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Health06:44 · 8h ago

Israeli Woman Recovers After Rare Guillain-Barré Syndrome Leaves Her Paralyzed

N12Center
Translated & summarized from N12 by baba
The story · English

Roan Salem, a 33-year-old accountant from northern Israel, was diagnosed with Guillain-Barré syndrome, a rare neurological disorder in which the immune system attacks the peripheral nerves. Initially experiencing numbness in her hands, her condition rapidly deteriorated over days, leading to paralysis, inability to swallow, and respiratory failure. She was hospitalized, intubated, and sedated for eight days in intensive care at Emek Medical Center.

Following stabilization, Salem underwent 50 days of intensive multidisciplinary rehabilitation involving physiotherapy, occupational therapy, speech therapy, psychological support, nursing, and social work. She relearned basic functions such as swallowing, sitting, standing, and walking. Despite significant progress and regaining independence, she continues to face challenges, especially with swallowing, and her full recovery may take months to a year.

Dr. Afif Saida, head of rehabilitation at Emek Medical Center, explained that Guillain-Barré syndrome affects about one to two people per 100,000 and can range from mild weakness to severe paralysis and respiratory failure. He noted that most patients experience a single episode, but rare cases may relapse. Salem’s case was among the most severe seen at the center, but her determination was key to her recovery.

Salem recounted how she initially mistook her symptoms for a viral illness during a stressful period and delayed seeking urgent care. After diagnosis, she received immediate treatment with intravenous immunoglobulin. She emphasized her resolve to return to life despite the difficult rehabilitation process and ongoing symptoms. Medical experts advise prompt evaluation for anyone with new neurological symptoms following Guillain-Barré syndrome.

Salem was discharged home about two weeks ago, where she faces new challenges adapting to daily life without the constant hospital support. Her story highlights the seriousness of this rare disease and the importance of early diagnosis and comprehensive rehabilitation.

Read the original at N12
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