Showing posts with label Simply Amazing.... Show all posts
Showing posts with label Simply Amazing.... Show all posts

Monday, March 26, 2007

Miracle Monday!

I met Christy King and her husband, Rob at WakeMed while Zoe was there. These people are totally amazing!!! I have posted about her before, but decided to post her on Miracle Monday, because their daughter, Sophia is such an incredible little miracle!! Christy, Rob and Spohia were recently featured in our local newspaper, the News & Observer. Here is the story as the newspapers wrote it.... GET SOME KLEENEX!

Christy King went into labor the morning of Aug. 26. It was not a happy occasion.

Barely 23 weeks into her pregnancy with triplets, King and her husband, Rob, had been warned that challenging times lay ahead.

Each of their children would weigh in at just over a pound. The infants' skin, lungs, eyes and digestive and circulatory systems would be woefully unprepared for life outside the womb. The Kings, first-time parents, would not be able to touch their babies. Doctors and nurses would use extreme care handling them.

If the babies lived, each one would likely need multiple surgeries and other interventions, but even the most advanced care might not save them. Survivors could be blind, deaf, brain damaged and afflicted with at least some neurological, physical and developmental problems.

Neonatologists at WakeMed asked the inevitable and painful question: Did the Kings want doctors to do everything possible to keep their triplets alive? Or would they prefer the infants receive no medical care and instead be allowed to pass on as their parents held them?

The question put the Kings, who live in North Raleigh, at the center of one of medicine's most emotionally charged and difficult ethical debates. How early is too early to try to save the youngest and most fragile premature infants, and how should decisions regarding their care be made?


Nationally, 30 percent of 23-week preemies, at best, survive with intensive care. Some hospitals, including WakeMed, typically provide these preemies with routine life support only, such as mechanical ventilation. Whether to provide more aggressive care -- or no life support at all -- often depends on the parents' wishes.

Christy and Rob King, who had a couple of days' warning before Christy went into full labor, agonized over their choice.

"As a mother, I was already in love with them," Christy King, 36, said of the two girls and boy she carried. "The selfish part of me wanted them . But as a mother, I did not want them to suffer just to make us feel better."

The Kings decided they wanted each triplet to be placed on a mechanical ventilator. But if there were clear signs the infants' bodies were failing, they would not seek further care. The couple saw no point in forcing their children to endure painful, invasive treatments that might extend their lives for a few days or weeks but would not ultimately change their final prognosis.

Roman Catholics, the Kings asked their priest to come to the hospital the day of Christy King's cesarean section. As his wife lay in recovery, Rob King stood with the triplets as the priest baptized each baby.


One of the Kings' girls, Natalie Rose, was in trouble within 12 hours of her birth. Close to midnight on the night of Aug. 26, the Kings learned their daughter's lungs were not working properly, even with help from the ventilator. The neonatologist on duty told them they would soon need to make a decision about ending support.

Then, an hour or two later, the same doctor came back into the hospital room with more bad news: the Kings' son, Robert Jr., was fading fast and was not expected to make it through the night.

A nurse appeared at the door with a wheelchair to take Christy King, followed by her husband, into the nursery. They stopped at Robert Jr.'s incubator. As the nurse gently disconnected the baby from his ventilator, Christy King asked that her husband be allowed to hold him first. Rob King held the small bundle for a while, then passed the baby to his mother.

Christy King gave the boy back to his father, who held the baby as he died. A nurse put Natalie Rose in her mother's arms. To Christy King, her face seemed no larger than a golf ball. Doctors and nurses stood around the couple in a circle, honoring the babies' passings.

"They were in tears for us," Christy King remembers.

When the babies were both gone, the Kings went to their remaining triplet's incubator. Christy King spoke to her daughter, Sophia Marie.

"I said to her, 'Little girl, this life has so much to offer. Mommy will never leave you. I will fight this with you,' " King recalled.

