Living with MS: ‘We need to change misconceptions’ around the needs of patients

Although multiple sclerosis is one of the most common diseases of the central nervous system, it remains little understood among the general public, patients and medical experts said on World MS Day. The degenerative disorder, which is caused by inflammation in the nerves of the brain and spinal cord, is most commonly diagnosed between the ages of 20 and 40 and is twice as common among women than men. Symptoms range from minor, such as tingling in the arms or legs, to severe – including a complete lack of movement. They develop without warning and in some cases subside within a few weeks. But in other patients the damage can be permanent. Emirati father of two, Sultan Al Shamsi, 31, was diagnosed with MS in 2014, after he insisted that doctors perform a brain scan. At the time he was suffering from severe fatigue and could not move one arm. “I kept telling doctors that I did not feel OK and they kept insisting that I was fine,” he said. An MRI scan showed he had MS and Mr Al Shamsi’s fight began. With progressive MS, there is a steady pattern of deterioration until an individual is completely incapacitated. Before that point, however, many patients can appear completely normal because only one third have a persistent disability. But that does not mean they suffer any less, as the nerve pain can still be acute and the waves of fatigue and other invisible symptoms are debilitating.

Pain of being ignored

Because MS patients often have no symptoms at all – and don’t require a wheelchair or a walking cane – their calls for help too often remain unheard and ignored. Initially, Mr Al Shamsi did not inform his employer of his illness, but as his symptoms worsened in 2018 he had no choice. “I had to tell my employers because I needed some flexibility. I told them that I was suffering and showed them all my medical reports,” he said. “No-one believed me and they refused to understand that I had a disease where there are days where I am fine and others when I am not.” Mr Al Shamsi went as far as asking for assistance from local authorities to help explain to his employers that he had special requirements, but to no avail. “My employers took it as a personal attack against them,” he said. “They told me that they had employees in wheelchairs and with disabilities who were fine. “We are a special category of people with special requirements. Every day is different with MS. We don’t know what symptoms to expect and when, or if we will get better,” Mr Al Shamsi said. “We can’t be compared to people of determination [the expression used by the UAE to describe people with disabilities] and don’t want less hours, but only some flexibility and to be understood.”

Increasing cases of MS

World MS Day was established by the Multiple Sclerosis International Federation in 2009, and is observed every May 30. It seeks to unite the global MS community of more than 2.3 million people “to share stories, raise awareness and campaign with and for everyone affected” by the condition. Reliable nationwide figures are not available but it is known there are about 2,000 residents in Abu Dhabi and 2,000 in Dubai living with the condition. The auto-immune disorder affects approximately 64 per 100,000 people in the UAE, according to a 2019 research article published by scientists at the Sheikh Khalifa Medical City in Abu Dhabi. This figure is more than twice the World Health Organisation’s global prevalence estimate of 30 people per 100,000. Dr Ahmed Shatila, consultant neurologist at Sheikh Shakhbout Medical City in Abu Dhabi sees about one new MS patient each week and highlights the importance of early diagnosis. “MS is a chronic disease and yes it can cause significant disability but we also have very good treatments available right now that can change the course of the disease.