Corey Chambers Real Estate Newsletter July 2024 | The California Home

The California Home
The California Home

Celebrate ‘Your’ Independence… TOO!

July 4th 1776 is a momentous day in history for all FREE

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. 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 www.ReferralsHelpKids.com 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 888-240-2500.

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 www.ReferralsHelpKids.com 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. Being a 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.

New Treatment for Down Syndrome Regression Disorder Helps Bring Darci Back to Herself

by Parker Danowski

The Special Olympian and her mother find answers and rapid improvement at CHLA.

Track and field star, bowler, floor hockey player, health coach, cooking show host, public speaker—all these words describe Darci.

Growing up with Down syndrome, a genetic condition that results in intellectual disabilities and developmental delays, never kept Darci from staying busy. She excelled in leadership roles and in team settings in her home state of Alaska and participated in mainstream school life.

“In high school, she was in the marching band,” Dana says. “She was varsity high school basketball manager, and she traveled with the team independently, without me. She went to an after-school program where they learn job skills up until she was 21. After that, she got a job with Special Olympics.”

Working for the largest sports organization in the world for individuals with intellectual disabilities, Darci filled an important role.

“Initiatives Assistant,” Darci says proudly. This position involved assisting with clubs at Special Olympics Unified Schools. Beyond her job, Darci was deeply involved with the organization as an athlete, playing multiple sports, and as a public speaker at Special Olympics games and PR events. As Dana says, “You gave this girl a microphone and she could light up a crowd.”

Darci was also the first Special Olympics athlete to become a certified health coach for the organization in Alaska, teaching other athletes how to maintain a healthy lifestyle and hosting a YouTube cooking show. She would even travel with the Seattle Seahawks when the football team would visit Alaska.

Then, in early 2022, things started to change. First, Darci began to mysteriously lose weight. Next came confusion. “Darci would unload the dishwasher and take a spatula and try to put it in the fridge,” Dana says. “She would stand there and she was able to verbalize, ‘I’m confused.’” It quickly got worse.

Darci was also the first Special Olympics athlete to become a certified health coach for the organization in Alaska, teaching other athletes how to maintain a healthy lifestyle and hosting a YouTube cooking show. She would even travel with the Seattle Seahawks when the football team would visit Alaska.

Then, in early 2022, things started to change. First, Darci began to mysteriously lose weight. Next came confusion. “Darci would unload the dishwasher and take a spatula and try to put it in the fridge,” Dana says. “She would stand there and she was able to verbalize, ‘I’m confused.’” It quickly got worse.

“The week of April 11 is when it hit with a vengeance,” Dana explains. Darci stopped eating and began hallucinating. “There was one time it was so bad that I had to stop the car on the highway because I thought she was going to jump out.”

The weight loss ramped up. Darci lost 30% of her body weight and was down to 89 pounds. She lost her ability to bathe or dress herself. An accomplished 28-year-old, Darci was estimated to be functioning at an 18-month-old level. “It was getting pretty scary,” says Dana.

She brought Darci to various medical providers in Alaska, but they could not diagnose her. “I had always heard that this population [those with Down syndrome] was underserved medically, and I had never experienced that personally,” Dana says. She has worked in health care for 31 years and is Manager of Therapy Services at Alaska Regional Hospital. But she was shocked at how difficult it was to get a straight answer from the providers she and Darci were seeing.

One gastrointestinal specialist told Dana that he couldn’t help Darci if she chose not to eat, and Dana had to reiterate that Darci wasn’t choosing not to eat. When they saw a neurologist, Dana was told almost immediately that Darci must have schizophrenia.

“I was like, ‘Based on what diagnosis are you saying that?’” Dana recalls. “This doctor said that her speech was fluent. Darci was mute at that point.”

Dana was able to bring Darci to a psychiatrist who prescribed an antipsychotic medication, which eliminated Darci’s hallucinations. But her other symptoms continued as Dana persisted in her search for answers.

“We did have one primary care provider [PCP] who had known Darci since we transitioned from pediatric care at 18,” she explains. The doctor was also having trouble diagnosing Darci, but Dana says she offered something the other providers didn’t: hope. “She was the one person who was like, ‘I don’t know what it is, but we’re going to find it.’”

And eventually, they did. Dana researched Darci’s symptoms on her own. “I was just plugging in anything that I could find that would match Darci’s symptoms. What kept popping up were Dr. Santoro’s articles. I was like, ‘Oh my gosh, this is what Darci has. I’ve got to pursue this path.’”

