Home » Blog » Entertainment » The real reason why the murderer PASSARIS was kept alone in the cell for 23 years

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Investigators have revealed, for the first time, the real reason why Greek murderer Konstantinos Passaris was kept in solitary confinement for more than 23 years. No other prisoner would have been subjected to a similar detention regime, at least since 1989.

After the double assassination on the night of November 24 to 25, 2001, when he fatally shot two security guards of a currency exchange in the center of Bucharest, Kostas Passaris was sentenced to life imprisonment. From the first moment he was put behind bars, the Greek criminal was kept in solitary confinement, regardless of whether he was in pretrial detention or in a maximum security penitentiary.

Moreover, for a long time, the prisoner, considered particularly dangerous, was released only separately and with chains on his hands and feet. Recently, his detention regime was changed, from maximum security to closed, and he was moved to the Craiova Penitentiary, where he had been previously incarcerated.

Sources from the National Administration of Penitentiaries (ANP) declared, for thoughtthat the inmate was housed alone in the room and is subject to close supervision by sp

Cancer fighter ｜Wen Songnan, who suffers from a rare “Ewing’s sarcoma”, is optimistic about fighting cancer and raising medical expenses in public: My family needs hundreds of thousands in the short term , which will be enough to cover my medical expenses for several months.

Cancer fighter ｜ Wen Songnan (Koba), the host of the J2 program “Abnormal Love Research Institute”, was diagnosed with the rare “Ewing’s Sarcoma” (Ewing’s Sarcoma) last October, which is about 6 × 6 × 4cm A large malignant tumor (Ewing’s sarcoma) was located near the disc bone between the vertebrae.

Written by: CK@Medical Inspire │ Photo source: instagram@koba_mcn

Cancer fighter ｜Wen Songnan, who suffers from a rare “Ewing’s sarcoma”, is optimistic about fighting cancer and raising medical expenses in public: My family needs hundreds of thousands in the short term , which will be enough to cover my medical expenses for several months.

After Wen Songnan was diagnosed, he stopped working and was actively treated. He went through several rounds of chemotherapy and electrotherapy, but his condition kept relapsing, and he had to kneel and sit due to severe pain. He said that when he learned he had cancer, he didn’t feel anything special, but he was very calm:

Due to his illness, Wen Songnan’s income decreased after he stopped working, and the medical expenses were expensive. He publicly raised money for medical expenses on social media. He also said that the cost of X-rays is the biggest burden at the moment, because public hospitals have to wait half a year for reports, while private X-rays cost tens of thousands to twenty

Opal Sandy was treated shortly before her first birthday and, six months later, she can hear sounds as soft as a whisper and is starting to talk, saying words like “mom” and “dad.”

The therapy, which is administered as an infusion into the ear, replaces defective DNA that causes their type of deafness, which is hereditary.

The girl is part of a clinical trial that is being carried out in the United Kingdom, the United States and Spain.

Doctors in other countries, including China, are also exploring very similar treatments for OTOF gene mutation that Opal has.

Difficult decision

Her parents, Jo and James, from Oxfordshire, a county in the south of the United Kingdom, say the results have been incredible, but acknowledge that allowing Opal to be the first to try this treatment, made by Regeneron, was extremely difficult.

“It was really scary, but we had been given this unique opportunity,” Jo told me.

His sister, Nora, five years old, has the same type of deafness and copes well with a electric cochlear implant.

Instead of increasing the volume of sound, as happens with a hearing aid, this implant gives the patient the “feeling” of hearing, directly stimulating the auditory nerve that communicates with the brain, bypassing the damaged hair cells that detect the sound. sound in a part of the inner ear known as the cochlea.

Instead, the therapy uses a modified and harmless virus to introduce a functional copy of the OTOF gene into these cells.

Opal received the therapy in her right ear, under general anesthesia, and had a cochlear implant placed in her left ear.

Just a few weeks later, he could hear loud sounds, like clapping, in his right ear. AND after six months, His doctors at Addenbrooke’s Hospital in Cambridge confirmed that the ear had a almost normal hearing for soft sounds, even very quiet whispers.

“It’s