Christmas is a time for parents to be happy for their children’s excitement. But this doesn’t apply to Ray and Tina Cleveland, as their daughter Holly is suffering from a rare disease that causes her heart to stop and leaves her breathless for about 30 seconds, when she gets over excited.

This is two-year-old Holly’s first Christmas since she was diagnosed with the disease and both her parents are very worried, even though they were assured the toddler’s heart will always start beating again. In fact they put up the Christmas tree and started “celebrating” early so that little Holly could get used to all the excitement gradually.

“We even put our tree up early to try and get her used to the twinkly lights before they started appearing everywhere. It’s heartbreaking to see her little face light up and then have to immediately calm her down again. I’ve even avoided asking her what present she wants because I don’t want her to get too excited when she sees it,” Holly’s mother, Tina, explains.

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Haunted houses, cockroaches or any kind of bugs for that matter, snakes, you name it, there’s nothing in this world that will freak this woman out.

I can’t even imagine what it would be like to never experience fear, but there is someone out there who really is fearless, due to a rare disorder, called the Urbach-Wiethe disease, which destroyed a part of her brain called the amygdala, where researchers believe the feeling of fear is born. A 44-year-old woman, whose identity hasn’t been revealed for reasons of confidentiality, suffering from this rare disease, has become a case study for researchers at the University of Iowa.

Scientists have tried everything to provoke her fear – spiders, live snakes, tours of haunted houses – but nothing seems to work. As a matter of fact, she has been exposed to very dangerous and scary situations in her day to day life, for example being held at gun point or knife point, or even life threatening domestic violence, but none of it caused her to be afraid. While it may sound like some cool superpower, her lack of fear and response can also be very dangerous for her as it comes with a lack of preservation instinct.

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For the last three years, doctors have been trying to figure out what makes Twinkle Dwivedi‘s body ooze blood through her eyes, feet and even her head, but she remains a medical mystery.

When Twinkle’s case first appeared in the international media, many hurried to call her a fake, but after countless tests and procedures, including blood transfusions, doctors are still baffled by her strange bleeding. A group of medical specialists, led by dr. George Buchanan, recently traveled to North India to investigate the 14-year-old Twinkle, but all they have been able to say was that “she really suffers from a condition we have never seen before.”

The young teen remembers her disorder first appeared when she was just 11, and her classmates started mocking her and calling her disgusting. Although her bleeding didn’t hurt at all, she felt scared and alone, because no one would come near her. At first she would cry when she saw her clothes soaked with blood, but now she just keeps quiet, and prays she will eventually get better.

Despite her parents efforts, who took her to see the best doctors, Twinkle Dwivedi still bleeds from her eyes and pores, up to 14 times a day. Read More »

A German toymaker has designed a series of cuddly toys, each suffering from serious mental illnesses like depression and hallucination.

36-year-old Martin Kittsteiner, from Hamburg, says the idea to create the bizarre toys started from a joke between him and his girlfriend, who has a lot of stuffed toys, but he soon started to see the potential of the idea. Each of his cuddly toys has its own disease and symptoms, and comes with a medical history, referral letter and treatment plan. Martin hopes his unique creations will help families with children suffering from mental illnesses.

You can order your very own mentally ill toy from Martin Kittsteiner’s website, for $40 each. There, you can also play a mini-game and try to diagnose the toys’ problems.

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33-year-old Yvonne Simon, from Essex, Great Britain, has a rare type of allergy that makes her shopping sessions real-life nightmares. You could say she can’t stand money.

Yvonne has already been labeled as the most allergic woman in Britain, due to the many things that cause her allergic reactions. Among the things her body can’t stand are deodorant, perfume, paint, fizzy drinks, minerals in bottled spring water, chocolate, onions, car fumes, hydrocortisone cream, nuts, bleach, fish, tea, coffee, oranges, tomatoes, latex, talc, newsprint dye, coins, banknotes, pasta, sunflower oil, dairy products, wheat, bread products, white rice, porridge, white sugar, sweets, cigarette smoke, nickel, gold, silver, food colourings, sulphates, calcium chloride and rainwater. And these aren’t even the worst ones…

Like most women, Yvonne loves to shop, but in the last few months she had to cope with excruciating pains, every time she bought anything. It was like her body was punishing her for spending money, and in a way, it was. After extensive tests, doctors found out Yvonne’s body is also allergic to the dye in bills, and also metal coins. And, if that wasn’t bad enough, she is also allergic to latex, so she can’t wear rubber gloves to handle money.

