Because Alistair has profound learning disabilities, epilepsy, schizophrenia and severe autism. He has no awareness of danger and an unstable gait, meaning he is very likely to fall and cause serious injury when not supported. Alistair will also self harm and become aggressive when he feels nervous and doesn’t have someone there to help him and make him feel safe.

By providing trolley’s in such disrepair it demonstrates a lack of respect for SEND families. They are a health and safety hazzard and they represent a total disrespect and lack of provision which reflects badly on the businesses that operate there. They ignore the rights of disabled children to be able to sit safely and comfortably, access the facilities there and be treated equally. The facilities for disabled adults are adequate so why not show the same respect for our disabled children. I have asked for 3yrs for these trollies to be replaced or repaired but have been ignored or excuses have been made. Enough is enough now and parents of disabled children what to be listened to and our children treated with respect they deserve.

The Derbyshire Unemployed Workers’ Centre (DUWC) received a grant of more than £41,000 annually and a further £50,000 from Public Health to carry out tribunal representation work for people challenging decisions by the Department for Work and Pensions regarding benefit reductions and withdrawals. But the funding from the County Council will come to an end on March 31. Colin Hampton, co-ordinator of the centres for the past 33 years, said: “DUWC, irrespective of who is in government, gives a voice to those who come to seek our help." “You would think those in power would welcome this feedback but it appears that this authority would rather not hear what they have to say." “The centres have many funding streams and even more supporters. We will be embarking on a massive fundraising campaign to bridge the gap left by the Council’s cynical move.” Thousands of Derbyshire residents use the service, which has offices throughout the county. It also comes at a time when the centres are dealing with the full digital roll out of universal credit. Please visit our website for more information about the service: http://www.duwc.org.uk/

If this erroneous decision is not rescinded then it would create a two tier urgent care system that would exclude, workers, visitors and those that participate in the full range of sporting fixtures that happen in the area from accessing and using the urgent care centre: putting untold pressure on KGH A&E and the East Midlands Ambulance Service.

Over the year 2016-2017 nearly 174,000 allegations were closed and 149,450 (86%) of tip offs were incorrect allegations. Over the financial years 2015-2016 and 2016-2017 332,850 cases were closed following reports by members of the public (of benefit fraud). Of these 287,950 were found to have no or little evidence to substantiate the claim (87%) We need to stop the culture of hunting out benefit fraud, as most of the time the allegations are incorrect. Going through this process has a detrimental effect on disabled and chronically ill people’s mental and physical health. We believe that if the public are to remain involved in reporting on alleged benefit fraud then they should not be allowed to do this anonymously and should have to give at least their name and national insurance number. This will help to make people think about their actions before picking up the phone, will help to reduce bogus allegations, and will make improvements to this culture of thinking people on benefits are scrounges and that disabled/chronically ill people are faking (when in fact they are probably faking being well most of the time). If someone is found to be a serial malicious reporter then they should be fined and banned from giving tip offs again. The general public have a slim view and understanding of what disability/chronic illness ‘looks like’ resulting in more reports of benefit fraud and disabled/chronically ill people being scared to leave the house for fear they’ll be reported increasing isolation in communities and fears that your neighbour is spying on your every move. Let’s stop feeding this narrative. Please help us make some positive changes to the benefits system. Together we rise! Faye Dempsey, Ellie Hicks, Alison Morton Articles of interest: www.theguardian.com/commentisfree/2018/feb/01/spy-on-your-neighbour-britain-demonisation-benefit-claimants-disabled-people www.independent.co.uk/news/uk/politics/benefit-fraud-public-tip-offs-legal-action-police-no-evidence-dwp-work-pensions-department-a8144096.html

In King's Lynn, one of only two local residential respite units which supports many children with disabilities and Complex Needs has been earmarked for other usage. The remaining unit has only four beds and cannot accommodate all the children affected by this decision. Although Norfolk have a legal obligation to provide short breaks for disabled children, the council has still decided to shut it down. Residential Respite such as Morley House is essential to the well-being of these disabled children (who have already been assessed as needing the highest level of support) and their families who depend on the time to give other siblings or family members support, and access parts of everyday life (such as shopping, medical appointments and household maintenance it is difficult or impossible to do safely while caring for their disabled child). They allow children to make friends and try activities and days out which other children take for granted. Without access to Morley House, many of these children will be denied what every child should have, a life with friends where they can enjoy experiences in a safe environment with people who can understand and support them. In addition to the use as a residential respite unit, Morley House is also used to house educational boarders from the local Complex Needs School. This provision is part of their education. For my family and many others Morley House is a lifeline, the only place we know our child is safe and well looked after which enables us to relax and meet the needs of our younger child and give her the everyday experiences we cannot safely provide while caring for our older daughter, daytrips to the beach or even visits to the homes of family and friends are impossible apart from the times our older daughter is in respite. We need your support to reverse this decision and ensure our children and the many children who will come after ours still have access to this essential service.

Dr Glen has renewed her application to add Plains, Caldercruix and Hillend to her practice area and is hoping to achieve this by August 2018 with agreement from Lanarkshire NHS. The Primary Care Department of NHS Lanarkshire gave assurances in Caldercruix in January 2014 at a public meeting that there would continue to be GP services in Caldercruix at dedicated premises.The present service is well short of the assurances given to Alex Neil MSP in 2014 about a commitment to having a GP in the village. Assurances were also given to the Scottish Government that a GP would be in place in the village. The NHS is under pressure and Dr Glen is able to offer appointments in a permanent building with nursing and administrative support all ready to run for the benefit of local villages.

