The Kiss Of Life(Quite Heartwarming)

shadowshiv

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May 29, 2007
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After having read the article about the 61 year old pedophile that was given the suspended sentence, I clicked onto another article at the same site. While the other article made me shake my head, this article made me smile.:) The article is from dailymail.co.uk.

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The kiss of life: This is the moment a mother paid a tearful goodbye to the 14-month-old daughter doctors said was about to die... miraculously, she started BREATHING again.

This tender kiss from a mother to her child is invested with a weight of unendurable sadness. It is a parent’s last embrace; the moment when Jennifer Lawson said a final goodbye to the cherished daughter she believed was dying.


Sad: This is the moment a tearful Jennifer Lawson thought she was kissing her daughter Alice goodbye forever - until a miracle happened




Doctors had told Jennifer there was no hope for 14-month-old Alice, who had succumbed to a virulent form of meningitis just over a month before. The disease had triggered kidney failure, then a catastrophic stroke. Alice lay in a coma in her hospital bed, dependent on dialysis and hooked to a ventilator.

The fragile threads that held her to life would soon be severed. Her life-support machine was about to be turned off, and a transplant team stood by. Jennifer had decided that from her daughter’s premature death some good should come. Her organs would be donated to help another child live.

And so she prepared for the unimaginable: the final farewell to her little girl.

As she cradled her daughter’s head in her hand, leant forward and pressed her lips to Alice’s forehead, all her teeming, agonised feelings were distilled into one thought: ‘How can I ever carry on without her?’

Today, she grapples for words to describe her pain. ‘I just tried to tell her how much we loved her; I hoped she could hear and understand. I talked to her as if nothing was wrong, but I felt delirious. It was so unreal. I felt the warmth of her; saw the pink in her cheeks. She just looked like a sleeping baby.

‘The past and the future merged in that moment. I told her how proud I was of her; that she had fought for so long and could rest now. And I lay next to her.

‘I was in a daze. They had told me she would die that morning; that they were turning the machine off because she would never breathe on her own. So I tried to tell myself she was already gone, that it was only her little body lying there. But it doesn’t work. You hold on to hope until there is none left.

‘The doctors had arrived for her organs. Suddenly they had unplugged everything and there was Alice, lying on her bed with the lights dimmed. They had given her morphine and then we were left alone, just me, Alice, and her dad, my partner Phil.


‘So I kissed my little girl. She felt so warm and cosy I couldn’t imagine she was about to die.’

Jennifer’s instinct was to prove right. What happened next was a miracle.

Alice did not die.


Smile: Alice, centre, pictured with mother Jennifer and sister Taylor, is a fun-filled child - which is a testimony to her fighting spirit

When her life support machine was turned off on March 24, 2010, she began to breathe on her own: her tenacious little spirit would not be vanquished.

Neither Jennifer, 31, nor Phil Lloyd, 36, could quite believe that their 14-month-old daughter had not slipped seamlessly from her coma into everlasting sleep.

‘The truth did not dawn on us to begin with,’ recalls Phil, ‘but then a nurse came in and said the strangest thing. She said the organ donation team were leaving; that they wouldn’t be needed after all. Then a doctor came in and told us Alice was breathing without ventilation. They’d been watching her monitors in a separate room; they’d seen her rally.’

As Jennifer recalls: ‘It was as if a bubble of despair had been popped. The sick feeling of being stifled just dissolved. Lovely Alice was with us again. We did not allow ourselves to feel joy — we did not yet know she was permanently out of danger — but the relief was indescribable. We felt we were witnessing a miracle.’

It is now two-and-a-half years since Alice lay on the brink of death. Today, aged three-and-a-half, she is a beautiful, doll-like child with china-blue eyes, rosy cheeks and an ever-ready dazzling smile.

She lives with Jennifer, a former massage therapist, Phil, who used to run an online fancy dress shop, and her elder sister Taylor, eight, in a neat semi in Gainsborough, Lincolnshire. The family’s puppy, a Westie called Alfie, bounds exuberantly around the sitting room.

Both Phil and Jennifer, who have been together for ten years, have now given up work to share the care of Alice. The legacy of septicaemia has left her with one leg shorter than the other; she cannot yet walk unaided but is formidably tenacious. The illness deprived her of speech, but she is learning to talk again. Her words are halting; she supplements them with sign language. When she sits on the floor, surrounded by her soft toys, her beam of pleasure lights the room.

