by Zane Groenewald | Dec 4, 2025 | Campaign, Featured
Photo above: John and Judy, and Great Dane, Charles.
Marlands, Germiston, Johannesburg – What began with a tiny, dying puppy on a doorstep has grown into one of the East Rand’s most heartfelt grassroots rescue initiatives. Today, Recycling for Animal Welfare (RAW) — a registered non-profit organisation — is asking the public for support to keep their rescue work going alongside the recycling efforts they have carried out faithfully for years.
Paul: The Puppy Who Started It All
Eight years ago, a freezing, limp puppy later named Paul arrived at the home of Judy Knox (54) and her partner John Ancill (60) in Marlands, Germiston. Severely ill and minutes from death, Paul was rushed to the vet — who later said he would not have survived had he arrived even an hour later.
For months, Paul fought for his life, surviving Parvo, tick bite fever, and gastro. Judy and John stayed beside him through every drip, every setback, every shaky breath.
Against all odds, Paul survived. And when he finally recovered enough to be adopted, they both knew he was already home.
Paul became RAW’s very first rescue — the little soul whose courage shaped the heart and purpose of the organisation.
On 18 July 2025, Paul passed away from liver cancer after eight deeply cherished years. His loss was heartbreaking, but his legacy lives on in every animal RAW helps today.
How RAW Was Born — Turning Recyclables Into Lifesaving Care
In 2017, Judy and John wanted a sustainable and dignified way to fund veterinary care for animals in crisis. They had never wanted to ask for donations — they preferred to earn the money needed to help each animal.
So, after their full-time day jobs and every Saturday, they began collecting glass and cardboard across Johannesburg’s East Rand — Germiston, Boksburg, Benoni, Edenvale, Kempton Park, and wherever they were needed. Armed with their small Hyundai i10, they filled it to the roof every week.
Their first load earned R50, but it confirmed that even the smallest beginning could grow into something meaningful.
With the help of a local vet and their small team — Monique (46) and Patrick (77), lovingly known as “G-Dad” — RAW has since recycled more than 750 tons of glass and 75 tons of cardboard. Every cent earned goes directly toward sterilisations, vaccinations, emergency treatment, and rehabilitation.
A Growing Need — And Why They’re Asking for Help for the First Time
Despite their enormous effort, recycling yields very little:
- 50c per kg of glass
- R1,20 per kg of cardboard
- 2–3 weeks of collecting = about R1,200
Animals continue arriving every week — frightened, abandoned, injured, or desperately ill — needing urgent veterinary care. RAW’s vet bill now exceeds R50,000, and their account is on hold.
For the first time since RAW began, Judy and John have launched a BackaBuddy fundraising campaign to help cover the growing gap between what recycling brings in and what the animals urgently need.
The campaign will help top up what they already earn through recycling, making sure the vet bill is covered even when emergencies arrive faster than the glass and cardboard can.
Campaign Link: https://www.backabuddy.co.za/campaign/support-recycling-for-animal-welfare
This doesn’t replace their hard-earned efforts — they will still be out collecting after work and every Saturday, just as they’ve done for years.
The campaign simply gives their rescue work a little extra support, so no animal has to be turned away.
So far, almost R10 000, has been raised from 18 donors, a touching beginning — but far more support is needed to reopen their vet account and continue their rescue work.
In Paul’s Honour — RAW Launches Their Monthly Giving Campaign
The BackaBuddy campaign is dedicated to Paul — the brave little dog whose survival inspired RAW’s mission.
Through monthly supporters, Judy and John hope Paul’s legacy will continue helping other animals get the second chance he fought so hard for.
Call to Action: Help Keep Paul’s Legacy Alive
RAW is asking the public to stand with them in honour of the puppy who started everything.
You can help by:
- Making a once-off donation
- Becoming a monthly supporter — the most powerful way to ensure RAW never has to say “no” to an animal in crisis
“Every rand goes straight to the animals — their treatment, their healing, their safety,” Judy says. “We will never stop recycling. This campaign simply helps us bridge the gap so we can keep saving lives, just like we saved Paul.”
