Oral Answers to Questions

Debate between Jim Shannon and Kevin Foster

Wednesday 24th April 2019 Commons Chamber

[Kevin Foster]

It is vital that those who stand for office are representative of our society. As a Government, we are taking action to achieve that through a £250,000 fund for disabled candidates in the forthcoming English local election in May. That will help to create a level playing field for disabled and non-disabled candidates.

[Jim Shannon (Strangford) (DUP)]

T7. Will the Minister further outline what discussions have taken place with social media outlets, such as Facebook, Snapchat, Twitter and others, to strike the delicate balance between freedom of thought and opinion, and security and freedom from cyber-bullying?

[Kevin Foster]

The hon. Gentleman alludes to the fact that there is a delicate balance to strike between ensuring that people can freely express opinions and ensuring that the Government do not get involved in regulating opinions. It is about making sure that facts are accurate. That is why we are working with colleagues in the Department for Digital, Culture, Media and Sport on the online harms White Paper to ensure that we can tackle those challenges and strike the right balance on freedom of speech.

Mental Capacity (Amendment) Bill [Lords]

Debate between Jim Shannon and Kevin Foster

Ping Pong: House of Commons
Tuesday 2nd April 2019 Commons Chamber

[Kevin Foster]

My hon. Friend makes a strong point. We should not just assume that once a DoLS is in place it will be there for life. For some people, it may apply during a particular period of treatment or time, and things will fluctuate for some people if they recover to a point at which a DoLS is no longer appropriate because they are able to make their own decisions. As he says, the appropriate records must be kept to ensure that that is properly reviewed and borne in mind, so that a decision cannot be made that someone should be subject to this forever. There should be a rolling review, to ensure that those in charge of caring for a person and those overseeing the care are satisfied that it is still the appropriate measure, given its impact on the person’s life.

I do not wish to prolong the debate, given that there is consensus across the House, which is welcome. The Bill will be better for having these substitute amendments, inspired by the Lords amendments, and on that basis, I hope the House will endorse them.

[Jim Shannon (Strangford) (DUP)]

It is always a pleasure to follow the hon. Member for Torbay (Kevin Foster), as I do on many occasions. I agree with what he said. First, I thank the Minister for her commitment, for our comprehensive discussions and for making herself available for each and every person who wished to have input into this process, and hopefully the changes that the Government want to see will be passed.

The Government have gone to some lengths to ensure that this Bill replaces and improves existing legislation surrounding the deprivation of liberty as a matter of pressing urgency. The current system is not fit for purpose—many people in this Chamber and outside it feel that—and this legislative change by the Government is what we want to see.

The Bill implements the Law Commission’s recommendations, introducing a new system for people who lack capacity and need to be confined for care and treatment, ensuring that the system protects vulnerable people, is person-centred and includes a strong role for carers and families. I have had a chat with the Minister about this, and the Bill will also ensure that supported people and their families are supported and included throughout the process. That is very positive.

The supported person will be afforded their rights throughout the process by an appropriate person. The appropriate person will normally be a family member. Carers and families will be given a stronger role, with an explicit duty to consult them and the supported person. As someone who cares, along with my mother and son and others, for my brother Keith, who was in a motorbike accident some 15 years ago, I know the importance of the carer’s role across the whole process.

Synthetic Cannabinoids: Reclassification

Debate between Jim Shannon and Kevin Foster

Tuesday 6th November 2018 Westminster Hall

[Jim Shannon (Strangford) (DUP)]

I congratulate the hon. Member for Mansfield (Ben Bradley) on securing this debate on a subject very close to our hearts. Many others who would love to be here also support the aims of the hon. Gentleman and other speakers. I will talk about a specific case that the Minister is aware of. It is a success story in that Government policy has helped very much.

Members will know that I am a most sincere advocate for my young constituent, Sophia Gibson, who was prescribed medicinal cannabis. I watched the struggle of my constituents as they fought with every breath to legally get the help that their child needed, and today young Sophia is a different child. I want to put on the record my thanks to the Minister for his endeavours to make sure that that happened. He had the opportunity to meet Sophia Gibson, my parliamentary aide and me to talk about this matter. I know that he industriously, personally and sincerely pushed the matter for Sophia and I thank him for that. I also thank the Government for their help to make that happen. Without that help and intervention, we would not have the Sophia we have today. Like me and everyone who helped, the Minister has a photograph of that young girl who has now come on greatly.