Heartbreaking: Alice was expected to die, and when doctors turned her life support machine off they thought it was the end - all except tiny Alice

Jennifer will never forget Valentine’s Day 2010, the day Alice fell ill.

‘Alice was a healthy, happy child, just starting to take her first steps,’ she recalls. ‘She’d never had more than a minor chest infection, so I wasn’t really worried when she became sick and off-colour.’

She phoned her GP who prescribed medicine to bring Alice’s temperature down, diagnosed a viral infection and sent her home. But then alarming symptoms developed. Jennifer noticed purple marks appearing on Alice’s stomach. ‘They were literally spreading before my eyes,’ she recalls. She rang the hospital. An ambulance arrived in minutes.

Alice was rushed to hospital in S****horpe. Doctors pumped her full of antibiotics. Tests disclosed that she was suffering from meningococcal meningitis and septicaemia. She was dispatched immediately to intensive care.

Jennifer remembers: ‘Everyone started shouting, and running around her with syringes and machines. We were taken to a family room, where Phil and I sat side by side in silence.

‘I just went numb. I couldn’t process it. Everything happened so fast. I felt I was outside my body, looking down on the scene. I don’t think I even thought about the word “meningitis” when they told us.’

Next day, Alice was transferred to the children’s hospital in Sheffield while Taylor went to stay with Jennifer’s sister. Jennifer recalls how she and Phil followed the ambulance in a taxi: ‘It was awful, being separated from Alice. I felt the loss of her closeness like a physical pain. She was with strangers, lying helpless in the ambulance. Phil and I couldn’t even speak.

‘When we arrived at the hospital in Sheffield I caught a glimpse of Alice in intensive care, with her pink blanket and her little pony toy. I shouted to the doctors, “Please don’t give up on her!” and burst into tears.

‘Her little face was swollen. You could hardly make out her features. We felt utter disbelief. But she needed us to be strong for her. We clung to the positives — she was safe, in the care of doctors who could help her.’

Thereafter, Jennifer and Phil kept a constant vigil at Alice’s bedside. First she was attached to a life-support machine. Then one of her kidneys failed. She was put on dialysis. Then she developed septicaemia. It caused a severe infection in her knee and back. She was put into an induced coma.

Jennifer struggled to remain calm. ‘I hardly left her side,’ she remembers. ‘I’d gently wash her face, put lip balm on her sore dry lips, hold her hand. Phil and I would sing the familiar songs she liked, act out scenes with her teddy bears, and we fastened balloons to her bed.’

‘I thought: “How much more can a tiny person take?'
Next, their gravely-ill daughter was transferred to the Queen’s Medical Centre in Nottingham. There, in the hospital’s renal unit, she seemed to rally. Doctors began to talk about a kidney transplant.

Alice’s parents allowed themselves a flicker of hope. But then her blood pressure rocketed, her eyes glazed over and her breathing became laboured. These symptoms were the harbingers of a stroke: Alice was rushed back into intensive care.

‘When we were told Alice had had a stroke, we didn’t quite believe it. It’s something you associate with elderly people,’ recalls Jennifer.

‘She had an MRI scan. Then they said she’d need a shunt fitted to drain the fluid from her brain. We heard snatches of the doctors’ conversations; phrases like “devastating bleed”. Phil became convinced she’d never pull through.

He recalls: ‘I thought: “How much more can a tiny person take?” ’ He clasps his head in his hands and bats back tears. ‘From that point, I started to prepare for the worst.’

Jennifer, however, clung on to hope: ‘I never said goodbye. You always hope and pray. I spent a lot of time in the chapel at the hospital, it’s the only thing you have left to do. When you’ve got nobody else, you ask for help there. I’d pray, “Please let her get through this.” ’

But then the thin thread of Jennifer’s optimism was stretched to breaking point. ‘A nurse burst into the waiting room and told us that Alice’s heart had stopped beating. Going down to the theatre in the lift was horrendous, but as soon as we got there, a doctor came out saying, “She’s back!”’

The yo-yoing of their emotions was almost unendurable. Then, when Alice went back to the ward it seemed as if hope had abandoned them. The little girl was in a deep, impenetrable coma.


‘She was not responding. I would feel a rush of excitement because she moved her arm, then nurses would tell me it was just a reflex muscle reaction. When the doctors did their rounds they walked past us. It seemed they’d given up.’