Support RAW here: https://www.backabuddy.co.za/campaign/support-recycling-for-animal-welfare
by Tessa Van Rensberg | Dec 3, 2025 | Campaign, Featured
Benoni, South Africa — Two young siblings, 21-month-old Sadie Krause and her six-year-old brother Jesse, have been diagnosed with one of the world’s rarest immune disorders, DOCK8 Immunodeficiency Syndrome. With the only curative treatment available overseas and costing up to $1million per child, the family is urgently appealing for public support to save their lives.
Sadie and Jesse are among fewer than 300 known DOCK8 cases globally, and specialists believe their diagnoses may be among the first formally identified in South Africa.
“When Sadie and Jesse were diagnosed with DOCK8 Immunodeficiency Syndrome, we discovered just how rare this disease truly is, and how little information exists, especially here in South Africa,” says Dominique Nelson-Esch, aunt of Sadie and Jesse.
“With only 250–300 known cases worldwide, DOCK8 is one of the rarest primary immunodeficiencies in the world. As a family, we have spent months searching for answers, consulting countless doctors, and piecing together information that often wasn’t available in one place.”
Understanding DOCK8
DOCK8 Deficiency is caused by biallelic mutations in the DOCK8 gene — Dedicator of Cytokinesis 8 — responsible for helping immune cells move, adapt, and communicate properly. When the gene malfunctions, the immune system becomes severely compromised.
Children with DOCK8 face:
- Persistent skin and lung infections
- Chronic viral illness
- Severe eczema and allergies
- Higher cancer risk
- Extreme vulnerability to everyday germs
For Sadie and Jesse, this means a daily routine of:
- Weekly immunoglobulin infusions
- Ongoing antiviral and antibiotic medication
- Bleach baths for viral skin disease
- Regular hospital visits
- Strict isolation when anyone is ill
- Home-schooling for safety
- Cancelled outings, birthdays and gatherings
Paediatric pulmonologist and clinical immunologist Dr Ashley C. Jeevarathnum, who is overseeing their care, explains:
“Children with DOCK8 do not have a fully functioning immune system. They are highly vulnerable to severe infections, chronic viral skin disease, progressive lung damage, and certain cancers at a young age. Without definitive treatment, the condition is fatal.”
Even with so much happening around them, Jesse remains kind and watchful, and Sadie’s laughter still fills the room.
A Diagnosis That Changed Everything
Parents Lee-Ann and Clayton spent years seeking answers as their children battled severe infections, skin complications, and unexplained illnesses.
When the diagnosis finally came, it brought clarity — but also the devastating reality that South Africa cannot provide the only lifesaving treatment their children need.
To help manage the overwhelming medical and administrative demands, the children’s aunts —
Dominique, sister of Clayton and Claire, sister of Lee-Ann established the Sadie & Jesse DOCK8 Foundation.
“It has taken so many childhood moments,” says Dominique. “And yet Jesse remains a gentle, protective big brother, and Sadie’s giggles still light up the room even on the hardest days. Their spirits remind us what’s at stake — the chance to grow up, to dream, and to live the childhood every child deserves.”
The Only Lifesaving Treatment — Overseas
The only curative treatment for DOCK8 is an allogeneic haematopoietic stem cell transplant (HSCT) — one of the most complex medical procedures in the world.
Due to the condition’s severe rarity, South Africa does not have a formalised DOCK8 transplant programme, and the procedure must be performed at international centres with proven DOCK8 expertise. Most successful transplants have taken place in the United States and Europe, with survival rates of 80–85% when completed early.
The cost, however, is staggering:
R20 million to R30 million per child
“When we learned about the astronomical costs per child, it was terrifying,” says Dominique. “No family can shoulder that kind of cost alone. Asking the public for help wasn’t an easy decision, but it felt like the only way forward and to give the kids a real chance at life.”
