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Fred's Story
Mary Lou Allocco
Jim Kane
Michele Hood
David
Keegan
Jessica
Loulou
Linda Edwards
Jerry Berkesch
Bill Westerman
Joe and NaDeen Sierra
Megan
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Fred and I have participated
in the American Heart walk for about eight
years now. We get the information flyers they
send out and I read articles they run in the
AARP magazine etc. After reading about the
CRP blood test in the AHA material and seeing
it again in the AARP magazine in 2004 we decided
to add that to our annual physicals. Fred was
56 years old and in good physical condition
other than moderate high cholesterol. After
the blood test came back 9.2 on a possible
scale of 1-10 we were very concerned as was
his cardiologist (our primary care Doc) Fred
had not had any shortness of breath or chest
pain, absolutely no indication of a problem.
The next step was a thallium stress, where
the ejection fractions were not what they
should have been either; next step was a
heart cath. After the doctor checked Fred
out and saw what good shape he was in, he
indicated that he really did not expect to
find anything wrong. Thanks to the blood
test we continued with the testing and there
was a 90% blockage in the centraflex artery.
We would have had no idea and Fred could
have experienced a cardiac event at any time.
Thank you American Heart Association for
your research and educational materials.
Fred had the balloon procedure and a stent
placed in that artery and has no problems
since.
I can’t tell you how many friends
I have shared this information with and hope
that you will too.
God Bless each of you,
Fred and Linda McCoy
Palmetto, Georgia
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Mary
Lou Allocco
Impossible
There has never been a more
perfect person than my mama.
It's simply impossible.
Through her flaws; she is flawless.
With imperfections, she is pure
Pure...that is how you can describe my mama.
Her skin is porcelain, her words are diamonds
and her touch is gold:
for the longer you know her, the richer you
grow
although you may still be poor in the eyes
of those who don't know her.
If only they knew what a miracle they were
missing.
You do not need money to be happy, or expensive
cars, or fancy clothes.
Just ask Mama's flannel vest and make-shift
shorts.
They will tell you it was an honor to be
loved by the most perfect person
(and the happiest at that)
Her life was not what an observer would call
ideal
...yet she never did sit in the stands.
She was running (or so she called it) and
stumbling and crying
and all the while smiling.
With every scratch she grew stronger
and weaker
With every fight, she made me prouder
and more humble,
until the sudden realization came that she
was worn out from being perfect.
I thought it was impossible...
My time to touch and hug her is gone, but
I can still cry to her;
I can't hear her voice, yet she goes on teaching.
She doesn't give me words of wisdom as she
did before,
but her words are forever in my heart.
I love her and she was taken, yet every day
I am blessed.
Blessed with the knowledge that the most
perfect person
taught me everything I know.
I am who I am because of my mama and that
is an honor.
I will run as fast as I can to see her again
but for now, she told us to be happy and
smile.
And I will be happy as long as I keep every
last diamond
and every last ounce of gold sealed in my
heart and actions.
I am relieved to know that at the end of
all of this
we will be together again and, that single
thought keeps me going.
Radiating happiness was one of my mama's
greatest talents
and to live unhappily is
simply impossible.
Copyright © 2005 Laura Therese Allocco.
All rights reserved.
Photo: Laura with her mother Mary Lou
Allocco
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Jim Kane -
My name is Jim Kane, I am 51 yrs. old and
had a heart transplant on 11-16-1992 at
MGH in Boston. My heart was destroyed by
a virus in 1988 and I waited until 1992
for a heart. I give thanks everyday for
my donor (David 16 yrs. old) and his family,whom
I have met and become friends with. They
donated their son's organ in order to give
myself and others the Gift of Life. I also
give thanks for my wonderful wife, who
is my hero. I never returned to work after
my transplant, because my job as a school
police officer was very dangerous. But
it enabled me to stay home and enjoy my
2 sons as they grew up Allowing me to coach
them in baseball and see them thru middle
school, high school, college and now graduate
school. Thank God Everything has not been
all roses. I have had minor rejections,
large weight gains, colon cancer in 96,
surgery for melanoma on my shoulder in
99, various aches and pains. But I wouldn't
trade it for anything. In 2002 I decided
I had to get back in shape and worked hard,
lost 35 lbs (down to 242) and attended
the US Transplant Games for the first time
since
1994, I played in the basketball tourney
(4th place), ten pin bowling and ran (walked,jogged
) the 5k organ donation race in 90 degree
heat.(4th in my age category) I also ran
11 races, 3-5 miles from July-Nov. If I
could do that anyone can if they put their
mind to it. Any questions or comments E-mail
me at jkane1992@hotmail.com.
I plan on being around for 10 more years.

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Michele--Pelzer, SC
My name is Michele (Stewart) Hood, and
I am a kidney/pancreas transplant recipient
as well as a member of a donor family.
I was diagnosed at 20 months old with Juvenile
Diabetes (or Type One diabetes) and was
required to take daily insulin injections.
Before I received my transplant I had been
on up to 6 or 8 shots a day. My blood sugars
ranged from 16 to over 700. In addition
to coping with my blood sugar, I also fought
high blood pressure, high cholesterol,
pancreatitis, and vision loss.
During 1998 I had two eye surgeries to
repair a detached retina and remove a cataract.
Unfortunately, the doctors were unable
to keep the retina attached, resulting
in blindness in the left eye. I was put
out on disability at the age of 26, due
to failing kidneys, partial blindness,
and other problems stemming from diabetes
and high blood pressure. I was prepared
for dialysis by having two surgeries to
prepare an access, which I used only 5
times. I was also prepared for the need
for a transplant. The doctors explained
that it was best, if possible, to receive
both a kidney as well as a pancreas with
me having type 1 diabetes. I received the
call on February 4, 2001, that I was to
come to Charleston for a transplant. I
had the transplant the next afternoon.
It took me 4 months to regain my energy,
and now I go as much as possible. I have
a lot of time to make up for that I in
a sense lost while I was sick. My husband
never truly knew how much energy I really
had, and my family tried to warn him that
he had no idea what he was getting into.
I try to keep going to help others that
are/will be in need for a transplant, because
so many did it for me.
I have been very blessed in my lifetime.
