Geelong and Surfcoast Doula Services

Geelong and Surfcoast Doula Services Geelong and Surfcoast Doula Services has been providing experienced and certified doulas to the greater Geelong area since 2010.

10/04/2026

This tiny beautiful goddess Sarah Bradford supported by her partner John, birthed all 9lb3oz of her beautiful baby recently while her daughter's watched on... This is an incredible gift to pass onto our daughters & son's.
Women can do amazing things, especially when they are at home, in their own space, doing their own thing, in their own sweet time. Misty and I were blessed to both hold space for her and her family until she needed more, more of our hands, our hearts, our words through the tough moments. 🙏
Thanks Misty Barth for such precious footage.

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These women - on this International Women's Day I want to acknowledge these inspiring legends that are the team. They go...
08/03/2026

These women - on this International Women's Day I want to acknowledge these inspiring legends that are the team. They go on call for weeks on end, miss out on family birthdays, celebrations and school concerts, to disappear in the middle of the night to witness mummas unfurl on the hardest and most empowered days, moments and time of their lives... What do we do? We hug, hold, massage, dance, breathe, build comfort, create labour stations, feed, supply support tools, fill baths, empty baths, wipe tears & cry, encourage, empower, hold space, in/out of the shower, heat packs, accupressure, aromatherapy, provide herbs, and not just to the birthing mums.... And often all of this in the first hour & repeat until that babe is in their arms... This can be for 6hrs and sometimes it's over 30hrs. We are honoured to share such intimate space with families and love what we do so families can do what they do!
Pictured is Erin Mirkovic Wilson , myself, Misty Barth & Penny Morcombe

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06/03/2026

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March is Pregnancy After Loss Awareness Month, a time set aside to hold space for families who are navigating the tender, complicated path of pregnancy after miscarriage, stillbirth, or other perinatal loss. It’s a month to gently acknowledge the reality that joy and grief can exist side by side… and that both deserve to be seen and supported. 🫶🏻

For many parents, becoming pregnant again after loss is not simply a “fresh start.” It is a step forward while still carrying the memory of a child who is deeply loved and missed. Studies show that 50–80% of women become pregnant again within 12–18 months following a perinatal loss, statistics don’t capture the emotional weight of that journey. Behind each number is a family learning how to hope again while protecting their an already broken heart.

Pregnancy after loss can feel like walking a delicate line between fear and hope. There may be moments of deep happiness and excitement, followed by waves of anxiety that can blindside from nowhere. Early appointments can feel overwhelming. Milestones may bring both relief and renewed worry. Even sharing the news with others can feel complicated. đź’”

If you are pregnant after loss, it’s important to know that whatever you are feeling is valid. The fear. The joy. The hesitation. The love. The grief that still lingers. Emotions often shift throughout the pregnancy… intense in the early weeks for some, easing over time for others but there is no “right” way to move through this experience.

This month, we honour the strength it takes to try again, the courage it takes to hope again, and the love that connects every part of the journey. By speaking openly and offering compassionate support, we can help ensure that no parent feels alone while navigating pregnancy and parenting after loss. ✨🫶🏻

18/02/2026

We talk about the baby blues like they’re just “a few tears.”

But within days of giving birth, a woman experiences one of the most dramatic hormonal shifts a human body can go through.

Estrogen and progesterone, hormones that were sky high during pregnancy plummet rapidly.

That drop doesn’t just affect mood.

It affects:
• Sleep
• Anxiety levels
• Temperature regulation
• Tearfulness
• Mental clarity
• Emotional sensitivity

She’s not being dramatic.
She’s not “too much.”
She’s not unstable.

Her body just went from pregnant to postpartum in a matter of hours.

And while she’s navigating that crash, she’s also:
Bleeding.
Healing.

Breastfeeding a newborn.
Running on broken sleep.

So no, she doesn’t need criticism.

She needs protection.
She needs softness.
She needs someone to hold her the way she’s holding everyone else.