The family’s medical scheme has been vague about what they will cover. To date, more than R120,000 has already been paid out-of-pocket just to stabilise the children.
“This is not experimental or optional — in the correct hands, HSCT is curative,” Dr Jeevarathnum emphasises. “The diagnosis is real, the medical situation is urgent, and the funds requested are for proven, lifesaving therapy.”
Community Support Grows
In response to the overwhelming financial burden, Dominique and Claire launched a BackaBuddy campaign that has gained remarkable early momentum.
More than 300 donors have already contributed over R300,000, sending messages of love, encouragement, and prayer.
“With grateful hearts — to everyone who has followed Jesse and Sadie’s journey, shared their story, sent words of encouragement, or given so generously, thank you,” says the family. “Your love and support carry this family through the hardest days.”
Why Every Donation Matters
The financial need extends far beyond the transplant itself, with ongoing costs for weekly immunoglobulin, specialist visits, medication, home-schooling, medical supplies, transport, counselling, and many hidden day-to-day expenses.
“It all adds up,” the family explains. “Every contribution brings them one step closer to the lifesaving transplants they urgently need.”
The public is invited to help Sadie and Jesse receive the urgent medical care they need by donating here:
https://www.backabuddy.co.za/campaign/sadie-jesse-krauses-stem-cell-transplants
All funds go directly toward the children’s treatment and long-term care
by Simbulele Jezile | Nov 25, 2025 | Campaign, Featured
In just one year, KwaZulu Natal siblings Charity “Shaz” Gumede (31) and her brother Sabelo “Sabz” (30) have faced two life-threatening diagnoses. Shaz survived a near-fatal case of Stevens-Johnson Syndrome in 2024, and Sabz was diagnosed with Stage 3 Choriocarcinoma in 2025. With their mother leaving her job to care for both children full-time, the Gumede family medical crowdfunding campaign has been launched on BackaBuddy to help appeal to cover mounting medical costs and keep their household afloat.
Despite the fear and financial strain, the siblings continue to meet each challenge with a disarming mix of courage, humour and hope — determined to turn their darkest year into a story of survival, family, and quiet resilience.
Two Siblings, Two Rare Diagnoses and One Remarkable Bond
Despite experiencing two extremely rare medical crises within months of each other, the Gumede siblings have chosen a path defined not by fear, but by connection. Their home remains a place of warmth, laughter and mutual support — a testament to their deep bond as they navigate uncertainty together.
“We’ve been through a lot, yes,” says Shaz, “but we’re choosing to focus on the fact that we’re still here. We’re still laughing. We’re still us.”
“This year didn’t go according to plan,” adds her brother, “but we’re trying to meet it with as much heart as we can.”
Shaz’s Story: A 1% Chance at Life, and a Return to Herself
When beautician Shaz developed Stevens-Johnson Syndrome in 2024, doctors made it clear that survival was unlikely. The rare and catastrophic allergic reaction burned 75% of her skin, attacked her lungs and organs, destroyed her nails and hair, and left her blind.
She spent eight weeks in a coma while her mother, Nombuso, left her job and sat by her bedside every single day, praying, tending to her wounds and refusing to leave her child alone.
“When I woke up, I couldn’t walk, I couldn’t see, and I had no memory of what happened,” Shaz shares. “It felt like being born into a nightmare… but being alive at all was a miracle.”
Today, she lives with partial sight — about 5% vision in one eye and roughly 35% in the other. Her skin remains fragile, her nails never grew back, and her respiratory and digestive systems were permanently affected. Despite this, Shaz speaks about her recovery with gratitude and gentleness, not grief.
“I survived,” she says simply. “And that’s something worth celebrating.”
As part of rebuilding her physical wellbeing, she now requires medically essential procedures to restore her nails and teeth, along with lifelong specialised dermatological treatment to support her skin and comfort. These treatments form part of what will help her feel whole again.
