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<div>Hi my name is Katie, I'm raising funds for my auntie and her 4 sons who lost everything to a massive house fire yesterday morning (30/06/2026).
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<div>I'm posting this with permission from my auntie so she doesn't have to worry about anything other than her son (who's currently in a coma fighting for his life in Alderhey Children's Hospital). I can give updates on her son IF and only WHEN my auntie is ready for them to be public knowledge.
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<div>Currently I've sorted everything but furniture to put into their new home. They have a home lined up for whenever they're ready, I've sorted clothes, some cash, food however I can't fund an entire house of furniture by myself.
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<div>There's four people living in that house that only left with the clothes they were wearing and our two beloved dogs who lost their lives. Unfortunately there's absolutely nothing that can replace our 15 years of great memories in that home.
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<div>So I'm raising funds to help my auntie with filling her new house with furniture and the costs that come with living out of a hospital for the foreseeable.
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<div>I just want to thank the neighbours who supplied clothes for my cousin who came out with none, shoes and socks for my auntie after she'd burnt her feet climbing the roof and the emotional support you all provided at the time.
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<div>Any help at all (whether it's a donation or sharing the gofundme) would be greatly appreciated.
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Help Coby have the best send off

<div>Onthe 7th December 2021 our life’s we’re blessed with a 4lb2oz angel we called Kalbi. After birth we were given the news Kalbi had numerous health conditions one of them being A AVSD (two holes in his heart). Kalbi fell Unwell in February 2022 and was admitted to alderhey hospital after 18 days in Blackpool. It was found Kalbi had influenza, bronchitis, sepsis and was in fact in heart failure and After 2 trips to the operating table Kalbi managed to fight and fight through. And staff at alderhey helped Kalbi get back to being the strongest happiest little boy we new and was allowed to come home with his brothers where he belongs on the 1st June 2022 . After a lovely 3 months at home Kalbi then became unwell again, after a short stay in Blackpool he was then transfered again back to alderhey hosptal, Kalbi has undergone full open heart surgery and Remains in alderhey for the time being where he will recover before going home to his family, my self (kalbis mum) and his brothers and the rest of our family and friends are organising numberous events to help raise money to give back to the hospital who saved our boy ❤️
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<div>one of those evens being the cutting and donating of his big brother kailos hair, Kailo will be cutting his very long hair and donating it to the princess trust charity that makes wigs for other children and raising money to give to alderhey.
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<div>Any donation would be very much appreciated ❤️❤️
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Kalbis story ❤️

<strong><a href="https://www.instagram.com/charliesfight/" target="_blank"><br />Charlie's instagram page</a> ‌ <br /></strong><strong><a href="https://www.facebook.com/groups/265101867249571/" target="_blank">Charlie's army Fb page </a> <br /></strong><strong><a href="http://www.Charliesfight.org" target="_blank">www.Charliesfight.org</a> ‌<br /><br />help us to save our baby boy! </strong><strong><br />#charliesfight  #charliesarmy #parentalrights #raredisease #whatif<br /></strong><br />Our gorgeous little 11 month old boy Charlie has a devastating disease called mitochondrial depletion syndrome. Me and his Daddy Chris are both carriers of a faulty gene. (This was unknown to us until Charlie was 3 months old) <br /><img src="https://d2g8igdw686xgo.cloudfront.net/17867326_1489365216.1335_funddescription.jpg" alt="17867326_1489365216.1335_funddescription" />He was born on the  04/08/16 (4th of August) perfectly healthy but then he started to decline. We took him into hospital at 8 weeks old and none of us have been anywhere near home since. We have been with Charlie day in, day out &amp; watched our poor baby get weaker and weaker, he now needs a ventilator to breathe but we have never lost hope throughout all this time! After endlessly researching and speaking to Dr's all over the world <strong>we found hope</strong> in a medication that may help him and <strong>a Dr in America has accepted him in his hospital</strong>. It hasn't been tried on anyone with his gene before (he's only number 16 in the world ever reported) but it's had success with another mitochondrial depletion syndrome called TK2 which is similar - it's helping children to get their strength back and live longer! We strongly feel as his parents that <strong>Charlie should get a chance</strong> to try these medications. He literally has nothing to lose but potentially a healthier, happier life to gain. <br /><br />Charlies condition is caused by a disruption in the mitochondria, the part of the cell that provides energy to his muscles, kidneys and brain. There is a new treatment available which is a nucleoside bypass therapy, which could potentially <strong>repair Charlie's mtDNA</strong> and help it synthase again by giving him the naturally occurring compounds that his body isn't able to produce. It's oral medication so nothing invasive or harmful.<br /><br /><strong>We are running out of precious time with our baby</strong>, he can't have this treatment in the UK so our only hope now is to get Charlie to America  - this will obviously cost us a ridiculous amount of money, money we unfortunately don't have enough of. <br /><br /><strong>If we don't raise enough money then we wont be able to go to America for treatment</strong> <strong>and Charlie will die</strong><strong>!</strong> Great ormond street hospital have already taken us to court to try and gain permission to turn off our baby's ventilation which will result in Charlie's death :( They don't think it's in his best interests to go but we think it's in his best interests to have a chance to improve.<br /><img src="https://d2g8igdw686xgo.cloudfront.net/17867326_1489364525.1565_funddescription.jpg" alt="17867326_1489364525.1565_funddescription" /><strong>The court date is April 3rd and it will be held in the high Court in London.</strong><br /><br /><strong>We just CAN'T let our baby die when there is something that might help him! We won't give up on him</strong> because he has a rare disease. He deserves a chance and he deserves a life as much as anyone else. We understand that rare diseases don't get enough funding for research but why should that be a reason for a child to die?! He's here now and this could help our baby.<br /><br />If Charlie receives this treatment and it does work like the Dr in America thinks, <strong>it won't be just Charlie's life that has been saved, it will be many more children in the future, who are born with this horrible disease</strong> and it will open up other trials on other mitochondrial depletion syndrome's.<br /><br />We need to change things and show how determined parents can forge a path for other families encountering similar obstacles. <strong>We need to find treatments for incurable diseases. We need to give other people hope. We need to start saving lives.. hopefully starting with Charlie xxx</strong> <br /><br />#charliesfight #charliesarmy #savealife<br /><br /><img class="not-resizeable" src="https://d2g8igdw686xgo.cloudfront.net/17867326_1485817987.0053_funddescription.jpg" alt="17867326_1485817987.0053_funddescription" width="100%" /><br /><img class="not-resizeable" src="https://d2g8igdw686xgo.cloudfront.net/17867326_1485818064.2255_funddescription.jpg" alt="17867326_1485818064.2255_funddescription" width="100%" /><br /><img class="not-resizeable" src="https://d2g8igdw686xgo.cloudfront.net/17867326_1485818248.3024_funddescription.jpg" alt="17867326_1485818248.3024_funddescription" width="100%" />

Charlie Gard #charliesfight 

Chanise Williamson

Chanise Williamson

Chanise Williamson

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