Down's Syndrome (Children and Adults) Bill - Second Reading of the entire bill

Supports the Bill, highlighting its educational value and the need for better awareness. Cites statistics: 47,000 people in the UK with Down’s syndrome; discusses issues such as negative language around diagnosis, health challenges, education barriers, and inappropriate social care.

Supports the Bill, citing its potential to improve targeted legislation for those with Down’s syndrome. Highlights importance of tailored education choices and age-appropriate social care services.

Alex Norris commends the right hon. Member for North Somerset for his initiative to use a private member's bill slot on Down’s syndrome issues, highlighting it as human rights legislation aimed at empowerment rather than charity. He acknowledges that 47,000 people in the UK live with Down’s syndrome and advocates for a four-nations approach moving forward. Norris emphasises the importance of individualised support beyond statistical data, mentioning his family's involvement to personalise the discussion. He stresses the need to remove barriers to progress and tackle stigma, advocating for better mental health services alongside physical health advancements. Additionally, he queries the Minister about the alignment with the Health and Care Bill regarding clinical commissioning groups and housing provision for people with Down’s syndrome.

Intervened to highlight difficulties in identifying mental health issues among those with disabilities like Down's syndrome, suggesting a need for more nuanced approaches in treatment and identification.

The speaker supports the Down Syndrome Bill, highlighting her personal connection to someone with Down’s syndrome. She emphasises the need for tailored services and guidance for those with Down's syndrome, advocating that public authorities must be obligated to have due regard for this guidance in carrying out their functions. She also mentions the importance of involving people with Down’s syndrome and their families in developing such guidance.

Mr. Liam Fox concluded by thanking his colleagues for their support and emphasised that the bill is not a panacea but a vital step forward in addressing societal values. He also highlighted the importance of ensuring legal redress to make the rights enshrined in the bill effective. Additionally, he stressed the global leadership role of the UK by being the first country to legislate on this issue and underlined the empowerment of individuals with Down’s syndrome as full citizens demanding quality services in health, education, and social care.