I have facial disfigurement and I have encountered discrimination and hate crime throughout my life. Society judge by my disfigurement. I encounter staring, negative comments, and sniggering. I have failed employment interviews. I have encountered bullying. I have been stopped from driving due to new ruling with DVLA after 30 years of safe driving with a congenital defect.

When you're at a time where you're mentally distressed, to the point you need to be in hospital, knowing where you are plays a bigger role than you'd think. If you know you're up the road from your house, or a short bus ride away, it gives you peace of mind. You know you're family and friends will be able to visit you, and bring you things you might need. It also means you can have effective home leave before being discharged. Now imagine, you're being sent 100miles away from your home, to a place where you probably don't know anyone. What if no one in your family drives? You become alone and isolated, at a time where being around people who love you matters more than anything; but you're all alone instead. There are kids being sent far away! Some as young as 12. If you're far away, and you are in a unit where you can't use your mobile, how are you meant to stay in contact with friends? What if you're in that hospital for months? Having no familiarity makes you sink even lower. It is essential that more is done to improve the current bed crisis.

The anxiety caused by worrying that benefits will be cut can make a range of conditions worse by increasing stress and anxiety. making work related activities voluntary for people in the support may help them feel more comfortable and encouraged and give them better success in getting off benefits. the added anxiety will prevent people accessing the support the green paper aims to offer. those with mental illnesses will be affected very badly as the additional stress and anxiety could exasperate the problem however encouragement to voluntarily get involved in work related activities could help some people to gain the confidence to get back into work and come off benefits.

This is an issue which needs to be addressed in order to help the development of children with disabilities. Having recently visited a store with my 7 year old nephew, who has down syndrome, we were shocked to discover that there was not a single section designated to children whose needs differ from normal children. They require sensory toys, often with lights and sounds to aid their development but all that is available in store is similar toys designed for babies and small children not for older children who despite having a disability still need to work on skills such as counting, just through different means.

Disabled people like myself are being left to try and tidy up there property without any help from the authorities, which is causing a lot of Stress and needless suffering for all Disabled People in similar positions to myself, with Disabilities that affect how a person functions, like walking, preparation of food and Mental Health Problems which can cause communication breakdowns quickly without the appropriate help.

These checks are important to anyone who has a job working with the sick, disabled, or children. All care/support workers, nurses, and teachers cannot legally work in the uk without a current DBS check. However the government currently has a back log of over 150.000.00 people (and rising) who cannot start work in much needed services such as the NHS and community support as they are still waiting for their DBS.

Holders of NHS Tax Credit Exemption Certificates are disadvantaged by low incomes and sometimes by medical conditions. This might make keeping track of the certificates expiry date difficult and treatment may be unknowingly accessed when the certificate has recently expired. The current system enforced by the NHS Business Services Authority targets vulnerable people in various ways. Firstly they do not send any reminders when the certificate is due to expire - can you imagine if insurers took the same approach! Secondly if your card has expired and you receive medical treatment, even though you might still meet the criteria to be eligible for free treatment you will still be fined. I found this out first hand. Thirdly this fine is approximately 200% of the cost of the medical treatment. I offered to pay the cost of treatment but that wasn't enough, the NHS are demanding a 200% fine - how is this fair? Lastly when you are told of the fine the letter tells you that if you still met the exemption criteria to call them. I tried this and when you call they reprimand you for the certificate expiring and are not interested that you were still exempt. If the financial industry worked in this way the ombudsman and or government would take action to resolve this. The NHS is actively discriminating against vulnerable people and making their situation worse. How can this be legal? It certainly isn't ethical and I want to start this campaign to protect others who find themselves in this situation. Please sign and demand a fair and just situation for vulnerable people.

At the moment there is no set national legislation for rights and responsibilities for taxi companies towards guide dogs and their owners. This is currently dealt with on a regional level and not a national one. Nationally, there are no penalties in place to deter these companies, or their drivers from refusing guide dogs with their owners. Our aim is to impose penalties on drivers and the companies that they work for if they refuse anybody with a guide dog. Refusing guide dogs and their owners by taxi companies leaves individuals in a precarious and vulnerable position, especially if they are out at night. This needs to be stopped.

There are charities that are doing amazing jobs getting into schools to run mental health awareness sessions but it is not regular enough or even existent in some schools. I struggled hugely growing up in school and struggled with mental health but did not know what was wrong with me until I experienced a mental breakdown at around 15 years old. I have trained with 'Mind' as a youth wellbeing trainer and delivered mental wellbeing sessions in schools and it really is needed permanently.

Since the introduction of the Care Act, many local authorities are reassessing people's ability to pay for their own care and/or support. My daughter relies on her support worker to help her to live independently. For the last 6 years she has received funding from the Local Authority to pay a support worker to help her cook meals, shop, keep her flat clean, deal with correspondence, go to medical appointments and get out and about. Without any warning or discussion, it stopped on the same day she was visited to 'check' she was receiving the right amount of benefits. A subsequent letter informed her that after the general living allowance was deducted from her benefits, there was enough income left to pay for her own care. The Government 'say' that she needs £x amount to live on then our Local Authority say she can live on less than half the benefit amount. It is very wrong and very soon you will be talking to someone who is affected by these assessments (parents of disabled adults, people with aging parents and/or people who need care). Please support this campaign to force Local Authorities to ignore disability benefits when assessing people's ability to pay for their own care so they can exercise choice and control over their lives.

The forums are made up from elected representatives from the 9 regions in England. These representatives talk to government and other Organisations such as the NHS & CQC to give the opinions and voice of people with a learning disability. Without the forums, the voice of people with a learning disability will be lost. We are worried that when the government stop supporting and listening to people with learning disabilities others may stop too. More people with a learning disability could end up isolated and alone with nowhere to turn. Please sign this petition and show our local MPs how important the voice of people with a learning disability is. We would really like them to speak up for the people in their communities that have #NoVoice. We want MPs to tell government that their local community think people with a learning disability should be included at a local, regional and national level. We think the Department of Health should reconsider funding the vital work of the forums. http://nationalforums.co.uk/

This very important because we need to help our children cope in society, prepare our children for a happy and meaningful life. My daughter is 12 years old, though out her primary school days struggled with going to school, crying a lot, her anxiety levels were through the roof. Only when my daughter was in year 4 the school had noticed my daughter had communication problems I was never told about until year 5. When my daughter was 3 years old I had taken to the GP, she was very violent so our GP referred my daughter over to the community paediatric services I got my local MP involved. After all those years of stress, anxiety, we finally received a outcome, on the 6th Dec 2016 my daughter was finally diagnosed with Autism Spectrum Disorder.