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<div><strong>Give Bella More Time</strong>
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<div>Bella is 23 years old, newly engaged to the man she adores, and desperately needs more time.
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<div>Just before Bella was admitted to hospital, Ben asked her to marry him. She said yes.
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<div>They absolutely adore each other, and one of Bella’s biggest dreams is now to marry Ben and have that incredibly special day together.
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<div>But instead of planning their future, Bella is facing something no 23-year-old should ever have to face.
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<div>Bella has a rare form of spindle cell sarcoma. After major, life-changing surgery and cancer treatment, we have received the devastating news that her cancer has now spread extensively to her lungs.
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<div>Without another effective treatment, we have been told that Bella’s time could be very short, potentially just months or even weeks.
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<div><strong>But we have a reason to hope.</strong>
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<div>Bella previously received a targeted cancer treatment which worked incredibly well. It dramatically shrank her tumours. Sadly, she eventually had to stop taking it because of the side effects.
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<div>Her medical team is now hoping to treat Bella with entrectinib, another targeted treatment that we desperately hope could work for her again.
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<div><strong>But there is one enormous obstacle.</strong>
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<div>Bella cannot get this treatment funded. If she is going to have it, we have to pay for it ourselves.
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<div>The cost is huge. Bella’s previous treatment cost approximately £14,000 for just 56 tablets. We simply cannot meet costs like these without help.
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<div>Bella is clever, kind, caring and has an absolutely wicked sense of humour. Even through everything she has endured, she is still our Bella, making people laugh and surrounded by people who absolutely adore her.
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<div>We know there are no guarantees with any cancer treatment. But we have already seen Bella respond incredibly well to this type of treatment once before.
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<div>We have to give her the opportunity to try again.
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<div>How your donation will help
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<div>The money raised will primarily be used to self-fund Bella’s treatment, medication and associated medical costs. Funds may also be used for her care, support, travel, equipment, comfort and wellbeing.
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<div>If circumstances change or funds cannot be used for the proposed treatment, they will continue to be used for Bella’s care and benefit, and we will keep everyone supporting her updated.
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<div>If you can donate, however large or small, thank you from the bottom of our hearts.
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<div>And if you cannot donate, please share Bella’s story. Every share could put her story in front of someone who can help.
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<div>Please help us give Bella the chance to receive this treatment.
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<div>The chance to marry Ben.
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<div>The chance for more precious moments.
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<div>The chance for more time.
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<div><strong>Please help us give Bella more time. </strong>
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Help Give Bella, 23 years old, a Chance at More Time

<div>Our mum means the world to us. She is a loving mother, grandmother, friend, and the kind of person who has always put others before herself.
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<div>We are creating this fundraiser to help ease some of the financial pressures during an incredibly difficult time. As a family, we are facing challenges that no one ever expects, and we want to ensure that our mum receives the support, comfort, and dignity she deserves.
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<div>Any donation, no matter how small, will help with expenses and allow us to focus on what truly matters—spending precious time together and supporting one another.
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<div>If you are unable to donate, simply sharing this page would mean so much to us.
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<div>Thank you from the bottom of our hearts for your kindness, support, and prayers during this difficult journey.
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<div>With love and gratitude,
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<div>Iain 
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My mum Mary 

<div>Ive set up this go fund me for sophie she has had the most horrendous thing happen to her and has been through such a hard time she is such a kind strong loving girl and doesn't deserve what has happened ❤️ anything would help and anything made will go towards treating sophie 
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<div>Thank you so much  
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Fundraising money for sophie

With the permission of sonny’s mum and family I am setting up a fundraiser to put special touches to Sony funeral <br />. this beautiful baby boy put up the most amazing fight and sadly lost his battle at 6 years old to Dipg a brain tumour.... we want to make his day as amazing as possible and any money raised will<br />go directly to kelly and Jordan.... sonny was a much love baby brother to Star 11 and Hudson 8.... please share

Raising funds for our sonny boys amazing send off

<div>Hi my name is Sara-Mia I am fundraising for my little brother Cayden
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<div>He is 13 years old and an identical twin, he attends a special needs school with his twin brother, Cayden has autism and mobility issues over the past couple of years he has slowly lost his ability to walk further than 20 steps and is very conscious of the way he looks while walking so has stopped wanting to go out at all, he is currently using a wheelchair that needs someone to be pushing him at all times, he wants to be able to go and play with his friends and brother independently. My mam has worked very hard to provide everything for us all our whole lives but has had to give up her job in community care to give full time care to Cayden whilst he is awaiting more scan results on his spine and hips. Any donations as small as €1 go towards the chair and any alterations that need to be made to our family car and maintenance of the chair thank you
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Help Cayden get a motorised wheelchair