If you know a postpartum mama right now, please love her a little harder 🤍 I beg you 🙏🏻

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18/02/2026

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She slept on a folding bed next to a dying baby for four days straight—and changed medicine forever.
For most of human history, if you were born too early, you died. There was no other outcome. No fight to be had. Premature babies would arrive, struggle for air, and within hours, simply stop breathing. Doctors wrapped them in blankets. Nurses held them. But no one could give them the one thing they desperately needed: a way to breathe.
The killer was called Hyaline Membrane Disease. In tiny, underdeveloped lungs, the air sacs lack a crucial substance called surfactant. Without it, the lungs collapse after every breath. The baby gasps. The chest heaves. The skin turns blue. Eventually, the body exhausts itself and gives up.
Even in the 1950s, in the best hospitals in America, doctors could do almost nothing. There were no neonatal intensive care units. No ventilators small enough for a two-pound body. Oxygen alone wasn't enough. Medical staff watched baby after baby die, knowing they lacked the tools to stop it. Most doctors accepted it as tragedy, not emergency. Premature birth was simply considered unsurvivable.
One woman refused to believe that.
Dr. Mildred Stahlman was a pediatrician at Vanderbilt University in Nashville. She had trained in Sweden under world-class researchers and returned with an audacious idea: that premature babies with failing lungs could be saved if someone could breathe for them until their lungs matured.
Everyone thought it was impossible.
Through a research grant, Stahlman set up a laboratory next to the hospital nursery. She obtained a prototype negative-pressure ventilator—the same type used for polio patients—but miniaturized for infants. She pioneered the use of arterial blood gas monitoring in newborns, inserting catheters to measure oxygen levels in real time so she could adjust the machine moment by moment.
But no one had ever successfully kept a premature baby alive this way. There was no protocol. No manual. No proof it could work.
Then came Halloween night, 1961.
Martha Humphreys was born two months early. Her lungs were failing. She had severe Hyaline Membrane Disease. Under every known standard of care, she would die within days.
But Martha's father was a medical student at Vanderbilt. He and his wife understood the risks—and the possibility. They gave Dr. Stahlman permission to try.
Martha was placed in the tiny ventilator. Dr. Stahlman set up a folding bed in the lab and refused to leave. For four days and four nights, she stayed at that baby's side. She monitored blood gases. She adjusted pressures. She watched every single breath the machine delivered to those fragile, collapsing lungs.
On the fifth day, Martha Humphreys was weaned off the ventilator.
She was breathing on her own.
She survived.
That moment didn't just save one baby. It created an entirely new field of medicine. Dr. Stahlman had proven that mechanical ventilation could save premature infants. What the world had considered impossible was now real.
From that single success, she built one of the first modern Neonatal Intensive Care Units in the world. For twenty-five years, she directed the Vanderbilt NICU. She trained over eighty specialists from more than twenty countries. She developed mobile transport systems to bring critically ill babies to equipped hospitals. She became president of the American Pediatric Society and received its highest honor.
And Martha Humphreys? She grew up healthy. She became a registered nurse. And she spent her entire career working in the very same NICU that saved her life.
Dr. Stahlman never liked being called a pioneer. "Everything is built on the backs of somebody else," she said. She was a small woman with sharp blue eyes, gray hair in a bun, and legendary devotion to her patients. Those who worked with her said she had "the courage of a lioness."
She also understood that medicine alone wasn't enough. She advocated fiercely for education, housing, and healthcare access, knowing that preventing prematurity mattered just as much as treating it.
Dr. Mildred Stahlman turned 100 years old in July 2022. She passed away in June 2024, having devoted her entire life to giving the smallest, most fragile human beings the one thing they couldn't give themselves.
A breath.
Today, hundreds of thousands of premature babies survive every year because of the work that began with one woman, one machine, and one baby girl born too soon on a Halloween night in Nashville.
Every NICU in every hospital in the world carries her legacy: that no life is too small to fight for, and that the right person with the right courage can change what the world believes is possible.

15/02/2026

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Belmont, VIC
3216

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