Appealing For Your Donation - To support families affected by Neuroblastoma
Mitchell’s Miracles is delighted to offer financial grants directly to families with children diagnosed with childhood cancer Neuroblastoma. We understand that once hospital treatment starts, financial pressures can begin to mount and part of our role is to lessen that burden.
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How we offer help to families
In response to this need, we offer grants to families (with parents/carers who are employed, self-employed and unemployed) across the UK and applications can be made to access help with the following:
● transport to and from hospital ● household utility bills ● mortgage ● rent ● food expenses in hospital ● hospital parking, toll, congestion charges ● loss of income ● clothing ● furniture ● bedding ● Cost of living |
Access our help by clicking on the buttons below. They will take you to forms that once submitted will be reviewed by our dedicated staff - asap.
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If you are in need of emotional support, you are not alone! Send an email or call Lisa Denison, who heads up this service. Alternatively, click on the emotional support button above and complete a form.
Here are some of the amazing brave children we have proudly supported. If fundraising to support our families is something you would like to explore, we would love to hear from you!
Tramaine is just 3 years old and was diagnosed with stage 4 Neuroblastoma in 2021. Tramaine has already endured all of the front line treatment and is now currently receiving antibodies on a trial at The Queen's Medical Centre. How we’ve helped Mitchell's Miracles have supported Tramaine and his family over the last two years, providing financial grants to help buy Tramaine clothing, bedding and furniture and support with transport costs to and from hospital appointments. |
Tramaine Donachie, 3 years old, from Nottingham
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Freddie Rumsey
From Walton on Thames |
Freddie was diagnosed with Low-Risk Neuroblastoma in September 2021 at Great Ormond Street Hospital. Freddie has already received chemotherapy and will be needing ongoing physiotherapy support, as sadly the tumour compressed on his spine which has caused nerve damage to his leg and foot and is unable to walk. His mummy has given up her career to care full time for Freddie. They have a long journey ahead of them, which involves many appointments and hospital stays. How we’ve helped Mitchell's Miracles will be providing ongoing financial and emotional support to help the family through this very difficult journey. |
Skyla Hassal
From Merseyside |
Skyla was diagnosed with Neuroblastoma at just 6 months old in 2021. She is currently having regular scans every 2 months, as she hadn't responded to the previous chemotherapy treatment. Skyla's mum explained to us that due to the tumour compressing on her spine, she is currently unable to walk. How we've helped Mitchell's Miracles are supporting Skyla and her family with the help of living costs and supporting them with transport to and from hospital. |
Dulcie is just 5 years old. In September 2021, her parents were given the terrible news that their daughter has stage 4 Neuroblastoma cancer. Dulcie has started chemotherapy at Birmingham children's hospital and will continue with her treatment for a minimum of 18 months. How we’ve helped Mitchell's Miracles will be providing ongoing financial and emotional support to help the family through this very difficult journey. |
Dulcie O'Kelly
From Telford |
George Brown
From Birmingham |
George was diagnosed with stage 4 Neuroblastoma in April 2019, and is being treated at Birmingham children's hospital. George's parents were given the heart-breaking news of a third relapse which has really hit the family hard emotionally and financially. Scans and tests are still on going, to determine the best treatment plan.
How we’ve helped Mitchell’s Miracles is supporting George's family with ongoing emotional and financial support during this extremely difficult time. |
Kayla Buttle
From Norwich |
Kayla was diagnosed with stage 4 Neuroblastoma at the start of this summer, 2021. She has just completed the first course of chemotherapy called 70 days rapid cojac. Her stem cells have also been removed from her body, for harvest, which are the building blocks for her bone marrow to recover after such intense treatment. After she has received a high dose chemotherapy, they will be given back to her after. Following on from this, she will need further treatment, which will mean long stays in hospital.
How we’ve helped Mitchell’s Miracles is supporting Kayla’s with financial support for: travelling to Great Ormond Street hospital from Norwich, food costs in hospital, extra clothing and extra childcare for Kayla’s siblings. |
Xavion Blue-Michael
From London |
Xavion was diagnosed with stage 2 at just 7 months old in November 2020. At Great Ormond Street Hospital he has endured chemotherapy and very complex surgery to remove the growing solid Neuroblastoma tumour which was compressing his spine. Xavion has been left with little movement in his legs due to the nerve damage caused by the compression and now receives physiotherapy at the Royal National Orthopaedic hospital for children who have spinal injury and he now needs to wear a spinal brace. How we’ve helped Mitchell's Miracles have provided two separate financial grants to his family to help with travel expenses as well as providing emotional support. |
Milo Phelps
From Gloucestershire |
Milo was diagnosed with Neuroblastoma in April 2021. He has undergone front-line treatment including chemotherapy, radiotherapy, stem cell transplant and Antibodies at Bristol children's hospital. "Quote from his mummy" Milo is resilient, he smiles lots, and even at his most poorly time he would smile at his family through teary eyes whilst his tongue peeled and his tummy lining dissolved from the chemotherapy.
Milo has two sisters aged 4 & 8, who adore him, but struggle so much when they go to hospital, as they worry they may not get back to seeing their brother for day's /weeks at a time. Sadly Milo's parents have had to stop working, which has had such a huge impact on funding the travel costs to and from hospital, and with the rising prices of energy and fuel, they reached out to our charity for support. How we’ve helped Mitchell's Miracles was able to provide ongoing financial assistance to cover the transport costs to and from hospital. |
Harry Deeba
From Norwich |
Harry was recently diagnosed with stage 4 Neuroblastoma. He is currently receiving hospital care at Addenbrookes Hospital. Harry's parents have a 70-mile round trip to the hospital which is having a negative impact on their income.
