It is a pleasure to serve under the chairmanship of Mr Paisley. The Minister thanked Julie Marson for securing the debate and expressed condolences to Simon and Andrea, who were present. She acknowledged that cancer diagnosis in young adults can be challenging due to its rarity, with just under 4,000 cases diagnosed annually in England. GPs often lack experience dealing with non-specific symptoms. However, there are numerous opportunities where further investigation could reveal the problem, but Jess's case highlights issues with delayed diagnoses despite multiple visits and symptoms. The Government has allocated £2.3 billion to roll out community diagnostic centres enabling direct referrals for patients with non-specific symptoms without hospital referrals needed initially. Additionally, non-specific symptoms pathways are being introduced to facilitate early diagnosis through discussions involving diagnostic equipment and expertise. A target of 75% of cancers diagnosed at stages 1 or 2 by 2028 is set, aiming to address all cancer types including rarer ones with no known origins. The Minister also mentioned piloting a nurse specialist route for patients needing further support or diagnosis. She discussed the possibility of implementing a flag system in GP practices based on frequency and persistence of symptoms but noted technical challenges with independent IT systems among GPs. Training programmes are being rolled out by Macmillan Cancer Support, CLIC Sargent, and Cancer Research UK to educate primary care teams about cancer diagnoses in young people.