Sabz’s Story: A Young Actor Confronts Cancer With Grace
Just as the family was adjusting to Shaz’s new needs, her brother began noticing unusual symptoms. After months of tests and consultations, he was diagnosed with Stage 3 Choriocarcinoma, a rare and aggressive germ-cell cancer.
His first chemotherapy protocol initially brought hope, but soon stopped responding. He has since begun a more intensive treatment plan that brings both physical strain and financial pressure. As an actor, his diagnosis adds another layer of challenge, as the visible effects of the tumour and the side effects of treatment have halted his ability to work.
“There are hard days, of course,” he says. “But I watched my sister face something unimaginable, and she showed me what fighting looks like. So now it’s my turn to fight.”
The ongoing co-payments for his treatment continue to rise, and his future healthcare needs remain open-ended.
A Mother’s Steadfast Love
At the heart of the family is their mother, Nombuso, who has shown quiet strength in every chapter. She left her job the moment her daughter fell ill, and months later found herself travelling again to support her son through cancer treatment. She manages medication schedules, hospital visits and emotional care with unwavering calm.
“She’s our hero,” says Shaz.
“She’s the strongest person we know,” adds Sabz.
Her constant presence has been the family’s anchor, but it has also meant that, for many months, the household has had a limited source of income.
Why the Family Needs Help
The Gumede family is now trying to balance two rare medical conditions, ongoing hospital visits, reconstruction needs, co-payments and everyday living costs without any income. Their medical aid has supported them as far as possible, but shortfalls, specialised treatments and the realities of day-to-day life have created financial pressure beyond what any family could manage alone.
To keep the siblings’ medical journeys on track and maintain stability at home, the family has launched a verified BackaBuddy campaign with a goal of R800,000. So far, 260 donors have contributed more than R52,000, sending not only financial support but messages of kindness and encouragement that the family treasures dearly.
“We’re incredibly grateful,” says Shaz. “Each donation, even R20, feels like someone saying: Keep going.”
“This support reminds us that South Africa still cares,” adds her brother. “And that’s something we’ll never forget.”
“We’re scared sometimes,” says Sabz, “but we’re showing up for each other every day. That’s what keeps us going.”
To Support the Gumede Family
Visit their verified BackaBuddy campaign:
https://www.backabuddy.co.za/campaign/surving-steven-johnson-sydrome
by Tessa Van Rensberg | Nov 18, 2025 | Campaign, Featured
Dr Shenaaz Essa, an anaesthesiologist with a special interest in paediatrics at Tygerberg Hospital in Cape Town, has launched a new storybook and colouring pack designed to help young surgical patients navigate their hospital journey with compassion and warmth.
Recognised as one of the Tygerberg Hospital Children’s Trust’s supported programmes, Themba and the Sleep Fairy Project was created to support children who arrive in theatre frightened and unprepared – a designation that will help extend its reach across public hospitals countrywide.
And now, thanks to a heartwarming matched-funding partnership with Gift of the Givers, every act of kindness is doing double the good, ensuring thousands more children walk into surgery feeling braver, calmer, and more supported than ever before.
Helping Children Understand a Scary Process
In many public hospitals, young patients go into surgery without understanding who they will meet, what the equipment does, or why they need anaesthesia. For a child, that uncertainty can be terrifying – leading to heightened anxiety, higher medication needs, and more difficult recoveries.
“Calm children cope better,” says Dr Shenaaz. “When they understand what will happen, their anxiety drops, and their wake-up experience is much smoother.”
The book gently walks children through the surgical process in age-appropriate language, from the moment they arrive in theatre to the moment they return to the ward.
The book explains the steps of surgery in a clear, age-appropriate way, from the moment a child arrives in theatre to the moment they return to the ward.
Included with each book is a box of crayons so children can colour while waiting, a meaningful addition for many young patients who arrive with no personal belongings.
