Hypermobility Stories

Orla has battled with Extreme Hypermobility since she was 3 years old. It affects her life dramatically - she goes to daily physio sessions and can bearly walk, let alone run or take part in any sport. Her joints click and lock in positions they really aren't meant to be in, and it hurts her. Lots. one day she meets a boy. He is different. Unique. Special. And she likes him a lot. What will her destiny hold?

This is a story about me, the writer. It's something I'm struggling with right now. I'm going tell you about my struggles. It's related to a disease. I don't know what it is yet but I want to write my journey just so I won't go crazy till then. Shutterstocks picture on the cover

this is my journey as a chronically ill person who is still trying to find a diagnosis

Winifred is a young girl that has the weight of the world on her shoulders. No she isn't fretting about prom or a boy or even homework. She is enduring an invisible illness, alone. Take this short story trip with Win as she give you a glimpse of her world with a chronic invisible illness with a twist of fantasy.

My story of finding out I have Ehler-Danlos Syndrome Hypermobility type.

In an Alternate Universe where Kakashi has a child... Hatake Tsukiko knows she's different. Aside from the obvious of being the child of Hatake Kakashi, they need more help than the average shinobi, which is why she was placed on Interrogation Specialist Morino Ibiki's first genin team. Morino Ibiki works hard to keep Tsukiko engaged and in a safe and comfortable environment when learning. When the third teammate, Minamoto Ryouichi, starts bullying Tsukiko for being so different, leading to physical violence against her, Ibiki is left without choice but to throw the boy off his team and even strip him of his shinobi rank. After gaining another genin-Ibiki's own son-they are sent away on their first C-Rank mission. However, Team Ibiki is not ready for the mission to turn sour... CWs: • Murder • Blood • Transphobia/Exorsexism • Bullying • Injury • Panic Attacks/Mental Health • Reference to suicide • Mentions of vehicles - NO AI WAS USED IN THE CREATION OF THIS STORY. All of it is fresh, directly out of my head, unhinged bullshit (^: - SCAM COMMENTS NOT WELCOME

So I was born with dyspraxia and Hypermobility. This is just some of the worst parts of my life.

The Science of Listening is a series of essays detailing the diagnosis and treatment journey for Ehlers-Danlos syndrome.

And then I remembered the strange doctor and his even stranger children. The progression of my condition and the coming to terms with my mortality. My hand gripped onto his, "Does this mean you won't run from me anymore?" I dared to glance in his direction. Into his beautiful eyes I fell as I felt him lift my hand and place his firm, yet smooth, lips against it. His southern twang came out as he spoke, "No, ma'am." ~~~~ A story in which a girl with a deadly condition gets the chance at a happily ever after. Versión española : @traduccionesmapache This story technically has an end as I've posted the plans I had for the last 12 chapters. Though this may be an unsatisfying end.

Simple statements from my mental breakdowns

What do you think of when you hear hoofbeats, a horse probably, what about a zebra? Did you know all zebras are unique, like a fingerprint, not one zebra has the same stripes as another. In the same way, anyone who's a horse is normal, has normal sickness and can carry on with life. A zebra, contains all the rare people, all the rare diseases that go unnoticed because everyone thinks of a horse first. This story is about a girl who's a zebra, she's not normal, she doesn't know it yet and no one can change who she is not even herself. Find out how she finds out, lives and enjoys her life. This is a tribute for the May awareness for Ehlers-Danlos Syndrome! My way of raising awareness. The picture is made with fused.

Young Whisper is suffering. Life is harder for her than most people. When she has to join a new school in a new town and leave everything behind, how will she cope?...

Cover made by @vintagegrace In the Fabray household, Quinn was the leading lady-the perfect, polished star. Megan was just the understudy, waiting in the wings of a life she wasn't sure she was allowed to lead. While Quinn got the nose jobs and the spotlight, Megan got a pink wheelchair and a list of diagnoses that felt like a life sentence. Megan Fabray's life was measured in hospital stays and the shadow of her sister's perfection. To her parents, Quinn was the dream; Megan was the fragile reality they didn't know how to fix. Megan was the daughter defined by a growing list of diagnoses and medications. Across town, Paige Hudson was lost in the noise. While Finn was the hero of the gridiron, Paige was a girl of silence and missed cues, navigating a world that felt too loud and too fast. They were both side characters in their own families-until the Glee club stage gave them a place to finally speak up, and a reason to look at each other. Paige Hudson knew what it was like to be "the weird one." While her brother Finn was the town's golden boy, Paige was a puzzle with missing pieces, struggling to find her voice through the fog of ADHD and autism. They had spent years as background noise in their siblings' legacies. But as the Glee club curtain rises, they're done being footnotes. This is their story-the messy, beautiful, and difficult melody of finding where they truly belong. The two young girls were often the understudies left waiting in the wings, two girls whose presences were only felt by the quiet hum of Megan's health and Paige's special needs. They were both often a step behind society's standards of what they had to be. TW: Mental health, chronic illness, disability, bullying, LGBT, panic attacks, health issues.