Showing posts with label Lila Rae. Show all posts
Showing posts with label Lila Rae. Show all posts

Tuesday, October 26, 2010

Heaven is Celebrating Today…..Lila Rae’s Heavenly Birthday

 

lilarae

I've lost my baby daughter,
Though not misplaced.
I feel she's somewhere
Bound by neither time nor space. 

Perhaps she sits before the Throne
With radiant face.
She could be dancing happily
Like little girls do
With golden taps beneath
Each precious little shoe.

I know she must love music,
So I'm sure it's true.
I'm grateful that in Heaven
She is healthy and strong
And that she's lulled to sleep each night
By Heaven's song,
But I wish I could hold her;
Is that terribly wrong?

I sang so often to her
While she was with me
And I will go on listening
For her harmony.

How sweet to know
I'll hear it In eternity.

Lisa L. Easterling
Copyright 1990

LilaRae_thumb[4]

Missing you today and everyday my sweet baby girl.  But we keep our pink balloon in sight, reminding us your presence is always soaring near.

Love you so much,

Mommy

Tuesday, September 28, 2010

Lila Rae’s Birthday Gifts and More

 

2010_0904October20090066

LilaRae1 Our Lila Rae

On Lila Rae’s birthday we did ALL the things we do for our precious angel’s big day!  At church, the flowers at the Altar and the wreaths on the front door were dedicated in her honor.  We had her special birthday dinner and dessert.  We took her flowers and sent her and Jesus some balloons (pink of course). 

Her day was VERY special.  It always is.  BUT.  This year was different.  She was giving us a gift!

On this day, out of God’s hands, we were given a home!!!  Now for months we have been working on this project……waiting for the day to close on our new home.  And of course the FIRST day that was available for ALL involved was September 13th, my baby girl’s birthday.  You cannot tell me that that isn’t the work of our Lord and Savior!  So we like to think of our new home (a much needed home) as a gift from our Lord with a little help from his angel Lila Rae (smiling!)  I AM ONE PROUD MOMMA!!!!  To know that my baby girl is not only sitting in the right hand of our God but is actually working with Him to show her love for us.  (yes I am crying….but what Momma wouldn’t be?!)

What a beautiful thing it is to see God’s involvement in our lives.  How He continues to show His love and grace is amazing to me.  I am so thankful He interwove(?) my Lila Rae and our home.  You know I couldn’t figure out why God had been prolonging the closing on our home.  I would get upset and wonder if we were even doing the right thing.  But Cory and I knew God’s hand was in it and we just had to wait on His time.  NOW I know why and I am so thankful He waited….waited for Lila Rae.

What a special day my Lord made………

 house

Our new home!

 

 Whatever is good and perfect comes down to us from God our Father, who created all the lights in the heavens.  He never changes or casts a shifting shadow.

James 1:17

Monday, September 13, 2010

Our Heavenly Angel is Four

 

LilaRae

Today is a very special day!  The birthday banner is hanging outside, the cake is in the oven, and the special birthday menu is ready to be prepared!

The only thing missing is our baby girl!

Birthday party plans should be in the making.  Everyone is tuned up, ready to sing her her song.  The balloons have been ordered and her flowers are as perfect as she is.

The only thing missing is our baby girl!

Oh how I wish this day was filled with the laughter of our Lila Rae.  Having her here to celebrate her birthday is something we’ll never have.  She will always be the missing link to our family.  Physically. 

But we know that she is with us  in other ways

She is our guardian angel that protects her sisters and brother.  She is in the warm smile or laughter I receive from other babies.  She is in the extra hug or “I love you Mommy” that I get from my girls or Whit.  She is in the beauty ALL around us.  She is always in our thoughts.  On our minds.  In our life.  There isn’t a day that goes by she isn’t thought of.

Thank you God for this beautiful gift You so richly blessed us with.  We will always treasure this day and the beauty, our Lila Rae, shared with us all.

Happy Birthday Lila Rae!  We love you!

You made all the delicate, inner parts of my body and knit me together in my mother’s womb
~ Psalm 139:13 from NLT

God is good….ALL the time,

~jct~

Sunday, February 14, 2010

Our CHD Angel



Sweet Lila Rae
A glimpse of sweetness,
Precious moments of love,
Then our sweet little Lila Rae,
Was taken to heaven above.
God shared with us a miracle,
to hug, hold, and love.
He gave to us, our Lila Rae,
with blessings from above.
Her stay with us was very short,
her heart was just too weak.
So God took his precious angel
to sit at Jesus' feet.
We'll meet again in heaven,
with no sickness, and no pain.
There we'll see our angel, Lila Rae,
and her precious smiles again.
Cheryl Mullis
In memory of our beautiful Lila Rae on this last day of CHD Awareness Week 2010.
Please don't forget all those babies effected by these defects. Remember them and their families in your prayers. Thank you.
God is good....ALL the time,


