Parents Express Gratitude in a Heartbeat for the Strength of Stanford’s Pediatric Network
Child celebrates another “heart-aversary” after undergoing open-heart surgery nine years ago at only two months old.
Child celebrates another “heart-aversary” after undergoing open-heart surgery nine years ago at only two months old.
Former patients and their families traveled from all over California to celebrate 50 years of pediatric heart transplants and 35 years of pediatric lung transplants at Stanford.
Woman achieves 40-year anniversary of heart transplant with the same donor heart.
A multispecialty Stanford heart team takes heroic measures to ensure a good outcome for a complex heart transplant.
Knowing what you may be carrying in your genes could literally save your or a family member’s life, including your child’s life.
Elodie was diagnosed with coarctation of the aorta—a rare heart defect that is present at birth but often does not create symptoms until later in life.
Joseph Sanchez-Munoz is special. He has had three transplants—a kidney, liver and heart—at three different points in his life. And now, he’s honoring his donors on a national stage.
One of Santa’s favorite elf received a Berlin Heart, a ventricular assist device (VAD) that acts as an external heart pump attached by tubes, which sustains a child whose heart may be too weak to work on its own. Of course, this version was shrunk down to elf size.
Josh, a 24-year-old from Discovery Bay, California, has Danon disease—a rare genetic condition that weakens muscles in the body, along with the heart.
A rare genetic condition meant a lot of uncertainty for an unborn baby. A multispecialty Stanford Medicine Children’s Health team came together to find answers.
Stanford fetal heart, heart surgery and CVICU teams come together to treat baby with uncommon heart defect.
Stanford Children’s heart doctors perform unifocalization to repair Hayden’s toF with pulmonary atresia and MAPCAs.
It started as a simple persistent wet cough, something Eloise (Ellie) McCloskey’s mom, Aubrey, noticed before spring break of second grade, and it quickly escalated from there. After a week in the hospital and an echocardiogram and tests, the family received the news. Ellie had dilated cardiomyopathy—a disease of the heart muscle—and her heart was slowly failing.
Sky Mattan Gopin is a miracle baby. He went from needing a heart transplant to near-normal heart function in just a few months’ time—without heart surgery.
A Stanford Medicine Children’s Health pediatric heart transplant patient is riding on the Donate Life Rose Parade float to raise awareness for organ donation. This is her story.
Stanford doctors provided specialized heart and ENT follow-up care for preschooler.
Novel Interventions in Children’s Healthcare (NICH) Program supports families of babies with chronic health needs.
Stanford Medicine Children’s Health gives kids with advanced pulmonary hypertension another option besides lung transplant.
Highly specialized Complex Biventricular Reconstruction Program offers exciting alternative for kids with single ventricle hearts.
Elisabeth Martin, MD, and Raji Koppolu, NP, encourage those who are just starting their career to enjoy each step of the journey.
Novel heart-lung procedure gives toddler a chance at a full life. Heart team combines two highly complex specialties in an unique surgical procedure.
Stanford doctors use uncommon practice to save Becker muscular dystrophy patient.
Smallest baby at Stanford Medicine Children’s Health to have heart stent placed for tetralogy of Fallot.
Resilient teen becomes Stanford Medicine Children’s Health’s legendary 500th heart transplant.
COVID-19 is daunting for all parents, but even more so for parents of children with a heart condition.
Family of teen was told she couldn’t be saved, but doctors at Stanford Medicine Children’s Health offered solutions.
Baby born with a very rare condition received expert care culminating with a heart transplant from one of the best heart teams in the country.
A multidisciplinary approach pins down the best care for a complex, rare heart condition.
Quick-witted teen gets treated for a rare genetic heart condition, and arrhythmia by one-of-a-kind cardiology team at Stanford Medicine Children’s Health.
An inquisitive teenager and a determined cardiologist work together to treat a rare type of pediatric arrhythmia which required a different approach.
Even successfully treated congenital heart defects require lifelong monitoring and specialized treatment.
A determined mom fights to find lifesaving treatment for her son’s Williams syndrome.
Treating pediatric ICD patients and their parents through family-centered care.
Innovative Ozaki valve repair technique reverses heart failure and improves functioning.
Patient with rare heart disease thrives thanks to a fighting spirit and a highly knowledgeable care team.
Not the youngest, but possibly the smallest baby in the nation to receive an ICD.
Our hospital’s annual Connecting event provides education and support for patients and families coping with the psychological impacts of heart devices. This year’s well-being theme focused on music.
When Ben Thornton wheeled onto the court for the Bay Area Outreach and Recreation Program’s youth wheelchair basketball West Coast Conference Championship at Stanford, it was a game he was certain to play with heart — the same heart, in fact, that he received at Lucile Packard Children’s Hospital Stanford nearly 12 years ago.
Shaun White, three-time Olympic gold medalist was born with a rare heart condition comprised of four congenital heart defects. Seth Hollander, MD, explains.
A rare heart support helped middle-schooler Ziyan Liu survive to transplant with a single ventricle heart.
For Oakland Raiders cornerback TJ Carrie, Valentine’s Day has a special meaning – it is the anniversary of his open-heart surgery to repair what doctors describe as a one-in-a-million heart defect.
