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 <strong>My name is Lee Hutchinson, and I am raising funds on behalf of Kole and his family.</strong>
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 Kole was born on 4 July 2024, weighing a perfect 7lb 8oz.
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 He was the final piece of his family's puzzle. After a short stay in NICU because of a few minor complications, his parents looked forward to simply watching their little boy grow up alongside his siblings, Koby and Ayla.
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 <strong>They could never have imagined that less than two years later, they would be fighting to save their son's life.</strong>
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 When Kole was around six months old, his family noticed he wasn't reaching the same milestones as other babies his age.
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 After many hospital appointments, Kole was diagnosed with BESS and Global Developmental Delay. As he grew, he also began showing signs of severe autism from a very young age.
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 His family had to adjust the future they had imagined for him. But one thing never changed.
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 <strong>Kole was perfect just as he was.</strong>
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 Whatever support he needed, his family would be there to give it to him for the rest of his life.
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 Then, on 28 April 2026, when Kole was just 22 months old, everything changed again.
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 Kole was diagnosed with Sanfilippo syndrome, often described as childhood dementia.
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 <strong>His family received the devastating news that, without effective treatment, Kole could begin losing the abilities he has worked so hard to develop.</strong>
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 The disease can progressively take away a child's skills as they grow. For Kole's family, that means facing the possibility of watching their little boy lose more and more of himself over time.
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 But his family is refusing to give up hope.
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 There are clinical trials taking place around the world, and they are doing everything possible to find an option for Kole.
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 They are also closely following a potential treatment currently being reviewed by the FDA. The family understands that the estimated cost of accessing treatment could be at least £2 million.
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 It's an enormous amount of money.
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 <strong>But right now, Kole has something incredibly precious on his side: time.</strong>
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 His diagnosis came while he is still very young, and his family wants to use every moment they have to search for treatment and give Kole every possible chance.
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 That's why we're asking for your help.
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 We don't expect one person to give thousands of pounds.
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 <strong>We're asking a community to come together. If two million people gave just £1 each, we could reach Kole's £2 million goal.</strong>
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 Every donation gets his family one step closer.
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 Every share puts Kole's story in front of more people.
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 And every person who helps gives this family more hope that they can access an option that could give their little boy more time.
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 <strong>More time with Koby and Ayla. More birthdays. More family memories. More ordinary days together. More time for Kole simply to be a little boy.</strong>
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 His family wants to be able to look back and know they did everything they possibly could for him.
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 Please help us give Kole every possible chance.
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 If you can donate, even £1 will help.
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 If you can't donate, please share Kole's story. One share could help us reach the next person who can.
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 Kole's family is fighting for his future. Let's show them they don't have to fight for it alone.
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 Thank you for reading, donating and sharing.
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 <strong>For Kole.</strong>
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Jacob Wynne

Anonymous

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zoe washington

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George Deehan

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Help give Kole as much time as possible

Help give Kole as much time as possible

Still £1,406 to go. Help us build momentum.