Monday, 3 November 2014
Monday, 22 September 2014
#chicktrain
Have you seen the #chick Train on Facebook?
#Chick is shared every Friday and is used to create awareness for not only Charleigh Jayne's Berlin Heart Fund, but also, to raise awareness for CHD (congenital heart defects) and for organ donation, donors and recipients.
SO when you see the Train on your timeline, give it a share, it takes 2 clicks and together, we can all be heroes!
Much Love
Team Chick xxxxxx
Tuesday, 15 April 2014
#chickband
SOLD OUT!!
500 #chickbands
500 proud owners
£500 to start the Charity Fund
We have now placed an order for some more, and we will have some
seasonal special limited edition ones coming too.
With all the support we have been receiving for Charleigh Jayne’s
Berlin Heart Fund, it’s hard not to get a little emotional. To know that she
touched so many people in her short time here.
So in the next edition of our blogs, you will see stories of people
who met Charleigh, who have very special memories of her.
Thank you all for your continued support.
The CJBHF Team xxx
Thursday, 3 April 2014
Have you got your #chick on?
Have you got your #chick on?
You can order your wrist band via our website www.charleigh-jayne.webs.com
Or tweet your order to @cjbhf
Or via the Facebook page www.facebook.com/pages/Charleigh-Jaynes-Berlin-Heart-Fund
Here are some of our followers who already have theirs, can you spot yours?
Monday, 31 March 2014
Heart Warriors
It is with a very sad heart that I write this post.
As I write this I am not sure of the outcome, but I am hoping it isn't the worst. As many times we have done before, I am praying for a miracle.
Throughout the journey of a heart transplant for a child, you form friendships, a support circle, and bonds with others on the same journey as yourself. This not only helps you, but helps everyone around you.
The tail end of this support, newly formed friendships and bonds is that you ride your own roller coaster, but you also board theirs. You ride the waves of relief and good news, but you also battle the undercurrents of bad news, long recoveries and sometimes death.
There is just one thing on my mind when it comes to this. WHY?
Why? is the Transplant list so long?
WHY? have the government not changed the infant rules BEFORE?
Why? does this have to happen to the ones you love?
and most importantly WHY is everyone not on the list?
So with the questions unanswered we will have to answer them ourselves?
An Army of Heart Mums, Dads, Sisters and Brothers, Aunties and Uncles.
An Army of Doctors, Nurses, Play specialists.
An Army fighting for one thing. One Outcome. One life does not have to end for nothing when it can start 7 more.
Please, if you read this, and have not already signed your organ donation register, wherever you are in the world. Become a hero today and sign it.
And if you have Facebook, or twitter, share this blog, and you might convince one person to sign the register but you will have saved another 7 lives too :)
Charleigh Jayne's Berlin Heart Fund
As I write this I am not sure of the outcome, but I am hoping it isn't the worst. As many times we have done before, I am praying for a miracle.
Throughout the journey of a heart transplant for a child, you form friendships, a support circle, and bonds with others on the same journey as yourself. This not only helps you, but helps everyone around you.
The tail end of this support, newly formed friendships and bonds is that you ride your own roller coaster, but you also board theirs. You ride the waves of relief and good news, but you also battle the undercurrents of bad news, long recoveries and sometimes death.
There is just one thing on my mind when it comes to this. WHY?
Why? is the Transplant list so long?
WHY? have the government not changed the infant rules BEFORE?
Why? does this have to happen to the ones you love?
and most importantly WHY is everyone not on the list?
So with the questions unanswered we will have to answer them ourselves?
An Army of Heart Mums, Dads, Sisters and Brothers, Aunties and Uncles.
An Army of Doctors, Nurses, Play specialists.
An Army fighting for one thing. One Outcome. One life does not have to end for nothing when it can start 7 more.
Please, if you read this, and have not already signed your organ donation register, wherever you are in the world. Become a hero today and sign it.
And if you have Facebook, or twitter, share this blog, and you might convince one person to sign the register but you will have saved another 7 lives too :)
Charleigh Jayne's Berlin Heart Fund
Monday, 17 March 2014
What does Organ Donation Mean to you?
What does Organ Donation mean to you?
Unless you have been directly effected by the need for a donor organ, its not on the top of the to do list.
You never imagine, the long wait, the nerves, the stress, that call.
Once upon a time, there was this beautiful little princess, she was on day 254 of a Berlin heart, waiting for her call.