<div>Hi.
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<div>Without going into too much detail, Emma has had to come back to the uk without the one thing that keeps her alive… her furbabies who are currently in the USA. Zura and Zion are mummy’s babies, they panic whenever she is not there. It’s going to be a long road, it’ll take a lot of travelling and expenses for Em but she is determined to bring her babies back. Anyone who watched or knows Em will know those doggies have had and will continue to have the most amazing life with her, they’re treated as royalty and they adore Emma more than life itself. It is possible to bring them home and I know we can do this. So please for those beautiful faces on the front of this page, any amount would be so appreciated to help towards the costs to get them here to the UK. If this isn’t possible there is another way but we will still need the funds to get them to Delaware as a last resort, either way.. they’ll be home to their mummy where they belong ♥️
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Please help bring Zura & Zion home to their Mummy♥

ZeZe Vanilla 

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<div>We are reaching out to you with broken hearts to share Arthur’s story. On the 15th of August 2023, Arthur was diagnosed with a very rare brain tumour called AT/RT which has spread aggressively throughout his brain and spine.
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<div>Arthur is a 4-year-old boy and a big brother to his baby sister Annie who was only 10 months old at the time of diagnosis who had to move in and live with immediate family since Arthur’s diagnosis…… Mum, Dad and Arthur had no choice but to move to Nottingham. Arthur is always full of fun and always spreading joy, kindness, and laughter wherever he goes! Unfortunately, he has being diagnosed with an extremely aggressive stage 4 cancer. A diagnosis which has shaken the family to its core.
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<div>Sadly, this diagnosis has led to Arthur having 2 major brain surgeries including an 11 hour resection of the initial tumour where 75% of it was removed. The second surgery was to have an Ommaya Reservoir drilled and fitted in his skull and brain to directly allow multiple injections of chemotherapy to the remaining 25% of his tumour. Both surgeries were successful, however, the remaining 25% of the tumour is wrapped around the main stem of his brain and is simply too dangerous to operate on without having a devastating impact on Arthur’s future life. Arthur then had to undergo further surgery for a third time to have a central line fitted to the major arteries of his heart to directly treat him with high doses of chemotherapy…….
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<div>Following this, Arthur started his first round of 12 weeks intense chemotherapy. After a complex first round of chemotherapy Mum, Dad and Arthur had to pack up their bags and move to Birmingham for Arthur’s radiotherapy at Queen Elizabeth, which consisted of him being put to sleep for 30 days every single day…… but before radiotherapy could start Arthur had to be tattooed and also have body and face mask made specifically to him; so that they could absolutely be sure that they delivered the high doses of X-Ray beams to the right places without room for error when treating the whole brain and spine……. Arthur successfully completed his radiotherapy on the 29th of December and was then transferred back to Queen’s Medical Centre in Nottingham where he started his second round of chemotherapy on the 2nd of January 2024.
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<div>In the last 7 months Arthur has been put to sleep around 50 times and we have lost count of the amount of blood and platelet transfusions he’s needed. He’s had shingles, infections, fevers, 2 emergency lumbar punctures, countless MRI and CT scans, heart scans, kidney tests, hearing tests, allergic reactions the list goes on……
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<div>As a result of treatment, he is often neutropenic which leads to Dad injecting him daily to stimulate Arthur’s bone marrow to make more blood cells quicker to fight infections, which can be tragic whilst undergoing such intensive treatments.
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<div>The journey ahead is long and challenging, emotionally and financially…… both Mum and Dad who are self-employed haven’t been able to work since the diagnosis in August. The endless medical treatments, scans and consultations being miles away from home results in having to stay hotels and air B&amp;B’s and with cost of living, the bills don’t stop and are adding up placing a burden of worry on their shoulders.
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<div>This is where we can make a difference! We have set up a GoFundMe campaign to rally support for Arthur, Annie, Mum and Dad to alleviate some of the mental and financial stress they are experiencing. We want to allow them to have the best quality of life whilst having to undergo devastating daily battles and missing out on being a family unit without baby Annie for the past 7 months.
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<div>As a family we want to make it possible for them to make amazing memories together and to raise money for Arthur and Annie to make all his wishes come true and hopefully give him the quality of life he deserves!
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<div>I’m sure everyone can appreciate that this is an exceptionally difficult time for Arthur and the family and although we are reaching out for help and support, we do also ask that their privacy is respected.
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<div>Despite being in the face of adversity Arthur is STILL STANDING, YEAH, YEAH, YEAH!
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<div>his favourite song LOL!
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<div>Here's how you can help:
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<div>Donate: Every contribution, no matter how small, makes a significant impact. Visit our GoFundMe page [insert link] to make a secure donation.
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<div>Share: Spread the word! Share Arthur’s story on social media, email, and within your networks. The more people who know about this campaign, the closer we get to reaching our goal.
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<div>Encourage: Leave a supportive message on the GoFundMe page. Your words of encouragement mean the world and provide strength during this difficult time.
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<div>Arthurs family have always been there for others, and now it's our turn to be there for them. Let's come together as a community and show our support in their fight against this challenging illness!
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<div>My Sincere thanks Darcy O’Connor…….. All the funds will be received directly to myself and I will then transfer them to Arthur’s Mummy (Kristy Kidd) for them to make this amazing little boys life as special as it possibly can be!
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HELP Arthur (THE KING) Fight Brain Tumour & Cancer

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