A 22-year-old Armenian woman who supposedly cries up to 50 jagged-edged crystal tears every day has been accused of faking her “biochemically and anatomically impossible” condition by placing glass shards in her eye sockets.

For most people, crying is the result of great pain or suffering, but for Satenik Kazaryan, a young woman from the Armenian village of Spandaryan, the act of crying itself is a source of excruciating pain. That’s because she allegedly cries solid crystal tears with jagged edges that scratch her eyes as they come out of the eye sockets. The 22-year-old first started crying crystal tears a few days ago, while visiting a dentist. It felt kike sand had gotten in her eye, and when she went to visit an ophthalmologist about it, the doctor extracted several crystals from her eye. Since then, her life has become a living hell, as she claims to cry around 50 crystals a day.

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For the past three months, Riley Horner, a teenage girl from Illinois, has been waking up every morning thinking it’s June 11. To make matters worse, her memory resets every couple of hours, so she can’t even remember things she did or people she met that very day.

Riley’s troubles began after she got accidentally kicked in the head by a teenager who was crowd-surfing during a dance at the FFA State Convention. She was taken to the hospital, but doctors there only diagnosed her with a concussion and sent her home with crutches. Tests showed no brain bleed, tumor, or anything else out of the ordinary, but Riley’s family soon noticed that there was something wrong with her. It was like her brain was suck in the past and refused to make any new memories. But apart from her memory constantly resetting, Riley has also experienced dozens of seizures in the last three months.

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Gemma Cairns, a 32-year-old woman from Scotland, can’t remember the last time she experienced total silence. Even in the absence of outside noises, she can hear everything going on inside her body, from blood pumping through her veins, to the movements of her eyes.

Cairns has been able to hear noises coming from inside her body for as long as she can remember, but she only realized it was unusual after mentioning it to her mother as a teenager. She’s been looking for explanations ever since, but until three years ago, doctors couldn’t properly diagnose her condition and only prescribed her medication for blocked ears and nasal problems. Nothing worked, and the young woman had to get used to the idea that she would never learn what was wrong with her. Luckily, she moved to Glasgow in 2016, and was able to see a specialist who finally diagnosed her with bilateral superior semicircular canal dehiscence.

The rare condition means that Gemma is missing part of a tiny temporal bone in both her ear canals, which impacts both her hearing and her balance when moving around. Doctors recommended that she undergo surgery as soon as possible in order to fix the problem, but after getting her right ear fixed last September, she will have to wait until next month to hopefully experience silence for the first time.

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Marie McCreadie was just 13 years old when she lost her voice to what doctors could only assume was a freak virus. 12 years later, she was shocked to discover that her sudden loss of voice had been caused by an old coin stuck between her vocal coins, which prevented them from vibrating. This is an old story that is once again getting a lot of attention because of Marie McCreadie ‘s newly published book, “Voiceless”, in which she details the traumatic experience of losing her voice at a young age and regaining it after 12 long years.

When 13-year-old Marie  – then Marie Heffernan – suddenly lost the ability to speak one day in 1972, doctors put it down to a bad bout of bronchitis, but even after recovering from the illness, she still couldn’t utter a sound. They performed all kinds of tests but nothing appeared to be wrong, so they eventually put it down to a virus and told the 13-year-old girl to just go back to school and lead a normal life, as a mute. She was frightened and confused, and her parents didn’t really know how to handle things in the beginning either. Luckily, Marie and her friends started finding new ways of communicating, like passing written notes to each other, which was fun and made getting used to a voiceless life easier. Things got worse as time went by and her voice didn’t recover, but the other children’s reactions were nothing compared to the treatment she got from her teachers.

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Imagine hearing someone chewing a piece of bubble gum loudly and being overwhelmed by a feeling of anger, disgust or panic. Sounds like loud chewing or slurping can be hard to put up with for most of us, but for people suffering from a rare condition called misophonia, it’s virtually impossible.