After the transplant, I was able to get
married to a wonderful man that helped
me through the difficult times. We also
bought a new car and house within a year
of having the transplant. Our house is
beside my husband's family. God placed
us there for a reason. Bo's father passed
away July 19, 2002, which was only
5 months after we moved in next door to
them. He had a massive heart attack.
He and my mother-in-law had discussed that
they would agree to organ/tissue donation
in the event of the other's death. He donated
a tremendous amount to help so many now
and in the future. If you ever had the
chance to meet “Pop”, as I called him,
you would know this was exactly what he
would have wanted.
I am often asked how I have gotten through
all of this. I tell that there are 3 things.
The first and foremost is f aith in
God. Second is a great family support system.
Laughter is the third thing-without it I
would have cried. I now go out and do volunteer
work with the gift of life trust fund in S
outh C arolina. It is a very rewarding
thing in my life. I talk to people at churches,
civic groups, health fairs, etc. One of the
things that I enjoy tremendously about doing
the volunteer work is that I am also able
to go into the schools and talk tot he young
people. I tell those that are diabetics or
that have family members who are diabetics
that they are looking at their future or
their family member's future if they are
not taking care of their diabetes the way
that they should be. I was not a "perfect
angel" when it came to mine, but I also stress
that when I tell people about it.
My hope is that I can at least change one life through
what I do now. I have told my family that if this is
not what god intended for me to do, then I am enjoying
it along the way. I have had students come up to me
and tell me that they had never thought about what
a difference that the decision to be an organ/tissue
donor could make, and that they appreciated me showing
them/changing their minds or lives. comments like those
have brought me to tears so many times. As I said,
it is very rewarding and I enjoy it tremendously.
Don't forget to thank those that have helped you along
your journey in life. most importantly be sure to thank G
od for the blessings that he has bestowed upon you.
for they are as easily taken away as they are given.

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David -
I am a Baptist Pastor from Northern Ireland
who has spent the past year adjusting to
major illness. At the end of 2001 I was suddenly
diagnosed with heart failure. Now I am waiting
for a heart transplant. The following testimonial
is based on the letter I wrote to all my
friends in church and around the world; friends
who have been so faithful and encouraging
through this past year.
Christmas Day 2002 was filled with some
very mixed emotions. I love the Christmas
season and the opportunity it gives to
rejoice in Him who was rich but became
poor to make me eternally rich! No change
in circumstances can rob me of those riches;
not even the dramatic changes the past
year has brought to our lives. It was on
Christmas Day 2001 that I last preached
in Moira Baptist Church. I still find it
difficult to take in, that life can change
so suddenly but I bless God for everything
He has done. Let me share some of the things
I have missed in the past year but also
how God is working in everything for good.
I miss Church
I miss Moira Baptist Church so much. For
almost 7 years it was what I lived for;
even in this past year it has been constantly
upon my heart. Recently I have been able
to attend services more regularly; usually
one service each week. I was delighted
to be able to go to the Carol Service.
We were packed out; standing room only.
I enjoy the days when I am strong enough
to be able to greet everyone there. They
are such good people and have been a wonderful
support to us. I love to worship the Lord
there. I miss the fellowship. Friends call
but sometimes even too many visits are
tiring.
So I often find myself in a cell or a
desert or by a lonely brook. But just like
Paul or Moses or Elijah, I have found that
the Lord draws dear. In the secluded places
His presence has been precious. He has
taught me again the value of personal communion
with Heaven.
Hanging in my office in the church is
a picture of the walk to Emmaus; a reminder
that even in our disappointments, the risen
Lord Jesus comes personally to be with
us. One wonderful thing to come out of
a difficult year is the “heart-burning” experience
of a closer walk with Him.
I miss Preaching
I miss being a preacher. After 33 years
of preaching and teaching, it has been
a most strange experience to be kept away
from declaring the Word of the Lord. I
miss all aspects of pastoral ministry.
I believe that all my years of Christian
service have been preparation for the role
of a Pastor/teacher. Now the Lord has set
me aside from that; I trust His purpose
is to make me a better pastor.
But I thank the Lord that He has enabled
me to continue a degree of ministry this
year. I have been able to do a little visiting,
but more often the visitation and counseling
have been by telephone. Through the medium
of email and my websites (www.moirabaptist.org and www.2hearts.org.uk )
the Lord has opened doors for me to many
people at home and around the world. I
have had responses from those who have
found blessing through the meditations
and messages. I have been able to take
a more personal interest in God's work
in the wider world and be a “ Pastor” to
some of God's servants at home and abroad.
One of those servants from overseas has
graciously described me as “the Pastor
of my heart.” It has been good to discover
that God still wants to use me, even in “weakness”.
I miss College
I miss teaching in the Irish Baptist College.
It has been an enormous privilege over
the years to help prepare men and women
for serving the Lord in Ireland and around
the world.
This past year I became a student. I have
had to go back to “college” to learn new
lessons and revise some I thought I had
mastered. I had hoped that I could have
avoided one particular teacher – his class
is the most unpopular in college; nobody
chooses to be a student of his. It seems
his classes are always the longest. I have
seen some leave bitter and disturbed and
some never moved out of that class. I am
in his class now but I am not alone. My
Friend has been with me every day. He has
been through this class long before me
and passed it without a single failure.
I am learning things I could not have learned
from any other teacher. The teacher's name
is Suffering and my Friend is my Lord and
Saviour Jesus Christ. What am I learning? – to
walk by faith and not by sight.
I miss the Workshop
Here I am with more time on my hands than
I have ever had in my life; time to do
all those DIY projects in the house and
the garden; time to enjoy landscape photography
or wood-turning hobbies; time to take my
grandchildren to all those places we never
had time to visit.
But there is a limited landscape from
our window. Once our garden was on the
edge of the countryside but now is overlooked
by new two-story homes. Limited energy
restricts traveling: rarely do I travel
further than Lurgan or Moira. And as for
those practical projects! I just cannot
attempt them. I am thankful to be able
to use the computer and to do a little
oil painting, but the garage remains locked,
the lathe is silent and the projects wait
for me to regain my health.