“Some children arrive with no personal belongings at all,” says Dr Shenaaz. “Giving them something of their own restores dignity, sparks creativity, and helps them feel seen.”
Parents who have used the book say their children arrived at hospital noticeably calmer and more confident – proof of just how powerful small acts of kindness can be.
Inspired by What Doctors See Every Day
The project began during Dr Shenaaz’s final month of specialist training. After organising a mural in the recovery area at Tygerberg Hospital, she saw firsthand how a supportive environment can change a child’s entire experience.
Her work in both private and public hospitals revealed the stark contrast between the environments children experience – and how much emotional support is missing in under-resourced settings.
Working with colleagues illustrator Dr Annemie Burke and editors Dr Ramona Ramklass and Dr Graeme Wilson, all experienced anaesthetists, she spent nine months refining the story around the real questions and fears children express before surgery.
But for the team, this project is about more than a book.
“It comes down to dignity and compassion,” says Dr Shenaaz. “Many of these children come from environments where even basic needs aren’t met. Giving them a story, a kind character, or even their own crayons is a reminder that they matter.”
She believes deeply in the biopsychosocial model, emphasising that healing isn’t only physical – mental health, environment, hope, and emotional safety all shape a child’s ability to cope and recover.
“We want to give every child the best chance,” she says. “Sometimes, that begins with the smallest act of kindness.”
Kindness in Action: How One Small Gesture Can Change a Child’s Life
When asked what kindness means to her and her team, Dr Shenaaz offers a deeply human reflection:
“These children are the most vulnerable. A small gesture – a story, a colouring pack, a moment of compassion – can restore dignity and spark hope. Maybe it inspires a future artist, writer, or nurse. Kindness opens up possibilities.”
She recalls being moved by the film Patch Adams as a child – a reminder that the work of healthcare is not only clinical.
“Our impact is not just medical. It’s emotional, psychological, and social. When you give a child comfort, you strengthen every part of them.”
This is the heart of the Sleep Fairy Project – showing children they are valued, cared for, and never alone.
Matched Funding Doubles the Impact
The project’s BackaBuddy campaign has raised R6 000 from 13 donors, toward a R30 000 goal.
Through matched funding by Gift of the Givers:
- R30 supports 2 children
- R300 supports 20 children
- R1 500 supports 100 children
- 1 000 donated books = 2 000 books delivered
The first 2 000 packs are planned for distribution to public hospitals in 2025.
For Dr Shenaaz, seeing this ripple effect has been deeply inspiring.
“I am so privileged to have Gift of the Givers collaborating with us,” she says. “Acts of kindness are contagious. When people see generosity, they want to join in. It releases joy – not just for the giver, but for everyone involved.”
With the festive season approaching, she believes this is the perfect moment for South Africans to uplift children who may receive no other gift at all.
Reaching More Children Across South Africa
To ensure accessibility, the book is being translated into Afrikaans, isiXhosa and isiZulu, with French and Swahili versions underway for broader African use.
“Our goal is simple,” says Dr Shenaaz. “Every child facing surgery deserves to understand what is happening to them.”
Aiming for No Child to Enter Surgery Unprepared
For many young patients, this storybook may be the only emotional support they receive before going under anaesthesia. But with every act of kindness multiplied through matched giving – and with supporters joining hands across the country – that emotional safety net grows stronger.
“A small amount of information can completely change how a child experiences surgery,” says Dr Shenaaz. “Even reducing fear a little is meaningful. And it’s something every child deserves.”
The Sleep Fairy Project proves that kindness doesn’t need to be grand to be powerful.
Sometimes, it looks like a storybook, a crayon, a smile – or a donation that becomes two.
