HAPPY BIRTHDAY PRINCESS BRIANNON profile picture

HAPPY BIRTHDAY PRINCESS BRIANNON

I am here for Friends

About Me



------------------------------------ It's A Boy!!!
Build your own Blingee

------------------- .... ..I edited my profile at Freeweblayouts.net , check out these Myspace Layouts!

..

My Interests


imikimi - Customize Your World------------------- With all the things that have gone on in mine and Steve's life this song makes me feel all warm and fuzzy when I bellar it out ...It expresses how I feel about him and how he makes me feel..I LOVE YOU STEVE ALWAYS AND FOREVER! --------------------------------- PLEASE ADD THIS PAGE TO YOUR PROFILE FOR LITTLE LOGAN GOBLE JUST CLICK ON THE BANNER .. " ----------- THIS IS MY LIL MANZ LOGAN GOBLE HIM AND HIS FAMILY NEED SOME FINACIAL HELP AS WELL AS PRAYERS FROM EVERYONE...YOU SEE THIS LITTLE GUY WAS DIAGNOSED WITH ALOT OF PROBLEMS SHORTLY AFTER HE WAS BORN ..FOR THOSE OF YOU WHO CAN ..COULD YOU PLEASE HELP ..AND FOR THOSE WHO CANNOT ..COULD YOU PLEASE SAY A PRAYER ..THANKYOU...LOT'S OF LOVE TRISHA HIS STORY IS WRITTEN BELOW AND HIS DONATION PAGES ARE IN THE 3RD ROW IN MY FRIENDS LIST




Logan was born on 3-19-07 at Highlands Hospital in Kentucky.When Logan was born we had no ideal that anything was wrong.They left Logan with my daughter for around 2 hours before they took him back to check him.I had already came back home and a couple hours after getting home my daughter called and said something was wrong. They found he had the cleft palate,his respiration rate was high and he needed to be put on oxgen,Highlands has no NICU so Nine hours after Logan was born they released Jessica from the hospital because Logan was being flown out to UK Hospital in Lexington.After getting to UK they weren't sure why his respiration rates were high so they did a heart echo and found he had VSD,coarctation of the aorta,anomalous pulmonary of the vein,2 leaflets instead of 3. On March 30th he had his first heart surgery,coarctation of the aorta and he was put on the respirator.His respiration was still high,On April 13th they did a heart cath and due to what they saw on April 14th he had openheart surgery they patched the VSD,anomalous pulmonary vein repair.On April 20th they placed chest tubes in to drain the fuild.After all this there was several times they tried removing him from the respirator,but respiration was still high he could only stay off the respirator afew hours.

So they decided it would be best to send Logan to Cincinnati Childrens Hospital in Ohio on May 17th.Logan would improve some then take another backset.While in Cincinnati he had balloon dilation of a residual coarctation,and then was difficult to extubate,eventually requiring tracheostomy on June5.In addition,he had a gastric tube placement and Nissen fundoplication on June 21.

On the morning of June 28,Intending to write 10ml/kg to start,given his cardiac history(or 35ml).an ordering error was made,and 350ml was ordered.The nurse hung the fuild,and approximately 220ml(approximately 65ml/kg)had be infused before the error was recognized.After remaining stable 36 hours,given the uncertainty whether or not Logan needed on going diuretics,and his ongoing poor weight,his lasix was stopped.Logan went about 4 days without lastix,when he then developed respiratory distress on the evening of 7/3/07.After all this my daughter wanted Logan took back to UK.Logan finally started improving some and after 4 moths he was able to come home.

Logan still has the trache,feeding tube and is on oxgen he also has a blood clot in his leg.He will go to Cincinnati in Oct.16th at 6:30am at 7:00am he will be put to sleep and have a 3-D CT scan he will also see all 3 of his doctors in Cincinnati then on Nov. 9th he will go to have his surgery to repair his chin,they will be putting distraction pins in,he will stay in the hospital for about 3 days.He will keep the distraction pins in for around 3wks.At 15lb or 17lb the will place a speaking valve on his trache,then some time in ..hey will try to repair the cleft palate.Logan has never been able to make sound not even a cry except one time.He has never had a bottle.Logan has came so far but still has a long road ahead.

I'd like to meet:

Rebetha MAria 7yrs old April 10th 2008 1st grade ================================================== Samantha May Trisha Ann 6 yrs old April 10th 2008 1st grade---------------------------------------------------- AND HERE IS LITTLE LOGAN 1yr LATER........
Photo and video editing at www.OneTrueMedia.com --------------------------------- PLEASE HELP SKYLARS PARENTS BUY HER A HEADSTONE ..THIS LITTLE PRECIOUS ANGEL WAS ONLY 4 YRS OLD WHEN SHE PASSED AWAY ....NO CHILD SHOULD EVER BE TURNED AWAY ..LOVE TRISHAPLEASE DONATE TO GET SKYLAR~JADE
HER HEADSTONE....
ANY AMOUNT IS APPRECIATED...
SKYLAR~JADE FUND

Address is:

Bank of Wolcott
SKYLAR MAXSON FUND
116N.6th Street
Monticello,Indiana 47960
BANK PHONE# 574-583-5300(MONTICELLO BRANCH)
# 219-279-2185(WOLCOTT BRANCH)

IF YOU HAVE ANY QUESTIONS JUST CALL THE BANKS...

For cards and gifts:
Skylar~Jade Maxson
c/o ConnieJo Maxson
438 Walnut Street
Monticello,Indiana 47960



"HEAVEN'S RAINBOW GARDEN"

I went to heaven's rainbow garden,
And saw flowers on every side,
And loveliness too great to imagine,
Where no good thing was denied.