And yet I have found myself in a workshop – God's
workshop. He is fashioning me for a purpose
that He has in mind. I have felt the squeeze
of the Potter's Hand; I have known the
heat of the Refiner's fire; I have been
shaken as the Sculptor has chipped away
the bits in me that are not pleasing to
Him. The process is ongoing and sometimes
He gives me glimpses of what He wants me
to be and assures me that “ He knows the
way that I take; when He has tested me,
I shall come forth as gold.” Job 23:10.
God never produces “seconds” from His workshop,
nor does He leave projects unfinished.
I miss Travel
We have never traveled on typical foreign
holidays, preferring holidays in Ireland
or Scotland. (Is Scotland foreign?) Very
kind friends sent us to the Holy Land some
years ago and our church paid for a holiday
in Florida in '96. In our days with CEF,
our work took us to quite a number of European
countries. In more recent times, kind friends
have taken us to minister in Romania, India
and Nepal. Those trips have been highlights
in our lives. If we were ever to travel
abroad again, we knew the places we wanted
to go.
But suddenly the door to such ministry
opportunities has closed; some likely to
be closed permanently because of the health
risks even after transplant. I remember
my first thought, as I listened to the
doctor telling me the nature of my illness,
was “ I can never go back to India”.
Whether I minister abroad again is in
the Lord's hand but He has opened a door
to the world for me. I am astounded at
the opportunities He has given me to minister
to hearts over the Internet and amazed
at the international nature of my prayer
support team. This message goes all over
the world; I am prayed for regularly and
faithfully in places as diverse as Australia,
USA, Canada, Peru, Brazil, Switzerland,
India, Pakistan, Nepal, Romania, Spain
and France, in addition to every corner
of the British Isles. I have found very
supportive friends through the Web and
have been able to minister to many who
in turn need support. These all are people
I would never have met or had time to help
if I had been a busy Pastor. I would ask
you to pray particularly for the ministry
of the 2hearts website. I want to be used
by the Lord to point others to the One
who never fails.
I miss Children
I have left children to the last. (When
have I ever done that?) Anyone who knows
me, knows that children have a very special
place in my heart. I have a host of little
friends; first my grandchildren, Adam and
Debbie, who are very special and whom we
love to have with us. Then there are all
those children in Moira Baptist; I have
had the privilege of holding more that
50 new babies born to church folk over
the past 8 years! I miss those times together
in Sunday morning services when I used
to be surrounded by a sea of little ones.
We would sit together on the platform steps
and talk about the Saviour. I miss those
special services when the focus would be
exclusively on teaching children.
Sometimes little children come to visit
me and bring their Mummy with them. Recently
I had very special visitors when my “little” friends
Jed and Ethan arrived together. (Very premature
babies who will always remain on my heart.)
Some days when I get out to church I feel
like the Pied Piper. Little ones want to
hug me, give me sweets or present pictures
that they have drawn of me or for me. I
know that many of them pray for me every
night. I was moved to tears when one nine
year-old girl actually said I could have
her heart! I know of street children, rescued
from the sewers of Romania, who pray for
my heart. I believe God is answering the
prayers of children. As adults, we look
on the challenges posed by transplant surgery
but children simply ask God for a new heart
for me, without all that hesitancy. One
of the good things God has taught me, and
used children to teach me, is the power
of prayer; we have seen the most amazing
answers to prayer this past year.
I never intended this message to be so
long. In writing to you, I have discovered
how much I missed last year but I have
also discovered how much I have gained.
Has this been a wasted year? Certainly
not.
The year ahead may be an even more crucial
one, but the grace that overflowed to us
in 2002 will not dry up in 2003. We have
buried some dreams this year and maybe
there will be more dreams to bury, but
the Lord knows my heart. I want only to
live for Him. I can never again sing without
sincerity “All for Jesus … all I am and
have and ever hope to be”. And if, through
my illness, I have helped one person this
year to have a deeper faith in God, them
it has been worthwhile.
Thank you for your love to Joanna and
to me. The Lord will reward you. Hebrews
6:10
Love in Jesus
David
UPDATE 9-29-05
Dear friends,
Some of you have been reminding me that
it is some time since I gave you an update.
I thank you sincerely for your concern
and for all your prayers since I last wrote.
There have been no major developments in my condition except that I continue
to gain strength and confidence. I have
had a really good summer, doing things
I have been unable to do for years. We
traveled to Ballycastle, to Bushmills and
to Newcastle (for those of you not from
Ireland, all are around an hour to an hour
and a half from home and all by the sea)
where dear friends loaned us their holiday
accommodation. We had our grandchildren
with us each time so there was plenty to
do!!! As long as I paced myself and kept
within my limits, I was able to cope most
days. I do not have so many bad days as
in the past but did have one last Sunday,
just to remind me what it used to be like!
On the whole I am keeping well. I saw my
GP yesterday for a check-up and he is very
pleased with my heart, lungs and blood
pressure and has lengthened the period
for my check-up to every 6 months, so that
helps with confidence.
I am able now to get out to church a bit more and have a little involvement in
church life. In fact I have been asked
to preach in Moira Baptist on Sunday morning
9th October. I would really appreciate
your prayers for that day. It will be my
first Sunday sermon for almost 200 weeks!
Pray for my voice to hold out. (one of
the problems is if I talk too much my voice
weakens) Pray that I will be able to do
it without stressing my heart and most
of all, pray that the Lord will be glorified. It will be emotional for me and for all my friends in Moira but I want the focus to be, not on me but on the Saviour and for the occasion to be a mighty testimony to God's grace.
Please pray for my church. It is beginning a series of studies during October to December on "Our Purpose in Christ Jesus".
It is based on the church in Acts 2 and I hope to help just a little with that.
The Elders have a great vision for the future of the church and it is thrilling
to see Moira Baptist Church moving forward. These are very exciting days. God
is blessing us with evidence of his grace in hearts and lives, a growing congregation,
more baptisms and new members. It is particularly encouraging to see the church
reaching out to the community in new ways and I am delighted to see the young
people getting even more involved in mission at home and abroad. Please join
us in prayer as we seek to find God's man to Pastor the Church.