How we’ve helped Mitchell's Miracles was able to provide Harry’s family with a grant that meant the costs of going to and from hospital were paid for. |
Lincoln Melling
From Liverpool |
Lincoln, was only 5 years old, when he was sent to Alder Hey children's hospital on the 13th of Feb 2019 with a lump in his tummy. He was diagnosed with stage 4 Neuroblastoma and very quickly started his treatment of 70 days of chemotherapy, high dose chemotherapy, radiotherapy and immunotherapy.
How we helped Mitchell’s Miracles was able to provide two separate grants to help with household utility bills and transport costs to and from hospital appointments. They responded to our help by saying, 'we can't thank the amazing work and contributions from Mitchell's Miracles. It was fantastic to hear from you today and we will keep you posted on Lincoln's progress and really can't thank you enough. My son will come out the other side’. |
Archie Wilks
From Newport |
Archie was diagnosed with stage 4 Neuroblastoma and is receiving hospital care at Addenbrookes Hospital. Due to the length of time he has had to spend in hospital, the emotional and financial impact on the family was heavy.
How we’ve helped Mitchell's Miracles was able to provide two seperate grants to help towards the parents’ loss of income and buy a single stroller so that they could travel around with Archie’s twin easier. |
Oscar Manktelow-Page
From Kent |
Oscar was diagnosed with Neuroblastoma in October 2018. We are delighted to announce that he is currently in remission, but still requires regular treatment of 3 monthly ultrasounds and 4 weekly steroids.
How we’ve helped Mitchell's Miracles was able to provide a grant to cover the costs of travel expenses to and from hospital appointments. |
Alfie Ward
From Southampton |
Alfie has battled with stage 4 Neuroblastoma for most of his life. After suffering from another relapse, he will start the minivan trial at University College Hospital, London and Southampton hospital. His long battle with Neuroblastoma has been an immense battle for the whole family; mentally, physically, and financially. How we’ve helped Mitchell's Miracles has been able to offer a financial grant to help towards the travel costs to and from hospital appointments and clothing for Alfie. |
Ireland Banham
From Ipswich |
Ireland was diagnosed with stage 4 Neuroblastoma in July 2019 and treated at Addenbrookes children’s Hospital. Ireland endured front line treatment for approximately 18 months. In addition to the financial strain the Neuroblastoma diagnosis had incurred, Ireland’s mother moved home. This resulted in having to travel 60 miles to and from hospital stays.
How we’ve helped Mitchell's Miracles was able to support Ireland and her family with two separate financial grants to help with their travel to and from hospital. |
Henry Stone
From Birmingham |
Henry was diagnosed with stage 4 Neuroblastoma. He courageously endured all the front line treatment including high dose chemotherapy, stem cell rescue and immunotherapy. Henry spent a very long time in hospital fighting against Neuroblastoma. He is currently stable and under frequent check ups to monitor his progress.
How we’ve helped We have supported Henry and his family with two separate financial grants which helped cover their transport costs to and from hospital and food expenses. |
Audrina Hatton-Wright
From Derby |
Audrina was diagnosed with Neuroblastoma in July 2018. She spent a lot of time in hospital receiving frontline treatment which included chemotherapy, surgery, radiotherapy. Audrina would like to one day work for NASA, absolutely loves Star Wars, and does a great Darth Vader impersonation! When her treatment finished she rang the bell in the hospital to celebrate this very special day. Her family are currently raising funds to take Audrina abroad for treatment to help prevent a relapse occurring.
How we’ve helped We supported Audrina’s family with a grant to help towards the travel costs to and from hospital. |
Maya Nash
From Folkstone |
Maya was almost four when her family were given the devastating news that she had stage 4 Neuroblastoma Cancer. Over a 20-month period, Maya has been bravely battling this cancer. Her treatment includes having: ten cycles of chemotherapy, additional high-dose chemotherapy, a stem cell harvest and transplant, 100% surgical resection of the tumour in her left adrenal gland, radiotherapy, differentiation therapy and immunotherapy at The Royal Marsden Hospital. Doctors believe that there is no active disease present, but Maya’s future is uncertain and knowing how aggressive her cancer is, the family are not comfortable applying a “wait and see” approach.
How we’ve helped Mitchell’s Miracles proudly supported Maya’s family with two financial grants, which went towards the numerous expenses incurred throughout their journey. The family were struggling financially to the point where they were going to lose their house and our financial assistance eased some of their pressure. |
Harris Morrison
from Isle of Skye, Scotland |
Harris was diagnosed with stage 4 High Risk Neuroblastoma on July 2020. After taking their son to hospital for what they thought was constipation and trapped wind, it took months to receive the confirmation that their son had cancer. Harris is being treated at the Royal Aberdeen Hospital and Aberdeen has become their new home.
How we’ve helped Mitchell's Miracles have supported Harris’s family with emotional and financial support throughout their journey. For 6 months, they received a monthly financial grant to help cover the costs of living away from home and buying essentials in their rented accommodation. |
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As a local children’s charity based in Romford, London, it is our aim to raise awareness amongst the local and UK population about the early signs and symptoms of childhood cancer Neuroblastoma
Our services can be accessed by people all over the UK. Our local areas covered include:
childrens charity romford | childrens charity cranham | childrens charity upminster | childrens charity elm park | childrens charity gidea park | childrens charity harold wood | childrens charity havering atte-bower | childrens charity noak hill | childrens charity north ockendon
childrens charity romford | childrens charity cranham | childrens charity upminster | childrens charity elm park | childrens charity gidea park | childrens charity harold wood | childrens charity havering atte-bower | childrens charity noak hill | childrens charity north ockendon