Jennifer and Phil prepared for the worst. They should gather the family, they were urged, and prepare to say their last goodbyes. There was nothing more the doctors could do.

They agreed she should be Christened. It was a short, perfunctory service and Jennifer recalls little of it. She only remembers clasping Phil and crying the whole way through. She also recalls worrying, needlessly, that she might have to sing.

‘Our parents came in to say their goodbyes,’ says Phil. ‘My dad said, “She’s not going yet”, but I remember thinking he’d accept it eventually, in his own time.’

Telling Taylor, then just six, that she would not see her sister again was heartbreaking. But even as they did so, they allowed for a little chink of hope.

‘We told her Alice might be going to Jesus, but we had to see if he wanted her,’ says Phil. ‘When you see a child’s face crumple in such a way, it stays with you for ever.’

Taylor had stayed with her aunt for the three-month duration of Alice’s hospital treatment. She had visited her sister often, ‘but I don’t think the implications of what we were telling her actually sunk in,’ says Phil.

He and Jennifer steeled themselves for their final goodbye to Alice on March 24. ‘We’d taken footprints of her hands and feet as mementos and I’d stayed up with her late the night before, virtually passing out with exhaustion in the early hours,’ says her mum. ‘Then, early in the morning, I’d gone to her bed in intensive care and taken some balloons with me. She loved balloons.

‘I fastened them to her bed then I kissed her. When I did, the world stood still for a moment. And then, of course, the miracle happened.’

When we look into her room at night and see her sleeping peacefully we pause for a minute and think how lucky we are
Alice pulled back from the brink. With relief came cautious elation. Then Jennifer and Phil had to adjust to the news that Alice would be disabled. With the new chapter came a fresh wave of strength. ‘Alice was just like a newborn baby again,’ recalls Jennifer. ‘She couldn’t control her head or sit up, but her kidney function was improving. That felt like a victory.

‘After a week, she was moved back to S****horpe; it felt like a step closer to taking her home. She had been fed by a tube, and when she took her first mouthful of pureed food it was another triumph. Then she started to reach for my hand. Half her face had been paralysed, but slowly, her smile came back.

‘We kept thinking how lucky we were and as she progressed, we focused on getting her stronger and preparing her for coming home.’

Duly, one May day two years ago, they brought Alice home. The joy they felt as they settled back into a new routine of family life was unsurpassed. Alice was infected by their excitement: ‘She started to make little squeals of happiness; they were her first sounds,’ her mum recalls.

Today, Alice attends a special school; recently, to Jennifer’s joy, she said ‘Mummy’ for the first time. There will be operations in future to lengthen her left leg, and both Phil and Jennifer intend to encourage her progress in every way. She’s still fed fluids through a tube in her stomach because she has not yet regained her capacity to swallow. Meanwhile, her kidney function has improved dramatically.

Each milestone is a cause for celebration. Alice is learning to count. She rides a specially-adapted bike; her paintings adorn the wall and her laughter fills the house. When Alfie lollops into the kitchen, Alice kisses the puppy tenderly on his nose.

It reminds Jennifer momentarily of that other kiss; the one she thought would be the last she would give her daughter.

‘When we look into her room at night and see her sleeping peacefully we pause for a minute and think how lucky we are,’ she smiles. ‘She really is our little miracle.’


Read more: The kiss of life: The moment a mother paid a tearful goodbye to the 14-month-old daughter doctors said she was about to die, before something miraculous happened | Mail Online



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I realize this is a long article, but it is worth reading.
 

shadowshiv

Dark Overlord
May 29, 2007
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After reading/hearing/seeing so much heartache happen in the news, it is such a breath of fresh air, it is so amazing, to hear something so uplifting, I just had to share it.
 

SLM

The Velvet Hammer
Mar 5, 2011
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After reading/hearing/seeing so much heartache happen in the news, it is such a breath of fresh air, it is so amazing, to hear something so uplifting, I just had to share it.

I get that way too. The news can drag you down so I keep an eye out for 'good news' stories. Post them when I can.
 

shadowshiv

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May 29, 2007
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I get that way too. The news can drag you down so I keep an eye out for 'good news' stories. Post them when I can.

Exactly. Good news (at least reported good news) is rare, and it is always a treat to be able to learn about it. It gives one faith that not everything is doom and gloom in the world.
 

