Home > Search Results: keywords:"Parkinson's disease Motory symtoms of Parkinson's disease Non-motor symtoms of Parkinson's disease Course of the disease Informal care"
Search:
Search Tips :: Advanced Search
Search collections:
Sort by: Display results: Output format:
National Repository of Grey Literature 2 records found  Search took 0.01 seconds. 
The issue of informalcare for a close person with Parkinson's Diseasefrom the perspective of caregivers
 Mašková, Monika ; Válková, Monika (advisor) ; Ondrušová, Jiřina (referee)
Diploma project, the issue of informal care for a close person with Parkinson's disease from the perspective of caregivers is focused on the intensity of care and access to services that could help informal caregivers in the care of their loved ones.In the theoretical section of Parkinson's disease I am describing, its development and changes that the disease brings along. Then I followed with the care of relatives person and support from the social system - the state. In the practical part I have chosen for my research a survey, which was attended by only a small part of respondents from informal carers. Care of long-term sick family member is very difficult. Caregivers feel tired and exhausted, they report that their own health becomes wors. Care also affects cares professional life and there leisure time. Although half of the respondents are still able to find time for their hobbies. Some carers have no idea about the possibilities of helping services and just minimum of them use these services.
Detailed record
The issue of informalcare for a close person with Parkinson's Diseasefrom the perspective of caregivers
 Mašková, Monika ; Válková, Monika (advisor) ; Ondrušová, Jiřina (referee)
Diploma project, the issue of informal care for a close person with Parkinson's disease from the perspective of caregivers is focused on the intensity of care and access to services that could help informal caregivers in the care of their loved ones.In the theoretical section of Parkinson's disease I am describing, its development and changes that the disease brings along. Then I followed with the care of relatives person and support from the social system - the state. In the practical part I have chosen for my research a survey, which was attended by only a small part of respondents from informal carers. Care of long-term sick family member is very difficult. Caregivers feel tired and exhausted, they report that their own health becomes wors. Care also affects cares professional life and there leisure time. Although half of the respondents are still able to find time for their hobbies. Some carers have no idea about the possibilities of helping services and just minimum of them use these services.
Detailed record

Interested in being notified about new results for this query?
Subscribe to the RSS feed.
Digital Repository :: Search :: Submit :: Personalize :: Help
Powered by Invenio v1.1.2
Maintained by admin.invenio@techlib.cz
This site is also available in the following languages:
Česky  English