Currently, reports from the UK are causing a stir. The reason is data from the British statistical authority, according to which there have been increasing deaths in connection with the intake of Pregabalin from 2018
Continue readingRecently, the DMSG Federal Association has been receiving an increasing number of inquiries from MS patients regarding the possibility of reimbursement for the Exopulse Mollii Suit by statutory health insurance companies, as well as by
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There are still MS patients who are unsure about sports and exercise, especially when it comes to intensive training. Therefore, I would like to emphasize once again that the old view that one has to
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In the diagnosis and monitoring of multiple sclerosis, magnetic resonance imaging plays a crucial role. Images of the brain show inflammatory lesions at different locations in MS patients, primarily in the so-called white matter of
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Especially in summer, it is a common question: “Am I, as an MS patient, allowed to be in the sun? Isn’t the sun harmful?” – Here, I can generally reassure you – sunlight is by
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Immunotherapy for MS is an important measure for many patients, but it is not the only strategy we use. Although immunotherapies are particularly important therapeutic measures in the early stages of the disease, this (apparent)
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I recently wrote on the topic of cortisone for MRI changes. The comments on the blog were so interesting that I wanted to pick them up and comment on them again.
Continue reading I have often written about the role of MRI. In reality, I often experience a distinction problem between clinical stimulus and failure symptoms (= MS relapse) and changes in the MRI (new lesions).
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In Germany, there is a diffuse fear of (Neuro)Lyme disease, a disease transmitted by the bacterium Borrelia burgdorferi, which lives in the digestive tract of ticks. Lyme disease is considered a “mysterious” disease, supposedly responsible
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People with MS often suffer from a sometimes very debilitating physical and mental fatigue, which is referred to in clinical practice as “fatigue”. Despite its importance for many MS patients, “fatigue” is not well defined,
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