-From Institutionalised Children Explorations and Beyond
This interview focuses primarily on
the mental health needs of children in care and, with this objective, has been
divided into three sections: exploring institutional care, family and
community-based care, and the context in South Asia, respectively.
Children in institutional care have
suffered significant trauma in separation, as well as with issues embedded in
dysfunctional families, prior to entering care. What are some of the impacts of
institutional care on the mental health of children? How do they influence
their growth and developmental outcomes?
The course of world
de-institutionalisation policies began when international child researchers
studied the effects of deprivation in Romania and Bulgaria in the 1990s
(Charles Zeanah, the Michael Rutter Group). These orphanages were substandard
and comparable to concentration camps. Children spent most of their time in
beds with no stimulation or physical or emotional interaction with caregivers.
As a result, the children’s brain development was severely impaired: low brain
weight, lack of brain network formation, stunting, dwarfism and extreme infant
mortality due to low brain activity.
Surviving children developed
‘institutional autism’, extremely aggressive or withdrawn behaviours, and some
developed a psychopathic personality. As an adoption expert and consultant for
Danish state, I saw many adoptive families break down, especially overwhelmed
by older children’s problems and their inability to attach to new parents. Many
children had to be replaced to specialised institutions.
What are some of the factors in
institutional care that lead to such outcomes? In your opinion, are these consistently
observed across care institutions globally? What are some of the developmental
markers for trauma that you consider important for placement?
Even though there is little
scientific evidence that group care is less effective than family-based care, the
negative experiences described above caused UNICEF to ask all countries in 2009
to close their orphanages, reconfirmed at the December 2019 declaration signed
by 193 countries.
The mindsets and role of caregivers,
and their continuous training, support and supervision, play an important role
in providing safe environments to children. Caregivers must see themselves as
parents and not only as care professionals; they should learn to perform
relational work and include children in daily activities; they should create
social and emotional bonds with each child; and act as secure attachment
figures and parental substitutes.
Sixty years of research in lifelong
success for placed children shows five dimensions of quality care: a long-term
secure attachment relation with one or two close caregivers and a long-term
membership of a group of peers; having friends is very important for developing
social networking skills as a care-leaver and an adult; one caregiver per four
to six children; educated and supervised caregivers.
Caregiver's well-being and knowledge
are directly related to their ability to provide loving care; social isolation
or overwhelming numbers of children is detrimental to secure care capacity and
agreement between shareholders in the child’s placement and attachment. If, for
example, divorcing parents fight over a child, or the foster family and
biological family, or caregiver staff and social worker are in conflict, the
child’s development and school performance declines. ‘Quality in care’ need not
necessarily depend on placement type.
Unfortunately, international policies are not focused on quality care standards, but only on de-institutionalisation. This creates a host of challenges. I am not for or against de-institutionalisation, but it has become an ideological mantra project as the cure for all problems, demonising group care in all its forms. In my view, challenges and the concept of improvement vary from country to country and from child to child. For this reason, I prefer an array of solutions and a longer time perspective in implementation.
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