The 2hearts ministry is busier than ever with support given to almost 70 families
around the world who face the trauma of heart illness. Nearly 25% of them are
heart transplant families. Let me share one example. Julie from USA is 18 and
has been told she needs a new heart very soon. She was taken to surgery a couple
of weeks ago, went to sleep thinking she was getting a transplant but at the
last minute the donated heart was discovered to be defective. She woke thinking
she had a new heart only to realize the truth. But she is a most lovely Christian
girl and her faith is remarkable. Please pray for her.
The website ministry continues to give
me opportunities to serve the Lord from
home. I am staggered at the impact, with half a million hits per year. Eternity
alone will reveal all that God has done. He encourages me from time to time as
people testify to finding spiritual help from the sites. I still manage the web
ministry for Moira Baptist as well as four sites of my own. My latest allows
me to indulge in my hobby of taking landscape photographs and even try to use
it to witness for the Saviour http://photo.2hearts.co.uk A
friend recently took my grandchildren and me up for a short helicopter flight
over our villages. What a thrill. Some photos are on the site. (No, I did not
ask the Doctor's permission! He might have said no! )
I manage five mission sites, a site for a very special little girl and have two
more ministry sites under development for friends. I help a good friend in Australia
who runs a support organization for heart children to produce some graphics for
her sites. And this week a dear brother called Aidan, who has a powerful ministry
in USA, has told me his webmaster is no longer able to help. I don't know yet
whether it is practically possible to help him but I cannot allow his web ministry
to fall apart. I'm out of breath just thinking about this. I've just counted
and there are 14 web sites I am already responsible for, in addition to others
in which I have a part !! And I have had no training; I am a rank novice with
basic resources and I do it all voluntarily. I would like to learn to do this
properly but I'm not sure if I can cope with the study required. Thanks to the
support of my church and a few friends, I can even provide free hosting for many
of the sites. This enables these missions to use their income directly in evangelism.
I was honoured recently to be invited to become a Trustee of a very special ministry
called Assisting Children's Evangelists Worldwide - a branch of Child Evangelism
Fellowship. It is the ministry of my long time friend Sam Doherty. He provides
training manuals and Bible lessons for more than 6000 teachers in 135 countries
around the world. All this literature is provided free. Much of it is also translated
overseas into 43 other languages and provided for a further 20,000 children's
workers. Please pray for the team as they continue to develop this ministry around
the world.
I continue to help where I can with other ministries in Romania and India. I
try to give pastoral support to Christian friends at home and abroad who face
great challenges. How I wish I could travel to them and have direct involvement,
particularly in India where there is such potential and so much need. But email
and telephone at least keep me in touch with dear friends and I do what I can.
So life is busy. If I was a pastor I could never do all this. I do not know what God has planned for my future ministry but I am amazed that He wants to use me. Last night a friend in ministry from USA, who is suffering terrible health and other problems wrote "It was so lovely to speak to you brother- what an encouragement you are to so many... Spurgeon - in a wonderful book...the writer said - he healed more though he was not a doctor- but because of how he suffered... and so yours will be known in eternity- that the Master chose this time to use you in lives of people you never would have met, or known ." I am humbled to think that God still has work for me to do for Him.
I know God has His perfect plan for me - it is often painful, in many ways puzzling, and even petrifying at times - but perfect. I do not know what the future holds. Three years ago the doctors said they would try through medication "to buy me a little time" - they suggested 6 months or perhaps a year. But God has the only timetable. "All
the days ordained for me were written in your book before one of them came to
be. How precious to me are your thoughts, O God! Psalm 139 I celebrated a big
birthday on Sept 11. Some friends totally surprised me with a very special party.
A few years ago I wondered if I would ever see this milestone. Isn't God good?
I appreciate your prayers for Joanna too. She keeps quite well but she still
carries so much of the load, doing practically all the driving and anything heavy
- all the hard, boring, unseen work without which I could not survive let alone
minister to others. She has been my rock through these years and I am convinced
her reward will be greater. I pray that I gain even more strength so that her
load will lighten a bit.
Thank you again for all you mean to us. Hebrew 6:10 God is not unjust; he
will not forget your work and the love you have shown him as you have helped
his people and continue to help them.
with love
in the grace of our precious Lord Jesus,
David
Update: 5/23/06
View Latest Newsletters
Part 1 - Part 2

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Keegan -
Here it goes:
Shortly after Keegan's birth he began having difficulty
breathing. His pediatrician was called in to examine
Keegan. She suspected a heart defect. When Keegan was
less than 48 hours old he was bayflited to another area
hospital where Hypoplastic Left Heart Syndrome was confirmed.
When Keegan was just five days old he underwent his first
open heart surgery. The Norwood Procedure. The surgery went well,
with no complications. All appeared well for a while. Keegan began
having problems just two weeks later and underwent his second open
heart surgery, an emergency surgery to repair a leaky valve and to
narrow the shunt that was placed two weeks earlier. This surgery
also went smoothly with no complications, but one month later Keegan
was still not thriving on his own and was being paced 100%. At this
time we were told the only option for our son was a heart transplant.
On May 12th of 2002 Keegan was moved again to another hospital who
specialized in transplanting infants. Keegan immediately began testing
to see if he was in fact a candidate for a heart transplant. He was,
and the next day he was placed on the national registry for organs
sharing. Next began the longest six days of our life. We waited for
roughly one hundred and thirty-four hours for Keegan's new heart.
Considering the average wait time for an infant organ we hardly waited
at all, but it seemed like an eternity. I received the call at 1
a.m. on May 19th that they found Keegan a new heart. He was immediately
prepared for surgery and had his transplant later that morning. He
had no complications and recovered very quickly. Keegan came home
two weeks later and is now a happy, healthy baby. We feel very fortunate
and blessed to still have Keegan in our lives. So many times in his
short life we have been so close to losing him. He is our hero, our
little superman, and we feel honored that such a special little boy
found his way into our arms.
Click
Here for Keegan's Before/After Transplant Photos
TO VERY SPECIAL PEOPLE:
We want to thank you, but what do we say, to let you know our true
feelings today?
To express our gratitude and show appreciation, to show you the heights
of our joy and elation.
Keegan now smiles and he coo's a lot, too.
This wouldn't have been possible for him without you.
We're so very sorry you suffered such loss.
We know your gift was given at such a great cost.
All of us want to thank you, each and every last one. We know
you are special for what you have done. With comfort and peace,
we ask God to bless you. Just know we are thankful to God and you,
too.
