29 results on '"Kavanaugh, Melinda S."'
Search Results
2. Variations and Patterns in Sleep: A Feasibility Study of Young Carers in Families with ALS.
3. Parental and child adjustment to amyotrophic lateral sclerosis: transformations, struggles and needs
4. How Far Have We Come? An Updated Scoping Review of Young Carers in the U.S.
5. What, how and when do families communicate about ALS? A qualitative exploration of parents’ and children’s perceptions
6. Young Carers, The Overlooked Caregiving Population: Introduction to a Special Issue
7. 'I Just Learned by Observation and Trial and Error': Exploration of Young Caregiver Training and Knowledge in Families Living with Rare Neurological Disorders
8. What, how and when do families communicate about ALS? A qualitative exploration of parents' and children's perceptions.
9. “Man, This Isn’t Easy”: Exploring the Manifestation of Parentification Among Young Carers of a Parent with Huntington’s Disease
10. "It's Put a Lot of Responsibility on Me to Make Sure That She's Being Taken Care of": Latino and African American Young Carers of Family with Dementia during the COVID-19 Pandemic.
11. “I Just Learned by Observation and Trial and Error”: Exploration of Young Caregiver Training and Knowledge in Families Living with Rare Neurological Disorders
12. “This could be me”: exploring the impact of genetic risk for Huntington’s disease young caregivers
13. “I am no longer alone”: Evaluation of the first North American camp for youth living in families with Huntington's disease
14. US data on children and youth caregivers in amyotrophic lateral sclerosis
15. Stigma experienced by ALS/PMA patients and their caregivers: a mixed-methods study
16. Adapting an intervention to support young caregivers of cancer survivors: A study protocol.
17. Unacknowledged Caregivers: A Scoping Review of Research on Caregiving Youth in the United States
18. Additional file 1 of Parental and child adjustment to amyotrophic lateral sclerosis: transformations, struggles and needs
19. Additional file 2 of Parental and child adjustment to amyotrophic lateral sclerosis: transformations, struggles and needs
20. Young carers and ALS/MND: exploratory data from families in South Africa
21. Skill, confidence and support: conceptual elements of a child/youth caregiver training program in amyotrophic lateral sclerosis – the YCare protocol
22. Young carers and ALS/MND: exploratory data from families in South Africa.
23. “This could be me”: exploring the impact of genetic risk for Huntington’s disease young caregivers
24. Feasibility of a multidisciplinary caregiving training protocol for young caregivers in families with ALS
25. Caregiving Youth Knowledge and Perceptions of Parental End-of-Life Wishes in Huntington’s Disease
26. Unacknowledged Caregivers: A Scoping Review of Research on Caregiving Youth in the United States
27. Feasibility of a multidisciplinary caregiving training protocol for young caregivers in families with ALS.
28. Application of the UN Convention Rights of the Child to young carers in the United States: US policies in international context.
29. “ It’d be nice if someone asked me how I was doing. Like, ‘cause I will have an answer ”: exploring support needs of young carers of a parent with Huntington’s disease.
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