with this quite a bit. Can you explain how it has affected your quality of life?” “I realize the research on Long COVID is slow to come, andIcan’t imagine how frustrating that is for you. Let’s see whatwecandorightnowtotreat someofyoursymptomsandimprove your quality of life.” Telling patients they look fine may make themfeel like you are doubting their illness, even if you are not. Somepatients maynotfeel like it is great newsthat test after test is negative whentheyknowsomethingis absolutely wrong with them. Online communities have become ahuge source of support for patients with LongCOVIDandotherinvisible illnesses. Hearing someone else describe the same symptomscanbe incredibly validating. Avoid dismissing these sources outright. Avoid starting with “at least,”which can sound dismissive or invalidating. Instead, explore how the illness impacts the patient’s life. Even without definitive treatments, providers can offer symptom managementandhope. Acknowledging the patient’s frustration while focusing on what can bedoneisempowering.

"Never-Words for Patients With Invisible Illnesses – Liza Di Leo Thomas, MD"

From:
When We Don’t Have All the Answers: #LongCOVID and the Need for Humility in Medicine

www.ochsnerjournal.org/content/25/3...

#invisibleillness #LongCovid #chronicillness
#hiddenillness #ChronicIllnesses

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Video

Patient thinks chronic fatigue is "just stress." Standard blood work comes back normal. Plot twist: Hidden chronic infections like Bud-Chiari disease that regular doctors completely miss. The Skolnikoff Method finds what others don't even test for.


#ChronicInfections #HiddenIllness

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Developing my writer's platform. An essay of learning to fail gracefully and with mindfulness when you have temporal lobe epilepsy. #chronicillness #hiddenillness
Sorry+2+Myself elejrnl.com?p=4194843

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Post image

Just because we don't always look ill, doesn't mean we are coping!

#fibromyalgia #chronicpain #hiddenillness #pain

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Image of a doctor with their head in the sand

‘Symptom Invalidation’ in Clinically Uncertain Diagnoses Can Leave Lasting Mental Health Harms
As a young child in the 1980s, Jiwa Farrell earned the moniker “Little Apple Cheeks” because her face was always so “cute and pink.” But by the time she was 6 years old, she had already begun recognizing that something else distinguished her from other kids besides her bright pink complexion.

“I had flu-like symptoms all throughout my childhood and always felt very fatigued,” Farrell told Medscape Medical News. “My muscles ached, my joints ached, and I remember thinking as a kid to myself, ‘If I feel this way and other people don’t feel this way, what’s wrong with me?’”
Read more here>>

Image of a doctor with their head in the sand ‘Symptom Invalidation’ in Clinically Uncertain Diagnoses Can Leave Lasting Mental Health Harms As a young child in the 1980s, Jiwa Farrell earned the moniker “Little Apple Cheeks” because her face was always so “cute and pink.” But by the time she was 6 years old, she had already begun recognizing that something else distinguished her from other kids besides her bright pink complexion. “I had flu-like symptoms all throughout my childhood and always felt very fatigued,” Farrell told Medscape Medical News. “My muscles ached, my joints ached, and I remember thinking as a kid to myself, ‘If I feel this way and other people don’t feel this way, what’s wrong with me?’” Read more here>>

Symptom Invalidation’ in Clinically Uncertain Diagnoses Can Leave Lasting Mental Health Harms

www.medscape.com/viewarticle/...

Image is screenshot from AMMES July newsletter

#ChronicallyIll #chronicillness #ChronicPain #Spoonie #hiddenillness #invisibleillness

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Post image

Haven’t enjoyed the onrush of a thunderstorm in quite a while, as here from #withinadream54321 #adream54321 #nursemusician #wellbeing #qualityoflife
#wellnessretreat #hiddenillness #mentalwellbeing

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📆 Tweaking my #drop schedule for my design collections—I'm looking at Wednesdays b/c who doesn't love #humpday? The latest drop will be later today (after I get back from #physicaltherapy) 🧘‍♀️✨ #disabledartist #disability #ehlersdanlos #invisibleillness #hiddenillness #artisforeveryone #art #artforall

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Free Spirit Circling Above
Free Spirit Circling Above YouTube video by Within A Dream

Carrie Elizabeth Joy & I have been weaving together our talents for #relaxation & #wellbeing. #adream54321 #withinadream54321 #yogamusic #meditationmusic #spamusic #soundscape #deeprelaxation #hiddenillness #nursemusician #fyp #viral #homemusicstudio #calmingsounds #slowdown
youtu.be/Whb6WG1pz1A?...

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Video

#aspookykindofbeautiful #adream54321 #withinadream54321 #wellnessmusic #meditationmusic #relaxationmusic #spamusic #nursemusician #yogamusic #wellbeing #qualityoflife
#soundscapes #twitchlivestream #livemusicstream #wellnessretreat #hiddenillness #mentalwellbeing

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#withinadream54321 #wellnessmusic #meditationmusic #hiddenillness #spamusic #nursemusician #wellness
#withinadream54321 #wellnessmusic #meditationmusic #hiddenillness #spamusic #nursemusician #wellness YouTube video by Within A Dream

Elements of Victoria
#withinadream54321 #wellnessmusic #meditationmusic #relaxationmusic #spamusic #nursemusician #yogamusic #wellbeing #qualityoflife
#soundscape #twitchlivestream #livemusicstream #wellnessretreat #hiddenillness #mentalwellbeing #elementsofvictoria #fyp youtube.com/shorts/QF6P1...

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GOING TO THE DOCTOR WHEN YOU HAVE A CHRONIC ILLNESS

What people think it's like
----------
pie chart showing:

Go to appointment
Get diagnosed
Receive treatment and support
Heal your body and get better

What it's actually like
---------
pie chart showing:

Waiting months for an appointment
Multiple/ongoing appointments Being left untreated
Treatments being ineffective and/or dealing with side effects
Worsening and/or new symptoms
Dealing with Medical gaslighting

@flexiblegonewrong

GOING TO THE DOCTOR WHEN YOU HAVE A CHRONIC ILLNESS What people think it's like ---------- pie chart showing: Go to appointment Get diagnosed Receive treatment and support Heal your body and get better What it's actually like --------- pie chart showing: Waiting months for an appointment Multiple/ongoing appointments Being left untreated Treatments being ineffective and/or dealing with side effects Worsening and/or new symptoms Dealing with Medical gaslighting @flexiblegonewrong

Going to the Doctor When You Have a Chronic Illness

#chronicillness #ChronicallyIll #hiddenillness
#invisibleillness

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Post image

#Exactlythis #Me #ME/CFS #Fibromyalgia #HiddenIllness #NoHope

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(Most) Doctors are all about helping the vulnerable until you ask them to put on a face mask. Weird. Maybe they should just admit their jobs are more about feeding their own egos than helping sick people
#covid #longcovid #chronicillness #hiddenillness

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Video

Let go #adream54321 #withinadream54321 #wellnessmusic #meditationmusic #relaxationmusic #spamusic #nursemusician #yogamusic #wellbeing #qualityoflife
#soundscapes #twitchlivestream #livemusicstream #wellnessretreat #hiddenillness #mentalwellbeing #letgo #release

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