Counselling and Support for Families with Inherited Cancer Syndromes

Monday, 22 June 2009 - 9:00 am - 5:00 pm

Monika Keller MD

Only in English / Ausschließlich auf Englisch


Target Audience:

Clinical psychologists, psychiatrists, genetic counselors, nurses involved in genetic counseling, any clinician involved in the care of families with familial cancer syndromes.


Workshop Objectives:

The workshop shall enable participants to:

  1. Describe topics that are important to families with an inherited cancer syndrome
  2. Actively address these topics within genetic counseling
  3. Identify families at elevated risk of psychosocial problems and to provide adequate support

Workshop Description:

Individuals at increased risk of cancer and families with inherited cancer predispositions (HNPCC, HBOC, FAP) represent a new group in the health care system and, in particular, in the field of psychooncology. This workshop aims at providing insight into some particular clinical features of inherited cancer syndromes, that should be actively addressed in order to enhance individuals’ and families’ adjustment during the phase of genetic testing and also beyond.

An overview is provided of psychosocial challenges families with familial cancer syndromes commonly are facing during the course of genetic counseling and testing. This includes the impact of the family’s previous experiences with cancer and death on their belief systems, on their personal theories of illness and inheritance, on developmental tasks and on family relationships and communication. Since experiential knowledge profoundly shapes current perceptions this knowledge needs to be actively incorporated in the process of genetic counseling, to ascertain that families can integrate the ‘genetic news’ within their experiential background.

Several case reports, each of them focusing on a specific problem will be presented for discussion with workshop participants (participants presenting own cases are welcome).

Based on clinical experience and on family systems theory, recommendations are provided and discussed for comprehensive psychosocial assessment and monitoring, that includes the identification of individuals and families probably at increased psychosocial risk and in need for further interventions.

An agenda is proposed how to establish multidisciplinary collaboration with clinicians and geneticists, and how to provide adequate counseling and support for families at risk of hereditary cancer syndromes within a multidisciplinary context.