There is a young 8 year old boy called Jack who was admitted to Alder Hey Children's Hospital on the 25th October 2017, SEVEN WEEKS AGO. Jack lives with autism and has mental health issues; extreme low self-esteem, suicidal. Jack has recently had a severe mental breakdown - hence the stay at Alder Hey Hospital. Jack was assessed as a tier 4 and has been waiting in hospital for a bed to come available in a children’s unit, for SEVEN WEEKS. Jack or his family have been offered no support from CAMHS in the past seven weeks. This is the reason why; Jack has been assessed by the Tier 4 team(in-patient CAMHS unit) and is waiting on an inpatient bed becoming available. This means they cannot work with Jack in his current environment (Alder hey hospital) only once allocated a bed within a unit, So, Jack does not fit the CRITERIA for tier 3 support (community), and can not access the tier 4 support until he is an inpatient in their unit. It is imperative that the government increase funding for children's mental health to prevent this level of waiting time and the dangerous gap that exists between accessible support in a crisis.

There is a young 8 year old boy called Jack who was admitted to Alder Hey Children's Hospital on the 25th October 2017, SEVEN WEEKS AGO. Jack lives with autism and has mental health issues; extreme low self-esteem, suicidal. Jack has recently had a severe mental breakdown - hence the stay at Alder Hey Hospital. Jack was assessed as a tier 4 and has been waiting in hospital for a bed to come available in a children’s unit, for SEVEN WEEKS. Jack or his family have been offered no support from CAMHS in the past seven weeks. This is the reason why; Jack has been assessed by the Tier 4 team(in-patient CAMHS unit) and is waiting on an inpatient bed becoming available. This means they cannot work with Jack in his current environment (Alder hey hospital) only once allocated a bed within a unit, So, Jack does not fit the CRITERIA for tier 3 support (community), and can not access the tier 4 support until he is an inpatient in their unit. It is imperative that NHS England fund more beds in children's mental health units to prevent this level of waiting time and the dangerous gap that exists between accessible support in a crisis.

Hallglen Sports Centre is the hub and heart of Hallglen Community but also caters for other areas in Falkirk. I have been involved with Hallglen Sports Centre for over 20 years now. The last 18 as the Chairman and the Lead Coach of Azami Falkirk Judo Club and have members of our club represent Scotland numerous times at home and in Europe. The club caters for a wide range of disabled people who have competed at a high level in disability competitions which has improved their lifestyle and confidence generally, but it is not just our Club who use the centre, there are numerous other groups and organisations that use the Centre on a weekly basis (Forth Valley Gymnastics, three different Cheer Leader and Dance Groups, weekly Yoga Sessions, two different Ju-Jitsu Clubs, two different Taekwondo Clubs, Karate Club, Balintawak and the main hall is booked most weekends for birthday parties and various other events. This is a busy centre with some weeks up to 1,000 people entering the centre. Could everyone please get behind this petition. There is nothing else in Hallglen or the surrounding area for community events and some place for children and young adults to go. Please support this petition. Gregor Gardner.

Not only will this have a devastating impact on the bank workers who are set to lose their jobs, these closures will also have a negative effect on the local communities of Biggar, Carnwath, Douglas, Dunns, Eyemouth, Hawick, Jedburgh, Lesmahagow, Melrose, North Berwick, Penicuik, Selkirk and Strathaven. Those who are older, in poor health, who cannot afford to travel further afield to do their banking, or who run small businesses will be hit hardest by these branch closures.

These disabled people cannot speak for themselves . The parents need these places because it is not only a stimulus for the person with the disability but also gives them some time for normality The council / SWYPT should clearly explain why these persons the most vulnerable in society are being targetted and what benefits this gives these persons by doing this. It cannot be at the detriment of their welfare which if it goes ahead as planned quite clearly will be. The MP’s should be in touch with local change and therefore should be championing these vulnerable persons to ensure they receive the best care The Tory government’s lack of funding for social care especially to those who do not and therefore cannot speak for themselves are an easy target .This is both callous and thoughtless from start to finish . It is paramount these persons get the best that society can give them . The young lady I know may not be able to speak nor can she walk , feed herself ,dress herself or look after her personal hygiene . But one thing she can do is light up a room with her infectious smile because she is such a beautiful young lady who is so loved and cared for. To think that by making these changes she may be affected and lose this wonderful trait is beyond comprehension. If only she could express her feelings and let everyone know how this will affect her wellbeing As for her parents they are both retired and have health issues. Do they really need the added stress of not knowing what will happen to their child and the worry associated with what is being planned This is becoming the norm all over the UK why do we not stand up to these contemptible people and say NO MORE . The vulnerable need our voice so let’s shout it out loud and clear . Stop these insane cuts on the severely disabled and start and make them feel loved and wanted and have the best life they can have . Not forgetting the parents and families who suffer when they feel their child is being neglected and that they have no voice and are invisible to the powers that be . I have shown this as a local issue as this is occurring in my local constituency but I firmly believe it is happening right now in numerous places across the UK and will continue unless we do whatever we can to stop it. Please can you give your support to the plight of these vulnerable persons