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Sabrina Perquis has cystic fibrosis. However, since her lung transplant in 2007, she has been living better and more than happy.
Thirteen years later, she still vividly remembers the moment when she first managed to do it breath deeply.
A DIFFICULT DISEASE TO LIVE
Cystic fibrosis is an inherited genetic disorder that affects cells in the airways, digestive tract, and sweat glands. In France, nearly 500 people die every year.
This was the case of singer Grégory Lemarchal, the great winner of the fourth season of the “Star Academy”. He died in 2007 and was among those waiting for a transplant, but to no avail.
Just like the latter, Sabrina Perquis is too affected disease. Only she was able to qualify for a lung transplant in time.
ALWAYS FIGHT
When she was born, doctors gave terrible news to Sabrina Perquis’s parents. With cystic fibrosis, they estimated its life span to be just 7 years. From that moment on, the host began a fierce fight against the disease. A fight which she mentions in a book called “I had to die at 7”.
As a child, the author spent most of his time in the hospital. A place where he is confronted for the first time with the harsh reality of life.
“I lost my best friend when I was only 11 years old. And at 11, when you’re a little girl, you tend to think about going to parties, birthday parties “,
he confided.
Another obstacle that the radio host had to face, the gaze of the people. Since cystic fibrosis is an “invisible” disease, it has been criticized several times by those who were not aware of its state of health.
Then, one day, his life changes. While on the set of the “Star Academy” to participate in a bonus, the woman receives a call. On the other side of the phone, the hospital.
Eventually, they found a compatible lung and the transplant could then take place. The operation lasted 11 hours and was a success. From 13% breath, Sabrina went up to 108%.
DURING A HEALTH CRISIS
Since its inception, Covid-19 has wreaked havoc in France and many other countries. A destructive plague especially for the most vulnerable individuals, namely the elderly and those suffering from diseases that can develop a severe form.
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“A month since my book was published, a month in which many of you have it in your hands. – Many have been able to discover my story and what I really am, some have discovered me, many of my relatives have rediscovered me, now many people understand … learn, realize … – It is strange for me to say that now you know who there is behind my smiles and my thirst for life is like a liberation that I have been waiting for for so many years, even if it is confusing to hear people, the journalists say the names of my relatives, to greet my mom’s courage wherever she goes, of my son, of my dad whom I never speak of, and of the first name of Naïta who is my guardian angel … – A month since my inbox is always full and your messages are all as beautiful as the others, messages that I love to read and reread, thanks for telling me your feelings as well as your stories … I really try to answer everyone but this is not obvious …, – I would have many thanks for you, for the your words and your countless messages, your sharing … thank you too to you for having lived my book … it is unspeakable, inexplicable … – There are scars that will not close but I love my life and today still, thanks to this book and thanks to you, you are offering me another great revenge …. To celebrate this month of birthday, I give you 2 extracts from important passages in my life … it is always available in the main bookstores and for each book a euro is donated to the association #gregorylemarchal @hugoetcie – Who has read my book here? give me a nice 🤍 good weekend 😘 – – #book #weekend #breakfast #morning # jedevaismourerà7ans #mood #goodvibes #combat # santé #muco #dondorganes #handicap
At first Sabrina Perquis had neglected the disease. Thinking it was no more serious than a mild flu. But over the months she realized the danger. That is why during an interview with Purepeople, the author wanted to warn all patients.
“Those who say they do not feel worried, I wish them not to know sickness, suffering or death, but to one day feel a great fear so that they become aware of it”,
he has declared.
A SECOND BIRTH
On November 10, 2007, Sabrina woke up after the transplant and was able to breathe deeply for the first time. For her it was like a second birth. So, 13 years later, he remembered this magical moment and posted an Instagram post to send a message to his subscribers.
“Do not wait to live, do not miss any opportunity (…) smile, love, vibrate, dare, be crazy, stop worrying about the details, … Shine, eliminate what obscures your path”,
he subtitled.
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13 years ✨🙏10 / 11/2007 When I think back to what I felt the first time I was able to breathe deeply … That famous day when I was born a second time … 2006 «I breathe stronger and stronger and at every cough, I have the impression that my life is about to end … but I hear this little voice that resounds in me stronger than anything else: “No Sabrina, you no. you will not die, you will not suffocate, you are much stronger … “. I lack so much oxygen that my lips are blue and I can no longer argue, it may seem sad but I am not unhappy, I like to hear the stories of my friends who bring me back to life … I know that soon my life too will have a new breath (excerpt from my book) Qlq weeks later, j ‘This time he enters this operating room without knowing my destination … will my next alarm bell be on earth or in the sky? ✨ 14.00 later I open my eyes, smile on my lips, I breathe with two new lungs, moved, excited, consoled and above all grateful … Once again I think of my donor, of this family that saved me, to allow me not to suffer more from one life to another. stop for breathlessness and give way to a wonderful life that will take my breath away✨❤️🙏 take care of yourself … Bcp does not realize what it is to live connected to machines, pipes, to be forced to endless hours of treatments … Waking up one day at home and the next day between the 4 walls of a hospital room for an indefinite period away from loved ones … I can’t wait to live, don’t miss any opportunity, this period ” in pause “is an example:; smile, love, vibrate, dare, be crazy, stop worrying about the details, … Shine, eliminate what obscures your path Life is beautiful but everything is fragile. ..✨🙏❤️ – #dondorganes # santé #cf #mucoviscidose #muco #life #greffe #combat #birthday #smile
SABRINA PERQUIES ON “WHY I LIVE?”
Grégory Lemarchal’s biopic allowed millions of people to retrace his journey and see how he lived with cystic fibrosis. However, according to Sabrina Perquis, the TV movie does not show everything. Find out his explanations.
Grégory Lemarchal | Photo: Getty Images
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