Will we listen? 2020 is the call we've all been waiting for. It feels like the opportunity to take responsibility for our part in this gigantic global shift. The waves of panic and fear have [...]
R A R E I must admit the words “Rare Disease” don't exactly feel right. Yesterday was world Rare Disease Day. I’m all for awareness, I’m a passionate advocate for our children - but rare [...]
Motherhood - what if? What if a mother had everything she ever needed the moment her child was diagnosed? What if a mother truly trusted her intuition at all times? What if a mother honoured [...]
You become many things the moment your beautiful child receives a diagnosis; an advocate, a medical researcher, an investigator, a carer, an administration executive, a taxi driver, a nurse, a doctor, an entertainer, a mind [...]
I am beyond excited to finally share with you some incredible news! A huge thanks to Virgin Australia for their approval of seating devices for infants and children with a disability. It's incredible when a company as [...]
When your friend's beautiful child has been diagnosed with something serious, it's difficult to know what to say or what to do. Here are some points that I've put together after speaking with hundreds of [...]
There is so much I want the world to know and understand about my daughter, because in creating awareness around diversity we can help break down any stigma attached to being “different”. I want the world [...]
Determined + Courageous + Strong & United. What a powerful theme for the PMGA conference and one that I started to witness unfold more and more as the hours went by. I was really [...]
HEY MAMA, POP YOUR EMAIL BELOW AND RECEIVE YOUR
A Guided Relaxation For Mums
