Archive | Why We’re Cool

Magnet Magic

Microsoft Word – Magnet Magicblog

Using magnets to treat babies and kids with hydrocephalus sounds like something from a science-fiction movie, but it’s happening here at CHOC Children’s. 

Hydrocephalus (or water on the brain) is a condition where there is a lack of absorption, blockage of flow, or overproduction of the cerebral spinal fluid (CSF) that surrounds the brain.  This can lead to dangerous buildup of fluid, increasing pressure inside of the head.

Some hydrocephalus patients need surgery, which usually involves placing a shunt into the child’s head to help drain the extra fluid from around the brain.

CHOC neurosurgeon Michael Muhonen, MD, was a primary investigator for clinical trials of Medtronic’s Strata Valve—part of a shunt system now being used worldwide to treat hydrocephalus.

Once surgically implanted in the brain, the settings on adjustable valves like Strata can be easily customized as the patient grows and changes. Dr. Muhonen uses a special magnet to change pressure settings in the shunt from outside the head. It’s noninvasive and totally pain-free.

Want to learn more about hydrocephalous and treatment options? Visit the CHOC Children’s Neuroscience Institute web site here.

Calling all hockey fans!

Alex with mascots #2

Want to be there when the Anaheim Ducks take on the Los Angeles Kings at home on April 8, 2011? The winner of the “Ducks Night Sweepstakes” will enjoy dinner at the Jack Daniel’s Club and game tickets for 10.

All you need to do is “like” CHOC Children’s Facebook page, then click  here (or on the CHOC Ducks Night tab on the left side of our Facebook page) to enter for a chance to win!

Join CHOC Follies Cast Member For Family Fun and Support of Pediatric Care

Martin Family

For over a decade, the CHOC Follies has earned a reputation as one of Orange County’s most unique and successful charity events. Some of the most prominent business and community leaders in Orange County have joined forces to put on a show like you’ve never seen before! This year, CHOC Follies XIV – A Funny Thing Happened on the Way to the Follies promises to be just as entertaining for the entire family. 

We recently talked to Paul-Dean Martin, a Follies cast member and director of the PDM Young Actors Workshop, an after-school program, about the upcoming show.

Q: How did you first get involved in the Follies?

A: I got involved last year and have been a fan ever since. I have two children, Phoebe, 7, and Max, 2, who are both CHOC patients, and thought here’s a way to give back to CHOC while doing something I’ve always enjoyed. This year I’ll be playing the role of Klaus Bruteman, an Austrian personal trainer.

Q: Why is this fundraiser so important?

A: The community should support this event for the fact that the proceeds go directly to the hospital.  I’m humbled by the people I’m surrounded with in this show.  They give so much of their time and support to such a great cause.

Q: What can we expect at the show?

A: The show is loosely based on the original and portrays various time periods. It’s very funny, entertaining and filled with talented performers; it’s put on by true professionals.

 The CHOC Follies will be held on March 31-April 2 at Orange Coast College, Costa Mesa. For more information or to purchase tickets, please click here:

 http://www.choc.org/events/event_detail.cfm?eid=730

Dr. Jim Cappon is Leading the Charge in Patient Safety

Dr. Jim Cappon is Leading the Charge in Patient Safety

As part of the team behind CHOC Children’s new state-of-the-art, seven-story, 425,000 square foot tower, Dr. Jim Cappon is literally transforming pediatric care from the ground up. Using his unique expertise as one of the nation’s first Medical Directors of Quality and Patient Safety, Dr. Cappon is implementing all the latest research and advancements in the emerging field of “safe design” in the construction of the new tower. From room configuration to infection prevention, CHOC Children’s will be the safest children’s hospital in the entire country.

Join us for more stories from our doctors, nurses, staff and donors at choc.org/noplacelikechoc.

