Corey Chambers Real Estate Newsletter July 2026

The California Home
The California Home
Your Referrals Help the Kids! Visit entar.com/kids

Celebrate ‘Your’ Independence… TOO!

Owning real estate, especially your own home, is a sure-fire celebration of independence. In today’s market, many homeowners really want to make a move but are finding themselves in a catch-22 – whether to sell first or buy first. They don’t want to end up getting stuck owning two homes or none at all. I am sure you will join me in saying we can’t blame them. I also believe that you agree that this is true for ourselves and others; homeownership is good for ALL. The more who can buy a home, the more who can sell a home, the more our economy benefits. And as Jimmy Carter said, “To be true to ourselves, we must be true to others.

Fortunately, I have a special program for Home Owners wanting to move and Buyers wanting to buy in Today’s market that turns the tables on this CATCH 22.

Over the last 12+ years of selling real estate, I have been able to develop and successfully implement a program that allows me to guarantee the sale of a property. Yep, you read that right. Actually guarantee in writing the sale of a home. Obviously, a program like this gives sellers GREAT PEACE OF MIND (a true celebration of independence from fear). I guarantee, upfront and in writing, that if their home does not sell at their price and within their time frame – I will step in and buy it myself.

The conditions are simple: the seller and I must agree on the price and possession date. Buyers benefit too because we are able to ensure they get the home they want and back up their purchase with a satisfaction guarantee: if they are not happy with the home, we will buy it back. This obviously is a win-win for all involved.

This is where you come in…

Your friends, neighbors, work associates, and family members who may be considering a move can now do so and celebrate true independence from the fear of getting stuck with two homes or none at all. And remember… Your referrals help the Children… As I share with you each month, we are on a mission to raise $25,000 for the Children’s Hospital Los Angeles Helping Hands Fund. We do this by donating a portion of our income. Children’s does great work in helping kids overcome cancer and other life-threatening diseases. In fact, Kids under their care are 300% more likely to enter into remission IF they can get into the recovery center. BUT the Recovery Center depends on sponsorships and donations to keep rolling. So, YOUR REFERRALS REALLY DO HELP THE KIDS…

Who do you know considering buying or selling a home you could refer to my real estate sales team? Not only will they benefit from our award-winning service, but we donate a portion of our income on every home sale to Children’s Hospital Los Angeles Helping Hands Fund. We also give to CHOC Children’s Hospital Orange County and Valley Children’s Hospital. I want to make it easy to refer your friends, neighbors, associates, or family members considering making a move, so here are your options:

1. You can go to entar.com/kids and enter their contact info on line or forward the link to who you know considering a move.

2. Of course you can always call me direct as well at 213-880-9910.

You and your referrals mean more than ever to my team and me. As we move forward in this new season, please know my team and I are extremely thankful for you and you’re being a special part of our business.

With all my appreciation.

P.S. The story of this young person enclosed may cause you to look at your loved ones differently. It did me. Check it out.

It’s easy to refer those you know considering buying or selling a home. Here are the Options Again:

You can go to entar.com/kids and enter their contact info on line or forward the link to someone you know considering a move.

Call me direct or pass my number on 213-880 9910.

Why I Support Children’s Hospital of Los Angeles

I grew up right here in Los Angeles. Born right nearby at St. Francis Hospital. I remember when I first heard about a young person close to our family suffering from a serious disease and getting treated for that at Children’s Hospital Los Angeles. It was then that I began to pay closer attention to the work they do at that hospital. Since then, I have learned that it is a collection of hard-working health care professionals, most making their home right here in the Los Angeles area, all coming together for a common cause. That cause is to help young people overcome unfortunate health issues that life sometimes throws our way. I also grew up in Orange County, graduation from Cypress High School. Being a Greater Los Angeles Area, California native, I take pride in supporting in any way that I can the good work these people do at Children’s. My team rallies around our annual goal of raising money and donating portions of our income to help Children’s Hospital in its quest to heal young people when they need healing. My team and I are committed to providing outstanding results for buyers and sellers referred to us by our past clients. I have discovered that Children’s Hospital Los Angeles shares similar commitments to their patients. And since their services survive on sponsorships and donations we are happy to contribute and proud to support them.

Living With Hypoplastic Left Heart Syndrome:
Beckett’s Journey

by Caitlin Kryl

When Beckett’s family found out he’d be born with a rare, complex congenital heart defect, they sought a second opinion and expert care at CHLA’s nationally-ranked Heart Institute.