To support the Sleep Fairy Project and help your act of kindness do double the good:
https://www.backabuddy.co.za/campaign/help-themba-and-the-sleep-fairy
Your contribution creates a ripple effect – touching not just one child, but every child reached through matched giving. And that is the true magic of kindness in action.
by Tessa Van Rensberg | Nov 14, 2025 | Campaign, Featured
Tiny Miracles: Jenna-Lee’s Journey of Love, Loss, and Hope This World Prematurity Day
Jenna-Lee La Cock (36) from Randpark Ridge, Gauteng, has lived through a journey that reveals the fragility of life – but also the extraordinary strength of a mother’s love. Her path to motherhood began with fertility struggles, continued through a life-threatening pregnancy complication, and today, she stands as the proud mom of two tiny fighters – Selena and Leona NICU Warriors, whose story brings powerful meaning to World Prematurity Day.
A Long and Hopeful Road to Motherhood
For Jenna-Lee and her husband, Uli, the dream of becoming parents began almost as soon as they married.
“Uli and I met a bit later in life, but from the moment I met him, I knew I wanted to have children with him,” she smiles. “We decided to start trying almost straight away.”
But months passed with no positive test. When Jenna-Lee stopped birth control after years of use, her cycle became irregular. A visit to a fertility clinic uncovered the reasons she feared: adenomyosis and anovulation, meaning her ovaries weren’t releasing eggs.
“It was tough hearing that, but we were determined,” she says.
After five rounds of ovulation stimulation, Jenna-Lee finally received the news they had prayed for – a positive pregnancy test.
“As the doctor moved the probe, we saw what looked like two gestational sacs,” she laughs. “The doctor started laughing, and when we realized – we laughed all the way home. Twins! We felt blessed beyond measure.”
The Day Everything Changed
On 18 August 2025, at 28 weeks and 3 days, Jenna-Lee woke up at 3am in excruciating pain – pain that no medication, no heat, and no shower could ease.
“I got dressed for work but couldn’t get past the agony. I woke Uli in tears, and we rushed to the gynecologist as soon as they opened.”
Blood tests revealed dangerously low platelet levels. Hours later, the diagnosis confirmed their worst fears: HELLP syndrome, a life-threatening pregnancy condition affecting the liver and blood. The only way to save Jenna-Lee and the twins was to deliver immediately.
“I went cold,” she remembers. “I kept thinking, ‘It’s too early – they’re too little.’ I was terrified and heartbroken, but I knew we had no choice.”
Because of the bleeding risk, she couldn’t receive an epidural or spinal block and had to undergo a C-section under general anesthesia.
“I drifted off praying for their safety,” she says softly.
When she woke up in recovery – weak and needing a blood transfusion – she learned that both babies had survived. They were tiny, fragile, and fighting for their lives.
Our Little NICU Warriors
Tiny but fierce, Selena (1.11kg) and Leona (1.1kg) began their journey as NICU warriors.
“Selena needed resuscitation and a ventilator. Leona needed CPAP,” says Jenna-Lee. “Selena later needed PDA surgery and battled pneumonia. Leona survived a life-threatening gut infection. They’re the strongest little humans I know.”
For the first weeks, the beeping of monitors and the hum of ventilators became the soundtrack of their days. Their parents visited daily – sometimes multiple times a day – despite exhaustion, pain, and emotional overload.
Now more than two months later, their journey has taken a new, bittersweet turn.
A Heart in Two Places: The Updated Journey
After more than two months of fighting, the twins’ story reached a painful and beautiful turning point.
On Day 76, baby Selena was discharged, finally strong enough to go home.
“She’s thriving at home,” Jenna-Lee says with a full heart. “Having her home is the biggest blessing.”
Selena at home with mum
But her younger sister is still in the NICU.
On Day 82, Leona continues to struggle with bottle feeding – something she must master before she can be safely discharged.
“We have tried everything – speech therapy, occupational therapy, paediatric advice, NICU nurses’ tricks, and every bottle on the market,” says Jenna-Lee. “We haven’t found the solution yet.”
This emotional split has been devastating.