The articles Dana had discovered were the work of Jonathan D. Santoro, MD, Director of the Neuroimmunology Program at Children’s Hospital Los Angeles. Since 2019, Dr. Santoro had been working to develop a novel treatment protocol for DSRD. He recognized that DSRD was often misdiagnosed as schizophrenia, early-onset Alzheimer’s disease or late-onset autism. He saw that physicians tended to be so focused on a patient’s Down syndrome that they wouldn’t fully investigate their individual symptoms.

“I just kept asking the question: Why are we treating these patients differently?” Dr. Santoro says. He became determined to better understand DSRD and identify new ways to treat it.

He tested patients with DSRD for conditions that could be affecting the brain and found inflammatory markers in the patients’ cerebrospinal fluid. Evidence began to grow that DSRD could be treated as an inflammatory condition.

This data led Dr. Santoro and CHLA to launch the first clinical trial for DSRD. A National Institutes of Health-funded collaboration with the University of Colorado and Children’s Hospital Colorado, the trial is investigating the safety and effectiveness of three potential treatments: lorazepam, a medicine that treats catatonia; an immune therapy called intravenous immunoglobin (IVIg); and Tofacitinib, a drug that suppresses an individual’s immune system.

By the time Dana reached out to Dr. Santoro, he was deeply familiar with DSRD. “He and our PCP connected and he gave her the diagnostics that we needed to run,” Dana says. Dana and Darci finally received a DSRD diagnosis seven months after the onset of Darci’s symptoms. “Then we went straight to Dr. Santoro  in California to initiate our treatments.”

Dr. Santoro recalls meeting Dana and Darci in person for the first time at CHLA. “The thing that I was most struck by was what Darci used to do,” he says. “I mean, she’s not just a typical young woman—she’s leading Special Olympics, she’s the upstanding citizen in her community, she just does so much. So to meet her and see this shell of a person—it was a very emotional visit between Dana and Darci and myself.”

Dr. Santoro initially prescribed lorazepam to address Darci’s catatonia. The first signs of improvement emerged during the pandemic. “We were still using masks,” Dana recalls, tearing up. “The first thing Darci did independently was she went and put all the masks by the door in a basket. That seems like a silly task—putting masks in a basket. But when you’ve gone seven months with just nothing—sitting on the couch and just being catatonic and not able to do anything—that simple task was just huge.”

The progress continued. Darci regained the ability to dress herself and eat on her own. Then, after Dana worked hard to obtain coverage from her insurance provider, Darci began IVIg infusions. “She’s been on that for about 16 months,” Dana says. “And we continue to see improvements.” The changes aren’t as drastic as they were when Darci started treatment, but every step forward is major.

Dr. Santoro also emphasizes that Darci’s providers in Alaska were open to discussing Darci’s progress, as well as his research. This helped immensely in monitoring Darci’s treatment between her visits to CHLA.

“We shared the literature and we talked about what to monitor for, and the doctors over there were really fantastic,” he says.

Through this experience, Darci has been attending a Family Outreach Center for Understanding Special Needs (FOCUS) in Alaska to re-engage in activities like community service. She has been involved with FOCUS since childhood, and they have played an important role in her DSRD journey. The FOCUS team brought Darci back to the space where she used to host her cooking show, and she has started to cook again.

Dana happily describes Darci’s present state. “Treatment’s going great,” she says. “Of all of the symptom clusters that are DSRD, most of them are gone.” The areas that they are still working on with Dr. Santoro are Darci’s speech and her internal motivation to independently perform tasks.

Dr. Santoro understands that while Darci is on a positive path, many others with DSRD need help.

“We get hundreds of emails a month from people all over the world,” he says. To support these individuals, Dr. Santoro remains committed to translating his research into new treatments as quickly as possible. “Being fast has really allowed us to totally change the landscape, and I think that will continue in the next couple of years as we get more and more data.”

As Dana and Darci look ahead, Special Olympics has assured them that there will be a position for Darci when she is ready to return. At the mention of this, Darci smiles wide and gives a thumbs up. Dana looks forward to Darci being able to organize the FOCUS  Halloween party and to dance at Special Olympics dances again.