Love from,
Keegan, his mommy and daddy, his grandparents, his great grandparents,
his great-great grandmother, his aunts, his uncles, cousins,
and all of his great big extended family.
This is not the end of Keegan's story this is only the beginning.
As he continues to grow, may he find great happiness and much
love.
Click
Here for Valentine's Day Photos |
CHD Quilt Project
I am sooo excited, Keegan's block has finally been completed. For
those of you who have no idea what this is here's the link that
tells about this project.
CHD Quilt Project
~Deanna Dempsey
Click
Here for Keegan's Quilt Photo & Photo
of Entire Finished Quilt
(Updated July 21, 2003)
Keegan's
First Birthday!!
Click
Here for Keegan's Birthday Photos
Photos of Keegan at 14 Months
Photos of Keegan at 15 Months
Photos of Keegan at 17 Months
Keegan's Halloween Photos
Keegan's Christmas 2003 Photos
Keegan's 2 years old pictures
Updated!
Please direct your browser to http://www.babiesonline.com/babies/p/pidders to
see
the changes!
New photos of Keegan - April 2006!!
Keegan has new photos - May 2007
Keegan just had his 5th heart birthday Saturday, May 19, 2007!

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Jessica
Hi, my name is Jessica.
When I was 4 years old I was told that I had an heart murmur. After
4 years of watching and seeing what would happen I had my first open
heart surgery. I had an ASD, VSD, and a cleft mitral valve. I managed
to do okay for a while, through elementary school, junior high, high
school, and two years of college. After my second year of college
I had a seizure and was hospitalized. I had open heart surgery about
a month later. I was sick on and off until my third open heart surgery
in December of the same year. Then I was doing okay but was still
in heart failure. In August of 2001 I started having ventricular
tachychardia. I had an AICD implanted and started feeling better.
Then in February of 2002 I was evaluated for an heart transplant.
I almost qualified. I was just not sick enough to qualify. Then a
month later I was tested again to see if I qualified for a heart
transplant. I got the same answer, which was no. I am now looking
into having the defribilator/bi-ventricular pacer. If I get that
then I either won't have to have a heart transplant for a while or
never. I am hoping science keeps up and can come up with something
instead of a heart transplant. That would make my day.

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LouLou
My Rebirth
Well, Kel, I might as well begin from the beginning.
In 1991, we decided to spend our 25th Wedding Anniversary
in Daytona Beach. The date was June 30, 1991. It was such a beautiful
weekend. I felt great! When I woke up on Sunday morning, the day
we were to come home to Ocala, I felt a small weight on my chest.
Didn't think much of it and never said a word to my husband. We
spent the morning at the beach and in the pool. Around 1 p.m.,
the weight became worse. We packed up the trunk and headed for
Ocala. I lit a cigarette while driving home. ( I decided I would
drive.) Halfway home and 4 cigarettes later, I felt so bad, I had
to pull over and have Carl drive the rest of the way. Halfway home
there were no hospitals in sight. We got home, emptied the trunk,
went inside the house and I went to my bedroom. I knew I was passing
out and getting sick and screamed for Carl. By the time he got
there, called for an ambulance and tried to help me, I had suffered
a very dangerous heart attack, damaging a large percentage of my
heart. I coded at Monroe Regional at 2 a.m. in the morning. Thanks
to an alert male nurse and our blessed Lord, I was brought back
to life. My heart was badly damaged. I was sent home a few weeks
later to rest for 3 months. I was told to sign up for Lifetime
Fitness Cardiac Rehab in October, which I did. I remember going
in to talk with the director and crying so hard because at 49 years
old, I thought my life was over. Before going back to work on November
1, 1991, I had lost 52 lbs., stopped smoking cold turkey, exercised
at least 1 hour 3 to 4 times a week and still was depressed and
scared. Each day I thanked God and asked him to keep me going.
I did keep going and kept my weight, no smoking and exercising
up for 6 years.
I was beginning to feel a bit tired once in a while
and short of breath. Not much I thought, but I did speak with the
doctor. He sent me for a test and told me the results. I was working
full time for State Probation and Parole, heading an inner school
Girl Scout troop, clowning around with a group from church at Shands,
etc., and also doing everything a woman does - house clean, wash,
etc. I was accomplishing this crazy lifestyle with only a 9 to
10% ejection fraction, despite all my work to keep healthy. He
really didn't know how I was doing all of this. I was sent to Shands
Hospital in Gainesville in August of '97. After being poked, probed,
stuck and dehydrated for 1 week of tests, I was told that they
could not accept me in the transplant program because I had arterial
disease. Three years prior to Shands, I had carotid surgery on
my right side with my left carotid 100% blocked. I was devastated!
They told me my working days were over.
On my return home to Ocala, I was beside myself.
I had been told I had 3 to 6 months to live, at that! I had just
begun to live a new segment of life. My first grandson, Zachary
Tyler Gehring had been born July 22, 1997. I wouldn't even live
to see him grow!
I prayed and prayed and in October of '97 my cardiologist,
Dr. McGhee and another cardiologist from MR sent all my test results
from Shands and also from them to the top surgeon at Tampa General.
My appointment was set up for December 11, '97. I met with him
in Tampa and after scrutinizing my records, he said I was a good
candidate and was placed on the computer for a heart. I was given
a pager and blood tests. We then went home to wait.
The Lord took over and carried me through those days.
On January 28, 1998 at 1:37 am, my phone rang next to our bed.
I was sound asleep. After ringing about 6 times, I answered. My
heart coordinator told me two hearts had come in with my blood
type and size. One was to go to me and one to someone who had been
hospitalized for a few weeks. They told me to be there by 6 am.
I was walking on clouds! The very first thing I did after hanging
up was tell Carl everything and he went out to alert the family.
I called my son, as he was the designated driver for me. I then
dropped to my knees. I started talking with the Lord. I told him
to remember the story of footprints in the sand. I asked the Lord
if he would carry me on his shoulders from here until the end because
I could not do this alone. Something came over me I will never
forget. My body became so relaxed. Everyone was crying in the living
room as my son and I walked out of the house. My mom was crying
so hard and asked me why I wasn't. I told her that the Lord was
in charge and he was carrying me now. After my transplant, when
the anesthesiologist came in to see how I was, he made mention
that I was the most relaxed transplant he had ever seen. He said
I was smiling when they brought me into surgery. We all knew why!