Sophia needed medicinal cannabis to have any semblance of a life. Her courageous mummy and daddy refused to stop pushing, and refused to give in and accept drugs that had horrific side effects and did not address the severe medical issues that their daughter had. I cannot speak highly enough of Danielle and Darren, the mum and dad who put it all out there to get their daughter the help that she so desperately needed. They did it in the right way. They followed the legal procedure and paved the way for others who need an opportunity to get that help. The path is still not smooth, and the Government are honing the procedure, but because of Alfie Dingley’s mother Hannah and because of the Gibsons, it is now a possibility.

I recently saw a picture of Sophia dressed as Princess Anna for her school Hallowe’en party. That might not be noteworthy for everyone, but it was noteworthy for Sophia’s family because it was the first party that she had been able to attend at school. That says it all about what medicinal cannabis has done for that young girl and for her mum and dad.

A post on the social media page Help for Sophia’s Seizures, which updates people on Sophia’s progress, encapsulates why I stood with Danielle and Darren in their battle for help for their child, as the Minister and many in the community did. It reads:

“Nearly 14 weeks on from when Sophia was prescribed medicinal cannabis with THC on the NHS and she has NOT been hospitalised from 10th July, seizure length and frequency are reducing and Sophia is so much brighter, has a lot more energy and her ‘wee rascal’ personality is shining through. Sophia recently had a cold that lasted 5 weeks and any other year day 2 of a cold and she was hospitalised with back to back seizures but this year it has been so much different and at last for the better. Our little princess is getting bigger, stronger and better each day and we hope this continues looking into the future. This was never to cure Sophia as her syndrome is genetic but about Sophia having a better quality of childhood and that is what she is doing.”

I am undoubtedly in the corner of those in the medical profession who know that nothing else is working, but I must say clearly that that is where I draw the line. I believe that honing the process means educating doctors to know the situations that call for the prescription of whole plant cannabis, which has no additional substances added to it. I am not a doctor—far from it—and I am not medically trained, but the fact that whole plant cannabis has been proven to make such a substantial difference to young Sophia’s quality of life tells me that more research is needed into whole plant medicine. That will enable medical professionals to have the information that they so need to prescribe whole plant cannabis to others in Sophia’s situation, in which the currently available drugs are not working and are even damaging her in the long term.

We must remember the impact that every seizure has, physically and mentally, on a child’s capacity. There are people whose lives would massively benefit from whole plant cannabis. Information must be available for medical professionals to understand the medication so that they can prescribe it.

[Kevin Foster]

I am listening to the hon. Gentleman’s speech with great interest. As always, he is a doughty advocate for his constituents. Does he agree that there is no contradiction in believing that Spice, as a synthetic cannabinoid for recreation use, should be made a class A drug, but that cannabis-based medicine should be allowed for specific purposes? The medicinal use of a drug is a different concept from its abuse for recreational purposes.

[Jim Shannon]

I wholeheartedly agree. I want to make sure that we understand the side effects, but the thrust of the hon. Gentleman’s intervention brings me back to a point that I have made clear throughout the debate: reclassifying cannabis to allow recreational use is something that I cannot support. Just as we use morphine under very select circumstances and in a controlled manner, but have rightly outlawed the use of heroin, it is right that we have classified cannabis products for medicinal use in select circumstances and in a controlled manner. That is the way I believe it must be.

I do not believe that we should allow recreational use of Spice or Mamba, or that we should advocate such use of any cannabis-derived product. Nor do I believe that legislating for medicinal cannabis means logically that we should legislate to allow recreational use, or to allow for those who believe that they can self-medicate.

We need to ensure that doctors understand the limitations of the change in legislation and can prescribe to someone whose case they know well and who is not responding to other conventional drugs. We need to ensure that people understand that the change in legislation does not give them carte blanche to grow their own plants. Finally, we need to ensure that children like Sophia Gibson who had no quality of life before medicinal cannabis was available can access medication that will enhance their life, as it has clearly done for Sophia, so that they can have a birthday party without ending up in hospital, attend school without having to drop out because they are not well, and have a semblance of normality. That is what I support and will continue to support, and there is a very clear difference between the two.