Thursday, February 11, 2010



Twas the night that you joined us...all eyes were on earth.
Awaiting with joy for a most special birth.
The angel's stood ready...for each need and care,
But all of them knew... that the Lord would be there,
And I labored on... and daddy was scared,
We waited...and wondered... and hoped we'd prepared.
We knew you were special...but so very sick,
Yet hope had grown in me... with every kick.
And soon it was time...into this world you came,
I heard a soft cry... then I called out your name....
And God held your hands...while the angels stood by,
Since I could not hold you...they hushed your soft cries.
One small angel looked to the father and smiled,"Can you truly teach hope... through such a small child"?"An infant so helpless...a baby so new...
"Oh please tell me Lord...is this what you will do"?
God looked from the angel...to the baby's sweet face,
"Through him my young charge... they will learn about grace"."I penned this child's journey...quite a long time ago,"And through his great courage...
such true love will grow". "Every hair on his head has been numbered you see.."
"It's my hope that through him... they will learn to see me.
"Oh my little one with a special heart...""Great love will see you through.."
"See look that is your family..""They've been waiting for you.."
"I send you to their waiting arms...for a time we'll be apart.."
"But I'll always be with you...for I live within your heart.
And so we held you in our arms...And thanked our Lord above..
In you...we see the miracle,of His undying love.
So when it's Christmas morning, And I watch my children play,
I'll need no great reminders,For I see my gifts each day.
Stephanie(Mommy to Braeden, HLHS)

Don't you see that children are God's best gift? the fruit of the womb his generous legacy? Like a warrior's fistful of arrows are the children of a vigorous youth. Oh, how blessed are you parents, with your quivers full of children! Your enemies don't stand a chance against you; you'll sweep them right off your doorstep.

Psalm 127:3-5

God is good ALL the time,

Wednesday, February 10, 2010

CHD Facts



  • The American Heart Association directs only $0.30 of every dollar donated toward research. The remainder goes toward administration, education and fundraising efforts. Of the $0.30 that goes toward research only $0.01 goes toward pediatric cardiology for CHD. Source: Children’s Heart Foundation

  • This year approximately 4,000 babies will not live to see their first birthday because of Congenital Heart Defects. Source: Children’s Heart Foundation

  • The cost for inpatient surgery to repair Congenital Heart Defects exceeds $2.2 billion a year. Source: Children’s Heart Foundation

  • Of every dollar the government spends on medical funding only a fraction of a penny is directed toward Congenital Heart Defect research. Source: Children’s Heart Foundation

  • Though research is ongoing, at least 35 defects have now been identified.

  • 4-8% born with CHD have Hypoplastic Left Heart Syndrome

  • 4-10% born with CHD have Atrioventricular Septal Defects

  • 8-11% born with CHD have Coarctation of the Aorta

  • 9-14% born with CHD have Tetralogy of Fallot

  • 10-11% born with CHD have Transposition of the Great Arteries

  • 14-16% born with CHD have Ventricular Septal Defects

  • Although some babies will be diagnosed during gestation or at birth, sometimes the diagnosis is not made until days, weeks, months, or even years after. In some cases, CHD is not detected until adolescence or adulthood. Source: March of Dimes

  • It is a proven fact that the earlier CHD is detected and treated, it is more likely the affected child will survive and have less long term health complications. Source: March of Dimes

Thanks again for taking the time out of your schedule to read over these facts. Who knows, maybe you can help someone you know one day through the information you received today.


Be strong and let your heart take courage, all you who wait for and hope for and expect the Lord!
Psalm 31: 24



God is good......ALL the time,

Tuesday, February 9, 2010

CHD Awareness Week


It’s a beautiful day up in heaven. Jesus is rounding up his tiniest angels, to go live on earth, and be born. One of the sweetest angels says to Jesus “I don’t want to leave, I like it here, and I will miss you”.
He reassures the scared little angel that everything will be okay, and that he is just going for a visit. He is still not swayed on this idea. So Jesus kneels down, and says, “How about if you leave half of your heart here with me and take the other half with you, will that be okay?” The angel smiles and says, “I guess that will work”.
But the little angel is still a little scared. He asks,”Will I be okay with only half of my heart?” Jesus replies,”Of course you will, I have other angels there that will help out, and you will be fine.” Then Jesus gives the angel more details about his plan.
He says “When you are born, your mommy will be scared, so you have to be strong, and when you feel weak just remember that I have the other half of your heart”.
“Enjoy your time with your family, play and laugh everyday.” “And when its time to come back to heaven, I will make your heart whole again. Always remember that you are not broken, just torn between two loves.”
Author Unknown



Sunday, February 7, 2010

Pulse Oximetry Screening on Newborns

Eight months pregnant with Lila Rae




this is one of the many tests that were performed on our Lila Rae. however, there are too many babies who don't get this simple screening. please take the extra measures to make sure this test is done one your little ones.

Pulse Oximetry Screening on newborns



A test that measures oxygen levels in newborns can detect "critical" congenital heart disease, but there are variables involved with the test that require more study before it is adopted for universal newborn screening, according to a new joint statement from the American Heart Association and the American Academy of Pediatrics.


A critical congenital heart defect is one a child is born with that requires surgery or catheter intervention in the first year of life, such as Tetralogy of Fallot and Coarctation of the Aorta, among others. The benefits of the oxygen test, called a pulse oximetry screening, outweigh the risks, but the best way to implement pulse oximetry screening is not well established by research.