In February of 2023, Lisa walked into her local maternal-fetal medicine center for a follow-up ultrasound.

She was just over 20 weeks pregnant with her second child, a boy. While a recent anatomy scan had hinted at issues with her baby’s heart, she’d been told it could just as easily be nothing.

Instead, she left with news that would change the family’s life forever: Her son had hypoplastic left heart syndrome (HLHS), a rare and life-threatening form of congenital heart disease where the left ventricle—the strongest chamber of the heart—is severely underdeveloped and can’t pump enough oxygen-rich blood into the body.

Essentially, he would be born with half a heart.

Lisa could barely process what she’d just learned. ‘I don’t know what any of this means,’ she thought. ‘Will he even be able to live?’

Finding the answers to her questions felt hopeless—until she and her husband were referred for a second opinionat Children’s Hospital Los Angeles.

While smaller medical centers may rarely see single ventricle heart defects like HLHS, CHLA’s Heart Institute is home to advanced programs designed to give every child with a complex congenital heart condition the best possible chance at a healthy future.

For families who receive a prenatal diagnosis, maternal-fetal medicine experts in the hospital’s Fetal-Maternal Center are often their first point of contact, helping to coordinate comprehensive, streamlined care for expectant mothers and their unborn babies.

Lisa recalls her first phone call with Nurse Care Manager Sheila Perez, RN, BSN: “That was when my perspective flipped. Here was this whole team of people, ready to care for us. I felt like someone was finally hopeful for us.”

Four months after that call, Lisa gave birth to her son Beckett.

Today, Beckett is an energetic 3-year-old—lovingly described as a “spitfire” who roughhouses with his big brother and enjoys any ride he’s tall enough for at Disneyland.

To a stranger, Beckett may look like the average toddler. In reality, he’s already had two open-heart surgeries, spent 149 days in the hospital, and will likely undergo another major procedure in the next year.

While scientific advances have greatly improved what it means to live with HLHS, the condition requires a three-staged surgical reconstruction, regular monitoring, and lifelong multispecialty care to manage complications.

“It’s been a hard journey—there was a time I thought I’d never smile again,” Lisa reflects. “But it’s also been beautiful in a lot of ways. I’m so proud Beckett is my kid.”

Here was this whole team of people, ready to care for us. I felt like someone was finally hopeful for us. — Lisa, mom of Beckett

Before Lisa was referred to CHLA’s Fetal Cardiac Clinic, she’d had a hard time understanding what life for Beckett—and her family—would look like after he was born. Her first appointment with Shuo Wang, MD, a cardiologist in the Fetal Cardiology Program, gave Lisa the perspective she needed.

“I went in not wanting to know any statistics, but actually, hearing about CHLA’s strong surgical volumes and outcomes helped,” says Lisa.

“As a pediatric academic medical center, our team is often the first to know about and implement new medicines, interventions, and tools that greatly improve the management of these conditions,” Dr. Wang explains.

Three statistics stood out to Lisa: CHLA’s cardiothoracic surgeons perform more than 700 surgeries on average each year. One in five of those heart surgery patients are newborns. And more than half of neonatal surgeries are high-complexity cases.

“Hearing those numbers provided a lot of hope going into a scary season,” says Lisa.

“Good counseling for single ventricle heart defects comes from an abundance of experience—and following patients long-term to understand what outcomes look like today,” adds Dr. Wang. “We do our best to empower families with the information they need to make their own decisions around their child’s care.”

As Beckett’s due date grew nearer, Lisa and Beckett’s care team arranged Lisa’s care with a neighboring delivery hospital and helped coordinate the intricate series of events following delivery.

Inside the womb, Beckett’s body was getting all the oxygen-rich blood it needed from the placenta. Oxygenated blood reaches the fetal heart via a special blood vessel, which typically closes on its own once babies are born. Then, the baby’s heart and lungs take over.

But since Beckett didn’t have a healthy left ventricle, his heart wouldn’t be able to support him on its own once that closure happened.

The minutes and seconds after his birth would be life-defining.

A group of subspecialists devised a plan to immediately stabilize the newborn using prostaglandin medication—the same hormone that flows through the placenta—to keep the fetal blood vessel open. This would allow Beckett’s heart to bypass his nonfunctioning left ventricle and force his right ventricle (the heart chamber responsible for pumping blood through the pulmonary artery to the lungs for oxygen) to do the job of two.