“It feels like your heart is broken into two pieces, and you cannot have both pieces together yet,” she admits. “Visiting your child, loving her, holding her – and then leaving her behind every evening – it’s a pain I can’t fully describe.”
Keeping their hearts together: a video call from the NICU to home brings comfort and closeness
Meanwhile, the next chapter has begun:
out-patient appointments and therapies, which their medical aid no longer covers because their savings are depleted.
“We want the best care for our girls, but we simply don’t know how we’ll afford what’s still ahead,” she says.
The Weight of Financial Strain
The financial pressure on the family has been immense.
- Their medical aid has disputed parts of Jenna-Lee’s hospital stay.
- Some claims for the twins’ care have been rejected.
- Uli lost his income for August while supporting his family at the hospital daily.
- Jenna-Lee is on maternity leave earning half her salary.
- UIF benefits are uncertain and limited.
- Additional unpaid leave will likely be necessary when both girls are home.
“This experience has brought so much fear and uncertainty, but every moment is worth it for my girls,” she says.
Community Compassion Through Crowdfunding
To help ease the growing financial burden, Jenna-Lee created a BackaBuddy campaign titled “Selena and Leona, Our Little NICU Warriors.”
So far, 15 donors have contributed R27,198 toward their R75,000 goal.
“The kindness we’ve received has lifted us up,” she says. “Prayers, food, messages, donations – every act of love has given us strength to keep going.”
A Message for World Prematurity Day – 17th November
This story unfolds as families around the world honour World Prematurity Day, a day dedicated to raising awareness for babies born too soon and the families who walk the NICU journey.
“Premature birth isn’t something you plan for – it’s something you survive,” says Jenna-Lee. “These babies are miracles. Their strength is unmatched. And parents in the NICU hold their fear, love, and hope all at once.”
Her message to other NICU parents is gentle and full of encouragement:
“It’s okay to have bad days. Don’t hide your struggles. But when you walk into that NICU, try to leave the fear at the door. Focus on love- that’s what your babies need most.”
Motherhood, she says, has changed her life forever.
“Being a mom to my beautiful girls makes me want to hand them the world. My purpose now is to guide them, protect them, and cheer them on as they grow into the strong women I already see in them.”
From a long fertility struggle to the emergency delivery of her twins at 28 weeks, from NICU alarms to first cuddles, from fear to fierce love – Jenna-Lee’s journey is a story of hope and unshakeable strength.
As one daughter settles at home and the other fights to join her, the family continues to rely on the kindness of those who believe in their story.
This World Prematurity Day, their journey reminds us that even the smallest babies can inspire the biggest courage.
To support Jenna-Lee, Uli, and their two little NICU warriors, visit their BackaBuddy campaign link here: https://www.backabuddy.co.za/campaign/selena-and-leona-nicu-warriors
Please share their story – because sometimes, a single share can bring a tiny miracle closer to home.
by Tessa Van Rensberg | Nov 12, 2025 | Campaign, Featured
Photo credits: Gift of the Givers
Building Sustainable Support for Those Who Need It Most
[Cape Town, 11 November 2025] — Gift of the Givers has announced the launch of Team Gift, a new monthly giving programme powered by BackaBuddy, designed to generate steady and sustainable support for their life-saving humanitarian work both locally and across the globe.
In a world where crises strike more often and with growing intensity, from conflict and hunger to drought and disaster, Team Gift gives ordinary South Africans a way to stand together consistently, ensuring no one is left behind when hardship hits.
Hope That Never Fades
Disasters, poverty, and limited access to healthcare continue to affect millions each year. Team Gift was created to provide consistent, reliable support, ensuring that when emergencies arise, help can arrive without delay.
The programme’s sustainable funding model allows Gift of the Givers to respond faster, plan further ahead, and maintain essential care long after initial relief efforts have ended.
From a Riverbed in Mozambique to a Movement of Hope
The inspiration behind Team Gift reaches back to 1990, when a young Dr Imtiaz Sooliman travelled with the Islamic Medical Association to Mozambique during a time of war and drought.
