A desperate mum claims she has to put her mentally ill son in handcuffs at home because of a lack of support from mental health services.
Joely Hignett says she has to physically restrain 24-year-old son Kyle Hignett, who has a borderline personality disorder and suffers from psychosis, to stop him from harming himself or others.
Joely who's from Warrington has released the video of Kyle sobbing and screaming to raise awareness of his condition - but said she feels 'let down' by the mental health system.
And a warning you may find this report by correspondent Amy Welch distressing.
TV medical dramas always portray the rush to help transplant patients by showing medics, racing against the clock, carrying donor organs packed in ice. While that's often the reality, new technology has done away with the special cooler pack in some cases.
Surgeons in Manchester are now using a machine that can keep the heart alive, and pumping, without ice. It means organs can be healthier when they reach the operating theatre, allowing more transplants to go ahead.
This report from our correspondent Rob Smith contains graphic close up images from the start.
A new drug treatment to help Duchenne muscular dystrophy sufferers walk for longer will not be funded on the Isle of Man.
The decision was made by the Department of Health and Social Care, who said this is based on advice from the IoM Clinical Recommendations Committee - because of the limited licence which the treatment has, more evidence to show that the drug is effective in slowing down the loss of walking ability would need to be submitted by the manufacturer.
Funding Translarna would cost the IoM Government an estimated £200,000 - £250,000 per year, which the DHSC said could not be justified.
When questioned by a local MHK, Kate Beecroft, regarding 7-year-old Finley Hesketh 's case, the Department's minister, Howard Quayle, replied that the drug will not be locally funded due to no evidence of effectiveness.
The National Institute of Health and Care Excellence (NICE) publishes guidance for the NHS in England and Wales. NICE has issued a draft recommendation that Translarna should be available on the NHS in England and Wales for patients with nonsense mutation Duchenne as part of what is, in effect, an extended study designed to provide data on clinical outcomes.
NICE is proposing that this NHS funded study (which they call a managed access scheme) should run for five years, after which the outcomes and funding will be reviewed.
The island's Committee concluded funding for a clinical study could not be a priority over other calls for resources.
The Department has a limited budget with which to fund all health and social care for the people of the Isle of Man. It is not possible to fund everything that may be requested which means that difficult decisions on emotive issues have to be taken.
A consultation meeting is being held later to discuss the future of Liverpool Women's Hospital.
NHS bosses plan to move services to a new unit, possibly at the Royal Liverpool in the city centre. But campaigners want the Women's Hospital to remain at its current site in Toxteth.
Skin cancer is the most common form of cancer in the UK, and rates are rising - with at least 100,000 new cases diagnosed each year.Read the full story ›
Holidaymakers bask in the mini heatwave as forecasters predict temperatures will reach a peak of 35C.Read the full story ›
Rachel Dorney had surgery at Tameside Hospital, but discovered she was pregnant days later following a bout of morning sickness.Read the full story ›
People could be inadvertently helping to create giant two ft rats that are immune to pesticides, a politician has warned.Read the full story ›
You might remember that on Granada Reports we've been following a chap called the cycling scouser after he pedalled 10,000 miles across 17 countries from Shanghai to Liverpool.
Andrew Rogerson then ditched his bike for his running shoes becoming the running scouser and completing 5 marathons in 5 days.
He's been raising money for a blood cancer charity and one little boy in particular.
Charlie Fearns is just 10 years old - he has leukemia and needs specialist treatment in America.
Sarah Rogers went to meet him on a very special day.
To donate to Charlie's Chance visit: Charlie's Chance
Family and friends of a six-year-old boy battling cancer for the third time are appealing for help to plan him a party to remember.Read the full story ›