This solution was temporary, however: The heart can only sustain this setup for a short period of time before risking exhaustion, unstable blood flow, and even heart failure.

Every child with HLHS is different. Each surgical approach is tailored to their unique anatomic and physiologic needs. — Dr. Cleveland

After receiving detailed imaging of his heart, Beckett moved to the Cardiothoracic Intensive Care Unit (CTICU) where he’d await the first of the three staged reconstruction surgeries: the Norwood procedure.

During the Norwood, surgeons close off the fetal blood vessel and rebuild the heart’s architecture to allow the right ventricle to pump blood to both the lungs and body. Newborn hearts are incredible fragile and small—no bigger than a walnut—which is one of the reasons the Norwood is one of the most complex, high-risk surgeries in existence.

“The fact that cardiothoracic surgeons at CHLA sometimes do multiple Norwood procedures a week was really reassuring for us,” Lisa says.

John David Cleveland, MD, Associate Chief of Cardiothoracic Surgery, explains how the team approaches decision making for each patient: “Any case that’s going into the operating room gets reviewed by our entire institute. A few days before each surgery, 3 to 4 cardiothoracic surgeons and more than 20 cardiologists of different subspecialties meet to align on a plan.”

Typically, the Norwood happens about a week after birth, but Beckett was healthy enough to receive it at two days old. “Every child with HLHS is different. Each surgical approach is tailored to their unique anatomic and physiologic needs,” Dr. Cleveland explains.

The time between each surgery, called the interstage period, can be exceptionally risky—especially after the Norwood.

Even for fragile newborns, years of scientific evidence point to the critical importance of babies spending as much time at home as possible. That’s why the Heart Institute established a specialized interstage monitoring program staffed by three full-time nurse care managers who meet with families regularly to monitor weight and oxygen saturation, while teaching parents how to monitor their child’s vitals at home.

“I was so thankful for the interstage program during that time,” Lisa says. “I called them so often, whenever I had a question.”

Dr. Cleveland explains that the connection between Beckett’s heart and lungs, his pulmonary arteries, were not growing quickly enough to provide his body with the oxygenated blood it needed to function properly.

In the early months of Beckett’s life, he spent more days in the hospital than at home—including a harrowing stay that required interventional cardiologist Darren Berman, MD, to perform an emergency catheterization procedureto open his pulmonary artery.

Not long after, his care team determined he’d need to remain in the hospital until the second of the three procedures: The Glenn.

The objective of the Glenn is to reduce the workload of the heart, connecting one of the body’s largest veins—the superior vena cava—directly to the pulmonary artery.

Because Beckett had undersized pulmonary arteries, he was considered a particularly high-risk patient, Dr. Cleveland explains. This required the surgical team to place additional shunts that would allow more blood to flow into his lungs and encourage his pulmonary arteries to grow.

“Our surgical approach for Beckett is not typical for the Glenn, but it made sense for him,” says Dr. Cleveland.

After additional hospitalizations following his Glenn procedure in January 2024, Beckett has managed to stay healthy out of the hospital.

He regularly meets with Dr. Berman and a multidisciplinary team of CHLA specialists to ensure his heart, brain, and body continue to develop adequately, and to gauge his readiness for the third and final procedure, the Fontan.

For Dr. Cleveland and the Heart Institute team, offering treatments that allow kids like Beckett to enjoy being kids is a major win. Still, they continue to pursue a future where management for HLHS is even safer, less invasive, and more effective.

One way the team is advancing HLHS research is by participating in a global consortium- Opens in a new window exploring the potential of umbilical cord blood to help kids’ hearts grow more effectively after the Glenn procedure.

“While our field has made incredible advances for HLHS, I hope that someday we have a better answer for these kids,” Dr. Cleveland reflects. “We continue to explore opportunities to do so.”

“It’s not an easy or comfortable path for families choosing to move forward with single ventricle surgeries,” he continues, “It is a wonderful testament to grace, mercy, and love imparted to a baby who hasn’t even been born yet.”

Recently, Lisa and her husband Chris teamed up with another CHLA family to raise funds for the hospital during the 10th Annual Walk & Play L.A.- Opens in a new window event.

On their personal fundraising page, Lisa writes:

“Beckett’s journey began before he was even born, when our prenatal care team at CHLA gave us the hope and strength we desperately needed… Since then, CHLA has quite literally saved his life… caring for him through every step with unmatched expertise, compassion, and love.”

