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BMJ 2005;330:885-888 (16 April), doi:10.1136/bmj.330.7496.885
Michaela Langgartner, specialist in training, Department of Pediatrics1, Ingrid Langgartner, technician2, Marcus Drlicek, pathologist, Clinical Institute for Neurology1
1 Medical University Vienna, Allgemeines Krankenhaus Wien, Währinger Gürtel 18-20, A-1090 Wien, Austria, 2 Department of Anesthesiology, Laboratory for Blood Groups, Landeskrankenhaus Kirchdorf, Hausmanningerstraße 8, A-4560 Kirchdorf, Austria
Correspondence to: M Langgartner (Michaela.langgartner@meduniwien.ac.at)
| The first 150 words of the full text of this article appear below. |
When someone goes on a journey there will be lots to tell afterwards, according to the above Austrian saying. This is how we feel about our description of the journey that is multiple sclerosis. We will not focus on its aetiology, diagnosis, or treatment, but we will concentrate on the experiences of a patient (MD), his wife (IL), and the impressions of one of their children (ML). Looking back on our journey together we will discuss and share our thoughts. A short description of our experiences at time of diagnosis (box 1) and a personal outlook on the future (box 2) are given here; a more detailed description of the journey is on bmj.com