It took 146 days in the hospital nursery and five major surgeries, but today Sophia at last lives at home with her parents. Bills for her hospitalization have reached about $800,000, most of which will be covered by the private insurance Christy King has through her work in sales for a major food distributor. Sophia breathes on her own and drinks from a bottle. She sleeps, cries and charms her parents. At seven pounds, she is now the size of a full-term newborn.

"We're really happy with where she is today," said Rob King, 32, a special-education teacher at Garner High School.

he Kings know there will be more challenges ahead, as Sophia grows and doctors get a better idea of what lingering issues her early arrival might have caused. The Kings already know that their daughter might have serious vision problems, which are common among preemies. With three eye surgeries already behind her, Sophia might be legally blind, doctors have warned.

But when Christy King thinks of her daughter's future struggles, she can't help but think with pride of what she has already overcome. She recalls that, in the beginning, doctors gave her a 15 percent chance of survival.

"I look at my little girl and, to me, she has the quality of life of any newborn," King said. "We are not here to convince people that they should save every baby. It's a personal decision, and everyone has to make it on their own. But if this is a 15 percent chance of life, it's pretty damn good."

Sophia now weighs 7 pounds 7 ounces! They are having a little trouble with her eyes, but they are seeing an eye specialist twice a month from the Governor Morhead School. Sophia is doing fantastic!!




Sophia's Daddy's wedding band fit around her wrist!!

Monday, March 19, 2007

Miracle Monday!




This picture was taken a few days before Jon Patrick went home. This is Jonnie and Zoe. And, all the nurses teased that they were betrothed. :)




This is my son Jon Patrick, he truly is my miracle baby. I was told that I couldn't have children and after waiting 20 years I was finally blessed with my beautiful little boy. Jon Patrick came into the world on October 20th 2006, at 33 weeks 0 days gestation. He was a big boy at 5 lbs 2 oz and 18 inches long. His lowest weight was 4 lbs 11 oz. We spent 4 weeks in the hospital at WakeMed and met a bunch of wonderful people. Jonny is now 20 weeks old and is 25 1/2 inches long and weighed 13 lbs 12.5 oz at his last doctors visit. He smiles a lot, but not when Mommy wants to take a picture of it. He is trying very hard to turn over he hasn't quite gotten there yet. His favorite things in the world are his thumb, his silky blanket. and his rainforest pack and play. He likes to watch the mobile and listen to the music. He gets so excited he talks, kicks his legs and tries to bat at the monkey bird and frog.

Monday, March 12, 2007

Miracle Monday!

Here is another mother that I meet in the NICU at WakeMed Raleigh. Here is yet another Miracle Baby. Every Monday I will be featuring a Miracle baby that survived from prematurity. I will feature a new mom every Monday until I run out of mom's, dad's and babies to feature. Please read Emma's amazing story....


