December 29th marked the tenth anniversary of Michael Schumacher’s tragic skiing accident.
The seven-time Formula 1 world champion is still suffering from severe after-effects that leave him unable to communicate and move.
Exactly ten years ago, on December 29th 2013, the accident occurred when Schumacher took a violent fall while skiing during his family vacation in Méribel in Savoie, shortly after retiring from Formula 1 racing.
His head hit a rock and his helmet shattered under the force of the impact.
When rescuers arrived, Schumacher, also known as “The Red Baron,” was stunned but conscious.
He was immediately taken to hospital, where he remained in a coma for several months.
On the evening of the same day, Grenoble University Hospital announced that the former champion had “suffered severe head trauma with coma upon arrival, requiring immediate neurosurgical intervention.”
Schumacher also suffered a brain hemorrhage, and his life prognosis was at risk.
When he woke up six months later, nothing was the same.
To this day, it is difficult to know the state of Michael Schumacher’s health, as his family is extremely discreet on the subject.
They keep him away from the media and do not reveal any information about him.
The Formula 1 world champion is now unable to walk or stand, and it is impossible for him to communicate with those around him.
Michael Schumacher is cared for 24 hours a day by a team of about fifteen doctors, nurses and physiotherapists.
A whole decade has passed since the accident involving Michael Schumacher, which occurred while skiing in the resort of Méribel in the French Alps.
Since September 2014, he has been living in a medical suite in his family villa in Gland, Switzerland.
“He is a prisoner of his own body,” said Gaëtan Vigneron, an F1 commentator for 30 years and an expert on the racing scene.
Michael’s younger brother Ralf revealed information to some local media, which was picked up by the Daily Mail: “I miss the Michael of old.
Life can be so unfair sometimes. Michael has been very lucky all his life.
Despite the danger: a woman with dwarfism boldly poses with her baby belly on the beach.
Most married couples get asked “when,” but Charli Worgan and her husband Cullen frequently received “why” questions.
The parents, who live in Sydney, are frequently in the spotlight due to their unique forms of dwarfism, most notably when Charli got pregnant with their first child.
After giving birth to their first child, the content Australian mother created a social media account to share updates on their family life with others. Little did she know how well-liked her account would become.
With two stunning daughters under their belt, Charli has amassed over 300,000 Instagram followers.
Charli recently revealed that she was fourteen weeks pregnant with her third child, but the announcement was bittersweet.
Charli has had to undergo thorough genetic testing during each pregnancy. Experts warn that if Charli and Cullen’s offspring inherit just one type of dwarfism, inherit both forms, or are of average height due to their genetic problems, the results might be fatal.
Charli expressed her disappointment at not being able to celebrate her pregnancy’s 12-week mark with her family, as most mothers do.
But at 12 weeks, I was preparing for a procedure called Chorionic Villus Sampling (CVS), which is similar to an amniocentesis, whereas most individuals are pleased to be able to announce their pregnancy. To check the embryo’s genetic composition, a big needle is placed into my abdomen to extract a sample of the placenta, which has a 2% miscarriage rate.
Their two daughters, Tilba, 4, and Tully, 2, each have one of the two varieties of dwarfism, so they waited to find out which of the four possible dwarfisms Charli’s third child would have.
In an Instagram post, Charli explained, saying, “Our child would be of ordinary height.”
Our child would have achondroplasia and be dwarfed similarly to me.
Our child would have geleophysic dysplasia, the same type of dwarfism that Cullen has.
As a result of inheriting both genetic defects, our child would be born with “double dominant dwarfism,” which is fatal according to every expert medical assessment. In the event that this had occurred, I could have decided to terminate the pregnancy or to go on and see how things turned out.
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