Vie familiale et fratrie Archives - Page 6 sur 9

Sep 18

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Stress Among Parents of Children With Severe Neurological Impairment in the Pediatric Intensive Care Unit

Sep 18

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Family Resilience Affecting Well-Being of Families With a Child With Profound Intellectual and Multiple Disabilities

Sep 18

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Do they agree? How parents and professionals perceive the support provided to persons with profound intellectual and multiple disabilities

Sep 18

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Care and support for persons with profound intellectual and multiple disabilities without parents: A qualitative exploration

Sep 18

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Digital participation of people with profound and multiple learning disabilities during the Covid‐19 pandemic in the UK

Sep 18

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Affirming Perspectives About Quality-of-Life With Caregivers of Children With Severe Neurological Impairment

Sep 18

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Parents’ tacit knowledge of their child with profound intellectual and multiple disabilities: A qualitative study

By jbberthier

Sep 18

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Asset-Based Health Care for Children With Severe Neurologic Impairment

By jbberthier

Sep 18

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Exploring the Experiences of Dutch Parents Caring for Children with Profound Intellectual and Multiple Disabilities: A Thematic Analysis of Their Blogs

By jbberthier

Sep 18

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The Role of the External Personal Assistants for Children with Profound Intellectual and Multiple Disabilities Working in the Children’s Home

By jbberthier

Sep 18

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Ashley, l’enfant Bonsaï. Inhibition de la croissance d’enfants très sévèrement handicapés : une réalité ou un fantasme ?

By jbberthier

Sep 18

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Séjours de répit à l’hôpital de La Roche-Guyon

By jbberthier

Sep 18

Love0

« Il est alarmant de voir combien de familles sont laissées en grande difficulté. »

By jbberthier

Sep 18

Love0

Quality of life among individuals with profound intellectual and multiple disabilities: crossed perspectives of institutional caregivers and parents

By jbberthier

Sep 18

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Déficience intellectuelle et vie autonome au Japon

By jbberthier

Sep 18

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Healthcare of Persons With Complex Developmental Disabilities From Three European Experiences: France, Italy, and Norway

By jbberthier

Sep 18

Love0

Le point de vue des familles. Table ronde réalisée par Loubna Chérif Kanouni Mekouar, Emmanuelle Petronzio et Xiao Hui Loo, animée par Jean-Claude Riou dans le cadre des journées du CRMH : Suivi orthopédique de l’enfant polyhandicapé, 9 juin 2023, Paris

By jbberthier

Sep 18

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L’expertise d’usage des parents d’enfant polyhandicapé

By jbberthier

Sep 18

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Être adolescent et polyhandicapé

By jbberthier

Sep 18

Love0

Les liens fraternels dans la famille d’un adolescent polyhandicapé, entre fantasmes destructeurs et créativité

By jbberthier

Stress Among Parents of Children With Severe Neurological Impairment in the Pediatric Intensive Care Unit

Family Resilience Affecting Well-Being of Families With a Child With Profound Intellectual and Multiple Disabilities

Do they agree? How parents and professionals perceive the support provided to persons with profound intellectual and multiple disabilities

Care and support for persons with profound intellectual and multiple disabilities without parents: A qualitative exploration

Digital participation of people with profound and multiple learning disabilities during the Covid‐19 pandemic in the UK

Affirming Perspectives About Quality-of-Life With Caregivers of Children With Severe Neurological Impairment

Parents’ tacit knowledge of their child with profound intellectual and multiple disabilities: A qualitative study

Asset-Based Health Care for Children With Severe Neurologic Impairment

Exploring the Experiences of Dutch Parents Caring for Children with Profound Intellectual and Multiple Disabilities: A Thematic Analysis of Their Blogs

The Role of the External Personal Assistants for Children with Profound Intellectual and Multiple Disabilities Working in the Children’s Home

Ashley, l’enfant Bonsaï. Inhibition de la croissance d’enfants très sévèrement handicapés : une réalité ou un fantasme ?

Séjours de répit à l’hôpital de La Roche-Guyon

« Il est alarmant de voir combien de familles sont laissées en grande difficulté. »

Quality of life among individuals with profound intellectual and multiple disabilities: crossed perspectives of institutional caregivers and parents

Déficience intellectuelle et vie autonome au Japon

Healthcare of Persons With Complex Developmental Disabilities From Three European Experiences: France, Italy, and Norway

Le point de vue des familles. Table ronde réalisée par Loubna Chérif Kanouni Mekouar, Emmanuelle Petronzio et Xiao Hui Loo, animée par Jean-Claude Riou dans le cadre des journées du CRMH : Suivi orthopédique de l’enfant polyhandicapé, 9 juin 2023, Paris

L’expertise d’usage des parents d’enfant polyhandicapé

Être adolescent et polyhandicapé

Les liens fraternels dans la famille d’un adolescent polyhandicapé, entre fantasmes destructeurs et créativité

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