“I want to advocate for the Government to recognise Lipoedema, as treatment needs to be subsidised by Medicare. For local GPs, awareness needs to be raised for diagnosis.”
How would your friends and family describe you?
Family orientated, outgoing and stubborn, a true Taurean.
When did you first suspect you had Lipoedema?
In Feb ‘21 my lower left leg was very swollen and bruised, so I made an appointment with a new doctor, as my doctor was on leave. This doctor was the one who said to me it may be Lipoedema and handed me a print out of Lipoedema symptoms. I had never heard of it up until then.
How did you first learn about Lipoedema?
When researching about Lipoedema I found Dr Lekich’s clinic and made an appointment in Melbourne in early 2022. It was very helpful to have my diagnosis confirmed at that appointment.
Do you recognise these symptoms in your family members?
I have no family history or other family members with Lipoedema symptoms.
What are the main challenges that Lipoedema has presented from an overall lifestyle point of view?
My lower limbs swell, are painful to touch and bruise easily. I also find it difficult to walk now like I used to.
Why do you think it’s important to advocate for awareness of Lipoedema?
I want to advocate for the Government to recognise Lipoedema, as treatment needs to be subsidised by Medicare. For local GP’s, awareness needs to be raised for diagnosis.