Dana also recognizes how much she and Darci have had to grow through this experience. “I think it has brought out a spirit of advocacy,” she explains. “I’m advocating for lifesaving care for her—and I’m telling this story so that any other physician, health care provider or parent can just know what this is so they don’t have to search for answers like so many of us have.”

Meanwhile, Darci is steadily resuming the activities she used to enjoy. She cooks again—making breakfast with her mom and preparing some favorite dishes (like runny eggs and hash browns, she says). She asks to listen to songs that she hasn’t heard in a long time.

“She recognizes that she’s not doing something, and she says, ‘I want to do it,’” Dana explains. “That’s Darci’s goal.”

Learn more about CHLA’s Down Syndrome Neurology Program.

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

www.ReferralsHelpKids.com 
or call Corey at 213-880-9910

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. 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 2024 | 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 18. 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 30 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 30 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. 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

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 www.ReferralsHelpKids.com 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


Genetic Testing Finds Lethal Heart Disease Lurking in Family

The painful discovery that a condition called hypertrophic cardiomyopathy was passed from a father to his three kids will ultimately help to protect all their lives. —  By Jeff Weinstock  (Courtesy CHLA)

If you were looking for a model of a double-edged sword, you couldn’t find one that cuts more sharply than Elias’ diagnosis of hypertrophic cardiomyopathy.

Soon after his disease was uncovered, Elias’ parents were sent to undergo genetic testing to see whether either of them had passed him the gene. The results ruled out mother Cecilia, but revealed that Rafael, Elias’ father, was the carrier.

“That’s when our story was just declining with bad news,” Cecilia says.

Viewed another way, Elias’ diagnosis may have been the very best bad news the family could have received. Or the worst good news. However you frame it, the consequences were at once devastating and fortunate, life-threatening and lifesaving.

A string of positive tests

The saga began only hours after Elias was born. A doctor’s stethoscope detected a murmur, suggesting some kind of interference around the heart, prompting an echocardiogram and an EKG to look further.

The tests indicated Elias had hypertrophic cardiomyopathy (HCM), a hereditary disorder causing thickening of the heart muscle that can obstruct blood flow into and out of the heart, potentially throwing the heartbeat off its regular rhythm and setting off fatal cardiac arrest. A local cardiologist reran the tests and came to the same finding. Elias’ heart was thickening rapidly, but this early in his life, there wasn’t anything to do beyond putting him on medication, a beta blocker to slow his heartbeat and prevent abnormal heart rhythm.

The one action that could be taken was to send Elias to the Heart Institute at Children’s Hospital Los Angeles so he could be seen by specialists in CHLA’s Cardiogenomics Program, which treats patients with inherited heart conditions. There, the team ran genetic tests on Elias and identified a gene mutation linked to hypertrophic cardiomyopathy.

That meant Elias’ older sister, Zulay, then 3 years old, needed to be examined. At the local cardiologist’s office, the same outcome ensued: A murmur was heard and subsequent genetic testing turned up positive for HCM, prompting another referral to CHLA.

In the span of five months, Cecilia’s newborn son, her daughter and her husband were all found to have a life-threatening heart condition, leaving her “an emotional wreck,” she says.

Different degrees of disease

In July 2020, a third child, daughter Emilia, was born, and she too was found to have the HCM gene. The three kids all show different progressions of the disease. Elias’ case is the most advanced.

“At 12 months old, his heart was incredibly thick,” says CHLA cardiologist Jennifer Su, MD. “It’s nowhere near as striking now as it was back then.”

Elias’ condition appears less dramatic because over the past five years his heart has grown but has not gotten any thicker, so its thickness is now more proportionate to its overall size. It’s a fortunate development, and unusual, Dr. Su says.

“We typically think of hypertrophic cardiomyopathy as a progressive condition. It’s quite unusual to see thickening up front and for it to regress over time. It’s not the pattern we would expect.”

Zulay’s heart, which had mild thickening initially, has behaved the same way. She was put on medication, but it was discontinued a year later after the disease showed no further growth.

Meanwhile, Emilia is on no medication as she has yet to show any manifestation of HCM other than the positive genetic test. “Emilia’s case is like what we would expect,” Dr. Su says. “We might not see it at first, and maybe in a few years we’ll start seeing it.”

Once a year all three kids—ages 3 (Emilia), 5 (Elias) and 8 (Zulay)—pile into the car to see Dr. Su for an evaluation. Between appointments with their local cardiologist and the visits to CHLA, they get monitored every six months.