On Saturday, MSNBC aired a two-hour documentary called “Heartbreak: Saving the Binghams”.
David Axelrod, MD attended the Oculus Connect 4 conference where he appeared as an expert on a panel about the applications of VR in healthcare.
Stanford University School of Medicine professors provide a unique boot camp for the next generation of cardiac specialists uses VR to teach complex heart anatomy.
Early Wednesday morning, after 512 days on the transplant wait list, 8-year-old Gage Bingham became the third child in his family to receive a new heart.
Marissa Eustaquio’s case was a mystery. After a strong recovery from heart surgery as a child, she’d been active for years, enjoying dancing, hula, gymnastics, running, and bike-riding.
Joey was born with several congenital heart defects, including a large ventricular septal defect (VSD), severe Ebstein’s Anomaly, and a coarctation of his aorta.
We introduced Hana Yago a few months ago when she was awaiting a heart transplant. Today, the Yago family of San Francisco are one step closer home and leaps and bounds closer to their “new normal.”
On the heels of his preschool graduation, 4-year-old Tyler Briend kicked off his summer vacation by traveling to Washington D.C. to speak with lawmakers about improving health care access for kids like him – patients living with complex medical conditions. Tyler, a patient at Lucile Packard Children’s Hospital Stanford, and his parents made the trip as part of Speak Now for Kids Family Advocacy Day, sponsored by the Children’s Hospital Association (CHA).
An implantable cardioverter defibrillator can help prevent the heart’s electrical system from malfunctioning — and help kids get their lives back.
Giving birth to her first child was a surreal experience for Tawny Aye — and not the way it is for most mothers.
In medicine we often refer to the “natural history of disease”— the normal course that a disease takes in an individual if no treatment occurs. In the case of congenital heart disease, the “natural history” was often death or, at best, survival with significant limitations. Fortunately, that history has changed.
Dateline NBC presented their 2nd national broadcast looking at the personal and medical journey the Binghams have faced, along with the many challenges ahead.
Our hospital expansion, opening in summer 2017, will provide a launching pad for expanding and renovating the current hospital next door. This will include creating room to grow the nationally-ranked Pediatric Heart Center, which will premiere a new and larger space in 2018.
Our implantable cardioverter defibrillator team provides lifesaving support for young people like Reina Villarreal, who suffers from an abnormal heart rhythm.
A Salinas teen faced a heart defect that could lead to sudden death, so our Heart Center leads the way in fixing a defect more common that most doctors realize.
Jordan Ervin, 6, had 26 areas of blood flow blockage from his heart to his lungs. Surgeon Frank Hanley repaired all of the blockages in one marathon surgery.
Baby Jackson Lane’s heart problems were “about as dramatic as you can get.” Famed surgeon Dr. Frank Hanley and his team stepped in to save Jackson’s life. “We are just so lucky that we found Dr. Hanley and that our son fought for his life,” said mom Elyse.
On Sunday, February 8, dozens of patient families with children that have congenital heart disease gathered to celebrate lives saved and CHD Awareness Week (2/7/15 – 2/14/15).
When a child’s heart is not making the right sounds, it can make parents very nervous. Alaina Kipps, MD, pediatric cardiologist in our Heart Center, explains that it’s actually very common and usually not as scary as you would think.
When parents of baby Isla found out at 16 weeks of pregnancy that their baby had a heart defect, atrioventricular septal defect, or AVSD, they traveled from the UK to the US to get help from pediatric surgeon Dr. Frank Hanley and cardiologist Dr. Stafford Grady.
One of the most complex birth defects of the heart—and one of the most challenging to repair—can now be easily understood through a groundbreaking, video-game-like graphic now available on the Stanford Medicine Children’s Health website. It’s the first in a series called “Moving Medicine: An Interactive 3-D Look at Conditions and Treatments.”
Christy Sillman is one of the many adult survivors needing lifelong, specialized treatment for her heart. Sillman brings special insights to her work as the nurse coordinator for the Adult Congenital Heart Program at Stanford.
A Minnesota doctor diagnosed Katie Grace, now 12, with idiopathic pulmonary arterial hypertension “IPAH,” at only 5 years old, and didn’t expect her to live. But the spunky lover of swimming beat the odds of that diagnosis, and received a rare heart-lung transplant in June.
This Wednesday, June 5, at 8 pm, Dateline NBC will present the fascinating story of the Bingham family’s medical journey at Packard Children’s. It should be one of Dateline’s most talked-about programs of the year.
For a child awaiting a heart transplant, the Berlin Heart offers a bridge to life. Packard Children’s helped bring this innovative device to pediatric patients in the United States, and achieved some of the early milestones for the most vulnerable patients.
Karina Gomez’s daughter, Kassaundra, was born in 2002 with a rare and life-threatening cardiac abnormality. At just 2 days old, Packard heart surgeons attached a tiny pacemaker to one of the two lower chambers, or ventricles, of her heart. Five months later, it was replaced it with a more advanced device wired to both ventricles.
In an extremely rare three-day series of transplants in May, three young adults received new hearts at the Children’s Heart Center at Packard Children’s, including an extraordinarily uncommon double-organ heart and liver transplant.