The Lord was with me all the way!
My bed in Transplant CCU was against a wall so I
could see out of a glass in the door to enter my room. The first
thing I saw when I awoke was my beautiful grandson held by my son
on the other side of the glass. Right then I knew I would come
through, I had to. My grandson will be 5 years old July, 2002.
I now have a granddaughter - Savanna Rose (Sissy for short) who
was 3 years this Jan. I am so blessed!
My first year after transplant was not an easy one.
One and one half months after transplant, one of the meds I was
taking actually ate through my colon. I was flown from Ocala Airport
to Tampa General on their helicopter. I had 3/4 of my colon removed.
In the fall of '98 I fractured the top of my femur which required
surgery and the placement of 4 pins. In November of '98, two weeks
after arriving home from the surgery, I felt ill one day, had a
slight temp and just knew something was wrong. I called Tampa and
by the time I got there a couple of hours later, I was in a very
serious rejection. I was in CCU for 2 weeks. Only my doctor and
I thought I would make it. Again, the Lord was there.
Since then, I have been just fine. I have learned
to be a fighter. The Lord will always be there for me, but I learned
I had to help also. And I did! I have a wonderful husband, Carl,
a great son, Greg, two beautiful grandbabies, a sister I don't
know what I would do without and lots of faith.
I have written my donor family twice now. I told
them what their gift gave to me and thanked them for the most precious
thing they could ever give. They have never written back acknowledging
my letters. I know how difficult it would be to relive a sorrow
over again and do not blame them for not writing. I believe they
are just happy to know what their gift gave me. I ask God to bless
them always.
I have gained weight, have bones that hurt, a stomach
that doesn't feel so good all the time after taking my meds, and
sometimes feel a bit out of it from those meds, too. BUT I AM ALIVE!
I HAVE SO MANY BLESSINGS NOW, I HAVE A HARD TIME COUNTING THEM
ALL! MOST IMPORTANTLY, GOD IS ALWAYS THERE!
If someone out there would like to write, my e-mail
is louloug@aol.com . I would
love hearing from any of you. I have met many wonderful new friends
on the computer. Kel is one. He always makes me smile! God bless
him. |

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Linda
Edwards
My name is Linda Edwards and
I was diagnosed with congestive heart failure when
I was 26 after having my first child and suffering
cardiomyopathy during childbirth. As a child, my
mother had passed away from CHF when I was 12,
she was 36. During the next several years I felt
pretty good and never really thought my heart condition
would be an issue until I got much older. Then
suddenly in 1998 at the age of 35 I started feeling
very tired and weak all the time and again was
told my heart was weak and would continue to get
weaker, eventually needing a transplant. Over the
next 2 years after one attempt of repairing some
valves with heart surgery, I found myself almost
too weak to move. During this time, my younger
sister passed away from CHF and I was taking care
of her three boys and my son - all teenagers and
- and I ultimately came down with a cold that turned
into bronchitis then pneumonia then in the hospital
in December of 1999.
I stayed in the hospital from December 1999 to February 3, 2000 when I
finally got the call in my room that I had a heart. It has been 3 years
since my transplant and like most people I have had some complications
but there are many more good days than bad and I get to see my son and
nephews grow up, something I never really thought I would be able to do.
As a single mother dealing with all of these issues, I have been very blessed
with the kind of perseverance and spirituality that only God could give.
Every day is a gift.
My Heart Sings
Submitted by Linda Edwards, borrowed from an unknown source on the Internet
and edited.
I walk alone, along a sandy beach, listening to the waves splash upon the
shore...
And I know from deep within, life goes on forever more.
I saw the bright skies above, with drifting clouds of white...
I felt the beating of my heart and smiled with delight.
The ocean roars on forever: How wide, how rippling, how deep...
Reminding me of how a family's loss gave a new life to me.
And when burdens overwhelm me, and I lose all my hope...
I hear a gentle whisper, and I know that I can cope.
Like the constant beating of my heart, life goes on and on ...
God's healing touch refreshes me, and I know I'm not alone.
Why does it take the dark clouds, to remind us that he cares?
When in truth all we need to do, is breathe a thankful prayer.
As I walk along that sandy shore, my heart begins to sing...
I owe my life to an unknown friend and God's grace in everything!

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Jerry Berkesch
I received my heart 7-18-95 at Henry Ford Hospital.
I am now 60 years old and on July 5 I will be
walking my daughter Kari down the aisle as she
marries her beloved Dan. I have now lived enough "extra" years
to see Kari graduate with highest honors from
the University of Michigan and actually be invited
to be one of the commencement speakers. My younger
daughter is a Junior at Michigan State and I
expect to see her graduate in two years. I am
on disability retirement and occupy myself taking
care of the house while my wife, Nancy, teaches
2nd Grade and I am also a volunteer speaker for
Gift of Life, the Michigan Organ Donation Agency.
Hope all is well with you!

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Bill
Westerman
Veteran basketball coach Bill Westerman works with players on the Kentucky
Bluegrass 16-and-under team in practice. Westerman is back on the sideline
after having a heart transplant two years ago.
A new heart and a new start
Two years after transplant, Westerman coaching again
Article Taken from The Kentucky Post
June 17, 2003
By Tom Ramstetter
Post contributor
Bill Westerman's story is an example of what is right with sports.
Westerman, two years after undergoing a heart transplant, has helped
guide the Kentucky Bluegrass AAU 16-and-under girls' basketball team
to the Kentucky state championship and a berth in the national tournament
July 7-13 in Cocoa Beach, Fla.
Westerman suffered from cardiomyopathy, a hereditary condition in which
cells in the back of the heart start dying. He was told he had two years
to live unless he got a heart transplant. He spent much of the past two
years in the hospital at the University of Kentucky.
"They sent me home to die," said Westerman, 53. "But they found a heart
a week or two later. I went back and they said I had a chance to come
out alive. I was in hospital for like two months (after transplant) and
so many of my players came to see me. There must have been 100."