SLM

The Velvet Hammer
Mar 5, 2011
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Exactly. Good news (at least reported good news) is rare, and it is always a treat to be able to learn about it. It gives one faith that not everything is doom and gloom in the world.

I've noticed it can have a real impact on the 'mood' on the board too when posted. Seems to take the edge off sometimes.
 

shadowshiv

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I've noticed it can have a real impact on the 'mood' on the board too when posted. Seems to take the edge off sometimes.

That is a good point. One cannot help but feel down when reading that numerous people are murdered, but perhaps reading an article about a life continuing regardless of the odds will pick up their spirits.:)
 

SLM

The Velvet Hammer
Mar 5, 2011
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That is a good point. One cannot help but feel down when reading that numerous people are murdered, but perhaps reading an article about a life continuing regardless of the odds will pick up their spirits.:)

Yes that but I also meant that if member's exchanges are getting a bit heated, I have noticed that starting a few humorous threads or posting an uplifting article can change that mood a bit too. Sometimes. ;)
 

shadowshiv

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May 29, 2007
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Yes that but I also meant that if member's exchanges are getting a bit heated, I have noticed that starting a few humorous threads or posting an uplifting article can change that mood a bit too. Sometimes. ;)

Another good point. We'll have to bring up the cudbear thread if that happens!;)
 

shadowshiv

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May 29, 2007
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Cudbear? I'm thinking that's CDN Bear after he gets old and his teeth are worn down.

LOL! No, it was actually the name of a thread created by a spammer a while back. It got a lot of action back then, but it has not been perused in quite a while.
 

TenPenny

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Interesting article.

Notice that both parents have given up work to look after their daughter. Obviously from England, you couldn't do that in North America.
 

shadowshiv

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Whenever I see a picture of a child holding a stuffed animal like this, I always get a lump in my throat. I think about how that could be their favourite toy, and it just makes me even more sad(thankfully happy in this case). I don't know why that's the case. I mean, it's just a stuffed animal, right? I just don't think of it like that, I guess.
 

SLM

The Velvet Hammer
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Another good point. We'll have to bring up the cudbear thread if that happens!;)

That was fun! We need a new cudbear, we're over due I think. ;)

Cudbear? I'm thinking that's CDN Bear after he gets old and his teeth are worn down.

No, no. Placental cudbears. If I'm not mistaken I think you were the one who told us what the heck it actually was, lol.

Anyway, that won't be CDN Bear after he gets old and his teeth are worn down, that will be, are you ready for it, gummi bears.LOL.

Interesting article.

Notice that both parents have given up work to look after their daughter. Obviously from England, you couldn't do that in North America.

It would be a benefit I'd support here. Can you imagine have to go into work when your child may be dying simply because you need to pay the mortgage that month?

Whenever I see a picture of a child holding a stuffed animal like this, I always get a lump in my throat. I think about how that could be their favourite toy, and it just makes me even more sad(thankfully happy in this case). I don't know why that's the case. I mean, it's just a stuffed animal, right? I just don't think of it like that, I guess.

Our stuffed toys are our first real comfort away from Mom & Dad I think. We attach a special meaning to them, many of us do anyway.
 

TenPenny

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Jun 9, 2004
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It would be a benefit I'd support here. Can you imagine have to go into work when your child may be dying simply because you need to pay the mortgage that month?
.

Can you imagine having to go into work when your child may want supper, just because you need to pay the mortgage?
 

shadowshiv

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May 29, 2007
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Our stuffed toys are our first real comfort away from Mom & Dad I think. We attach a special meaning to them, many of us do anyway.

That is a good point. Perhaps a link to our childhood?
 

lone wolf

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It would be a benefit I'd support here. Can you imagine have to go into work when your child may be dying simply because you need to pay the mortgage that month?
Cripe! It was hard enough just keeping my mind on the tasks at hand when our newborn was in neonatal ICU - a hundred miles away....
 

shadowshiv

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Cripe! It was hard enough just keeping my mind on the tasks at hand when our newborn was in neonatal ICU - a hundred miles away....

My youngest sister was born extremely premature. She was kept in an incubator, and it wasn't certain whether she would survive or not. She ended up having most of her small intestine removed, but she is still here with us and now happily married. I can't imagine how hard it would have been for my parents to have to go through that ordeal.