Now, Britain’s most allergic woman lives on a very basic diet, made up of filtered water, lentils, brown rice, carrots and apples. She hates being like this, and wishes there was something she could do about her condition, but right now it’s incurable, and because such a wide spectrum allergy is so rare, chances for an antidote are rather slim.

But, I suppose things could be worse, she could be allergic to something even more common like rain, right? Well, unfortunately, Yvonne Simon really is allergic to rain, and has to wear an umbrella, each time she goes outdoors.

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Ten-month-old Lei Lei, also known as the “Michelin baby“, has become somewhat of an Internet celebrity after photos of him were published on a Chinese government site.

The young boy had scientists scratching their heads, when he was brought to the hospital, earlier this month, on account of a fever. At just ten months, he weighs a whopping 20 kilograms, about the average weight of a normal six year-old. He is currently in a hospital, undergoing some tests that will hopefully reveal some hints about his abnormal size and weight.

Lel Lei’s parents say the boy has quite an appetite, and that he spends most of his days juts breast-feeding and sleeping. He also instinctively puts everything he touches into his mouth, and tries to munch on it.

The Michelin Baby is just the tip of the iceberg, as the obesity problem because more and more serious in China. As the country’s economy keeps growing, millions of people are becoming sedentary and developing weight problems. Over 60 million Chinese are obese, and over 200 million are overweight.

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A lot simpler and definitely more fun that traditional Yoga, the art of Laughter Yoga aims to keep people healthy through laughter.

It’s a known fact that laughter has a positive effect on our body and mind, but sometimes life gets you so down, you can’t find one reason to laugh. That’s where Laughter Yoga comes into play, because you don’t need a reason to laugh. This unusual form of exercise relies on the premise that your body can and knows how to laugh, regardless of what your mind has to say about it. You don’t need to know jokes, be happy, or even have a sense of humor to practice Laughter Yoga. It’s a body-mind approach, not mind-body.

Because laughter has proven a valuable asset in keeping healthy, Laughter Yoga aims to remind people that laughter is a powerful weapon against various diseases. But in order for it to work, practitioners have to laugh wholeheartedly for long periods of time (between 30 and 60 minutes), for no reason at all. You just have to leave all your problems and worries at the door, and laugh like a child with no care in the world.

Sounds like the kind of therapy I’d like to try, and statistics say it really works. In Asia, Laughter Yoga is already a popular practice used in prisons around the Philippines and by Indian policemen. It’s also becoming increasingly popular in the US.

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Seeing him rest on the steering-wheel of his toy truck, smoking a cigarette, you might think he’s a truck driver stuck in the body of a toddler, but Ardi Rizal is really just a two-year old boy who loves to smoke.

The 56 pound toddler, from Indonesia’s South Sumatra province, smokes 2 packs of cigarettes a day and sits on his toy truck all day long. There’s hardly ever a moment in the day when Ardi isn’t puffing away on a cigarette, and that’s the main reason why he can hardly move by himself anymore, let alone run along and play with other children.

His mother has desperately forced the toddler to quit, but he always got so angry that he started screaming and banging his head against the walls, saying quitting makes him dizzy and sick. He also asks for a specific brand of cigarettes, that costs his family $5.50 a day. While his mother is set on somehow getting Ardi to quit, his father says: ‘He looks pretty healthy to me, I don’t see the problem.’ Now this is what I call a “great” parent.

Although authorities have even offered the Ardi Rizal’s parents a brand new car, if they convince him to stop smoking, the parents don’t dare ask him anymore. Read More »

You could say it happened just like in Disney’s “Little Mermaid”, only in this real life case, the mermaid needed a little help from a surgeon.

The appropriately named Milagros Cerron, is a Peruvian girl,born with a rare condition, known as sirenomelia, or “mermaid syndrome“, which left her legs bound together, fro her heels, all the way to her groin.

The Little Mermaid, as she is known, in her native Peru, has just turned six years old, and she has made great progress. Dr. Luis Rubio, head of the surgical team that managed to separate Milagros’ legs, and rebuild her knees, hips and ankles, said she was doing very well, physically, but that she still has a long way to go.

The young girl, who’s name means “miracles”, in Spanish, has suffered three major operations, in the last five years, and she will need to have her urinary and sexual organs reconstructed, in two years.

