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About 2018-11-30T02:59:30+00:00

Soulful Support for Mums

Natalie_Feather_Small

Need to slow down and reconnect? Do you crave connection on your journey? Are you feeling overwhelmed?

Mothers need support, but the whole “it takes a village” takes on a whole new meaning with mums who are raising children with additional needs.

This is your space, an online sanctuary for you to gather what you need. You are raising a miracle with huge challenges and your voice needs to be heard. I believe we can truly reach our full potential, transforming loss and brokenness through love and light. Sharing my story has connected me to so many mamas experiencing challenges and are some of the most beautiful and courageous people I have ever met.

Community & Connection

I work with heart driven women just like you, who want to create a better life for themselves and their families.

You can dive straight in and check out the  THE REIGNITE PROGRAM, created by a mama of a beautiful warrior with additional needs, especially for mama’s of children with additional needs.

You can explore The Miracle Project an inspiring blog of women from all around the world sharing their journey.

As an International Speaker, Life Coach, Emcee and Advocate, I’m here to make a positive impact.

Together, we rise.

I’m based in Melbourne, Australia but travel the world.

Natalie

As Seen In

Disability. Brain-Injury. Special Needs. – it all weaves into the entire family’s journey.

My Story

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Every expectant mother has that little sliver of fear as she clasps her hands over her belly, hoping and praying that her baby will be born healthy.

I was no different and when I had a scan and they said they couldn’t find her foot and I needed to come back for another scan in a few days, my heart was in my throat as I instantly imagined the worst.

If only I knew then what was to come…

Read More

“The last of human freedoms – the ability to choose one’s attitude in a given set of circumstances.”

Vicktor E. Frankl

Latest Features

Soulful Support For Mums

What Rare Means To Us

February 28th, 2019|0 Comments

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 [...]

What if?

November 24th, 2018|0 Comments

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 [...]

The Adaptive Equipment Journey

November 6th, 2018|0 Comments

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 [...]

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