On August 16, 2006 I was diagnosed with a rare condition called HELLP Syndrome. It had progressed so fast my liver had began to shut down and my other organs were to follow. My platelets were also down to 50,000 (normal is 150,000 - 500,000). We were told that I was dying and the only way to save my life was to deliver the baby. (Delivery is the only cure to HELLP Syndrome). I was only 24 weeks along and Emma was measuring 3 weeks behind
in size. The C-section was performed the following morning on 8-17-2006 @ 6:00am. Emma only weight 14 ounces. She did well for a couple of days and than began to get worse. When she was a week old we were able to hold her for a few minutes. She was re-intubated the next day, it would be 2 more months before we could hold her again. She went into Kidney failure when
she was 10 days old. That was the scariest time of my life. We were told after 48 hours they would sit us down and give us our options. We already knew the truth..there were no options, there was nothing anyone could do. Her body was going to shut down. We were devastated. With just a few hours to go before we hit our 48 hour mark the doctors had discovered her blood
pressure was extremely low. There was no blood flow to the kidneys. They started medication immediately. Once her BP was normal her kidneys started to function again. I can not describe the feeling I had when we were told that she was doing great. I remember crying and telling God thank you. He had spared our little girls life. Her kidneys were in "overdrive" for a few
days but then she was back to normal. Over the course of the next week, Emma somehow developed a really bad yeast infection in her blood, which made her really sick. The doctors could not find the source of the yeast. They started antifungal medication, changed
her isolette and even tested my breast milk. They performed an EKG, and an ultrasound of her kidneys. They even had the opthamolagist come in to check her eyes. These were the 3 places a lot of blood flowed to.Nothing worked. Another medication was stared on top of the first, it was also unsuccessful. After speaking with the infectious diseases specialist he just said to continue both medication and eventually, hopefully it would go away. By this time Emma was almost 2 months old and was still on the ventilator. Doctors were afraid to take her off because "babies with infections do not like to breathe on their own". Finally they had no choice. Her lungs were being badly damaged from being on the ventilator for so long. They had already given her 2 series of steroids to try to help them and there was nothing left to do. To everyone's surprise she did great. She was still on oxygen but she was breathing on her own. The yeast
finally went away and she was up-graded to intermediate status. She was moved out of intensive care and was no longer considered critical. We were able to hold her again and finally got to a point where we thought everything might just be okay.

Emma continued to do well for another month or so. She was moved to an open crib and bottle feedings were started. We were actually starting to feel like parents to our little girl. We thought everything was great, life was finally getting to be a little bit easier. All we were doing now was
waiting for Emma to come off of oxygen and take all her feedings by mouth, then they would send her home. This was not the case. During a routine eye exam Emma was diagnosed with ROP (Reninopathy of Prematurity). It was progressing so fast, Laser eye surgery was necessary and performed the next day. After 2 weeks of waiting for the results, we finally got the news. It was unsuccessful. She was now in stage 4 and her retinas were detaching. We
were transferred to another hospital to see a specialist. She said that surgery needed to be performed immediately to save what little vision she still has. We were devastated. The good news was that Emma was doing well everywhere else. She was up to 5 lbs. and was taking all feedings by mouth. But now, after coming so far we were now facing possible blindness. 2 more
surgeries were performed on her eyes ( the first was also unsuccessful ). We came to a point where there was nothing left to do but watch how her eyes develope. Her right eye did great. We were told the ROP was gone and she should have normal vision in it. As for her left eye, she was legally blind. We were happy with the outcome. For a while we were afraid she would
never be able to see how beautiful she is.

We were transferred back to Wake Med on December 22, 2006. Emma came off of oxygen on December 24. For the first time she did great. She was 6 lbs., up to full feeds by mouth and required no assistance breathing. After 4 1/2 months, many sleepless nights, 4 surgeries, more blood and platelet transfusions I can even count, memories I'll treasure forever, memories I
wish I could forget, it was over. Emma came home to us on December 30,2006. She weighed over 6 pounds and was released with a clean bill of health. Today Emma is 6 1/2 months old and weighs close to 11 pounds. Doctors are very pleased with her progress. She does have serious vision problems and has already been given prescription eyeglasses but we are so happy with how far she has come. We spent 126 days in the NICU. Those were the hardest days of our lives, but, we made it through it, all of us changed forever. I truly believe Emma has taught us all something. Never stop fighting and always believe in miracles.































































































































Monday, March 5, 2007

Miracle Monday!

Olivia was 1 lb. 13 oz. and 13 1/4 inches long BEFORE

Ava was 1 lb. 12 oz. and 12 1/4 inches long --- BEFORE

Ava & Olivia AFTER 11 lb. and 11 lb. 12 oz with their big sister Allyson.
I am going to be doing a series of miracle Mondays featuring some of the woman that I meet in the Intensive Care Nursery at the WakeMed Hospital in Raleigh... here is my first.

