Invisibleillness Stories

Sovarielle was born into a legacy of music and magic-one of the legendary sound dragons of Whispervale. But everything changed the day an attack stole her sense of smell, severing her from the bond that connects dragonkind. Exiled by instinct and grieving the loss of her family and horde, she vanished into the human world, learning to navigate life through sound instead of scent. In dragon society, scent is everything. It guides memory, emotion, and-most importantly-connection. It is how dragons recognize their mates. Without it, Sovarielle is considered broken, untethered... alone. Years later, a single misstep leads her back into dragon territory-and into a storm of long-forgotten alliances, mythical creatures, and rising tensions. From sirens guarding sacred seas to secretive centaurs with ancient wisdom, Sovarielle's path is shaped by those who see her not as damaged, but different. And as feelings deepen between her and a dragon who seems to know more than he says, she begins to wonder: If dragons find their mates by scent... will she ever truly know if she's found hers? A map of the country is included in the prologue, showing dragon territories, human cities, and key locations mentioned throughout the story. For readers who enjoy diving deeper, I've also created The Scentmarked Archive, which includes an interactive map and expanded lore exploring ancient dragon territories, mysterious islands, siren legends, shifter homelands, and more. You can find the link to the archive and map in my bio. Thank you so much for choosing to step into this world with me.

I am: Sick These are my thoughts

Rants by a disabled person , mostly about things related to disability, but also my view as a disabled person on no-disabled topics and how I see the world.

This is why I'm bitter. Based on a true story.

This is my journey to getting a service dog! Disclaimer: Some mild language and rants! 🤣 I'm also older then I appear to be, I just look really young lol Invisible illness is just as real as a visible illness

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

"It's not like the movies that's how it should be," -Gina Porter *"Inspired" by the movie "Be Somebody" w/ Matthew Espinosa and "Starstruck" on Disney + -CW: mentions of diabetes and medical content. *Only on Wattpad

I write a lot about my seizure disorder in order to raise awareness for Epilepsy. It is so important that we understand this disorder so that a cure can be found. Being aware can save someone's life.

The reality of my disorder.

My battle with living life while battling multiple sclerosis, anxiety and depression. A life changing moment is one when you get a diagnosis of a illness without any cure. It makes you mad,sad, confused and really lost in a world where you no nothing and must make lufe altering decisions on the turn of a dime.

She's a girl with an invisible illness. Life is rough. Throw in a stalker with a secret, dysfunctional family, and high school. it's a ticking bomb. I hope you enjoy it but that being said don't kill me for late updates. Torture I'm okay with but murder is illegal ppl.

going through hell and back, she refuses to give up hope. read about the story of a girl going through hell more than once. based on the truth.

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.

This is going to be a collection of Celiac Problems and Celiac Wins. It's also going to include some stories and inspirational quotes. Welcome to the life of a Celiac.

17 million people around the world suffer from Myalgic Encephalomyelitis or ME and it is incurable and untreatable. The disease is called ME but Chronic Fatigue Syndrome or CFS is the name the CDC gave it. Doctors for the most part think that it is all in our heads; well it's not. ME is a neuro-immune disease that affects every aspect of your life. Diagnosed originally in September of 2012, this author was bedridden from October 2013 through August 1, 2015. this author couldn't go past her own back yard and that's on an extremely good day, her life came to a stand still and she couldn't move forward. In June of 2013, she graduated with her MBA and was supposed to start her Ph.D in early 2014 but that was not to be. In this batch of poems, this author hopes to show others that they aren't alone in this. She hopes that people will come together to raise awareness for this miserable illness. Her personal story of her life with ME can be found in the first chapter of this book in video form. The cover is of the Survivor Tree at the 9/11 memorial that this author took in 2011. To understand what ME really is please watch this 7 minute video and you'll see what life was like for me 24/7 365. https://youtu.be/qBriPTFOtmY So please take a stroll with her now, through her journey through ME......... ***All of the poetry here is original and written by me. All rights reserved © 2015 by Olga Pinsky***

June 2021 was supposed to be normal. A regular shift. A regular day. A regular breath. But in one moment - one strange, unexplainable rush of air as she took a breath - everything she thought she knew about her body, her future, and her life was about to change. What starts as "too much breath" turns into ER visits, unanswered questions, different tests, new fears, and a diagnosis that rewrites her whole identity: Myasthenia Gravis. This is the true story of a girl who looked fine on the outside, while her body was fighting a silent battle on the inside. A story about survival, grief, faith, and learning to live a life she never expected. This is her journey. This is her breath. This is the life she had to build... after everything fell apart.

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.

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.