Teddy Mascaro’s Journey

£248,010 donated of £238,000 goal

Teddy is a cheeky, funny and affectionate little boy, who adores cuddles, playing with his friends, and is obsessed with horses!

When he was just 16 months old he became ill, stopped crawling and his personality changed from lively and jolly to fearful and clingy.  Initially, doctors thought it was a virus or infection but in April 2018 a tumour was found in his stomach and he was diagnosed with high-risk neuroblastoma.

Brave Teddy has endured a long list of treatments including chemotherapy, radiotherapy and stem cell harvests. He has shown amazing spirit, handing out high fives to the doctors and nurses administering his medication.

Thanks to your donations, Teddy’s family flew to Barcelona in January 2019 to start immunotherapy, to clear any last remaining neuroblastoma cells in his body. His end of treatment scans showed the fantastic news that he’s got no evidence of any disease!

Teddy’ family also fundraised to be able to access a vaccine in New York that they hope will reduce the chances of his cancer coming back. The £238,000 target was reached in June 2019 and Teddy flew to the USA for treatment in a few weeks. They are continuing to raise funds in case he needs any further treatment that is not available on the NHS.

Teddy’s story

Teddy had always been very sociable and outgoing, so when he started to become withdrawn in February 2018, his parents Emma and Jamie couldn’t work out what was wrong. He was ill with what was thought to be a virus and had an ear infection for which he was prescribed antibiotics that knocked him a bit. From then on he just didn’t seem to be able to get fully well. His parents took him to the GP a few times who never thought it was anything more than a virus, not uncommon for a toddler who had just started nursery. After a month of being quite up and down, Teddy started not to want to crawl and became tired very quickly.

By Easter when the family were on holiday, his parents became really worried. Dad Jamie says: “It became clear that Teddy wasn’t well as he started spiking temperatures and didn’t want to get off our laps and play or swim or go near the sand. The doctor gave him a thorough check and prescribed more antibiotics, but by the time we got home, we knew it was something more. Teddy looked pale and his whole personality had changed.”

Emma took him back to the GP again, who listened to all she had to say about the previous month and while not sure what it was, confirmed something was wrong and referred Teddy to his local hospital. The family were soon hit with devastating news – straight away the doctor identified a large mass in Teddy’s stomach and that he needed a blood transfusion.

Emma says: “Despite the mass, we were shell-shocked and in total denial. I remember sending a message to work to say I wouldn’t be in the next day but would hopefully be back later in the week. Little did I know that I would be giving it up entirely to care for Teddy as he fought for survival. It started to dawn on us that the situation was bad when each doctor who came to see us over the next 24 hours looked at us sadly and said ‘I’m so sorry.’ At this point, we hadn’t been told it was cancer, but I suppose they all knew that it was. When it was confirmed by a consultant the next day I remember clutching Teddy and sobbing.”

As well as identifying the mass in Teddy’s stomach, blood tests confirmed he was extremely anaemic and would need a blood transfusion. Initially, the doctors thought it was a type of kidney cancer called Wilms but within days a specialist consultant confirmed from the CT scan it was more likely to be neuroblastoma. Teddy had surgery to insert a Hickman line and take a biopsy and bone marrow aspirate and a few days later his parents were given the worst news – it was confirmed that he had high-risk neuroblastoma.

At this time Teddy also started to go downhill fast, struggling to breathe, with his lungs full of fluid. Emma says: “It was the lowest point in our journey so far. We hadn’t seen him smile in at least a week and I started to think I would never see him smile again.”

Teddy deteriorated and was transferred to intensive care. But he pulled through and after a few rounds of chemotherapy, his parents started to see glimmers of the old Teddy reappearing. Emma adds: “Teddy started smiling and giggling again and developed his obsession with horses! Having spent weeks being terrified of the doctors and nurses, slowly his old sociable side came back and he started bonding with them by showing them his horse figures and books.”

A long list of treatments

Teddy went through frontline treatment in the UK, although immunotherapy – which aims to help the body’s own defences turn against the neuroblastoma cells using antibodies – took place in Barcelona.

The true extent can be seen in this post on Teddy’s Facebook page.

A vaccine in New York

After treatment, Teddy shows no evidence of disease. But high-risk neuroblastoma is a particularly aggressive and complex cancer to treat. If Teddy’s disease were to return his chances of surviving would drop to less than one in ten.

It means that Teddy’s family want to access the Bivalent Vaccine clinical trial at Memorial Sloan-Kettering Cancer Center in New York – treatment they hope will reduce the chances of relapse. Teddy flew to begin treatment in June 2019.

His family are continuing to fundraise in case he needs any further treatment that is not available on the NHS.

How you can help

There are many ways you can help Teddy: by making a personal donation; holding a fundraising event; getting sponsored to take on a challenge; or simply following and sharing Teddy’s story through his Facebook page, Team Super Ted or on Instagram.

Download our free Teddy resources (below) to support your fundraising, and click here for even more resources, including fundraising ideas, templates and guidance.

Campaign Poster

Event Poster

Sponsorship Form

To donate by text, send “TEDDY” followed by any whole amount up to £20 to 70085. This will cost your donation plus your standard network charge. It won’t matter if you leave a space before the number, if you include a ‘£’ sign or whether you use upper or lower case.

If you’d like help supporting Teddy’s campaign, please get in touch with the fundraising team on 0207 284 0800 and fundraising@solvingkidscancer.org.uk

Terms and Conditions for Journeys

All donations are paid into Solving Kids’ Cancer’s (SKC) general funds to further its general charitable purposes. The funds raised by this Journey are not restricted for the child’s use. However, the trustees of SKC have agreed to designate 90% of funds raised by this Journey to help the child and their family pay for potential future treatment costs and all other associated costs including travel and accommodation. We will use the remaining 10% to pay for SKC’s administrative and fundraising costs.

If the child no longer needs the funds, or if the trustees decide, at their absolute discretion, that the funds should be used for a different purpose, they may redesignate all or part of the 90% for SKC general charitable purposes. We are very grateful for your charitable donation.

For further information about SKC and how we spend donations, please contact info@solvingkidscancer.org.uk

Solving Kids' Cancer Europe a registered charity no. 1135601 and registered company no. 7208648.

Join our newsletter

For information and guidance on how Solving Kids’ Cancer manages your personal information please see our Privacy Policy

Privacy Policy (click to expand)

Follow Us

Useful links

Contact us

Solving Kids' Cancer

Tel: 020 7284 0800

CAN Mezzanine
49-51 East Road
London
N1 6AH

Contact us