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Chronic illness quotes to inspire, motivate, grieve, hope and laugh about. A community hub for the chronically ill to share and support.
Unfortunately, people still ask if fibromyalgia is real. With a range of medical evidence, we put this question to rest and explore the impact on sufferers.
Overcome FrustrationDealing with a chronic illness like Fibromyalgia, Chronic Fatigue Syndrome (ME/CFS), POTS, MCS or similar condition is full of frustration.Often people are not believed by family friends and even health professionals, they feel poorly understood and poorly supported.But we can learn to cope with these difficulties and finds ways to move past them. Start […]
"IF YOU WANNA BE MY LOVER...you have to come to terms with the fact my chronic illness is in fact chronic."
The official Chronic Pain India site. Know more about the Charitable Trust , Chronic Pain , chronic illness, invisible illness & disability.
The full list of chronic fatigue symptoms is shocking because the name has been misleading, causing much controversy. We expect fatigue but it's much more.
Nonprofit organization seeking to improve quality of life for people with POTS
A safe space for people with chronic illness where they can share deepest and darkest secrets anonymously.. “Spoonie Secrets: Issue #8” is published by Mary Gutierrez.
4.9 out of 5 stars - Shop Spoonie cards & gifts Trying To Understand created by WhyMePots. Personalize it with photos & text or purchase as is!
I know many people dismiss medical trauma, often not understanding that so many things surrounding medical treatment can be traumatic - the lack of control over your own body, traumatic procedures, medical gaslighting and mistreatment, the fear of losing your life, etc Your trauma is real, you are worthy of treatment and you are worthy of respect and understanding 💜
The answer might surprise you! The name does not fit the illness and fibromyaliga is NOT solely a pain symptom. We'll bust some myths for you.
Hello Spoonies, Well, the holidays are over, and you may have had to encounter your relatives during some sort of festive celebration thingie. I know there are spoonies who have wonderful, supportive families, but the majority of people I’ve met have at least one family member who is ... difficult. Maybe they lack empathy, or…
If you have ME/CFS, Fibromyalgia, POTS or other invisible illness, then chances are you find it frustrating trying to get other people to believe and take your choices seriously, especially family and friends. For years I have been giving people advice and find myself getting annoyed after all these years when I hear the suffering and frustration that people endure because their choices are not respected.
Cheyanne lives with Mast Cell Disease, which can trigger deadly allergies to anything. Read more about her in the "It's in My Blood" series.
Tell me you're chronically ill without telling me you're chronically ill - chronic illness memes inspired by the TikTok trend, "Tell me without telling me"!
It's been a string of bad days with depression, anxiety, fatigue, epilepsy, and more. But they made me realise something important on that one good day.
I am regularly contacted by people who have recently been diagnosed with Post Viral Fatigue or Chronic Fatigue Syndrome. They are often scared, worried and confused, but also hopeful and determined to return to their normal life. Their question is usually the same: what can I do? Having a diagnosis of PVF or CFS is […]
Thought of the day The worst thing you can do to anyone with a chronic illness is make them feel that they have to prove their illness. • • • • • #BNightsCRPS #CRPS #crpsawareness #crpswarrior #crpslife #crpssupport #chronicpain #CRPSisReal