The players came from his 30 years of coaching. Westerman started coaching
elementary school basketball and Knothole baseball in 1973, moved on
to junior high basketball and became an assistant basketball coach at
Notre Dame Academy in 1982. He became head coach at Holy Cross in 1993
and won 87 games in four years. He has coached the boys' basketball team
at Covington Latin, the women's soccer team at Thomas More College and
has started youth soccer leagues in Northern Kentucky.
When Westerman got sick in 1999, his coaching career was put on hold.
The heart transplant took place in May 2001, and after taking a year
to recover, Westerman got back into coaching last spring with the AAU
team.
After years in the insurance business, Westerman took a full-time teaching
position at Holy Cross last fall and coached the seventh and eighth grade
boys' basketball team. This spring, the girls asked him to coach them
again.
"It has been so much fun," Westerman said. "They have helped me. Dick
Maile coaches with me and he has helped me. I'm supposed to be the head
coach, but he does a lot, too. We've been friends for 15 years. We both
teach at Holy Cross and we were coaches at Notre Dame."
The team is made up of nine girls from local high schools and is only
the second team from Northern Kentucky to win the state tournament in
the age group. Boone County's Megan Fletcher and Tangie Sellers have
joined Amie Noll, Rachel Lantry and Cara Randal from Holy Cross, Notre
Dame's Danielle Wachs, Scott's Jessica Wendeln and Ryle's Renee Daily
on the team. Most of the girls were together last year when the team
finished as state runner-up. With older girls moving on, however, the
team dropped to the 16-and-under class and adopted the goal of winning
state and representing Kentucky at the national tournament. The girls
can't be older than 16 on July 1.
They played in five tournaments, including a trip to Detroit, and played
teams from Cincinnati and St. Louis to prepare for state. They beat the
Southern Sharp Shooters, 49-45, last week in Lexington to capture the
state title.
"Our record wasn't great," Westerman said. "I think we were 6-10 coming
into the state tournament. But we had never lost by more than six. When
we came down there, we really pulled together."
The key players are Noll, the team's point guard, and the inside combination
of Dailey and Sellers.
"Amie really took over and settled the team down in the championship
game. Dailey and sellers have really worked hard. All the kids are important
because we only have nine. We are playing a role-playing team; we've
had no bitterness about playing time. We ask them to do things and they
just do it."
Westerman's team lost early in the state tournament to the Sharp Shooters,
but regrouped and came out of the loser's bracket to win. The Bluegrass
defeated Central Kentucky team drew on its coach's experience to overcome
the odds.
"When you have that kind of team chemistry, you can do anything," Westerman
said.
The national tournament starts with pool play and the survivors of pool
play will then go into a one-and-out tournament. The team still has some
money to raise for the trip. The goal is to win some games in pool play,
but win or lose, the experience has already been a success.
"This was a blessing for me," Westerman said." I was supposed to die.
People around me helped me do it. Sports are not the biggest thing in
the world, but it is a character builder. This is for other people that
go through this. There is a light at the end of the tunnel and you can
get through it.
" I just wanted people to know that because someone decided to be a
donor, I've had the opportunity to coach these wonderful kids."

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Joe and
NaDeen Sierra
A sub note to the article -- In 2000 Joe became ill was diagnosed with
a brain
tumor that was caused from the transplant meds! Also he attended the 2002
Transplant Games at Disneyworld. He found the experience to be very spiritual
and calming to meet others like him.
http://www.qctimes.com/internal.php?story_id=1015893&l=1&t=Health&c=9,1015893

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Megan
Well, where do I begin?? Megan was our
miracle child from the start. We had wanted a child
for 17 years and the doctors all said I could not
get pregnant. I was saved but my husband was not
although he was a wonderful husband, he was not
saved. After 17 years of marriage he had gotten
saved and the very month he got saved is the month
I got pregnant, we were overjoyed! When I was about
4 months pregnant they did an ultrasound and told
us she was going to be born with all of her intestines
on the outside, that very night we prayed about
it. My husband got up the next morning and said
for me to call the doctor and have him do another
ultrasound because he said he knew the Lord had
healed the baby. I called the doctor and he said
he knew the baby's stomach would not be healed,
he said he had diagnosed over 200 of these and
he did not have a doubt that nothing will have
changed but we insisted. Three days later they
did another ultrasound, her stomach was perfect!!
God had healed her! Then, when I was about 5 months
pregnant they told us that she had fluid around
her kidneys and she would have to have surgery
for that as soon as she was born, once again we
prayed, by the time I was 8 months pregnant the
fluid was gone, the Lord had healed her kidneys
this time. Megan was born January 21st at 12:40pm
with the cord wrapped around her neck 3 times but
with no complications, once again the Lord had
watched over her. Megan weighed 7 lbs & 11
oz and was 19 inches long.
She was always such a healthy baby, never even so much as an ear infection.
She was so very smart, she was praising the Lord in church by the time
she was 6 months old. By the time she was 10 months old she was putting
2 words together, her pediatrician was amazed by how smart she was. One
day, about 6 months ago, I was at work and my mom called me saying Megan
had been throwing up and crying alot. I went home and took her to the local
hospital and they said she was dehydrated from a "little" virus, they transported
her to the hospital in the next town. All night I told them I felt like
something was not right. They kept saying it was just a virus, she would
be ok. The next morning her doctor came in and took an x-ray. She IMMEDIATLY
sent her by ambulance to T.C. Thompsons Childrens Hospital. When we got
there they called us in a little room and told us our little 11 month old
daughter whom we loved so very much had Cardiomyapathy, a virus that attacked
her heart, and that she had about 2 hours to live. We were devastated.
