An NHS children’s nurse is reaching out to the public for help as her three-year-old son requires urgent treatment overseas to combat his high-risk neuroblastoma cancer. The crucial treatment for Teddy Sloman’s condition has been discontinued for NHS patients in the UK, prompting his family to seek alternative solutions.
To fund the necessary treatment for Teddy, his mother, Sarah, who is also a pediatric nurse, aims to raise £250,000 to maximize his chances of fighting this rare and aggressive childhood cancer. Sarah emphasized the importance of accessing this treatment to prevent the disease from recurring and to provide Teddy with a hopeful future.
Teddy’s battle with high-risk neuroblastoma began last year when symptoms initially thought to be related to teething escalated, leading to a diagnosis. Following the discovery of cancer spread to his bone marrow, Teddy underwent extensive treatment at Noah’s Ark Children’s Hospital for Wales, including chemotherapy, major surgery, and other intensive therapies.
While Teddy has shown positive responses to treatment, the risk of cancer recurrence remains high, necessitating ongoing maintenance therapy. However, the anticipated treatment option is no longer available within the UK healthcare system, urging Sarah and her husband, Kramer, to explore international options. Their preferred plan is to procure the treatment directly from the manufacturer and administer it under local medical supervision.
As Teddy nears the completion of his current treatment phase, preparations for maintenance therapy are underway. To support Teddy’s journey and access the required treatment, donations can be made through the provided link. Time is of the essence for Teddy’s family as they strive to secure the necessary care to combat his condition and safeguard his future.
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