Oral Answers to Questions

Debate between Mary Glindon and Lord Cameron of Chipping Norton

Wednesday 10th June 2015 Commons Chamber

[The Prime Minister]

I welcome my hon. Friend to her place. I have to say that her election result was one I was dreaming of, and am very grateful for. She is absolutely right to raise this issue. In the past it has been too easy for some businesses to bring in workers from overseas rather than to take the long-term decision to train our workforce here at home. We need to do more to change that, which means reducing the demand for migrant labour, and that is part of our plan. So I can tell the House today that the Home Secretary has written to the Migration Advisory Committee asking it to report back on how to significantly reduce work-related migration from outside Europe. It is going to advise on restricting our work visas to genuine skills shortages and specialists. It is going to look at putting a time limit on how long sectors can claim to have a skills shortage, because frankly they should be dealing with that. We are going to look at a new skills levy on businesses who recruit foreign workers so that we can boost the funding to UK apprenticeships, and we are also going to look at raising salary thresholds to stop businesses using foreign workers to undercut wages. All these steps, combined with the measures we are taking within the European Union, can help bring migration under control, but also, more to the point, make sure that hard-working British people who get the skills and training can find the jobs that will help them build a better life.

[Mary Glindon (North Tyneside) (Lab)]

Q8. Six young boys with the devastating disease of muscular dystrophy will be in Downing Street this afternoon, supported by Muscular Dystrophy UK, to make a plea to the Prime Minister to help them access the Duchenne drug Translarna that they need now to stop them losing their mobility. Will the Prime Minister make time to see them and will he tell the House that these children can expect the positive answer they so desperately need now?

[The Prime Minister]

I thank the hon. Lady for raising this issue. Muscular dystrophy is a terrible disease and I hugely admire the courage shown by the sufferers and their families. Unfortunately, I will not be able to hold that meeting this afternoon because I have to go from the statement after Prime Minister’s questions straight to an EU summit in Brussels. I do remember meeting Archie Hill, who is one of the group, back in January. He is an amazing young boy—incredibly brave. The situation is that NHS England has now completed a consultation on how it prioritises investment in these specialised services, including drugs for rare conditions. It closed at the end of April and a decision can be expected in the near future. I recognise how vital it is to give those affected and their families a decision as soon as possible.