At 4am THAT call came, but some people are not that lucky, and should it be down to luck?
Why?
Why should you, or your loved one have to face every day waiting for death on the list?
Why should you have to wait?
Why cant there be an opt out service?
Why are there not enough to make a difference?
Why? Selfishness, perhaps, ignorance maybe. Lack of understanding, DEFINATLEY.
There is never a good time to discuss death and organ donation with young children, but what happens when a young child needs a donor organ?
When is it ok to loose a loved one? When is it ok to give a gift of life?
Last years statistics, they don't look too bad, but translate them into waiting lists, and funerals.
What cost do we have pay to get the Opt out system
Just going to leave you with this...
What would YOU do, if YOU were waiting for an organ?
Be A Hero, Save a life.
www.http://www.organdonation.nhs.uk/
Unless you have been directly effected by the need for a donor organ, its not on the top of the to do list.
You never imagine, the long wait, the nerves, the stress, that call.
Once upon a time, there was this beautiful little princess, she was on day 254 of a Berlin heart, waiting for her call.
At 4am THAT call came, but some people are not that lucky, and should it be down to luck?
Why?
Why should you, or your loved one have to face every day waiting for death on the list?
Why should you have to wait?
Why cant there be an opt out service?
Why are there not enough to make a difference?
Why? Selfishness, perhaps, ignorance maybe. Lack of understanding, DEFINATLEY.
There is never a good time to discuss death and organ donation with young children, but what happens when a young child needs a donor organ?
When is it ok to loose a loved one? When is it ok to give a gift of life?
Last years statistics, they don't look too bad, but translate them into waiting lists, and funerals.
What cost do we have pay to get the Opt out system
Just going to leave you with this...
What would YOU do, if YOU were waiting for an organ?
Be A Hero, Save a life.
www.http://www.organdonation.nhs.uk/
Wednesday, 12 March 2014
Urban Treasure Hunt Milton Keynes
So what is it?
We have hidden 2 #chick stones across Milton Keynes. They are accompanied with an envelope with instructions.
You will receive 1 photo and 3 clues on where to find the stones on Charleighs page.
Go and check them out find them then follow the instructions.
Love all at the CJBHF team xxx
Monday, 10 March 2014
Our Mission #chick
Charleigh Jayne
Berlin Heart Fund
This fund has been set
up to raise money for families with children on the Berlin Heart. The Berlin
Heart is a mechanical pumping unit which sustains the life of those waiting for
a transplant; it is often referred to as a bridge to transplant, and patients
on these devices would not survive without them.
Children on the Berlin
Heart often spend months at a time in hospital, the current record is 273 days on
this device, this does not include time before the Berlin Heart was chosen as a
means to ensure their survival, or the period in which the child recovers from
their transplant.
For the families of
these children it means that they are separated for extended periods of time
from their immediate family members. Usually accommodation at hospital is only
for one parent, some children have to travel hundreds of miles for this
treatment as currently the Berlin Heart is only available in 2 hospitals across
the country. This can cause financial hardship for the family as often the
second parent/carer will need to reduce working hours or give up working
altogether to care for other siblings, the parent staying continuously at the
child’s bedside is also unable to work. No parent should have to worry about
their bank account and bills whilst their child faces life or death.
The Charleigh Jayne
Berlin Heart Fund aims to provide financial help to the families of those
children, by helping with travel costs, utility arrears accrued whilst a child
is on the device, and help towards rent or mortgages and to support these
families to budget with the rising costs of a long term stay in hospital.
Our ultimate aim is to
raise enough money to provide accommodation so that all members of the child’s
family can spend time together at weekends, birthdays, religious holidays, and
so that the parent that is continuously at the child’s bedside can have members
of their family be with them. It is a long and hard journey on the Berlin
Heart; we believe that no person should be alone during this time.
The Charleigh Jayne
Berlin Heart Fund will also promote the importance of organ donation and
awareness of CHD at every possible opportunity.
#chick
#organdonation
#CHD aware
Update
Today is 10th March 2014.
So Charleigh's charity is being born, and from the depths of pain and loss, a legacy will arise.
Follow the story of Charleigh Jayne's Berlin heart Fund.
We promise to raise awareness for Organ Donation, and Congenital heart defects (CHD) by hash Tagging Chick wherever we can.
We will raise funds to make life more comfortable for families with children on the Berlin Heart machine, in The Freeman hospital and Great Ormand Street hospital.
