What is the New Era of Care without access?
It’s day three of Migraine Awareness Month and I probably should have posted something before now, but I’m really strugglingContinue Reading
It’s day three of Migraine Awareness Month and I probably should have posted something before now, but I’m really strugglingContinue Reading
Last week I addressed the Standing Committee on Health’s inquiry into how new drugs come to Australia. I told themContinue Reading
In the budget on Tuesday night it was announced that Emgality would finally listed on the PBS. This is aContinue Reading
One of the saddest things I have repeatedly encountered in advocacy is bullying.
Recently I revealed that I’d gone off Aimovig. Well, I cracked, and I’m now back on it. But it looksContinue Reading
I forgot how incredibly ugly migraine can be.
This morning I started International Women’s Day with a chat with Canadian migraine warrior Maya Carvalho. We talked about theContinue Reading
After two glorious years on this miraculous, life saving drug, I have given up Aimovig. I didn’t want to. I shouldn’t have had to. And I’m furious.
Do you think if I ask #LesMills really nicely they’d do a #migraine friendly group class of some kind?
It happened again. Another member of the migraine community, with a previously wonderful and now abusive partner unable to dealContinue Reading









