#Invisible Illness
Quotes about invisible-illness
Invisible illness is a term that encompasses a wide range of medical conditions that are not immediately apparent to the outside observer. These illnesses, which include chronic pain, mental health disorders, autoimmune diseases, and more, often challenge the conventional understanding of what it means to be "sick." Despite the lack of visible symptoms, those living with invisible illnesses experience profound impacts on their daily lives, often facing skepticism and misunderstanding from others. This tag represents resilience, empathy, and the courage to navigate a world that may not always recognize or validate their struggles.
People are drawn to quotes about invisible illness because they offer validation and a sense of community. These words can articulate the complex emotions and experiences that are often difficult to express, providing comfort and solidarity to those who feel unseen. For many, these quotes serve as a reminder that they are not alone in their journey, fostering a sense of connection and understanding. Whether seeking solace, inspiration, or a voice that echoes their own, individuals find empowerment in the shared wisdom and strength encapsulated in these poignant reflections.
Luckily, we are seeing less and less post-exertional malaise, the symptom that stops Danny’s body and brain recovering properly after expending any energy, even just watching TV.
I am so fed up of having to explain to people that Danny is not just tired; if only that were the case. We have lost friends, good friends, when we ran out of patience with explaining that Danny was off school so much, not because he had friendship issues or didn’t like his classes, but because he had an illness that seemed to be eating him up from the inside, despite it not really being visible on the outside.
If I say, “I have Chronic Fatigue Syndrome,” I’m likely to be discredited as a witness to my own condition. I’ve had doctors tell me there’s no such thing as Chronic Fatigue Syndrome. One doctor said: “Just drink some coffee.
I hope you are not saying that (ME)CFS patients are not as ill as HIV patients. I split my clinical time between the two illnesses, and I can tell you that if I had to choose between the two illnesses (in 2009) I would rather have HIV.
If I only could explainhow much I missthat precious moment when I was freefrom the shackles of chronic pain.
Because doctors can’t name the illness, everyone—the patient's family, friends, health insurance, and in many cases the patient—comes to think of the patient as not really sick and not really suffering. What the patient comes to require in these circumstances, in the absence of help, are facts—tests and studies that show that they might “in fact” have something.
Invisible illnesses exist - within body and mind (you just don’t always see the patients takingtheir pills).
He said that my problem was that I was perfectly healthy and had the illusion that I would be able bodied forever. I could only begin understanding his problem if I gave up that illusion and that would be very difficult, given how healthy I was. I understand, I mistakenly said, and he said no you don’t.
EDS is a scary and challenging diagnosis, but the consequences of not knowing are far greater than that of a correct diagnosis. EDS symptoms can range from the very mild to the extremely severe. One thing is certain, though: If I had received a diagnosis back when my symptoms were mild, I would be living a very different life now. Every single day, in my struggle to actualize the person I still can be, I cannot help but mourn the person I could have been.