“They didn’t just treat Beckett’s heart,” she continues, “They cared for our whole family and gave him the chance to grow, play, and thrive. Because of CHLA, Beckett has the life and quality of life we once only dreamed of.”

[CHLA] didn’t just treat Beckett’s heart. They cared for our whole family and gave him the chance to grow, play, and thrive. Because of CHLA, Beckett has the life and quality of life we once only dreamed of. — Lisa, mom of Beckett

Refer your friends, neighbors, associates, or family members who are considering making a move:

Visit entar.com/refer 
or call Corey at 213-880-9910

Lisa, Sawyer, Beckett and Chris

Copyright © This free information is provided courtesy of L.A. Loft Blog and Entar.com with the information provided by Corey Chambers, Broker, DRE#01889449 We are not associated with the homeowner’s association or developer. For more information, contact (213) 880-9910 or visit CoreyChambers.com Licensed in California. All information provided is deemed reliable but is not guaranteed and should be independently verified. Some photos and text have been created or modified by AI Artificial Intelligence. Properties are subject to prior sale or rental. This is not a solicitation if the buyer or seller is already under contract with another broker.

Corey Chambers Real Estate Newsletter June 2026 | The California Home

THE GIVING IT BACK AND PAYING IT FORWARD NEWSLETTER

corey-chambers-real-estate-newsletter-clients

Happy Fathers Day to… Everyone?

You guessed it:  Fathers Day is June 15. But why should I mention this to you?

Well, since you have been kind enough to be part of our business, I wanted to take the opportunity to give you a free gift on Fathers Day. Chances are that you are not a dad, but I am sure the dads won’t mind. So I am going to go ahead and give you (and those you know) TWO very special free gifts.

Yes, TWO Gifts.

Gift #1 We will sell your home at your price, or we will buy it.*

Yes, this is the guarantee I am most famous for. And you will know that, whether it’s a super awesome real estate market or a housing recession, I have not wavered from this guarantee. The peace of mind from a guarantee like this is a fantastic gift.

I can think of none better.  My team and I are committed to results. In fact, Results-Oriented is one of our core values. For more than 15 years, people have been coming to us when they want their home sold, at their price and with the least hassle. We look forward to the next 15 years of  Guaranteed Results for L.A. homeowners.  #coreychambers #realestate #news

Your Referrals Change Lives!

Go Serve Large!!! Investing In The People Of Our Great Community.

With The Corey Chambers Team, Your Referrals Really do Change Lives!

If you or a friend are thinking about selling, make sure to choose a real estate company you can trust!

A Real Estate Company That Gives Back!

Gift #2… Donations to one of the areas Leading NonProfits, CHLA Children’s Hospital of Los Angeles. In last month’s letter, I updated you on our goal of raising $25,000 for CHLA, CHOC and Valley Children’s. In case you missed it, we donate a portion of our income from home sales to help the kids.  Children’s Hospital Los Angeles is a 501(c)(3). a nonprofit institution that provides pediatric health care and helps young patients more than half a million times each year in a setting designed just for their needs. Its history began in 1901 in a small house on the corner of Alpine and Castelar Streets (now Hill St. in Chinatown) and today its medical experts offer more than 350 pediatric specialty programs and services to meet the needs of patients. CHLA provides more than $316.2 million in community benefits annually to children and families. As the first pediatric hospital in Southern California, CHLA relies on the generosity of philanthropists in the community to support compassionate patient care, leading-edge education of the caregivers of tomorrow and innovative research efforts that impact children at the hospital and around the world. YOUR REFERRALS HELP THE KIDS! Keep them coming!

Our goal: Raise $25,000 for Children’s Hospital Los Angeles!

Who do you know considering buying or selling a home you could refer to my real estate sales team? Not only will they benefit from our award-winning service and ironclad guarantees but the kids of Children’s Hospital will benefit too! Just give me a call or pass my number on to anyone you know considering buying or selling. My number is 213-880-9910.

Your Referrals help the Kids!

Life moves fast for some and we are eager to make the Home Selling and Buying experience a smooth rewarding one. Over the last two decades of helping thousands of families sell their home and/or buy another, we have met some wonderful, loving, caring people. People like you! As we move forward this Summer, please know we are A Real Estate Company That Gives Back!

Thank you in advance for your referrals! My number is 213-880-9910.

Go Serve Big!!! 