My identical twin girls, Ava and Olivia were born via emergency c-section on Aug. 15, 2006 at 27 weeks 3 days - three months before they were supposed to enter the world. Ava was 1 lb. 12 oz. and 12 1/4 inches long and Olivia was 1 lb. 13 oz. and 13 1/4 inches long. It is still unknown why I went into labor early. They were born at Raleigh WakeMed hospital where they spent the next 135 days (over 4 months) in the Intensive Care Nursery. They were very sick when they were first born and we didn't know if they would even survive. Ava and Olivia both had severe lung problems, suffered from apnea and bradycardia episodes, had several blood transfusions, developed infections, were on several courses of antibiotics and other medications, Ava had two spinal taps, and they both had a variety of other preemie problems. Towards the end of their stay in the hospital, they developed severe feeding problems. Nothing we tried seemed to help. They both ended up having a surgery to insert a gastrostomy tube (feeding tube) into their stomachs. This enables us to give them the nutrition they need even if they refuse to eat.
On December 28, 2006, Ava and Olivia both came home from the hospital. It's been quite an adjustment to say the least! We have been very fortunate to have our families who have stayed here for extended amounts of time to help out. Big sister Allyson loves her baby sisters and is always wanting to help push them in the swing or unexpectedly wake them up from naps.
Ava needed an additional surgery on Feb. 6th to repair a hernia. Her right ovary had become trapped in the hernia and needed to be fixed. When the surgeon went in, he discovered that the ovary had come out of the hernia on its own, but that Ava had an additional hernia on the other side. So she had two hernias repaired.
They still continue to struggle with their feedings. It looks like this may be a long-term problem that will take some time to overcome. However, with the gastrostomy tubes, they get the nutrition that they need and are gaining weight. They are both around 12 lbs. now. We feel so very fortunate that they are still here with us and that we're able to finally see them smiling and cooing at us. It's so wonderful to have our whole family together and complete.

Monday, February 26, 2007

Miracle Monday!

Skydiving miracle: Man falls two miles




I read about this story, and was amazed that this guy survived!! Check out his story! It's pretty incredible. Some of you may have heard about this already, but I thought it deserved a spot on my blog for Miracle Monday.

http://www.msnbc.msn.com/id/17113222/?GT1=9033

Tuesday, February 20, 2007

Miracle Mondays!

Ok, I have decided that from now on, Mondays I will post a story about a miracle or something amazing that has happened. It will be titled... "Miracle Monday".
This post is near and dear to my heart because all of you know that Zoe was born 10 weeks premature. My mom sent me this story about a woman who gave birth to a baby when she was only 21 weeks pregnant, and the baby SURVIVED and is going home in a couple of days!!! How amazing! See picture below, and click on the title of this blog to read the story! It's simply amazing. God had/has his hands on this little one! She weighed in at a little bit less than 10 OUNCES!!! Check it out!


Friday, January 26, 2007

Christine's Story...

Oh, my goodness am I thankful! I met a woman while Zoe was in the Intensive Care Nursery at Wake Med Hospital in Raleigh, NC... what a phenomenal hospital, by the way! Anyway. I meet this woman named Christine. She was originally pregnant with triplets, but went into labor and had her babies when she was only 23 weeks pregnant! Sadly, 2 of her babies passed away. Sophia survived. Though Sophia was only given a 15-20% chance of survival, Christine and her husband, Rob stayed amazingly strong through it all! I remember several times watching Christine with Sophia, and I could tell what an amazing person she was/is! I am not quite sure how she pressed on, but she did. I know that Sophia's fighting kept her going every day.
Despite odds against her, Sophia has made it through everything, and is now HOME!!! Christine's due date was only a few days before mine... December 23rd. Sophia is now home, and has been for 1 week exactly! Way to go Sophia! Please read more written by Christine...




