Introduction
Making a submission to government inquiries and consultations is an important way that rare disease organisations can raise issues of concern and advocate directly to government on behalf of their communities. This short course has been developed by government relations, advocacy and health communications specialist, Tania Jayesuria.
In line with Action 2.1.4 of the National Strategic Action Plan for Rare Diseases, this course contributes to developing the capacity of rare disease organisations to represent and advocate for people living with a rare disease and their families.
This course is ideal for:
- Rare disease organisation leaders interested in lodging submissions to government inquiries and consultations
- People living with a rare disease who are interested in lodging submissions and no formal support group exists
After completing this course, you will:
- Have a better understanding of best practice tips, strategies and tools for writing impactful submissions at the Federal/Commonwealth Government level
Please note: this course is available to RVA Partners only. Click here for more information about becoming an RVA Partner.
Introduction
During these uncertain and challenging times due to COVID-19, effective advocacy is more important than ever. With so many competing issues and voices, it’s essential that the rare disease community make their voices heard.
With this in mind, Rare Voices Australia (RVA) has developed this online learning resource to assist you in amplifying your rare disease advocacy using the National Strategic Action Plan for Rare Diseases (the Action Plan).
The Action Plan was launched in February 2020 by the Minister for Health and Aged Care with bipartisan support. The Action Plan was developed ‘by the rare disease sector, for the rare disease sector’ and is a powerful tool that you can use to amplify your advocacy.
This learning resource provides information, case studies and examples to highlight the power of the Action Plan in advocacy.
Once you’ve completed the course, you will:
- Understand the context and background to the development of the Action Plan.
- Recognise the key features of the Action Plan that amplify advocacy.
- Be able to use the Action Plan to amplify your advocacy.
The content is self-paced so complete the modules when it best suits you. You can test your understanding throughout and upon completion of the course, you will receive a certificate.
You will need to complete Module 1 before moving onto Module 2. After reading and watching all of the content, you’ll be asked to test your knowledge in a short quiz.
Please note: this course is available to RVA Partners only. Click here for more information about becoming an RVA Partner.
Introduction
Illuminating landmarks can be a powerful way to mark awareness days such as Rare Disease Day. Illumination activities showcase a united front and shine a light on rare diseases as a collective (Rare Disease Day) or for a specific rare disease. Additionally, illuminations help to raise awareness and may result in people and families living with a rare disease feeling seen and heard.
The more local and national buildings and monuments that are illuminated, the stronger the impact!
Once you have completed this course, you will:
- Understand the basics of illuminating landmarks.
- Be aware of the key factors to consider when reaching out to potential landmark contacts.
- Know how to maximise the impact of illuminations organised.
The content is self-paced so complete the modules when it best suits you. You can test your understanding throughout and upon completion of the course, you will receive a certificate.
Rare Voices Australia (RVA) thanks RVA Partner, Fragile X Association of Australia, and rare disease advocate, Andrew Bannister, for working with RVA to develop this resource and for sharing their learnings and tips so generously with the rare disease community.
Please note: this course is available to RVA Partners only. Click here for more information about becoming an RVA Partner.