Thursday, August 22, 2019
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Sidra Medicine helps bedridden teen with DMD to sit up again

Sidra Medicine helps bedridden teen with DMD to sit up again

Tribune News Network
Ali was bedridden for two years. But, now he can sit in his wheelchair and go out to enjoy the cool winds and chirping of the birds in the garden.
It was a determined multi-disciplinary team of Sidra Medicine that has helped the bedridden teen with Duchenne Muscular Dystrophy (DMD) sit up again and enjoy the wonders of everyday life.
Duchenne Muscular Dystrophy (DMD) is a rare muscle disorder that affects approximately one in 3,500 male births worldwide. It is a genetic condition usually recognised in boys aged between three and six.
DMD is characterised by weakness and wasting (atrophy) of the muscles of the pelvic area, followed by the involvement of the shoulder muscles. As the disease progresses, muscle weakness and atrophy spread to additional muscles of the body, including the trunk and forearms, eventually affecting breathing capability. The disease is progressive and most affected individuals require a wheelchair by their teenage years.
Sidra Medicine, with a multidisciplinary team-based approach, specialises in the care of children and young people with DMD providing high quality and cutting-edge services -- from pediatric intensive care, surgery and therapy services to post-operative and long-term care.
Ali is a young person with DMD. Due to the rapid progression of the disease, he was wheelchair bound by the time he was in his early teens. Despite spinal surgery at another healthcare institution in 2017, Ali’s condition continued to deteriorate. He became more immobile and was confined to his bed. He developed severe contractures where his muscles became tight, making it painful and difficult for him to move.
As a result, Ali required full support to move his body and was not able to sit up in his wheelchair.
Being bedridden and immobile for two years had a significant impact on his physical and mental health. Ali was admitted to the paediatric intensive care unit (PICU) at Sidra Medicine in mid-November of 2018.
Dr Manu Sundaram, attending physician at the PICU, said: “Ali was admitted with a chest infection and required non-invasive ventilator support throughout the day to help him breathe. Once he recovered from his chest infection, it became very clear that he would require full-time ventilator support for his long term care. It was recommended that Ali undergo a tracheostomy – a necessary surgical procedure that would facilitate Ali’s breathing.”
Dr Patrick Sheehan, the division chief of Paediatric Otolaryngology, Head and Neck Surgery at Sidra Medicine, performed Ali’s tracheostomy in late November 2018. Ali’s procedure involved creating an opening in his neck to place a tube into his windpipe, allowing air to enter his lungs.
During Ali’s time at the hospital, he was taken care of by a multidisciplinary team from PICU comprising specialists in occupational therapy, physiotherapy, respiratory therapy,and speech and language therapy. The team, which also included dieticians and child life specialists, created a customised daily care schedule to support Ali in regaining his weight and strength, to help him with a range of movements and for him to speak with a tracheostomy.
Over four months at the Sidra Medicine PICU, with the care provided by the highly specialized multidisciplinary team, Ali slowly regained his strength and eventually was able to sit up in his wheelchair once again. The transition from being horizontal for nearly two years to being able to sit up, had a major impact.
“Once Ali regained his ability to sit and talk – he was keen to go out on his wheelchair and spend time in our lovely healing gardens and interact with people. It was a wonderful transformation. We are really proud of his progress and his endurance,” continued DrSundaram.
Upon his discharge, Ali, who through speech therapy at Sidra Medicine learnt to speak with the tracheostomy, managed to share a simple and powerful message with the team who helped him: “Thank you.”


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