Melody Therapy at CHOC Improving Lives For Patients With Heart Disease

Melody Therapy at CHOC Improving Lives For Patients With Heart Disease

In honor of American Heart Month, we’re highlighting the CHOC Children’s Heart Institute including stories of our brave patients, as well as our amazing experts and some of the cutting-edge procedures they are using in caring for infants and children with heart defects/disease.  We recently spoke to Dr. Farhouch Berdjis, medical director of the CHOC Cardiac Catheterization Lab, about the new Melody Transcatheter Pulmonary Valve (TPV) Therapy, a less invasive procedure which can delay the need for open heart surgery.

Q: How do heart valves function?
A: The heart has four chambers. As the heart beats, normal heart valves repeatedly open and close fully to ensure that blood flows forward through the heart’s chambers. A narrowed or leaky heart valve can cause dizziness, chest pain, weakness, and can lead to serious medical problems.

Q: What is the Melody therapy and what makes it so unique?
A: The Melody therapy treats narrowed or leaking pulmonary valve conduits without open-heart surgery. With this therapy, a thin, hollow catheter or “tube” holding a specially designed heart valve is inserted into a child’s vein in his leg and guided to his heart. The heart valve is attached to a wire frame that expands with the help of a balloon to push the child’s blocked pulmonary conduit open. CHOC is one of a few hospitals in the United States currently using this state-of-the-art, FDA- approved procedure to treat the pulmonary valve.

Q: How will patients and families benefit from this procedure?
A: This therapy can be an alternative to surgery for some children who have already undergone previous heart surgeries. Patients can expect less scarring, less stress to their circulatory system, and an overall speedy and positive recovery both physically and emotionally.
To learn more about the Melody therapy, please contact Dr. Berdjis’ office at 714-547-0900. To learn more about the CHOC Children’s Heart Institute, click here: http://www.choc.org/heart/index.cfm.

CHOC Teens were Celebs at the Jingle Ball

Jingle Ball

This year, CHOC patients Jocelynn and Cynthia got an all-access pass to KIIS FM’s Jingle Ball at Nokia Theater LA Live. Check out this cool video:

CHOC and Disney Celebrate It's a Small World

In partnership with Disneyland Resort and CHOC Children’s, Sylvania helped brighten the holidays for a special little girl named Adela and her family. Adela Jauregui, 8, a patient at CHOC Children’s, along with some Disney friends, helped light up the It’s a Small World ride at the Disneyland Resort to celebrate the start of the holiday season.

NICU Mom Shares Her Journey

NICU Mom Shares Her Journey

In our continued recognition of National Prematurity Awareness Month, we asked one of our NICU moms to answer a Q & A regarding her current journey. Janelle agreed – hoping her responses would help another family experiencing the same thing.  Her daughter Isabella Rose was born at just 28 weeks gestation in August 2010, weighing two pounds, two ounces.  This strong, beautiful baby girl is still growing in our NICU – with the support of her loving family and CHOC staff.
What brought your child/your family to the CHOC NICU?

After about a week of feeding in the HOAG NICU, Isabella’s tummy was distended, and an X-ray revealed a diagnosis of necrotizing enterocolitis, a serious infection of the intestinal wall. She was transferred to CHOC Children’s Hospital that same night, in case she would need to have immediate surgery.

Briefly describe your experience dealing with a child in the NICU.

Bella is my first child, and her early arrival was a complete surprise during an otherwise perfect pregnancy. In the beginning, I was in shock, I had a hard time talking about what had happened and even getting out of bed to go see her the first few days, it was all too surreal. Once I was able to see her face and hold her, though, the bond was instant.

They call the first couple weeks the “honeymoon phase” and she did so well that the nurses were calling her a rockstar and telling me she would likely go home early. I was, of course, excited but also holding my breath a little for any upcoming surprises in the long road ahead.

I wish I could say that made what happened next easier, but it didn’t. I don’t think there is any way to prepare for having your tiny, but growing and healthy baby suddenly end up in a critical “touch and go” status.

During the next three months at CHOC, our daughter would go through one hurdle after another. Her vitals would fall steadily for days, then the doctors would do something to help her turn the corner, and she would recover faster than I really ever thought possible, more than once. She was on multiple types of ventilators, had three surgeries, half a dozen blood transfusions and she fought through it all with such grace and strength, it took my breath away.
What are things you’ve done to cope with having a child in the NICU?

