Your first meeting with a professional in the field of children’s disability may be about choosing a service that’s right for you and your child. Or it might be with a professional you’ve already chosen to work with. Either way, you’ll want to come out of it satisfied with the results and clear about what is going to happen next.
The answer depends on the professional and her role. But it is likely to include discussion about whether the service is suitable for you and your child.
Sometimes this may require a detailed assessment of your child’s situation. You may need to provide reports from your doctor or other specialists and give detailed information about your child and your family.
A bit of preparation beforehand will help you get the most out of your first meeting.
What can I expect from the professional at the first meeting?
At the first meeting, you might expect the professional to:
What kinds of questions might the professional ask me?
Expect the professional to ask questions. These will depend on what areas the professional is helping you with and how much information has been provided before the meeting. Some likely topics are:
Should I expect written information?
Many services and professionals will have brochures about what they do and how they work. Some will give you brochures about other services, handouts about your child’s disability, or possible treatments or tasks for you at home. For example, a speech pathologist may give you handouts about exercises to try at home between sessions.
Many parents find it useful to have verbal information backed up with the same information in writing. You can always ask for written information.
People employed to deliver services to a person with a disability must have relevant skills and competencies based on formal qualifications. Don’t hesitate to ask for information about the professional’s background and experience, including qualifications.
Questions you may want to ask include:
When you leave the first meeting, it’s really important you’re clear about what has been discussed, that you understand the information given, and know the next steps to take. Be up front about asking questions and repeating things back to the professional to make sure you’ve understood correctly. Feel free to ask for further explanations in words you can understand.
Make sure the professional is taking your needs and those of your family into account. If you’re worried you’re being pushy, remember that you’re speaking for and listening for your child – with experience you’ll get better and better at it. Don’t agree to anything you feel uncomfortable with or don’t understand.
Content funded by NSW Department of Ageing, Disability and Home Care
Carers Australia, (n.d.) Services for you. Retrieved May 20, 2007, from http://www.carersaustralia.com.au/index.php?option=content&task=view&id=67
Galil, A., Bachner, Y., Merrick, J., Flusser, H., Lubetzky, H., Heiman, N., & Carmel, S. (2006). Physician-parent communication as predictor of parent satisfaction with child development services. Research in Developmental Disabilities, 27, 233-242.
Moore, T. & Larkin, H. (2005). More than my child’s disability. A comprehensive literature review about family-centred practice and family experiences of early childhood intervention services. Glenroy, VIC: Scope (Vic) Ltd.