We are finally home after 146 days - it feels really good! Just now learning to live on little sleep.
Sophia - Five months and one day old

5lbs 11oz

After being born at 23 weeks & 0 days we proud to say that we got the word. "Our little miracle" will be home by the end of the week. After two hospitals, five major surgeries( two eye surgeries), three minor surgeries, too many blood transfusions, countless needles & IV's our little girl is coming home. She was born into a shell of a baby & right before my eyes as turn into a beautiful baby girl. I have watched this little girl fight so hard for life - just to be here for her Mom & Dad. She doesn't even know how good this world can, but yet she wants to be apart of it. What a zest for life!!!!

The past couple of months Rob & I lives have changed, but for the better. We have seen the circle of life & now know the meaning. We have witness a true miracle & have been apart of it. The day after Sophia was born we were told that she had about a 15-20% chance of living. She would more than likely come home on oxygen & with a feeding time. Well, she is coming home with nothing. We are still praying for the best with her little eyes. Only time will tell.

Through this experience we have meet a wonderful group of people at Wake Med & UNC Hospital. Without the care of this staff Rob & I know that we would not have our daughter. The life of a NICU baby is a life we know nothing about. It's like another world. The pain & suffering that this babies go through. This nurses have become my good friends & I'll never forget the unbelievable care they have shown my daughter. Also, to all the new Moms that I meet along the way thank you, for making each day a little easier. This is amazing group of woman that love there babies. It always helped seeing all of you everyday & knowing what each one of was feeling. We are the last to go home from our group, but will always have a connection.

Rob & I are very proud of the fight that Sophia has done & we know that Robert & Natalie are watching over her. I'm never going to know why all of this had to happen. I'm not sure there is a reason why. I just know my Pop is up there taking good care of them & teaching them a love of the water.

I would like to thank everyone for there support & prays over the past couple of months. We are very lucky to have all of you as friends & family. Can't wait to introduce you to her little girl. This journey(nightmare) is coming to an end & I'm ready to start the next journey as a Mom to my little Peanut.

Love,
Rob & Christy

Intensive Care Nursery



Nobody can understand the life of an ICN parent unless you have lived through it. All of us always told each other as we sat rocking our babies that "we would never wish this one anyone", but let me just tell you... every one of those babies in the ICN are miracles!! While in the ICN I learned so much about babies, and what they go through, and what they need. It was definitely an amazing experience. You form such a tight bond with your nurses! They are there while you're laughing or crying. Through your happiness and your sadness. Those nurses are the core to that ICN. If it weren't for them, it wouldn't be the same. Taking that walk to the ICN for the first time was so very scary! Seeing your baby, whom was just in your stomach kicking and thriving is now hooked up to ventilators, nasal cannulas, IV bags, feeding tubes, pulse ox machines, heart monitors, and sometimes there are more tubes than that! See other women's babies suffering, or seeing the babies that weigh just over a pound is very heart wrenching! I can say one thing, though... you form such a bond with the woman in that place! They understand your feelings. They know exactly what you are going through. They are going through it themselves after all. Having that bond with those mothers helps you get through it! I can say this, having a baby in the ICN definitely makes you a much stronger person, and a much educated mother! Having Zoe in the ICN for a mere 5 weeks had made me appreciate life. Appreciate the kiddos I have. Appreciate the fighter that Zoe was/is. Appreciate woman like Christine who had to endure the back and forth trips to the ICN a lot longer than most woman in there! Please read Christine's story...

Tuesday, October 17, 2006

It's a GIRL!




Yes, I know what everyone must be thinking! What?!?! You had your baby ALREADY? But....

Yes, we did. Unfortunately, I went into labor during my dad's birthday dinner and then proceeded to go to the hospital. In getting there I found out that I was 6 centimeters dilated and there was nothing they could do but wait and let the baby come! It was very scary, but, we were told the outcome was excellent! She is healthy! She is on the ventilator, but expected to come off of it any time now.

So, here is the announcement...

Michael, Shealynn and Angelina welcome,

Zoe Rae Benner
Born: 10/17/06 @ 2:41 AM
Weight: 3 LBS. 4 OZ. and 17 Inches Long
Zoe was born 10 Weeks too soon!

Original Due Date: 12/26/06