Jean is 68 years old and lives in Edinburgh. She was born with arthrogryposis, a condition which affects the joints and muscles and prevents development/growth in the legs. Jean is 4 foot 5 inches and wears heavy callipers and surgical boots weighing 3kgs. Each step is a challenge and for the past 20 years Jean has relied exclusively on her specially adapted Motability car to lead an independent life. Recently due to new guidelines for Personal Independence Payments, she has been told that she is no longer entitled to a car. This is unacceptable. Everything Jean undertakes is adapted, adjusted and limited by her physical handicap. Her balance is poor due to no ankle or knee flexion, she struggles with cobbles, uneven ground, steps, kerbs and slopes. If one of her callipers breaks, she is 100% immobile. Public transport is not an option. Boarding a bus requires the use of both arms, leaving no option for carrying any shopping. The height of the seats leaves her legs dangling unsupported, causing swelling and pain. It is of the utmost importance that Jean is permitted to maintain her independence through the provision of a specially adapted car. Her condition will never improve. Taking her car away will leave Jean housebound and reliant on the help of others. To deprive Jean of her car after 20 years, at the time of her life that she needs it most, is cruel and unnecessary. Under the new PIP guidelines Jean’s mobility was reassessed and she was deemed to walk with a “good gait”. The assessment was conducted by target-driven private contractors employed by the DWP. Given her medical condition and profound disability this assessment is evidently deeply flawed. Edinburgh West MP Christine Jardine said that assessments were often “box ticking exercises with no understanding of peoples’ situations”. This certainly rings true for Jean. There is no doubt that Jean should qualify for the enhanced rate of the mobility component of PIP. Please help us persuade Sarah Newton to support Jean’s case by signing and sharing this petition.

Because currently I have a 4 year old daughter with Down syndrome that now exceeds the limit on a baby changing table, therefore leaving me to either put her in danger by using the changing table, changing her on the floor which is a huge infection control risk and undignified OR change her in a pram (which she will soon outgrow) or my car?! I can’t be the only parent in this predicament.

I’m a mother, but no one has ever called me mummy. I’ve resuscitated my child, but I’ve never put a plaster on his knee. I’ve not been fined for taking my child out of school for a holiday, but I’ve been fighting to get him into school for almost four years. I’ve gone for months at a time with little sleep - but not with a baby, with a child who stops breathing. There are no family days out, because there’s nowhere to change my immobile and incontinent teenager. For four years, I have to sedate my child to travel because his wheelchair doesn’t fit and causes him pain. I’ve said goodbye more times than I can count - not for a school trip, but because I was told he would die. Our first community nurse told me to visit a morgue so I could get used to the idea of seeing my son in a freezer. I was told by a care company manager that if I complained about her staff, she’d ensure my son was put in a home. They were asleep when he wasn’t breathing, they overdosed his medications and they forcibly strapped him down to his own bed to stop them needing to move him. I’ve had to plan and write down all of the details of my child’s funeral. We have lost our home, jobs and self esteem - sponging from society, because care and education has not been sufficiently funded to allow us to work - to support our own family. I was a teacher, I fought for the children of others, I loved my job. Now, I have to fight for my son and his rights, to be his ICU nurse, to try to find time to be his mum when I’m so tired and so sad. My husband cared for people with MND or dementia, supporting them and their families until the end of their lives. Now he can only support us. Our lives revolve around keeping our son alive, well and comfortable.

This RAF air station is part of our national heritage from the Dambusters right through to today and the Red Arrows. It should be turned into a visitor centre and kept for the nation.

In September Thetford Academy are cutting funding to Lewis Coaches so that they no longer run the bus service for our children to get to school. I have no other way of getting my 12 year old to and from school. And many other parents are in the same position. Please don't compromise the safety or education of our children.

Woman have the right to find out if anything is wrong with their bodies! 25 is much to high of an age to wait for a smear test, girls of 19 and younger have shown sgins and symptoms of cervical cancer. If the problem got caught in an earlier time frame rather than having to wait till the age of 25, the problem could be treated sooner.

Important for the local community to socialise

Be heard in the fight to kill drivers speeds before they kill one of us or one of our own!

At the moment traders south of the Border can refuse to take such notes causing much embarrassment and frustration for visitors. Even the Scottish Secretary Mr Mundell, MP for Dumfriesshire, Clydesdale and Tweeddale, in 2009!! said: “Many people, myself included, have tried to pay with Scottish banknotes in England, only to find them questioned. This is exasperating. And when a Scottish note is refused, that can even leave Scots in restaurants or petrol stations unable to pay for what they have bought.” Nearly ten years after Mr Mundell`s attempt at a private bill nothing has changed. I don`t know a single Scot who has not experienced this embarrassment or indeed a single English person who has been welcomed to Scotland by being told your sterling is not welcome here. The time has come to stop this antiquated discrimination and bring in new law to stop it.

Under the Equality Act 2010, a house cannot be refused to be let to someone because of disability, gender, race, sexual orientation or religion; these are known as protected characteristics. However - with suitable disabled accommodation being very sparse among social housing - downstairs toilet facilities, first floor apartments, bungalows, etc, are being refused to be let to potential tenants on the basis the potential tenant is in receipt of a government subsidy towards rent. These subsidies are awarded because individuals are unable to work due to disability, yet disabilities are a “protected characteristic” under the Equality Act. No matter whether you are willing to provide references, admin fees, bonds, or consent to a credit search. Due to lack of social housing, disabled people are being pushed into the private rental market yet being discriminated against and refused housing there too. No person should be discriminated against for something that is beyond their control; where else are disabled people supposed to live? It’s a daily struggle to live in a house that’s not suitable, I think it’s abhorrent that disabled people are being refused to rent in the private sector because they receive a government subsidy towards rent. Take a look at properties for rent near you and see how many say "no DSS"! Imagine how difficult it would be for someone disabled looking for somewhere to live. It is discriminatory. Please take a moment to sign this petition!

Vulnerable children with complex needs are being placed in small and restrictive isolation booths for long periods of time - sometimes the whole day and even full school weeks. This is often for trivial offences such as uniform issues. Parents are sometimes not told or informed euphemistically that their children are in the ‘ inclusion unit’ This is damaging the mental health of young people and the potential long term effects need to be properly researched. We need to have a debate in parliament about this dubious practice.

There are currently only two outdoor basketball courts accessible to the public in the whole of Wakefield which has more than 300,000 residents.It is important to support children/young people to achieve their potential and to build stronger communities. Culture and sports play an increasingly important role in transforming Wakefield, building more Basketball courts will bring about positive change and can help tackle (ASB) Anti-social behaviour while improving the health and wellbeing of the district. 70.5% of residents in Wakefield are considered overweight/obese compared to 64.8% being the national average. Health benefits of playing basketball 15 minutes a day can reduce risk of heart disease, asthma, strokes, chronic illness and also keeping your weight under control. Anti-social behaviour (ASB) has increased by 11%  and racial hate crimes have risen in light of the brexit. Basketball can help brigde the gap between communities and ambitions for young people, as well as giving the opportunity to improve health & fitness. 'It is the mind which creates the world around us' George gissing