Greg's speech in support of Dr Liam Fox MP's Down Syndrome Bill:
Greg Smith (Buckingham) (Con): I rise to speak entirely in support of this Bill receiving its Second Reading today, and hopefully travelling at pace through its whole passage through both Houses and to Royal Assent before World Down Syndrome Day on 21 March next year.
As my right hon. Friend the Member for North Somerset (Dr Fox)—whom I warmly congratulate on bringing this Bill forward—has set out in his superb opening speech, the Bill is so important as it aims to improve services and life outcomes for people with Down’s syndrome, amounting to some 47,000 people across the country.
The Bill will particularly make England—I share my right hon. Friend’s ambition in time for it to be our whole United Kingdom—a better place to grow up and live with Down’s syndrome, bringing fairness to a group of people who, I am sorry to say, are too often marginalised. It will promote the rights and welfare of people who have Down’s syndrome at all levels of society, and raise awareness and understanding of it. Fundamentally and importantly, the Bill will force education, health and local authorities in England to take people with Down’s syndrome into account when providing services, and will establish a national strategy for equality.
Of course, most children with Down’s syndrome will learn to read and write, and go to a local mainstream school like other children. They will also rightly take part in many other activities that are on offer to all. Life should be as broad and fun-packed as that of any other child. Yet clearly, many daily challenges remain for those impacted by Down’s syndrome.
One constituent of mine, Kate, contacted me about her two-year-old daughter who has Down’s syndrome. My constituent wrote: “She is a bright, funny, gorgeous, amazing little girl. But already in her short life I have struggled to get her the help she deserves and needs. Covid has obviously played its part, but the issues are more ingrained. I am looking to the future and can see the battles ahead, the fights I know I will have. This needs addressing. It shouldn’t be like this.”
Those are wise words from my constituent. I very much hope that the Bill will make life better for my constituent and so many other families.
The Bill will transform the lives of people living with Down’s syndrome, and it is especially welcome that the Government have committed their support to it and will equally consult widely on the proposed guidance, ensuring that the voices of those with Down’s syndrome, their families and carers are heard, and that the guidance is fit for purpose. That is essential. Provisions in the Bill will enable adults with Down’s syndrome to live, work and join in with confidence and independence, fully included in society alongside their friends and peers.
Critically, I am hopeful and confident that the passage of the Bill will go a long way to destigmatise—we heard that word before and it cannot be restated often enough in this debate—Down’s syndrome and to re-educate both the public and professionals about the advances, including in life expectancy, that have occurred in recent decades.
As my right hon. Friend said in his opening remarks, for the first time people with Down’s syndrome are beginning to outlive their parents. If we do not make provisions for this, I fear that there will be tragic consequences in the future when it comes to care.
I entirely support the Bill and am delighted that the Government equally support it. I look forward to seeing it progress rapidly through Parliament.
