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  ME/CFS AUSTRALIA (SA) INC

Registered Charity 698

Email:
sacfs@sacfs.asn.au

Mailing address:
PO Box 28,
Hindmarsh,
South Australia 5007

Office:
266 Port Road,
Hindmarsh,
South Australia 5007
Ph: 1300 128 339

Office Hours:
Wednesdays, 10am-3pm


FIBROMYALGIA HELP:
Contact
Fibromyalgia SA
at the
Arthritis Foundation of SA
118 Richmond Road,
Marleston 5033
Ph: (08) 8379 5711

ME/CFS Australia (SA) Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.

Disclaimer

ME/CFS Australia (SA) Inc aims to keep members informed of the various research projects, diets, medications, therapies etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives.

Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services.

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ME/CFS Australia (SA) Inc Youth Policy
Introduction
Youth Inclusion in Education Policy
Mission Statement
Goals



ME/CFS Australia (SA) Inc Youth Policy is also available as a PDF file (youth.pdf – 15KB).


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ME/CFS Australia (SA) Inc Youth Policy (continued)

Goals

I. Improved access to educational facilities
II. Information to youth and parents
III. Consultation with membership
IV. Additional opportunities for achievement
V. Tertiary systems

I. Improved access to educational facilities

The basis of our INCLUSION policy is to encourage educators from both government and non-government/independent sectors to become sympathetic to the needs of young people with CFS. This includes a readiness to understand the condition and the disruptive effect it may have on ongoing schooling. We would like young people to have educational choices, and the opportunities to attend mainstream schooling as well as Open Access Schooling. We would like young people to be supported by flexible policies that allow children to combine open access studies and mainstream schooling backed up by the availability of counseling in the choice of suitable curriculum.

  1. To develop an awareness of the educational needs of young people and to liaise with appropriate educational bodies and to promote access to equal educational opportunities.
  2. To encourage educational systems to advocate on behalf of curriculum choices.
    1. Secondary Level, both Open Access and DETAFE Policy Levels.
      1. In partnership with and acting as a resource for central DETAFE Policy staff to develop educational material to for use by the schools and community.
      2. Input through participation in parental management groups at Open Access College.
      3. Promote liaise between open Access and DETAFE policy units in the training of staff at the level of services provision in the area of hierarchical management superintendent levels, counseling services and to the Attendance Branch policies, to manage opportunities for children who have chronic disabilities.
    2. Liaise with SABSA for equitable assessment processes for students who have a chronic recognized medical condition.
    3. Encourage schools to promote CFS in curriculum areas such as health, domestic science, personal improvement courses (where strategies in managing absences from and return to school could be discussed) and sport. Again consultation and partnership in program development is a desired objective.
    4. Lobby for improved facilities for students in mainstream schooling – access to phones for lessons, a quiet (non-punitive) rest area etc.
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II. Information for youth and parents

  1. The Society will assist youth and their families to negotiate the most appropriate curriculum choices, by providing information on changing DETAFE policy as it becomes available to us. The Society will continue to promote the needs of our members towards equitable and flexible educational choices.
  2. The Society will encourage promotion of its activities and parental resource contact people, through publications such as Open Access Magazine.
  3. Appropriate information will also be provided via the Talking Point and SAYME publications and Web sites.
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III. Consultation with membership

It is envisaged that the Society will seek to involve as many of their members particularly the SAYME group and their parents, as well as country members in developing policies and programs to meet the needs and interests of youth.

A special task force of committed members may be formed to promote the interests of this group. Such a group would work closely with the Society Committee of Management, and with other relevant groups such as the Grants Committee, in obtaining funding to pursue objectives.

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IV. Additional opportunities for achievement

The Society will also aim to create opportunities for youth to achieve success, in leadership and recreational pursuits outside of the formal education system. Involvement in the Duke of Edinburgh Award scheme is one such program the Society hopes to offer to its youth membership.

The Society may well decide to implement an annual best practice award process to those schools (including country and private sector) which exhibit a responsive program- or a pro-inclusion stance for children who straddle the fences of open access and mainstream schooling. The aim would be to recognize and reward endeavours by staff in schools who are willing to put some effort in meeting the special needs of children who have chronic fatigue.

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V. Tertiary systems

Another component of an inclusion policy would be the readiness of tertiary institutions to offer a flexible entry program for those students wishing to embark on a course of tertiary study. Some individual work has already been instigated with Flinders University and it is hoped that the Society may be able to extend such possibilities in the future.

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