Corey Chambers, Broker DRE#01889449

P.S. Check out the story enclosed of this amazing young person whose life was given back thanks to CHLA.

CHLA Your referrals help kids!

A real estate company with experience, proven results, and a give-back philosophy!

Refer your friends, neighbors, associates or family members considering making a move:

You can go to entar.com/refer and enter their contact info online, or forward the link to someone you know considering a move.

Of course, you can always call me direct as well at 213-880-9910

Why I support Children’s Hospital of Los Angeles

I grew up right here in the Greater Los Angeles Area, born in Los Angeles County at St. Francis Hospital. I remember when I first heard about a young person close to our family suffering from a nasty disease and getting treated for that at Children’s Hospital Los Angeles. It was then that I began to pay closer attention to the work they do at that hospital. Since then, I have learned that it is a collection of hard-working health care professionals, most making their home right here in the Los Angeles area, all coming together for a common cause. That cause is to help young people overcome unfortunate health issues that life sometimes throws our way. Being a Los Angeles Area California native, I take pride in supporting in a way that I can the good work these people do at Children’s. My team rallies around our annual goal or raising money and donating portions of our income to help Children’s in their quest to heal young people when they need healing. My team and I are committed to providing outstanding results for buyers and sellers referred to us by our past clients. I have discovered that Children”s Hospital Los Angeles shares similar commitment to their patients. And since their services survive on sponsorships and donations, we are happy to contribute and proud to support them.

Sincerely,

Corey Chambers

*seller and Corey must agree on price and time of possession. Corey Chambers, Broker DRE#01889449


A Lifesaving Move for Ella: One Family’s Journey With High-Risk Neuroblastoma

Ella and her family moved from Virginia to California so she could receive nation-leading treatment for high-risk neuroblastoma at CHLA. Medicaid coverage for children made accessing that treatment possible. —  by Sara Jones  (Courtesy CHLA)

Ella was just shy of 2 years old when a hug changed everything

It was June 2020—still the early days of the pandemic—and already a season full of changes for the family. 

Ella had become a big sister to her little brother, Francis, just two weeks prior. Her parents, Megan and Marcus, had recently transitioned out of the military and were pursuing law school.

Megan’s mom was visiting the new family of four at their home in Virginia. While hugging Ella, she noticed a lump on the right side of her granddaughter’s abdomen and pointed it out to Megan.

“I immediately knew it was not normal,” Megan recalls.

Marcus and Megan took Ella to the pediatrician that same day, who referred Ella to their local emergency department.

“It all happened so fast,” says Megan. “I was home with Francis and my mom, and Marcus texted me from the emergency department saying, ‘It’s something. They’re not sure what yet, but it’s not looking good.’”

Megan rushed to join Marcus and Ella at the hospital. That’s when doctors told them that Ella had cancer.

“It was shocking,” Megan recalls. “I’d just taken a video of her running around, being a kid.”

“Watching it back, you’d have no idea that we were about to find out our daughter has cancer. We had so many questions.”

Because of how Ella was presenting—happy, energetic, healthy, other than the lump in her abdomen—doctors were almost certain it was Wilms tumor, the most common type of pediatric kidney cancer.

In line with the standard protocol for this condition, Ella immediately went into surgery to remove the tumor and the affected kidney.

When the tumor came back from pathology, however, it turned out Ella didn’t have Wilms tumor—she had stage 4 neuroblastoma.

Neuroblastoma is a relatively rare, fast-moving, and difficult-to-treat pediatric cancer that affects about 700 kids in the U.S. each year. It develops from immature nerve cells in the body, and most often affects children ages 5 and younger.

Scans showed that the cancer had already spread to Ella’s abdomen and femur.

“I immediately started researching top hospitals in the country for neuroblastoma,” says Megan. “A family friend [Quynh Dao, NP] is a nurse practitioner at CHLA. So the whole time we were in Virginia, I was texting Quynh, and once the pathology came back, she put us in touch with Dr. Marachelian in the Cancer and Blood Disease Institute.”

Araz Marachelian, MD, MS, Medical Director of the Neuroblastoma Program, is one of the nation’s preeminent experts in neuroblastoma. Within a week of receiving the diagnosis, Ella and her family were on a flight to Los Angeles to meet Dr. Marachelian and her team.

Standard protocol for high-risk neuroblastoma typically involves multiple rounds of high dose chemotherapy followed by a stem cell transplant to help restore healthy blood cells, then a combination of radiation and immunotherapy.

