Background: 22q11.2 deletion syndrome (22q11DS) is the most common microdeletion syndrome. Parents of emerging adults with 22q11DS have an intense and ongoing involvement in their child\u27s life. This study explores the lived experience of parents in relation to their child becoming independent and establishing intimate relationships. Method: Interpretative phenomenological analysis was used to explore the positive and negative experiences of five parents of emerging adults with 22q11DS. Results: Supervised independence overarched four subordinate themes. These themes highlighted the difficulties experienced by parents attempting to relinquish control whilst still experiencing a need to keep their child safe as their child negotiated a com...
University of Minnesota Ph.D. dissertation.December 2017. Major: Family Social Science. Advisor: Ta...
Most children with chromosome 22q11.2 deletion syndrome (22q11DS) have an IQ in the range that may a...
22q11.2 DS is characterised by its variability, rarity and variety of features ranging from congenit...
Objectives: 22q11.2 deletion syndrome (22q11DS), a complex genetic syndrome associated with more tha...
Masters Coursework - Master of Clinical Psychology (MClinPsych)Introduction: Many people with intell...
Research Doctorate - Doctor of Philosophy (PhD)The negative psychological impact of having a child w...
The presentation of 22q11.2 deletion syndrome (22q11DS) is symptomatically variable presenting diagn...
Individuals diagnosed with 22q11.2 deletion syndrome (22q) have many barriers and quality of life is...
- Background: The predominant focus of extant literature exploring maternal experience of developmen...
Introduction: Despite a growing body of intellectual disabilities literature around the transition i...
This is an accepted manuscript of an article published by Taylor & Francis Group in International Jo...
Background: 22q11.2 deletion syndrome is a rare multisystem genetic disorder with over 200 associate...
This study seeks to develop understanding of the experiences of being a parent with 22ql 1, of child...
Data from parents and young adults were collected as part of a 20-year follow-up of chil-dren with d...
The development of autonomy is one of the developmental tasks young adults are faced with, but for y...
University of Minnesota Ph.D. dissertation.December 2017. Major: Family Social Science. Advisor: Ta...
Most children with chromosome 22q11.2 deletion syndrome (22q11DS) have an IQ in the range that may a...
22q11.2 DS is characterised by its variability, rarity and variety of features ranging from congenit...
Objectives: 22q11.2 deletion syndrome (22q11DS), a complex genetic syndrome associated with more tha...
Masters Coursework - Master of Clinical Psychology (MClinPsych)Introduction: Many people with intell...
Research Doctorate - Doctor of Philosophy (PhD)The negative psychological impact of having a child w...
The presentation of 22q11.2 deletion syndrome (22q11DS) is symptomatically variable presenting diagn...
Individuals diagnosed with 22q11.2 deletion syndrome (22q) have many barriers and quality of life is...
- Background: The predominant focus of extant literature exploring maternal experience of developmen...
Introduction: Despite a growing body of intellectual disabilities literature around the transition i...
This is an accepted manuscript of an article published by Taylor & Francis Group in International Jo...
Background: 22q11.2 deletion syndrome is a rare multisystem genetic disorder with over 200 associate...
This study seeks to develop understanding of the experiences of being a parent with 22ql 1, of child...
Data from parents and young adults were collected as part of a 20-year follow-up of chil-dren with d...
The development of autonomy is one of the developmental tasks young adults are faced with, but for y...
University of Minnesota Ph.D. dissertation.December 2017. Major: Family Social Science. Advisor: Ta...
Most children with chromosome 22q11.2 deletion syndrome (22q11DS) have an IQ in the range that may a...
22q11.2 DS is characterised by its variability, rarity and variety of features ranging from congenit...