Many of my clients have suffered at the hands of the Department of Worry and Persecution. Let's make them pay for their cruel treatment of those with both physical and mental health difficulties. People have commited suicide when their benfits have been stopped or cut and have to go through a long process to get redress. It is not fair and is not part of a society and government who should be looking after those in need, not harrasing them.

Because Universal Credit is driving up demand for foodbanks ---- This petition is being run by a Member of Parliament - 38 Degrees is independent of all political parties.

"Over 30,000 people are locked up in prison-like conditions every year, with no time limit on how long they can be held. This is not for having committed a crime. It is purely because they do not (yet) have the correct immigration papers. The majority of people detained are eventually released, but many never really recover from the trauma. It’s a terrible waste of money (£125 million a year), and a waste of lives. Immigration detention is a wholly unnecessary, unjustifiable practice, one of the most harmful aspects of the UK’s “hostile environment” for migrants and a shameful civil rights abuse that cannot be ignored." Quoted from the 'These Walls Must Fall' Campaign Website (http://detention.org.uk/)

Tony has Downs syndrome and is partially sighted with no sense of direction. Our mother Margaret passed away recently. He has lived in the house all his life, and he has the support of the local community to keep him safe. Our Mother was his carer; I am now going to fill the large hole left by her passing and take care of him. I have offered to give up my tenancy in the same borough to move in and provide care for my brother. Due to the house having three bedrooms (Not large) one of which is used as his dependency room. We are being told that we can not stay at the property as it would be under-occupied by one room. The upheaval and loss would be detrimental to his health and well being.

Cole Thomson is only 6 years old and has uncontrolled focal epilepsy of which he has now become drug resistant. He has tried 16 different types of medication and had his first brain surgery when he was only 2 years old. To date nothing has been able to stop his seizures. Unfortunately there has been a steady decline in his health since May this year. Coles speech, vision, movement and memory are all continuing to deplete and he has also developed Todd Paralysis, which is extremely distressing for his 9 year old brother Dylan when he takes an attack as well as his parents, grandparents, other family members and especially 6 year old Cole himself. Currently the next step in Scotland is invasive testing, which for Cole would potentially be in the first quarter of 2019. He has a 1 in 100 chance of not surviving the operation, to see if he is a suitable candidate for further exploratory brain surgery. We are looking for your help to enable a step in between which could negate the need for surgery by allowing him legal access to cannabis based medicine. After speaking to Coles mum we became increasingly concerned at the amount of unlicensed, untested products being offered to her on the black market to apparently “help Cole”. Coles parents are unwilling to take the risk with any of these products. This does not take away from the fact that they’ve been offered unlicensed products by numerous different sellers and shows that currently there is a market feeding off of the fears of vulnerable families, who are desperately looking for answers to improve their children’s quality of life or indeed save it. We are looking to support the family by putting a campaign forward to you The Scottish Government to enable Cole to gain legal access to prescription cannabis based medicine. This would be the step before invasive surgery which would give him the opportunity to try a more natural drug which has a very high success rate for children like Cole all over the world. Please support our campaign to Save Cole Thomson by allowing him to get prescription cannabis based medicine.

The lack of provision of social care in the UK is leading to immense distress for all people affected by dementia. According to the Office of National Statistics, people with dementia are dying prematurely as a result of austerity. Carers are not supported and are overwhelmed by the burden of unpaid care. 'Local authorities... which perform vital roles in providing a real social safety net have been gutted by a series of government policies... The Government has remained determinedly in a state of denial' (From the report by the United Nations Special Rapporteur on extreme poverty and human rights in the UK)

It's important because people are being forced into universal credit disabled made fit to work and cant work people looseing their homes under universal credit people are committing suicide under universal credit children are going to school with empty stomachs under universal credit people are suffering please I am asking and the people are asking the European court to take action on the un profesor philip Alstons damming report against the conservatives our human rights are being breached and abused please we beg you to scrap universal credit now

The building will make a big advance towards ending rough sleeping in Brighton & Hove by 2020 and be self-financing with housing benefits and volunteers. The building at 1-2 Morley Street, known as 'PsychoSocial', is currently unoccupied, meaning it would be easy for the council to purchase. It is also in a great location, as it is close to an excellent health centre, thereby lightening the load on A&E at the hospital. We've had two major successes so far in improving and increasing the amount of night shelters for Brighton's homeless. First of all in 2017, we won a campaign for Brighton and Hove Council to commit to opening night shelters for rough sleepers. Then we won a campaign for Brighton and Hove Council to have shelters open 365 days a year. These achievements only cam after thousands of us signed a petition. Brighton Centre should be open this November (2018) but by the middle of winter users will have to relocate to other venues. Now, we need a permanent shelter for Brighton's homeless, and Morley Street is the perfect location.

