
Born with a hole in her heart, Baby Kendreya thrives thanks to heroes and angels
Compassionate doctors and other NGOs stepped in, ensuring urgent care and transportation before the risks increased at nine months.
Now healthy and thriving, her grateful parents celebrate her second chance at life.
Two Durban parents, Paroosha Naidoo and Kevin Pillay, are grateful to the guardian angels who helped their baby Kendreya undergo the heart surgery that saved her life.
Kendreya was born in October last year to the happy parents from Chatsworth, but their joy was replaced with anxiety in those first few weeks as they watched her struggling to breathe.
'Her stomach would sink with every breath, like her little body was working overtime just to breathe,' Kevin said.
Kevin would drive Paroosha and Kendreya between hospital appointments and tests, sleep in the car while mother and baby waited to see doctors and juggle his night shifts.
Baby Kendreya was then diagnosed with atrioventricular septal defect, or AVSD - a congenital heart defect. She had a large hole in the heart, which affected her blood flow.
'Her heart couldn't pump properly, causing fluid to build up in her lungs. That's why her tummy caved in when she tried to breathe,' said Kevin.
READ | Shumi the pangolin's incredible journey from poaching victim to wildlife freedom
In a race against time, surgery needed to happen before nine months, otherwise the risks would increase. An appointment scheduled for March this year fell through due to resource constraints at Inkosi Albert Luthuli Hospital, and it was unclear when another surgery could be scheduled.
The two parents prayed for a miracle. In stepped a team of guardian angel doctors who are prepared for such scenarios.
'A light in a dark time'
The parents searched for help and found Dr Wilhelm Lichtenberg and the Young Hearts Africa Foundation. Since its inception in 2023, the foundation has helped 30 children with the same symptoms that Kendraya was experiencing.
'At first, it felt too good to be true, and we were almost worried it might be a scam. But Dr Lichtenberg responded, asking only for medical records, never money. It was a light in a dark time,' said Paroosha.
As they consulted the foundation, Kendreya's condition worsened. She was fatigued, lost her appetite, and started passing blood.
'Babies with AVSD often experience rapid breathing, difficulty feeding, excessive sweating, and poor weight gain,' said Lichtenberg. 'If left untreated, the extra blood flow can damage the lungs, leading to heart failure.
The timing of surgery is critical. The risks increase after six months because the lungs can suffer irreversible damage from the extra blood flow. Early repair gives babies the best chance to grow and thrive.
Unable to access private healthcare, Lichtenberg ensured that Kendreya would get the surgery she needed in Cape Town.
'When the Young Hearts Africa Foundation reached out about Baby Kendreya's urgent case, the Netcare Foundation and Netcare Christiaan Barnard Memorial Hospital immediately prioritised her AVSD repair,' said Mande Toubkin, Netcare's general manager of trauma, transplant, and corporate social investment.
'There's a huge need for specialised paediatric heart surgeries - they are complex, resource-heavy, and absolutely essential for giving these children a fighting chance.'
Images suppled by MNA on behalf of Netcare.
'Holding her for the first time after surgery'
Young Hearts Africa reached out to Wings and Wishes. They help remove transport barriers for disadvantaged children to get medical treatment and joined the effort by providing the necessary airline flights for Baby Kendreya and her parents.
And so, Baby Kendreya received life-changing help in the nick of time during a surgery in Cape Town thanks to the help of guardian angel doctors and NGOs - an emotional journey for the grateful parents.
'Dr Lichtenberg and Dr Vosloo are our heroes, our angels - our only option, and we can't express our appreciation to the Netcare Foundation, the Young Hearts Africa Foundation, and everyone involved,' the grateful parents said.
'She has healed so quickly and been so active since the operation. Kendreya is fascinated by the world around her,' Paroosha added.
Now back home in Durban, Kendreya's family is filled with gratitude for the care and support that saved their daughter's life.
'As parents, you experience every emotion imaginable, but holding her for the first time after surgery, feeding her, and seeing her fight back made it all worthwhile,' said mom Paroosha.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Medscape
an hour ago
- Medscape
Can Treating Siblings Aid Azithromycin's Effect on Infants?