After five cycles of chemo at CHLA, scans showed the cancer in Ella’s abdomen and femur was almost completely gone—but her care team discovered a brand-new spot that had developed in her skull.

“Hearing Ella’s cancer had spread was almost worse than the first time I heard her diagnosis,” Megan recalls. “I just lost it.”

Ella has a particular genetic mutation called MYCN amplification. Megan knew what the data showed: Many kids with this mutation don’t respond to treatment after relapse.

The family met with Ella’s care team to discuss their options. Dr. Marachelian explained that Ella was eligible to participate in a new clinical trial at CHLA. This particular trial was investigating an alternate treatment regimen that had the potential to help kids with Ella’s exact gene mutation.

“A lot of doctors may have encouraged us to continue with the standard of care, not taking into account that Ella is unique; she had several factors that put her at high risk were we to continue with protocol,” says Megan. 

“Dr. Marachelian looked at Ella as an individual, shared her thoughts, and encouraged us to decide as a team. And that’s what we did.”

Ultimately, they elected to take Ella off protocol and enroll her in the trial.

“It was the biggest, hardest, and best decision we ever made as a family,” Megan reflects, “But I still believe to this day that the trial is why Ella is clear.”

CHLA is home to one of the nation’s largest neuroblastoma programs and serves as the global headquarters for the New Approaches to Neuroblastoma Therapy (NANT) Research Consortium—the only clinical trial consortium focused on developing new treatments for kids and young adults with neuroblastoma.

Through NANT, families like Ella’s may access clinical trials that test investigational therapies and treatments not available elsewhere. The trial, led by Children’s Oncology Group, included a relatively new targeted chemoimmunotherapy regimen which had only become available for neuroblastoma five years before.

Megan is still amazed at the results: After just two cycles, Ella was clear. 

Ella continued the clinical trial regimen for a year, still with no evidence of disease. Then she returned to standard protocol for a few more months of immunotherapy and radiation. 

She rang the end-of-treatment bell in June 2022.

“I truly felt a part of the team through the whole process,” Megan adds. “And we feel Dr. Marachelian is part of our family now because of what she has done for our Ella.”

Ella’s care at CHLA was supported by California Children’s Services (CCS). CCS is a state program largely financed by Medi-Cal, California’s Medicaid program, and helps children with the most serious and complex medical conditions access specialized care. 

As veterans, Megan and Marcus had military health coverage, but that coverage did not extend to their children. 

“For us, Medicaid was exactly what it was designed to be: a bridge during the hardest moment of our lives,” says Megan.

Ella has had no evidence of disease since January 2021.

When Megan is asked how she would describe her daughter today—now an elementary schooler and big sister to two—the first word that comes to mind is “extraordinary.” 

“Ella is so confident and social,” Megan says. “She’s determined, she’s articulate, and I’m just so proud to be her mom. Most importantly, I’m happy we have more time with her. I credit much of that to CHLA.”

While Ella remains cancer free, the family has channeled their experience into helping advocate for others facing pediatric cancer. 

“Going through this journey with Ella motivated me to give back and get involved behind the scenes,” Megan says. “Without Medicaid, we don’t know what would have happened. The question is whether other families in similar situations have access to that same chance.”

Megan has since joined the CHLA Foundation’s Board of Trustees as Chair of the Patient and Family Advocacy Committee. She and Ella have traveled to Sacramento and Washington, D.C., multiple times to share Ella’s story with lawmakers, highlighting the importance of supporting pediatric academic medical centers and expanding state and federal resources for children’s health.

“CHLA’s experts saved Ella’s life,” says Megan. “Speaking up is one way I can help protect care for the next child.”

Find out more about the Cancer and Blood Disease Institute.

  —  Story and photos courtesy Children’s Hospital Los Angeles

How you can help:

Refer your friends, neighbors, associates or family members who are considering making a move:

Visit entar.com/refer or call Corey at 213-880-9910


Copyright © This free information provided courtesy L.A. Loft Blog and Entar.com with information provided by Corey Chambers, Broker, DRE#01889449 We are not associated with the homeowner’s association or developer. For more information, contact (213) 880-9910 or visit Entar.com Licensed in California. All information provided is deemed reliable but is not guaranteed and should be independently verified. Some text and images created or modified by artificial intelligence. Properties subject to prior sale or rental. This is not a solicitation if buyer or seller is already under contract with another broker.