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Living with gMG
The levels of fatigue and weakness gMG patients experience are unpredictable and can change from hour-to-hour across the day.1–3 Multiple aspects of people's lives are impacted by the symptoms, including different emotional, physical and social aspects.*1 This makes planning future activities, socialising, working and simple daily tasks more challenging.1,2
* Based on a qualitative, cross sectional, non-interventional study involving interviews with 28 people living with gMG.

Almost half of patients living with gMG struggle with clinically meaningful anxiety, and more than a quarter experience depressive symptoms.*†4

* Based on a study to evaluate the predictors of HRQoL in 80 patients living with gMG in Brazil.4

‘Clinically meaningful’ was defined as a Hospital Anxiety and Depression score of ≥ 9.4

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ADL, activity of daily living; gMG, generalised myasthenia gravis; IADL, instrumental activity of daily living.
Jackson K, et al. Understanding the symptom burden and impact of myasthenia gravis from a patient’s perspective: A qualitative study. Neurol Ther. 2023;12:107–128. Law N, et al. A lived experience of myasthenia gravis: A patient led analysis. Neurol Ther. 2021;10:1103–1125. Meriggioli MN, Sanders DB. Autoimmune myasthenia gravis: emerging clinical and biological heterogeneity. Lancet Neurol. 2009;8(5):475–490. Braz NFT, et al. Muscle strength and psychiatric symptoms influence health-related quality of life in patients with mysthenia gravis. J Clin Neurosci. 2018;50:41–44.
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