They let us go back to ICU to see her, she was hooked up to about 14 different
IV'S and she was on a breathing machine. By this time there were about
50 friends and family there. We all began to pray fervently. Her 2 hours
turned into all night then they said she would not make it through the
night. She did. They tried 3 times over the course of 3 weeks to get her
off of the breathing machine and finally the 3rd try she was able to come
off of it. She did great and they let her come home. She was home about
3 weeks and started getting sick again, her doctor once again had us take
her to TC Thompsons, with each passing day she got worse. She was in heart
failure once again. The last day she was there they put her back on the
breathing machine, she had been there about 2 weeks this time. The day
they put her back on the breathing machine they took her by life flight
to Atlanta Childrens Hospital, to wait for a heart. She was immediatly
put on the transplant list but we were told she was the sickest child in
icu. They had her sedated and paralized so she did not use any of her own
strength, she could not afford to, she was our little angel and she was
dying. Every passing day Megan got worse, we kept praying, we never gave
up on her although we told God if it was in his will to take her home we
would understand, that was the hardest prayer I ever prayed. One day they
called us up there to tell us that Megan's kidneys were failing and they
were going to have to put her on "ECMO" a heart , lung & kidney machine,
we had no choice, they told us all they were doing was buying time, hard
words to hear. They scheduled this for 7:00 P.M. but before 7:00 came Megan
went into cardiac arrest at about 3:00 P.M. They did CPR on her several
times and put her on ECMO right then. They came and told us she had died
several times but they got her back. They kept telling us she was not going
to make it, we kept praying and believing in our Lord and Savior Jesus
Christ. Megan's testimony was too mighty to let her go. Megan had been
on ECMO about 3 days when they came and told us her heart was so huge they
had no choice but to go in through a heart catherazation and pierce the
back of her heart to relieve the pressure but, he told us he did not think
she would ever survive this surgery, she was just too weak. Well, she made
it through that but while she was still in there she began bleeding from
somewhere and the doctors could not figure out where the blood was coming
from, he tried for several hours to stop the blood but they could not even
figure out where the blood was coming from. We were devastated. Once again
they said they felt sure she was dying. They came out and told us the only
thing they had left to do was have the heart surgeon come in and cut her
chest open to see if they could find out where the blood was coming from
but they felt sure when they did that she would just be bleeding from everywhere
and she would die right there on the table but if they did not do it she
would bleed to death for sure. They let about 20 of us go in and kiss her
good-bye, my husband got up there and kissed her and through his sobbing
I heard him say to her "Megan, I know you are with Jesus now and if you
want to stay with Him that's ok but if you want to come back to Mommy & Daddy
just tell Jesus" They carried me out of there. We went back to the room
where we had been waiting all day and got down on our knees and began praying
crying out to God as loud as we could to please save our baby. My pastor
went to the verse in the Bible that stops blood, Ezekiel 16:6 and he read
it and we all claimed it, 10 minutes later they came out and said the blood
just stopped!! They could not believe it! She was on blood thinners and
ECMO, which also thins your blood. The doctor said there was no "earthly" reason
why that blood should have stopped, but it did, we knew it was the Lord.
They never cut her open, it stopped right before the doctor cut her. (Abraham & Issac!)
They told us we could come see her in a little bit but they still did not
think she would make it through the night. One hour later they came to
get us again, they said they needed to speak to me and my husband alone,
you know what we thought! But we were wrong, we could not believe what
they had come to tell us, they had found our baby a heart! She got her
new heart the next morning around 8:00 am. We were told there would be
complications because she was so sick, there were none, we were told her
chest would be open, it was closed, they told us she would be on a special
venilator that shook you real hard, she was on a regular one, they told
us she would still be on ECMO, she was not! GOD IS GREAT! Well, we thought
our storm was over but when they started letting her wake up about 4 days
later they realized she had a "severe" brain injury from her heart stopping
so many times that one day. The neurology team said she was hopeless! WE
KEPT PRAYING! She could not bend her arms or her legs, she just looked
straight ahead, she would not respond to anything or anybody, we kept praying!!
8 weeks after her surgery, she came home! She is now moving her arms, moving
her legs, laughing, smiling and learning everything over again but she's
getting there and she's only 13 weeks post transplant!! GOD IS GREAT!!
UPDATE - June 18, 2003
Megan's therapist said this morning she can't believe how well Megan is
doing!!
Everybody that knows Megan good knows her favorite thing to say was "what's
that?" and this morning we were laying there with her and just out of
the blue me and Gene BOTH heard her say, "what's that?" Gene said , "did
you hear that?" I said I sure did!! Also, yesterday, my mom said when
I walked out of the room Megan said MOM VERY plain!! and she has just
been saying MA instead of mom!! PRAISE GOD PRAISE GOD!!! EVERYBODY PRAISE
GOD!!!!
Nobody knows what Gene and I have been through but we want to share
with the world what GOD can and will do if you only believe!!!
We love you all!!
Gene, Tammy & Megan
UPDATE - July 16, 2003
Gene & I would just like to take the time to thank you all for being
there for us during this terrible storm we endured. Megan still needs
prayer but I honestly believe God is going to COMPLETLEY heal her! John
Taylor told me something that has stuck with me through all of this,
he said "God does not do ANYTHING half way!" I will never forget those
words. I truly believe that! We love you all! We are now going to different
church's each Sunday speaking her testimony, this was our promise to
the Lord. We are now booked up 2 weeks ahead! We have not called one
person, God has sent all of them to us. Please don't ever forget what
the kindness you all showed to us meant to us! We love you all!
The Madden Family
UPDATE - September 3, 2003
Megan is doing far better than anyone ever dreamed she would! She is
now starting to say a few words here and there. She can now pick up
small toys and hold them for a while, (something we have prayed fervently
about!)
We put her back in her walker last night for the first time but she
had to have a little blanket to help hold her up, but it's a start!
Praise God she is once again raising her hand and praising the Lord
when we sing in church! She is no longer as afraid of everybody like
she was when she first came home.
We now know that Megan's heart came from a precious little 3 year old
boy named Bailey, Bailey lived in Kentucky and we have just recently
been told that his family wants to meet us! We are so excited about meeting
them!
We want to ask that everyone continue to pray for Megan's muscles, she
desperatly needs prayer for her being able to sit on her own and to walk
again!
And we ask that everyone remember Bailey's family in your prayers!
Thanks everyone for your prayers!
Gene, Tammy & Megan
Click
Here For Megan's Photos
Click
Here For Photos - Oct 2003
Click
Here For New Photos - Nov 2003
Click
Here For New Photo & Update - Jan 2004
Click
Here For Photos New Photos and Photo of Bailey - Mid Jan 2004
Click
Here For Photos of Megan's 2nd Birthday & More
Photos - July 5, 2004 Vacation
Megan's Site has been updated, Go To www.babiesonline.com/babies/m/miraclemegan |

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