Historias de Invisibleillness

She knew she was sick. Her doctors knew she was sick. But the one person meant to protect her never believed the treatment. When her mum chooses a new life over listening to medical advice, she's sent to live with her step-brother - the boy she grew up with, the one person who couldn't say no. At his flat, recovery comes slowly, measured in salt packets, careful steps, and days where standing still feels like success. When circumstances force him back to work, help comes from an unexpected place: a friend who asks questions, learns the condition, and stays - not because he has to, but because he wants to. Measured in Salt is a slow-burn chronic illness story about PoTS, medical neglect, learning to trust treatment, and the quiet kind of love that grows through care, patience, and choice.

a collection of poems about chronic illness.

How do you respond to discovering that you are suffering from a rare sleep disorder that will re-define life as you know it and turn your world upside down? My name is Caitlin I was diagnosed with a chronic illness. Find out how I survive day-to-day with an invisible illness that has no known cure and minimal treatments.

The things that I have learned so far about BPD and the disorder itself.

Lucy hasn't had the best of lives, growing up she was always in and out of hospital but the doctors never knew what was wrong with her until she turned sixteen and that was when her life came crashing down around her, she had just been diagnosed with her first chronic illness... Little did she know that this wouldn't be the last diagnosis she got. Although Lucy has to spend most of her time in the house due to chronic pain, she meets a boy named Joe who helps distract her attention from the rough patches in her life.

Not about and actual princess this is just basically my diary. I'm a girl recently turned 18 diagnosed with fibromyalgia at 14 I think... This book has not much of a structure just whatever I feel is important to me or things that strike me close to heart. So if you'd like to learn what's on the mind of a girl who is in literal pain 24/7 please continue reading. Thank you for your time.

Life is hard for everyone, it is almost impossible for someone with Fibromyalgia. Read the perspective of a fibro sufferer through my short stories, poetry, monologues and random thoughts as we journey through this together. Fibromyalgia: We fight more than you know, we feel more than we say. Stay strong and be kind to each other.

Hinata Shouyou, the hyperactive ray of sunshine of Karasuno. With his emotions put proudly on display constantly, nobody would ever guess that he could be hiding anything from them, until something happens during practice one stormy afternoon. something that could change how that little sunshine is seen by his peers forever.

Journal about POTS, rants and feelings about living with a chronic illness. Hoping to open peoples eyes to POTS syndrome and maybe even help some people out there.

Describing what it feels like to be the if, instead of the when, with something happening.

a collection of poems written by a sick girl through a never-ending journey.

Sometimes it feels like I'm black and white, and everyone else is in color. Other times it feels like I'm in color and everyone else is in black and white, and everyone is watching my every move, judging me, and trying to decide if I'm just asking for attention. The truth is, I would do just about anything that I could to get that attention to go away. I have Ehlers Danlos Syndrome, and being the only kid in my class with chronic pain is not easy. I have to fight to do everything that most people can do easily and no one realizes it. Instead, when I can't do something, people assume I'm exaggerating and I could do it if I just tried. So I want to share my story for anybody who is going through what I am.

I have had quite the ride these last three months. My symptoms were attacking me like crazy. It seemed as soon as I figured out a plan on how to go about fighting one, another symptom would come out of nowhere not just adding more stress to my body but also giving the other symptoms more to go on. July I was nothing but a sweat box. There was nothing I could do without literally needing to change my soaked clothes. It didn't matter if I was outside or in my air-conditioned house. All of the above caused me constant flare which caused my Anxiety to heighten to new all time highs. My Anxiety caused my depression to heighten leading to severe fatigue. Nothing I did could help me out of all of this. I would have moments of hope, where I would feel good and have energy. I had hopes that I had finally pulled out of all this, but then as fast as I felt better is as fast as I went back into this flare. I am trying my hardest to get out of this funk and feel a bit more like my normal self, but the fight is exhausting and sometimes needs a bit more energy then I can give.

Life of a schizo The mind, a shifting landscape of thoughts both profound and perplexing, carries me through a world that never settles. Moments of clarity flicker like crossing stars, only to be swallowed by the clouds of uncertainty. I stand at the edge of reality and illusion, where whispers weave themselves into the fabric of my consciousness, echoing truths I struggle to decipher. But there is beauty in the chaos. There is meaning in the shifting sands. To exist in this space is to navigate a reality unlike any other-to be both lost and found in the same breath. God bless Xian i love uuuu

I am: Sick These are my thoughts

She was fourteen when it arrived - silent, invisible, and merciless. In the sweltering heat of a Jacksonville summer, she was just a girl walking in her worn-out Converse shoes to the playground. Laughing with friends. Dreaming about eighth grade. But within days, her body began to betray her. Fevers, weight loss, rashes, and weakness-signs of an unseen war beginning inside her. Uninvited is the raw, intimate memoir of a young woman whose life was upended by an illness that came without warning and never left. More than a story of diagnosis, it's a portrait of survival-through pain and confusion, through hospitals and unanswered questions, through the quiet moments no one sees. From adolescence to adulthood, this journey traces not just the fight against a chronic illness, but the many battles life throws outside of it: identity, relationships, grief, endurance, and learning to live with something that was never supposed to be part of the plan. Told with unflinching honesty and quiet strength, Uninvited is a testament to what it means to lose control-and slowly, defiantly, reclaim your life.

(THIS BOOK ISNT SOMETHING I'M ACTIVELY WRITING AT THE MOMENT. I'M PUTTING IT UP FOR MYSELF, SO DONT WRITE COMMENTS ABOUT UPDATES BECAUSE I HAVE NONE PLANNED CURRENTLY.) Ashera turned 18 and thought that she had her future all planned out for herself. She graduated with an above average G.P.A. and got scholarships to two notorious Colleges for Musical Arts. Unfortunately everything comes crashing down around her when she gets saddled with an illness that has no cure. Scientists have been baffled by the cause for almost a century and her future looks bleak. It hurts her to even walk or stand on occasion, let alone think about attending classes. Everything hurts and she gives up on trying to live a relatively normal life. That is, until she met someone during one of her evening seclusion sessions near the Ocean. Her life turns upside down yet again. The question is: Were these new changes a good thing or has she merely traded one hell for another?