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Deborah Rickards

VPPRN GCA Patient-Partner and Patient Champion

Why do I participate in research?

My name is Deborah Rickards, I live in Fremantle, Western Australia. I was diagnosed with Giant Cell arteritis/ Takayasu arteritis approximately 8 years ago. This diagnosis came a year and a half after experiencing an at home cardiac arrest and was eventually found via a P.E.T scan.

I am keen to be part of the VPPRN as vasculitis in general is very misunderstood, even within the medical community. This is important to me (and others) as the more this disease/illness is normalized the more compassionate and empathy can be given to those who live life in this way. It is also important to be able to access research that allow for vasculitis to be further studied, which can only be of help to all of us!”

-Deborah Rickards

BETTER STUDIES | BETTER ANSWERS | BECAUSE OF YOU

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YOUR GIFT GOES TWICE AS FAR TODAY!

Double Match Day is here—help us celebrate 40 years by raising $40,000.

People living with vasculitis rely on support, research, and connection every day.

Today only, your donation will be matched dollar-for-dollar, helping us reach more patients, fund critical research, and ensure no one faces vasculitis alone.