TOPLINE: Mass administration of azithromycin to both infants aged 1-11 months and children aged 12-59 months reduced infant mortality compared with treating infants alone. Although the interaction effect was not statistically significant, mortality appeared to be lower among infants living with treated older siblings. METHODOLOGY: In this secondary analysis of a cluster-randomized trial, researchers evaluated whether mass azithromycin administration reduced infant mortality and examined how that benefit varied when an older sibling in the same household also received azithromycin. They included 98,969 infants aged 1-11 months with a minimum weight of 3 kg and no known macrolide allergies who received biannual 20-mg/kg doses of oral azithromycin or placebo from November 2020 to July 2023 in Niger. Participants were divided into three arms: infants and children aged 1-59 months on azithromycin (child arm), infants aged 1-11 months on azithromycin and children aged 12-59 months on placebo (infant arm), and children aged 1-59 months on placebo (placebo arm). The primary outcome was the community-level rate of all-cause mortality among infants aged 1-11 months after 2 years of azithromycin distribution, stratified by the presence or absence of older siblings (12-59 months) in the household. TAKEAWAY: The mortality rate of infants per 1000 person-years at risk was lowest in the child arm at 18.5 deaths (95% CI, 16.7-20.4) compared with 22.3 deaths (95% CI, 20.0-24.7) in the infant arm and 23.9 deaths (95% CI, 21.6-26.2) in the placebo arm. In communities receiving azithromycin vs placebo, mortality among infants aged 1-11 months declined by 23% (95% CI, 11%-33%). Of this reduction, 23.5% (95% CI, 1.2%-72.7%) was attributable to treating infants directly, while 76.5% (95% CI, 27.3%-98.8%) resulted from also treating children aged 12-59 months. Among infants with older siblings, the incidence rate ratio comparing child and infant arms was 0.78 (95% CI, 0.65-0.93), while it was 0.91 (95% CI, 0.73-1.15) for those without siblings (P for interaction = .26). IN PRACTICE: 'The main trial results support implementation of azithromycin MDA [mass drug administration] to infants and children aged 1-59 months to achieve the greatest benefit. The analyses presented herein further support this conclusion and suggest that the spillover mechanism may include treating older siblings,' the authors wrote. SOURCE: This study was led by Ahmed M. Arzika, MPH, Centre de Recherche et d'Intervention en Santé Publique, Birni N'Gaoure, Niger. It was published online on July 10, 2025, in JAMA Network Open. LIMITATIONS: Limited statistical power restricted the detection of interaction effects in subgroup analyses. Even in high ‐ mortality settings, deaths remain too infrequent to reveal significant differences between subgroups. The large simple trial design prevented the evaluation of cause-specific mortality. Thus, analysis of specific causes of death likely associated with spillover effects of the mass administration of azithromycin could not be determined. DISCLOSURES: This study received support from the Bill & Melinda Gates Foundation and National Institute of Allergy and Infectious Diseases of the National Institutes of Health. Pfizer Inc donated the azithromycin and placebo used in the trial. A few authors reported receiving grants from the funding organization. This article was created using several editorial tools, including AI, as part of the process. Human editors reviewed this content before publication.


Washington Post
an hour ago
- Washington Post
Everybody wants your 5-star rating. Even your ear surgeon.
The stitches in Cory Lonas's head were fresh. His mind felt loopy coming down from anesthesia; he couldn't hear. It had only been 24 hours since Lonas underwent cochlear implant surgery when, through bleary eyes, the 39-year-old saw an email come in on his phone. How would he rate his experience at the hospital? How were his interactions with the doctors, the staff, the food? Would he recommend the hospital to a friend?