I heard the angels, there singing,
With songs that I'd never heard,
As joy in the garden was ringing,
With rapture undisturbed.

Then I saw in the distance,
As a Glorious Light from afar,
A vision of our Loving Jesus,
Who heals every broken heart.

He was there in the rainbow garden,
Beside the fountain of Life,
To welcome all of His children,
And sing them songs of delight.

He was there with arms extended,
Reaching to give each a hug,
To give them treasures unending,
That could only be found in His love.

He was there to gather the children,
And remind them there'd be no fear,
As they came into His rainbow garden,
Where every sorrow would disappear.

Four-year-old Skylar-Jade Maxson loved her rainbow garden.

In fact, she spent most of her summer there, as the weather would allow, lying on a soft bed made up of layered blankets nestled in a crowd of impatiens, bright yellow and orange marigolds, purple and pink petunias, scarlet geraniums and the blushing blooms of the Mandevilla vine.

Skylar-Jade would often fall asleep in her rainbow garden, a place where she was always at peace and free from the torment of the brain tumor that had robbed her of the ability to speak and function as a typical child.

"I wanted a place I could bring her outside," said Connie Maxson, Skylar-Jade's grandmother and adoptive mother. "She loved flowers. She loved to listen to her wind chimes, listen to her birds, feel the wind. It was peaceful for her."

Though Skylar-Jade won't return to the rainbow garden at her Monticello home, ConnieJo will continue to tend and grow the garden - and spread the word about the inoperable brain tumor, known as a diffuse pontine glioma, that invaded Skylar-Jade's brainstem at the age of three.

Skylar-Jade passed away last Thursday night at age four, having been diagnosed with the tumor in May of last year. The particular type of tumor that victimized Skylar-Jade is rare and afflicts about five to 10 out of every 100 cancer diagnoses amongst children medical research states. It is considered inoperable because the tumor cells grow in and around healthy cells in the brainstem, interfering with critical functions controlled by that part of the brain.

When Skylar was diagnosed last spring she was given six months to live, and her family told most children live on average just one year past diagnosis. Twenty percent survive two years.

"No child has survived this tumor," said ConnieJo, resting on a swing on the outskirts of the rainbow garden Friday evening. "I'm going to continue to spread the word about this. If I can reach just one person who didn't know about this yesterday, then Skylar's life meant something. The world has to learn this attacks healthy children. too"

Skylar-Jade was indeed a healthy little girl prior to last May, when ConnieJo says she simply and suddenly lost muscle strength, the ability to maintain her balance and the use of her throat muscles. Misdiagnosis is often the case with children who are ultimately diagnosed with diffuse pontine gliomas, said ConnieJo, because the symptoms can mask the greater problem. Though she knows little can be done once a child has been found with the tumor, there is much room for research and a better understanding of it ConnieJo attests.

Life will be different for ConnieJo and Skylar-Jade's brother Tristan, 12, who ConnieJo also adopted, as they move away from a routine that involved constant visits with physicians, oxygen machines and attention paid to every breath Skylar-Jade took. Helping the family and their friends through their transition is Tammy Benner, a bereavement counselor with Serenity Hospice.

Benner has spent time getting to know the Maxson's since hospice became part of their lives shortly after Christmas last year. She testified to the strength of the family and said that though they will be grieving for some time over the loss of Skylar-Jade, sometimes what those in mourning need is just the presence of a familiar face or voice.

"There's no easy answers for a child (who dies). The most important thing is that a lot of people don't know what to say, but just being there is helpful. It's not always what you say."

Amber Biggs, a cousin of the ConnieJo said the family has been helped immensely by the hospice staff and have gained a greater appreciation for life and one another through Skylar-Jade's battle for life. Connie says her faith in God kept her strong for Skylar-Jade when she needed her most. It will keep Connie strong as her life continues without Skylar-Jade in the rainbow garden.

"I've watched God give her many miracles and we have lived on nothing but prayer for the last year. It held me up, holding a child, knowing she's leaving. And then, everything normalizes. My arms ache for her but she's showed us not to give up hope. You can be dying, but you can hope. God was there, part of my every day and he changed us forever."

"RELEASING SKYLAR-JADE"
Skylar-Jade, my little princess,
I embrace you now with tears,
Feeling with all my senses,
I must face my deepest fears.
For as I've held you near me,
And tried to ease your pain,
I have also cried for mercy,
As I was whispering your name.
I love you , little darling,
As I've loved you from the start,
But now I face your parting,
And my world is torn apart.
For I must now release you,
To the arms of God above,
So your purpose will continue,
In the fortress of His love.
I must release you to the Father,
And now trust His plans for you,
As His own sweet little daughter,
He is making whole and new.
So "good-bye," little darling,
I must release you for awhile,
But one day there'll be morning,
And we both will wear a smile,
At last, then home together,
No more parted in this way,
When we both are with the Father,
And our tears are wiped away...

to repost:
hit reply (dont hit send)
copy everything
go back to a new bulletin
paste everything & know you made a difference

Music:



Please send carepackages to Logan's Grandmother.
Teresa Johnson PO BOX 445 Weeksbury KY 41667
Do NOT send them to us! Thank you so much for your support and contribution to sweet baby Logan!

Movies:

----------------- Bulletin Message ----------------- From: Jayden Wants to Kick Cancer and Abuse In the Ass Date: Mar 1, 2008 5:48 PM
Copy this code to your website to display this banner!
..

My Blog

continued from the other one

ok I only have about 40 minutes till they get out of school ..this matter better have been resolved for real..cause tomorrow i won’t be as nice as I was today .......
Posted by HAPPY BIRTHDAY PRINCESS BRIANNON on Mon, 07 Apr 2008 11:42:00 PST