This is the fifth of our new series of periodic calls for #MEAction co-founders Jen Brea and Beth Mazur to meet other activists “face to face.” It’s an opportunity to ask big picture questions about the platform, brainstorm strategy, and offer suggestions for future directions.
We’d love this call to especially focus on connecting with activists in Australia.
![a multi-water colored image with the words, Severe ME Artists Project 2024 in white font outlined in black. the meaction action logo in the bottom right hand corner.](https://www.meaction.net/wp-content/uploads/2024/06/Severe-ME-Artists-Project-2024-1200-x-630-px-1-300x158.png)
Severe ME Artists Project 2024
Quick Overview: Submit one piece of artwork – image, writing, or video Label your artwork with your name as you want it to appear, an underscore, and the number of years with severe ME Example: Lastname_FirstName_14 FirstNameOnly_ No copyrighted material If you are submitting a video, it must be under two minutes. Submission due by
1 thought on “#MEAction Google Hangout: Australia”
I have only started ME/CFS advocacy work this year, mainly through the ME/CFS Australia Facebook website and have just become a Committee member of the ME/CFS South Australian Society. Canary in a Coal Mine was a catalyst for me becoming more involved.
Adelaide, South Australia is hoping to set up a world first clinic with research attached. I have been under the doctor whose protocol is being used and refined, so I have first hand experience with the treatment process which is ‘precision’ medicine: A step by step approach that is tailored to each individual’s biochemical profile.
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