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You have a lipoedema diagnosis … what now?

You have a lipoedema diagnosis … what now?

I ran a live chat titled “You’ve got a lipoedema diagnosis … what now?” as part of Lipoedema Awareness Month 2023. There are often posts in lipoedema support groups saying that someone has just got diagnosed and they have no idea where to start...
Lipoedema Awareness Month 2023

Lipoedema Awareness Month 2023

Lipoedema Awareness Month 2023 has a different flavour for me. It is the first year of me being on the Advisory Board of Lipoedema Australia, so I feel like I have a much larger responsibility to talk about it. I also feel the pressure to keep everything I say factual...
Lymphoedema Awareness Month 2023

Lymphoedema Awareness Month 2023

For Lymphoedema Awareness Month 2023 I decided to talk about the metaphysical side of Lymphoedema. Yes, compression, manual lymphatic drainage, exercise, healthy eating … blah, blah, blah. I talk about that stuff all the time. But let’s look deeper at what’s...
Lipoedema Awareness Month

Lipoedema Awareness Month

June is Lipoedema Awareness Month and I’ve been writing up a storm to help raise awareness. I had an article published in our local magazine, the Tawny Frogmouth – click here to read the magazine. I’m posting my original piece and a photo of the edited and...