Misophonia, also known as Selective Sound Sensitivity, is usually described as a strong emotional or physiological response to the presence or anticipation of certain sounds that are usually human-generated, like the sound of someone biting into crunchy foods, clicking noises, knuckle cracking, even breathing. While anger is the most common reaction recorded in misphonia sufferers, anxiety and disgust are also possible responses. But these intense emotions are also accompanied by a release of adrenaline which causes symptoms like raised pulse, shakiness, sweating and a raised heart rate. This makes dealing with experiences most of us consider mundane almost impossible for people with misophonia.

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Peter, a one-year-old cocker spaniel from Sheffield, in the UK, has earned the nickname “Fainting Pete” due to his bizarre habit of suddenly stiffening and falling over whenever he gets to excited or nervous.

Peter’s owners, Emma Clayton and Oliver Broomhead, adopted him from a family who could no longer look take care of him. They were told that the adorable pooch had been “fainting” ever since he learned how to walk, and despite seeing several veterinarians about his bizarre behavior, no one has been able to figure out what’s causing it. The English couple said that it occurs every time Peter sees ducks, enjoys his walks a bit too much or gets scared. Sometime he’ll just freeze and fall over for no apparent reason which lead doctors to believe that he is suffering from a rare neurological condition, although no one can say for sure.

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A 46-year old Thai woman recently issued a public cry for help after her breasts suddenly started to grow a few months ago, leaving her unable to work or even move around without using crutches.

Thai media recently presented the case of Lam Phrai Si Nuan, a 46-year-old woman from a village in the country’s Phitsanulok province, whose breasts started growing around 9 months ago and have no become so big and heavy that she needs crutches to walk. Mrs. Lam Phrai says she has seen doctors about her mysterious condition, and although they eliminated the possibility of cancerous tumors, they were unable to diagnose her or provide a treatment. Due to a precarious financial situation, the woman cannot afford a more thorough medical investigation and has appealed to kindhearted people for assistance.

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A 56-year-old woman from Baton Rouge, Louisiana, has been diagnosed with Transient Global Amnesia (TGA) after a terrible headache apparently caused her to completely forget the last 38 years of her life.

One day in early October of last year, Kim Denicola was leaving a bible study at a local church when she called her husband to complain about an excruciating headache and blurry vision. He told her to go to the emergency room, but some friends found her passed out in the church parking lot and rushed her to the hospital. The first thing Denicola remembers from after that incident is lying in a hospital bed and a nurse asking her questions she apparently had all the wrong answers to.

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A California man’s unexpected recovery has left doctor’s baffled. A day before his scheduled surgery to have a presumed brain tumor removed, a final head CT exam showed that the mass in his brain had miraculously disappeared.

Paul Wood, a resident of Lodi, in California, started complaining of excruciating headaches and dizziness several months ago, and received several serious diagnoses from doctors. A neurosurgeon at UC San Francisco told him that he had a brain bleeding, while a radiologist told him that his CAT scans showed a brain tumor. Both required risky brain surgery, but a day before the scheduled intervention to have the suspected tumor removed, a fresh CT scan revealed no sign of anything unusual in his brain. Doctors couldn’t, and still cannot explain what happened, but Wood is convinced that it’s nothing short of a miracle from God.

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An 11-year-old girl was recently admitted at the Quy Hoa National Leprosy Dermatology Hospital, in Vietnam, under suspicion of suffering from hematidrosis, a very rare medical condition in which people sweat blood.

The young girl, identified only as N., to protect her privacy, allegedly started sweating blood three or four months ago, when her parents claim she was very stressed about her exam for fifth grade. They didn’t take her to a doctor when the first symptoms appeared, but things gradually got worse, to the point where the girl would sweat blood 3 or 4 times a day and suffer from severe headaches.