It’s not an easy day for Cecilia. “Every time we go to the doctor,” she says, “I do fear hearing, ‘Hey, it got worse. This is going to be the next step now.’”

The annual assessment Dr. Su performs doesn’t stop at an echo and EKG. A Zio patch monitors the heart’s rhythm over a two-week period, and as the kids get older and can tolerate it, an MRI will be added to check for scarring, which would indicate greater thickening in the heart and more potential for arrhythmias. The most recent visit, at the end of March, showed no changes.

Dr. Su says there’s less to fear at this stage, as HCM often stabilizes in the time between infancy and adolescence and then starts to advance again. “Elias’ heart may become more severely hypertrophied as he gets into his teens,” she says.

To be clear, not having visible symptoms of hypertrophic cardiomyopathy does not negate the presence of it. It may be idle, but it’s there.

“Intrinsically,” Dr. Su says, “Elias’ heart has an abnormal genetic code that caused pretty significant hypertrophy when he was an infant. It’s not as severe looking at the moment, but certainly, especially considering his dad’s diagnosis, it may become a bigger problem.”

Defusing a time bomb

Rafael lived 26 years—he’s now 31—before his son’s diagnosis led to the discovery that he had hypertrophic cardiomyopathy. Initial tests showed such pronounced enlargement of his heart, doctors told him they were stunned he was still alive. “They can’t explain how I lived this long without any symptoms,” he says.

He was immediately prescribed a beta blocker, and after delaying surgery for years, on April 1 he had a device installed in his chest called an implantable cardioverter defibrillator (ICD). The ICD acts just like an external defibrillator, shocking the heart back into a normal rhythm if it detects an irregular heartbeat.

Rafael put off having surgery mostly from a lack of certainty that he needed it after playing contact sports in high school and college—which someone with HCM is advised not to do.

But he came around, understanding the operation was imperative, as his doctors likened his heart to a time bomb that could detonate without warning.

“I could be driving and I could have a heart attack,” he says. “Or working out, or just walking. There’s no way to gauge when it’s going to happen. I have to see tomorrow and see the next day and see many more years.”

Saving up a thank you

After the family’s diagnoses of hypertrophic cardiomyopathy, Rafael and Cecilia prioritized better health habits. Exercise is part of the effort, endorsed by the doctors. That wasn’t always the case, Dr. Su says.

“When I trained about 10 years ago,” she says, “the overwhelming recommendation was to restrict patients from high-intensity activity. There was a lot of concern for arrhythmias or risk for something happening.”

But that recommendation created sedentary children and adults who were developing disorders stemming from their inactivity—obesity, diabetes and coronary artery disease, which have no connection to hypertrophic cardiomyopathy.

“We told them not to exercise, and we can’t actually say we saved any lives or saw decreased likelihood of sudden death or arrhythmias,” Dr. Su says.

Current guidelines instruct doctors to discuss with families the benefits and risks of exercise based on the extent of their child’s disease, and then to together arrive at a plan.

“At this time, we recommend that Elias and his siblings participate in any recreational sport as long as they’re allowed to rest when they’re tired,” Dr. Su says. “There is a risk. We’re just not going to allow that risk to be very high.”

Even that thin level of risk leaves Cecilia to worry.

“I try not to let it get the best of me,” she says, “but with three kids and my husband all having the same heart condition, I can’t just be like, ‘Everything’s going to be OK.’ It’s hard not to think about it.”

Rafael struggles too. He still thinks often about being the source of the disease. “I wish I could take it from my kids,” he says. “I wish they didn’t have to carry that burden like I do.”

But he learned to look at his son’s diagnosis as a “blessing in disguise,” he says, as it tipped him off to his own disease and may well keep him around in his kids’ lives for many decades more. “If he was never born, I would have never found out.”

In time, he will deliver his gratitude to his son. “When he’s old enough to understand, we’ll have conversations. Every day when I hold him, he’s a blessing to me because he saved my life. He really did.”

  —  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:

www.ReferralsHelpKids.com or call Corey at 213-880-9910


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Copyright © This free information provided courtesy L.A. Loft Blog and LAcondoInfo.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 LAcondoInfo.com Licensed in California. All information provided is deemed reliable but is not guaranteed and should be independently verified. Properties subject to prior sale or rental. This is not a solicitation if buyer or seller is already under contract with another broker.