I want to highlight the sparsity of resources in the NHS for treating patients with eating disorders. This is a national issue but it has to begin somewhere. I mention anorexia in particular because it came into our family, but the same points apply to all eating disorders. The eating disorder charity BEAT states: "Anorexia has the highest mortality rate of any psychiatric disorder, from medical complications associated with the illness as well as suicide." So where is the funding? Where are the specialists? The Royal College of Psychiatrists report: “We are seeing waits of up to 16 months for non-urgent referrals. It is really worrying, because we know that the more quickly people start receiving treatment the quicker they are to respond to it.” Anorexia is an illness. Despite what some people might think, no-one chooses to be anorexic in the same way that no-one chooses cancer. It is a physical illness and it is a mental illness but it is also a neglected illness as far as the NHS is concerned. In the East Riding of Yorkshire, until recently, there was no provision for eating disorders. This year, CAMHS has established an Eating Disorder Service. What about those patients who are not children? Those patients like my own loved one. Four years ago, a beautiful, talented, artistic young lady whom I love with all my heart fell prey to anorexia and I watched in impotence as she shrank before my eyes. She was 16 and resisted medical treatment for the best part of a year. Once she accepted help, her GP was wonderful at keeping an eye on her and referring her to a general mental health therapist but there were no specialists in eating disorders or any specialist treatment. Early in 2017, when my loved one became so ill that she weighed 5 stone and had a BMI of 12, she was admitted to a gastroenterology ward at the general hospital. The doctors and nurses were marvellous but they were not experts in the treatment of eating disorders. However, they found her a place at a residential ED Clinic in Grimsby, 54 miles and a drive of an hour and a half away. Grimsby is not in East Yorkshire; it’s in Lincolnshire. Still, we were lucky. Did you see the programme, ‘Wasting Away: The Truth about Anorexia’, which told the story of news reader Mark Austin’s daughter? I watched in tears as their story unfolded in an almost carbon copy of our own. Now if someone in the public eye, with a doctor for a wife, had no clue what to do, and if help wasn’t readily available to them, then what chance did we have? Mark Austin's research taught him that there are only 200 beds for ED patients in Britain and his programme revealed a young woman from Nottingham who was sent to Edinburgh for treatment. Her mum had to make a 600 mile round trip to visit her. UK eating disorder statistics • 1.6 million people in the UK are affected by an eating disorder • 11% of the 1.6 million people struggling with an eating disorder are male • Eating disorders are more common in individuals between the ages of 14 and 25 years old • There are up to 18 new diagnoses of bulimia nervosa, per 100,000 people, per year • 1 in 100 women aged between 15 and 30, are affected by anorexia nervosa • 10% of people affected by an eating disorder suffer from anorexia nervosa • 40% of people affected by an eating disorder suffer from bulimia nervosa • The rest of sufferers fall into the BED (binge eating disorder) or OSFED (other specified feeding or eating disorder) categories of eating disorders • Research suggests that the earlier that eating disorder treatment is sought, the better the sufferer’s chance of recovery These UK eating disorder statistics are derived from data published by Beat and Mind. For the sake of the futures of our young people, we need to hold the government to account, locally and nationally, to keep their promises and to ensure that there is money in every local authority for ED Services.

Having seen my beautiful Bernese mountain dog collapse and shake with a heart beat pounding out his chest . No matter how much money I spend or what I do , i can not console my boy. It breaks my heart to see this, it’s for days on end because people can set them off whenever they want and what time they want , stress is not good for any human or animal, this affects us all.. Animals die from shock and fear . We are supposed to love and respect nature and our domestic pets not destroy them with fireworks . All I’m asking for is that we respect one another and come to a compromise to save our animals from the torture they go through around November . Please help !

The proposed road will force over 400 village school children and residents in the valley to breathe polluting, health harming, diesel freight traffic fumes. It would bring deadly traffic pollution and noise from freight vehicles into an environmentally sensitive valley that houses two primary schools. The list of long term effects of air pollution on children and the elderly is growing almost daily. Wales has a Future Generations Act designed to ensure we consider the needs of future generations, but this road, aimed at servicing the loss making Cardiff Airport which is actually owned by the Welsh Assembly Government, means the future health of Ely Valley school children and residents appears to have been abandoned. The Welsh Assembly Government is planning on spending £100+ million of taxpayers money on this road that will service their own business. The children affected by these plans have no voice. We must speak for them.

British tax payers are being required to work longer and pay NI & tax but state pension not increased, over 60’s who have worked all their lives have paid their tax dues to the country, majority never claimed a penny in benefits but are punished with state pension age being changed and likely will change again to pre war 70 years of age. It is not feasible for the majority of over 60s to stay in their current jobs I.e emergency and armed services, manual workers etc. When we do receive state pension it is another slap in the face that it is taxed, disgraceful country.