Medscape
4 hours ago
- Medscape
ART-Treated Children Remain at Risk for Vascular Disease
Children born with HIV and treated early with antiretroviral therapy (ART) continued to show elevated immune markers in adolescence, based on data presented at the International AIDS Society Conference on HIV Science. Although universal early ART has improved long-term health outcomes for children with perinatal HIV, data on long-term effects of ART exposure are limited, wrote Claire Davies, PhD, a researcher at Stellenbosch University, Cape Town, South Africa, and colleagues. 'Prior to 2008-2009, antiretroviral therapy for children living with perinatal HIV was withheld until HIV disease was advanced,' Davies said in an interview. 'The reasoning was that ART, having been developed from cancer chemotherapy, had significant toxicity and it was thought best to spare infants from those toxicities until benefit clearly outweighed risk,' she said. In 2009, the landmark CHER trial showed that apparently well infants living with HIV who were given empiric ART soon after birth had approximately 400% better survival compared with those with no intervention. 'Immediate worldwide implementation of this intervention has led to emergence of an entirely new disease profile: Since 2009, early initiation of ART has been standard-of-care for perinatally-infected infants,' Davies told Medscape Medical News . 'Since early-treated children living with HIV [CHIV] would then be spared from repeated opportunistic infections and years of ongoing HIV replication, it was hoped that they would also be spared from the enormous chronic inflammation that typically accompanied those infections,' she said. Chronic inflammation that persists over years is a powerful driver of cardiovascular disease (CVD), which leads to premature strokes and heart attacks in adulthood, she emphasized. The researchers reviewed data from 185 individuals aged 7-16 years who were part of a study of early ART in South Africa. The study population included 65 CHIV and 118 HIV-unexposed children who served as control individuals. The CHIV began ART within 3 months of birth and were deemed clinically well at the time of blood testing for biomarkers. The participants underwent a median of two measures of blood serum 4 years apart, yielding a total of 321 observations; 26 biomarkers were measured. After adjusting for multiple variables, the CHIV group had significantly higher levels of C-reactive protein, soluble CD14 (a marker of monocyte activation), and vascular endothelial growth factor than the unexposed children. The researchers also found specific effects in different age groups. Levels of Monocyte chemoattractant protein-1 (MCP-1), interleukin 6, and P-selectin in CHIV aged 6-8 years were significantly higher than matched control individuals, whereas MCP-1 was significantly higher in the CHIV group aged 13-16 years than control individuals. No other significant differences in biomarkers appeared between the groups. When the current study began, it was entirely unknown whether early-treated children living with HIV would suffer from the same chronic inflammation and consequent premature CVD, or to what extent early lifelong ART might prevent CVD in these children as they grew, Davies told Medscape Medical News . 'We hoped that by removing ongoing HIV replication and opportunistic infections, children living with HIV would be spared from the chronic inflammation that drives premature CVD in early adulthood,' she said. The researchers had hoped to find that early ART had a greater impact on preventing chronic inflammation, but the results showed otherwise, said Davies. The data should alert clinicians to the increased risk for premature strokes and heart attacks in adulthood for children treated early with ART, she said. For the study population treated with ART, their chronic inflammation can no longer be a result of ongoing HIV replication and opportunistic infections because these factors are no longer present, Davies told Medscape Medical News . 'We now need to understand what is driving their ongoing chronic inflammation so that we can find treatments to help reduce it, and in so doing, reduce their risk of premature strokes and heart attacks in adulthood,' she said. ART Alone is Not Enough 'While early ART dramatically improves long-term outcomes for children born with perinatal HIV, it remains unclear whether early ART alters the long-term inflammatory and immune activation profile,' said Jason E. Zucker, MD, an assistant professor of medicine and infectious diseases specialist at Columbia University Irving Medical Center, New York City, in an interview. 'These profiles are critical, as they are linked to future risk of noncommunicable diseases, such as cardiovascular and metabolic disorders,' said Zucker, who was not involved in the study. The current study fills a key gap by examining longitudinal biomarker data to assess persistent immune dysregulation in early treated children compared with uninfected control individuals, he said. Zucker said he was slightly surprised by the findings of extensive immune activation and elevated biomarkers, into adolescence, especially those associated with monocyte activation. 'The key takeaway is that early ART alone may not fully normalize immune activation in perinatally HIV-infected children,' he said. 'The data underscore the need for long-term monitoring and potentially adjunctive interventions to mitigate inflammation and reduce future disease risk, even among virologically suppressed youth,' he added. Some limitations of the study include the modest sample size and lack of any long-term clinical outcomes, Zucker told Medscape Medical News . 'Biomarker assessments, while robust, do not confirm clinical endpoints such as actual cardiovascular events, and future research should track these cohorts longitudinally into adulthood to determine whether the observed immune profiles translate into actual disease, and explore therapeutic strategies,' he said.