Thus, the organizations affirm that the test can be used at a physician's discretion, and call for more research to determine whether the test should become part of the routine assessment of all newborns in the United States.


In the research reviewed, the test's ability to detect critical congenital heart disease varied widely, from zero to 100 percent. According to the statement, most studies that have analyzed pulse oximetry in newborn screening were relatively small, and screening protocols differed with respect to both age at screening and cutoff levels for an abnormal screen. A normal oxygen reading is between 97-100 percent. Because oxygen levels in healthy newborns can vary considerably in the first 24 hours of life, the authors note that testing after 24 hours would appear the best strategy. False positive rates were just .035 percent in infants screened after 24 hours. "The statement is important because there hasn't been any strong guidance so far regarding the use of pulse oximetry as a diagnostic technique in newborns," said William T. Mahle, M.D., FAAP, chair of the writing committee and associate professor of pediatrics at Emory University School of Medicine in Atlanta. "Some hospitals across the country have adopted it and others haven't, so we wanted to review the available evidence and offer a consensus opinion on the topic."


The test potentially can identify significant or life-threatening heart defects that may otherwise go unnoticed or at least unnoticed before a newborn is released from the hospital, Mahle said. Early identification of certain defects is important, and can allow doctors to begin appropriate treatment or transfer to a specialty hospital.


Pulse oximetry was developed in the early 1970s, based on the fact that red blood cells that carry oxygen absorb different wavelengths of light vs. those that don't carry oxygen. Oxygenated blood cells absorb infrared light, while deoxygenated cells absorb red light. The test measures how much oxygen is in blood that flows through the arteries. Arterial blood oxygen levels are measured by a device with a thin wire, tipped by a small red light. The wire is taped to an infant's foot for a few minutes to obtain a reading. In older children and adults, pulse oxygen is often measured by a device clipped on a finger.


The overall cost of the test is reasonable, and is about the same as the cost of other newborn screening tests.


Source: American Heart Association, 07-07-09

Then the light of my blessing will shine on you like the rising sun. I will heal you quickly. I will march out ahead of you. And my glory will follow behind you and guard you. That is because I always do what is right.
Isaiah 58:8

CHD Awareness Week



CHD Awareness Week February 7-14, 2010
For those of you who don't know this is a cause near and dear to my heart. It was three short years ago that my sweet Lila Rae was diagnosed with a CHD. Unfortunately, she had a rare CHD, Hypoplastic Left Heart Syndrome, and died at 6 weeks of age.
This week I want to share with you some things about CHDs and its victims. So please check through out the week to learn something new about these defects.
Also, Cory and I will be wearing red ribbons this week to support the awareness. Please feel free to do the same!

  • Sometimes during early pregnancy, a baby's heart fails to form properly, resulting in structural abnormalities known as Congenital Heart Defects. Although some defects are genetic, in many cases the cause is unknown.

  • It is estimated that 40,000 babies with Congenital Heart Defects (CHD) are born in the United States each year. More than 1 million American children and adults with Congenital Heart Defects and Childhood Onset Heart Disease are alive today.

  • CHD is the most frequently occurring birth defect, and is the leading cause of birth-defect related deaths.

  • Although some babies will be diagnosed at birth, newborns are not routinely screened for CHD. The consequences of a late diagnosis can have serious, lifelong implications, so it is important for the public to be aware of the signs and symptoms in newborns, and children.

  • Some CHDs may not require treatment other than periodic visits to a Pediatric Cardiologist. Others can be treated with medications or repaired with surgery and/or procedures. Complex defects may require several surgeries and are never really "cured".
    Many cases of sudden cardiac death in young athletes are caused by undiagnosed CHDs and Childhood Onset Heart Disease.

  • It is estimated that more adults than children are living with congenital heart disease, and this population is expected to grow by 5% each year. Yet, many adults with CHD are not receiving adequate ongoing care from trained specialists. ***


* American Heart Association: Statistical Update 2001
** American College of Cardiology, 32nd Bethesda Conference: Care of the Adult With Congenital Heart Disease
***Report of the National Heart, Lung, and Blood Institute Working Group on Research in Adult Congenital Heart Disease, 2006







Wednesday, September 16, 2009

Sweetness in the Storm

As you know, Sunday was Lila Rae's birthday and well we have a few small traditions. Since I will never be able to give my baby girl a birthday party, buy her a prom dress, or shop with her for her wedding dress, I have my own little things that I like to give her. Every year Cory and I place a beautiful arrangement at the alter, of our church, in her memory. I always get wreaths to match but someone always beats me to the punch. One year my brothers gave them in her memory and this year our church was gracious enough to place them there in her memory. I thought they turned out beautifully! I wanted something that would be a good transitional arrangement....going from summer to fall. I LOVE these colors.



We have other Lila Rae traditions that I will share later this week. But what I wanted to show you this video of my precious little girls singing. I LOVE this song...you probably already know that! But Cora Jane and Vera Kate wanted to sing it in church on Sunday and so who am I to say no! I hope you enjoy it! I am a super proud Mommy. By the way, Whit was dancing away as the girls were singing...they are just the best!