Callum-Lee is a brave nine-year-old who loves watching wrestling and learning about dinosaurs.
He was diagnosed with neuroblastoma in June 2013 after months of illness and appointments. He has suffered two relapses since in January 2017 and most recently in August 2018.
With each relapse affecting Callum-Lees treatment options, the family are determined to keep his options as open as possible. This means they are fundraising in case he needs to access treatment not available on the NHS and potentially overseas. This could cost hundreds of thousands of pounds.
It is important to us as a family to get Callum-Lee the treatment he needs, so we are asking for help to raise the funds if needed, says Callum-Lees mum, Nicola.
In November 2012 Callum-Lee became unwell. He had a high temperature and pains in his stomach. By Christmas, he was still not getting better and his worried parents took him to hospital.
The doctor at hospital thought Callum-Lees stomach muscles were going into spasm and told Callum-Lees parents that he would refer him for further tests. But his condition worsened as they waited and his parents took him back to their local GP who referred them to the Royal Albert Edward Hospital in Wigan to see a paediatric doctor.
On 1st March 2013, Callum-Lee and his family visited the hospital where the doctor was concerned that Callum-Lees tummy was hard and swollen. Callum-Lee then had blood tests which doctors believed showed he had an infection for which they prescribed antibiotics.
Callum-Lee was discharged after a week. By June he was limping and unable to put any weight on his leg, he had stopped eating and even collapsed at nursery. Doctors diagnosed rheumatoid arthritis on 14th June and referred Callum-Lee to another doctor at Alder Hey Childrens Hospital in Liverpool. On 24th June Callum-Lee visited the doctor who diagnosed neuroblastoma after examining Callum-Lee for just fifteen minutes.
We were absolutely devastated, explains Callum-Lees mother Nicola.
We knew we had a poorly little boy on our hands but cancer was definitely not something we anticipated.
Callum-Lee went through chemotherapy and had surgery to remove the tumour, after which he had his stem cells harvested and transplanted back into his body to boost his immune system.
Callum-Lees scans came back with no evidence of the disease in December 2014 and life began to get back to normal.
In the two years, he was in remission we started to enjoy some sort of normality as a family. Callum-Lee went back to school and made new friends, and we went on caravan holidays, continues Nicola.
In January 2017 a lump appeared on the right side of Callums neck. I contacted his consultant who then sent him for an ultrasound scan and a biopsy - it was confirmed as neuroblastoma.
Since then Callum-Lee has relapsed twice and has gone through 12 months of chemo regime on the BEACON trial, followed by an oral chemotherapy drug to battle against this devastating childhood cancer.
Most recently in August 2018, the family were told the cancer had returned in his neck, in his spine and near his pelvis. Once neuroblastoma comes back, a childs chances of surviving for longer than five years drops dramatically to less than 10%. Its why Callum-Lees family are keeping all of their options open and fundraising for treatment he may need that is not available on the NHS.
Callum-Lee's fundraising campaign
Callum-Lee's family are determined to keep his options as open as possible. This means they are fundraising in case he needs to access treatment not available on the NHS and potentially overseas. This could cost hundreds of thousands of pounds.
To donate by text, send CALLUMLEE followed by any whole amount up to £20 to 70085. This will cost your donation plus your standard network charge. It wont matter if you leave a space before the number, if you include a £ sign or whether you use upper or lower case.
If youd like help supporting Callum-Lees campaign, please get in touch with the fundraising team on 0207 284 0800 and firstname.lastname@example.org.