I began a journal about the experience, dedicated and written to Isabella, so that when the time is right, she can hear about her dramatic entrance into the world from my perspective. Perhaps it will be when she becomes a mother herself, or maybe I’ll use it as a reason for why she can’t date until she’s 21.

I combined this journal with photos and video we’ve taken of her and put together a website to keep friends and family updated on her status. I’ve also gotten much more spiritually involved in my community.
What kind of support have you received from the NICU team?

The nurses and doctors became part of my family, and the rest of the hospital staff from the valets, to the security guards, to the receptionists became my best friends. Everyone is there for your child, and you feel truly lucky not only to be living in this country, but on top of that to be living in this area and have an establishment like CHOC on your side.

What advice would you give to other NICU families?

Everyone will tell you it’s a roller coaster, but you can’t imagine really what that means, and, on top of that, you never want to think that there are more free falls ahead.

One thing I wish I knew ahead of time is how resilient these babies are. They almost seem designed to withstand more than we can as adults, which was a completely foreign concept to me when I looked down at my two pound baby girl.

In the NICU, no one can provide the answer to the one big question: “When will my baby be okay and ready to come home?” The answer to every question will be “it depends on the baby.” But don’t let that frustrate you. Do your research and ask the challenging questions. Every course of action has a potential benefit and risk associated with it. Make sure you know what these are.

You know your child better than anyone, and the CHOC team respects your opinion as a valuable member of your child’s team. You are your kiddo’s strongest advocate, so fight for them.

There is no doubt that this experience changes you forever, as a person and as a parent; your perspective will never be the same. However, it helps to think of it as a crash course of the hardest part of parenting – the worry, the feeling powerless and wanting only what’s best for them. As one experienced mom put it to me – welcome to the club, this is just the beginning – wait until she’s driving!

Baby Connor Speaks Out for the CHOC Walk

It’s here!!! This Sunday is The CHOC Walk in the Park Presented by the Disneyland Resort. And this year’s CHOC Walk teams have been more creative than ever when it comes to raising support.

Team Babes in Disneyland is new to the CHOC Walk this year and captain Lisa Robertson enlisted the help of her adorable son Connor to encourage people to donate.

Check out this video:

Did you or your team make a video for this year’s CHOC Walk? Or are you planning to make one at the Walk on Sunday? Don’t forget to share it with your friends on Facebook and YouTube!

Then, visit Babes in Disneyland for insider tips on visiting Disneyland with young children, as well as ongoing coverage of this year’s CHOC Walk.

20 Reasons to Walk for CHOC

20 Reasons to Walk for CHOC

1.  It’s the 20th Anniversary of the CHOC Walk in the Park, presented by the Disneyland Resort!

2.  On October 17th, a crowd over 15,000 Walkers will be strolling with YOU down Main Street, U.S.A.

3.  Watching the sunrise at Disneyland is amazing.

4.  This CHOC patient: 

5.  It’s our biggest fundraiser of the year—bringing over $1.6 million to CHOC Children’s last year.

6.  Walking through the Disneyland Resort before it’s officially open is cool.

7.  This bear:

8.  You never know which Disney friends you’ll see there, cheering you on. Alice at the Mad Tea Party…Cinderella on King Arthur’s Carrousel…

9.   Meet some great VoluntEARS.

10.  This mouse:

11.  Get inspired by our amazing patients and their families.

12.  This little girl:

13.  This team:

14.  And this team:

15.  Our patients here at CHOC Children’s Hospital:

16.  Our new patient-care tower:

17.  Supporting cool technology that makes for safer medicine.

18.  You are sure to meet some pretty funny characters:

19.  Research that advances cares and cures.

20.  We’re making giant strides for tiny toes:

Want to learn more about the 2010 CHOC Walk? Click here.

Become a fan of CHOC on Facebook.