Any one is welcome to raise funds for Charleigh Jayne's Berlin heart Fund and you can contact one of the administration team by in boxing them on the facebook page, or emailing cjberlinheartfund@outlook.com
We thank those who have supported us from the start, that share our journey as we begin, and those who will come in time, to make this a new dawn.
Love CJ's Berlin Heart Fund Team xxx
So Charleigh's charity is being born, and from the depths of pain and loss, a legacy will arise.
Follow the story of Charleigh Jayne's Berlin heart Fund.
We promise to raise awareness for Organ Donation, and Congenital heart defects (CHD) by hash Tagging Chick wherever we can.
We will raise funds to make life more comfortable for families with children on the Berlin Heart machine, in The Freeman hospital and Great Ormand Street hospital.
Any one is welcome to raise funds for Charleigh Jayne's Berlin heart Fund and you can contact one of the administration team by in boxing them on the facebook page, or emailing cjberlinheartfund@outlook.com
We thank those who have supported us from the start, that share our journey as we begin, and those who will come in time, to make this a new dawn.
Love CJ's Berlin Heart Fund Team xxx
Friday, 7 March 2014
#chick on Facebook and Twitter?
#chick (click chick to see more)
Well here is her story in short;
Charleigh Jayne Thomson 7.5.10 -16.2.14 Light of our lives.
Christina Thomson, gave birth
to 3lb 4oz Charleigh On 7th May 2010.
After a
difficult pregnancy, the bay was expected to be low birthweight.
But
immediately after delivery there was an added shock - Charleigh’s tiny heart
was not working properly.
She had
a hole in the heart and her pulmonary valve is blocked, which means the heart
cannot pump the blood around her body.
Charleigh
was rushed to the neonatal unit, where doctors gave her drugs through a line in
her arm to force the heart to pump.
Without
that she would have died there is no doubt that the unit saved #chick’s life.
Charleigh
was then moved to Great Ormond Street for
an operation to repair her damaged heart.
Charleigh
was one of 350 lives saved every year at the unit, which urgently needs more
cots and more equipment.
After her first heart repair
she was sent home well, and with another operation to follow as she got bigger.
Charleigh Thomson was then left
fighting for her life after the operation to fix her seriously defective heart
went sadly wrong.
Doctors
in Great Ormond Street Hospital were pulling out all the stops to make 19 month
old chick survive long enough for a donor heart to be found.
She was
just so poorly. The doctors were fantastic and they done everything they
possibly could. But Charleigh’s only hope was an urgent heart transplant.
She needed a new heart as soon as
possible, but had to wait until one was found and watched her fading away while
they waited.
Doctors adjusted the medication keeping Charleigh
alive and decided whether she would be strong enough for a stopgap solution, a
mechanical Berlin heart.
The
problem was that the operation to give her a Berlin heart was even more
complicated than transplanting a human heart. The risks of the surgery, because
Charleigh was so ill, were horribly high.
At the last minute the Berlin heart
was attached to Charleigh, with hopes of a transplant to come.
Charleigh stayed hospital bound for 255 days on the Berlin Heart waiting
for a Transplant.
But it would not last forever; she needed a new heart fast before her
heath failed.
Charleigh was awarded MK prides Bravery award for her fight for life and
captured the heart of everyone who heard her story and they fell instantly in love
with her when they saw her smile.
She even captured the heart of Milton Keynes’
Olympic gold medallist Greg Rutherford, who made a special trip to Great Ormond
Street to visit the sick children. #chick had a special smile just for him.
Finally, in the early hours of the morning on
August 23rd 2012 the, came then call every one had been waiting for.
After a tough recovery Charleigh was allowed home,
no machines, no mechanical heart. A normal (ish) life at last.
Charleigh suffered some rejection and came through
this but suddenly during a second bout of rejection grew her angel wings on
February 16th 2014.
She is missed by all and loved by all, and will
leave a lasting imprint on this world.
Do your bit to help raise awareness for CHD
(congenital Heart Defects) and Organ donation, which blessed Charleigh with
another full year and 9 months with her family.
Light of our lives, help save a life, or seven!
Sign the Organ donation register, you may need one,
one day.
Follow her fund'a progress on Facebook.
Search for Charleigh Jaynes Berlin Heart Fund page.
R <3 I <3 P Princess Your Memory WILL Live on! I promise!!
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