While visiting Nacala Hospital, he noticed two frail children digging into a dry riverbed and drinking the muddy water that seeped through the soil. The image stayed with him, a painful reminder of how easily we take clean water and safety for granted, and how deeply ordinary people can suffer in times of crisis.
Determined to act, Dr Sooliman wrote about what he had witnessed and shared it through phone calls and fax machines, his version of crowdfunding at the time. Within just five days, friends and colleagues helped him raise $100 000 (USD), enough to provide 30 boreholes and vital malaria medication.
That first humanitarian mission became the foundation for Gift of the Givers, proving that when people unite around compassion, extraordinary things happen.
Today, more than three decades later, that same spirit of unity and collective giving lives on through Team Gift, a call for South Africans to join a community of monthly donors ensuring the organisation remains ready to respond whenever and wherever help is needed.
How Team Gift Works
From as little as R50 per month, donors can pledge recurring contributions via BackaBuddy, joining a growing global movement of consistent givers. All donations are pooled and distributed across Gift of the Givers’ key humanitarian projects, supporting food security, sanitation, healthcare, education, disaster response, and more.
Because the funding is stable and recurring, Gift of the Givers can plan ahead, reach further into crisis zones, and sustain life-saving support long after the headlines fade.
To celebrate the spirit of collective compassion, the organisation is calling on supporters around the world to be among the first 1 000 members of Team Gift — a founding community of monthly donors recognised for their commitment to ongoing, measurable impact.
Founding Member Benefits
When individuals join Team Gift as Founding Members, they will gain access to a range of exclusive benefits designed to bring them closer to the organisation’s life-saving work.
Founding Members will receive live, real-time updates through the Team Gift WhatsApp Community, including direct messages, photos, and videos from Gift of the Givers’ relief teams on the ground, offering a rare, behind-the-scenes view of humanitarian action in progress.
Photo credits: Gift of the Givers
Why Now
Unpredictable crises demand reliable compassion. Too often, projects fade once immediate relief ends, leaving communities vulnerable. Team Gift closes that gap, turning one-time generosity into continuous care.
Ronelle Mungaroo, Communications Manager at Gift of the Givers, explains:
“Team Gift represents the heart of our mission — a community of consistent givers who ensure that when the next crisis arrives, we are already prepared. Every monthly donation, no matter the size, helps sustain the lifeline that keeps hope alive.”
Catherine Swanepoel, Chief Growth Officer at BackaBuddy, adds:
“Recurring giving is one of the most powerful ways South Africans can make an impact. Through Team Gift, BackaBuddy is proud to support Gift of the Givers in building a community of everyday heroes who make long-term humanitarian work possible.”
Join Team Gift, Become a Founding Member
Gift of the Givers and BackaBuddy invite South Africans to transform compassion into action by joining Team Gift today.
About Gift of the Givers
Founded in 1992, Gift of the Givers is Africa’s largest disaster response NGO. The organisation has delivered more than R6 billion in humanitarian aid across 47 countries. Its wide-ranging projects include food security, water provision, healthcare, education, and disaster relief, as well as infrastructure improvements in disadvantaged South African schools and rapid local disaster response efforts that strengthen resilience at home and abroad.
The Gift of the Givers Foundation is the largest disaster-response non-governmental organisation of African origin on the African continent. The essence of its presence is to bring hope and restore dignity to the most vulnerable.
About BackaBuddy
BackaBuddy is South Africa’s leading crowdfunding platform, enabling individuals and organisations to raise funds securely for causes they care about.
Since its inception, BackaBuddy has helped raise over R610 million for thousands of campaigns across South Africa — supporting individuals, families, and charities in times of need.
Photo credits: Gift of the Givers
By powering recurring donations, BackaBuddy helps South Africans sustain meaningful change and provide steady support for critical initiatives like Team Gift.
