Date Held: 3 August 2023
During the briefing, we revealed our government affairs and advocacy strategy and discussed the role you could play. This briefing provides a comprehensive view of our government advocacy efforts and outlines how you can help step by step.
This includes step-by-step instructions and the below resources. Click on the image to download.
Summary:
Click on the image to download each resource.
Use the following checklist to help organise and plan your meeting with your MP.
We have developed a template meeting request letter for you to e-mail or send to your local MP and/or Senator. Feel free to amend the body of the email to suit your lived experience.
We have developed a template thank you letter for you to e-mail or send your local MP following your meeting with them. Again, feel free to tailor the body of the email to suit your lived experience and your own way of writing.
An infographic has been created about the need to address migraine in the workplace, especially for women who are already fighting for equal pay and workplace equity. You may print out this infographic and take it with you to your meeting or refer to it during your conversation.
When can I start?
Straight away (August 2023). We would like to get as many meetings conducted in August and September as possible in the lead up or during Migraine & Headache Awareness Week 4-8th September 2023. Will also hope to have PR coverage in early September.
What do I need to know about my MP and Senator?
Your MP and Senator website and social media channels are also a great way to see what they have been talking about recently.
What if I need to reschedule the meeting?
If you need to reschedule the meeting, speak with their office early and find a new meeting time that suits you both.
What do I do if my MP or Senator doesn’t want to meet with me?
MPs and Senators have busy diaries full of local community events, meetings with constituents like yourself, as well as parliamentary responsibilities. If your local MP or Senator is a Minister or Shadow Minister, then they can spend weeks at a time on the road developing policies or speaking with various groups within the sector.
If you do have trouble with meeting with your MP or Senator, reach out to Migraine & Headache Australia and we can work through it with the office directly. Often, it’s an issue of timing.
How do I stay in contact with my local MP or Senator?
Follow them on their social media handles e.g. Facebook, Twitter, or sign up to their newsletter. They may also signal during the meeting other ways that you can stay in contact as they may want to continue to hear about your experience living with migraine.
For any additional questions or issues, please contact us at info (at) brainfoundation.org.au or call us at 1300 886 660.
Migraine & Headache Australia is the only organization in Australia that aims to support the more than 5 million Australians affected by headache and migraine. 