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Despite the amazing scientific advances we have made in the last century, there are still many medical cases that can’t be fully explained. Vanishing Bones Syndrome sounds like something straight out of an episode of House MD, but doctors at the Royal Infirmary of Edinburgh in Scotland encountered a case of this bizarre condition in a 44-year-old woman.

Also known as Gorham-Stout disease, this extremely rare condition causes the sufferer to experience progressive bone loss. The disease is so uncommon that there has only ever been 64 recorded cases in medical literature since it was first described in 1838. In a healthy person, bones are constantly rebuilding themselves to help maintain their strength, and Gorham-Stout disease is believed to be a malfunction of this process; the bone breaks itself down faster than it can repair itself.

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In Sweden, hundreds of refugee children are reportedly suffering from a strange condition known as “resignation syndrome”. These children fall into a coma-like state; they don’t eat, speak, or even open their eyes. Sufferers of resignation syndrome are often left bedbound for years at a time.

Their appearances suggest they have been involved in some sort of accident or suffer from some sort of neurological illness, but sufferers of resignation syndrome have nothing physically wrong with them—they have simply lost the will to live. The condition is known as “uppgivenhetssyndrom” in Sweden, and it is thought to only affect young members of the refugee population.

Research has linked resignation syndrome with the stress and disappointment of having asylum claims rejected. In recent years, regulations surrounding asylum cases have tightened, and those refugees who were not fleeing from an active war zone were likely to have their applications rejected. These rejections could often take years to be decided upon, leaving refugee families in a state of limbo. For many children, the weight of rejection proved too much to bear and they would shut down completely, entering a coma-like state, seemingly on the edge between life and death.

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25-year-old Tomasz Nadolski, from Wroclaw, Poland,  suffers from a rare and cruel disease that has not only made his life a living hell, but also left him stuck in the underdeveloped body of a 12-year-old boy.

Tomasz’s health problems began when he was only 7-years-old. He would throw up after every meal and experience excruciating pain in his stomach, hands and feet. Because he couldn’t keep any food down, he lost a lot of weight and kids at school started teasing him about looking like a walking skeleton. For years, doctors couldn’t figure out what was wrong with him, and some of them even claimed that his problems were mental rather than physical. It took 16 years for Tomasz’s condition to finally be diagnosed, but, unfortunately, knowing what he was suffering from didn’t make the young man’s life any better.

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Looking at Xiao Cui for the first time, you could swear he is at least 80 years old, but in fact he is only an 18-year-old high-school student suffering from a very rare health condition that has caused his facial muscles and skin to droop, making him look a lifetime older than he really is.

18-year-old Xiao Cui is a senior at a top high-school in Harbin, China, but you couldn’t tell just by looking at him. He looks more like a pensioner than a young man in the prime of his life, but it’s all due to a mysterious condition that has been causing his facial muscles and skin to sag. In a Pear video that went viral in China at the end of last month, Cui says that he noticed the first symptoms during middle school, and that his face has been getting saggier ever since, to the point where he now looks many decades older than his classmates. Doctors have yet to understand his condition, let alone find a way to stop it or undo its effects, so Xiao has no option but to accept it and stay positive.

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O’Neal Mahmoud, a 3-year-old from an Arabic-speaking Druze  family in the Golan Heights, Israel, has amazed doctors with his ability to speak English with a British accent without ever having been exposed to the foreign language.

Named after legendary basketball player Shaquille O’Neal, O’Neal Mahmoud didn’t speak at all until he was 2-years-old. Then he started making these unintelligible noises, and at one point started speaking fluent English and using phrases like “my dear” and “oh my goodness”, which are hardly ever used in his home village, near the Druze town of Majdal Shams, in northern Israel. Stranger still is the fact that O’Neal doesn’t actually know the Arabic equivalents of the English words he speaks. A speech therapist and clinical linguist who examined the toddler concluded that his level of English was that of a three-year-old who grew up in an English-speaking family, while his level of Arabic – his native language – was far below that.

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