Quality of life, Coping and need for Support during the ALS disease trajectory
The overall aim of this thesis was to investigate quality of life, coping and emotional distress (i.e. anxiety and depression) among newly diagnosed ALS patients. An additional aim was also to investigate relatives’ experiences of the care for the patient and the support they received for themselves...
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| Format: | Doctoral Thesis |
| Language: | English |
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Uppsala universitet, Institutionen för neurovetenskap
2016
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| Online Access: | http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-283077 http://nbn-resolving.de/urn:isbn:978-91-554-9575-6 |