Sirenomelia is a rare congenital defect that occurs in one out of 70,000 births, and causes death in the vast majority of cases. There is just one other case, 17 year old American, Tiffany York, who has undergone successful separation surgery, before.

Born in a poor family, from a poor village in the Andes, Milagros Cerron is fortunate enough to have her health bills supported by the Peruvian municipal government. Read More »

Hemophilia is a serious condition,and over 2,000 Romanians suffer from it. To draw some attention to the hardships the 2,000 Romanians suffering from this disease, have to go through every day, the Romanian Association for the Problems of Hemophilia colored the water fountains, in the center of Bucharest, bloody red.

Passers-by did in fact notice the red water flowing in the fountains, but it’s going to take a lot more than this to inspire them to help hemophilia victims.

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It doesn’t happen very often, but people do grow horns. They’re called cutaneous horns and they are the result of a wide range of epidermal lesions. According to the World Journal of Surgical Oncology, cutaneous horns appear in men over 55 and women over 65. Rare as these cases may be, cutaneous horns have been around for quite some time, with the first documented case appearing in the 1500s. Let’s have a look at seven of the most recent cases of horned people: Read More »

35-year-old Kevin Easterday was born with a rare condition that prevented his spine from developing correctly. His legs were amputated, when he was only a baby, but that hasn’t stopped him from living life to the fullest.

A strange illness, known as sacral agenesis, made it necessary for doctors to amputate Kenny’s legs, when he was only six months old. Part of his shinbone was used to create the missing part of his spine, but Kenny lost the ability to walk. Believe it or not, Mr. Eastearday was able to live a rich happy life, regardless of his handicap.

During a documentary, Kenny’s father reveals he taught his son to walk using his hands, by telling him to imitate his mother, who “walks like a duck”. As a child, he was offered a pair of prosthetic legs, but he didn’t really find them very useful, so he always used his hands, or a skateboard, to get around.

Although he wasn’t expected to reach the age of 21, Kenny not only beat the odds, but enjoyed life, in the process. He learned to play pool, bowl, work, and even make love to his fiancee,Nicky. To top things off, the happy couple is waiting for confirmation that Desiree, their 7-year-old daughter, is actually Kenny’s daughter. Read More »

A Chinese hospital has released images of a 6-year-old boy who was born with 15 fingers and 16 toes. Since more isn’t always better, he’ll soon undergo surgery to have the extras removed.

With a total of 31 fingers and toes, the boy, who’s identity hasn’t been revealed, has beaten the previous record of 25. According to scientists, the excess of fingers and toes is a result of gene mutation.

Photos via ImagineChina Read More »

13-year-old Zara Hartshorn suffers from a rare skin-condition called lipodystrophy, which makes her look like an old woman and causes her daily grief.

It’s hard to imagine what it’s like having to cope with people staring at you like you’re some kind of freak, and being called names like “baggy face”, “monkey” or “granny”, on a daily basis. But, no one knows what Zara has to go through, better than her own mother, 40-year-old Tracy. She says she knew her youngest daughter inherited her dreadful condition, ever since she was just a few days old. All her other kids have it too, but the symptoms are much more severs in Zara’s case.

Tracy managed to protect her little girl until she had to go to school. That’s when the nightmare began. Schoolmates make fun of her and beat her up if she tries to talk back, adults stop and stare at her wrinkled face as if it’s her fault she was born with this yet incurable condition.

Lipodystrophy causes the fatty tissue underneath the skin to deteriorate, while the skin itself grows in excess, at an accelerated pace. Tracy, who experienced the same tragedies, when she was Zara’s age, had facelift surgery, but after only two years, the lypodystrophy symptoms were just as severe and now she had the surgery scars as well.

Modern medicine has advanced a lot since then, and Tracy is desperate to help Zara before it’s too late. Unfortunately, she can’t afford the proper skin treatment on a single salary. But if there’s ever a sure way her daughter could be spared all the torment, she’d do anything to save her.

via Mirror.co.uk

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Oddly enough, setting a man on fire isn’t necessarily a bad thing, on the contrary, it’s actually considered curative.

Although I wasn’t able to learn much about this strange medical procedure, fire treatment is apparently very popular during the winter months, in Chinese traditional hospitals. People believe this will keep them safe from illnesses like the flu and common cold.

The piece of cloth is sprinkled with flammable substance, probably alcohol,then set on fire and put-out with another cloth. It isn’t painful at all, and according to a video I found on Youtube, fire treatment is also a great way to lose weight.