Ability Bow is the only place in inner London that provides long term rehabilitation to help people who have a disability, an injury or a long-term health condition. For many it is be a life-changing experience. There are thousands of people that Ability Bow has helped over the last 10 years. Margaret is a stroke survivor who regained near full use of her body after doctors wrote her off. Albert had a spine broken in two places and learned to walk again. There are hundreds of stories like these here. We are asking for the assistance of a government partner to safeguard the future of this vital service. I do not know where I would be without this place. I started this campaign to raise awareness and make sure that people get the help they need to improve their lives.

As a mother of two young children, I have found myself in the position of having to carry a pram and still hold onto the other child, leaving me and the kids exposed to trips and falls. During the day the station may be quiet and there will be no individuals there to help you. This is not ideal especially if a parent has had a c-section. I have also seen many other parents struggle to navigate the steep staircase located at the station.

Kent Support and Assistance as it was called (KSAS), a Government Scheme funded £2.8 million pound in its first year and millions since, has just recently had removal the information of its phone service with the web page edited slightly to remove the multi million scheme's name too. You can only find information on the scheme by typing 'help in a crisis' or something similar into the KCC search bar with it's new name 'Home essentials in a Crisis'. The page has its header name changed and their number removed but is other wise the same. This seems to also be the case with other essential council services whereby you have to report/claim for help online not taking into consideration the vulnerable and those without internet access or the know how to use this method, the only choice given. This is something us a non funded organisation fill the faps with as they refer clients to us when turning people down for help was not informed of, nor any other sign posting agency we lisise with. We are already seeing the rise in cases coming to us before this at our Thanet 7 day Food Bank, non funded and run by community, something we have had to take the demand for with errors to this KCC service since it began in Spring 2013 following the abolishment of the DWP's social fund's Crisis Loans and Community Care Grants. As an organisation, we have previously fought to get waiting times down in their first year which was proven to be productive after being asked to meet with the scheme's commissioner when we swapped figures on how many people Kent County Council were helping in Thanet compared to our non funded 7 day food bank. The figures were shocking Our concerns were acted on after myself and vice chairman Robin were asked to meet the commisioner of the scheme and his colleague who travelled to meet us from Maidstone after we voiced our growing concerns through several channels Waiting times were at least 14 days often longer for a decision on helping with emergency food, gas and electric, by which time their situations had largely started to sort themselves but claimants were still receiving food and fuel from KSAS after we had supported them through their hardships within 24 hours which even the clients acknowledged to be a waste of the council money. The commissioner, Hugh Martyn listened to what we provide non funded and he called me the 'Gap Filler', he asked what we see as the need here in Thanet and was quick to act with waiting time reduced to a matter of days rather than weeks within weeks. This was funded £2.8 million pound in the spring of 2013 with further millions in funding year on year following from Central Government to provide a service to the people in need from Maidstone to the whole of Kent. Right now, the people of Kent are being let down hugely yet again. We will be gathering more figures and FOI's into exactly how many services have had their phone contact service removed. **If you would like to get involved or would like to share your story, please send us an email to [email protected] or [email protected] Kerry Keating and Robin Vaughan Lyons

Families where the spouse of a disabled adult are already on an extremely low income so having to pay the bedroom tax, which carers for children where for example one parent may be earning an adequate wage are already exempted from, is not only discriminatory, it leads to further financial pressure on top of the stress of being a carer.

Because genuine disabled people are often deprived of this service when they desperately need it.

It is continually used by the blind and partially sighted not only in Weston but from guest over the world with their blind dogs. It is used by local groups and the talking newspaper headquarters, as well as the public in the community. The staff are excellent the food is lovely. It is the only hotel in this are for the blind and partially sighted.

Whilst we welcome the move to schedule CBD as a medicine following clinical trials, it must be understood that completely removing it from the market with only 28 days notice is not sufficient time for patients to find alternative ways of maintaining their health. CBD is well documented through clinical research to be non-toxic and non-psychoactive and has no recorded negative side effects in humans, as well as being a powerful anti-inflammatory, anti-spasmodic and anti-epilepsy drug. This move will lead to more vulnerable patients buying untested CBD products on the illicit market, potentially bringing them to more harm or falling prey to unscrupulous cannabis oil scammers as it is an expensive product. Thousands of patients with hundreds of medical conditions ranging from acute to life threatening rely on CBD as a safe and non-toxic form of medical and therapeutic treatment. Patients who are buying CBD products have conditions such as Multiple Sclerosis, Parkinson's, Alzheimer’s, Crohn's Disease, Epilepsy, Fybromyalgia, Arthritis, Anxiety, Depression, Cancer, Polycystic Ovary Syndrome, Elhers Danlos Syndrome, and Chronic Pain. We petition the MHRA to please consider other means of approving CBD products so that patients do not suffer the consequences of this decision whilst stricter regulations are decided upon. Yours Sincerely United Kingdom Cannabis Social Clubs

I was born with head neck and facial disfigurement and only my left eye The right area where my right eye should have been was a beneign tumour. I passed my driving test in 1984 I have driven since within any problems. I am a community staff nurse In 2013 my licence was revoked as I failed the pheripheral vision test due to a congenital problem also due to my disfigurement the machine is not suitable for me. I feel Im being discriminated due to my disability. I am now being redeployed due to not being able to drive anymore. DVLA changed their rulings and policies in 2013 therefore I am not eligible to drive anymore

N.I.C.E. have recommended acupuncture for low back pain since 2009 and are now reversing their decision.The British Acupuncture Federation (BAF) which represents six organisations covering all styles of acupuncture can attest to its effectiveness for this condition based on proven outcomes. The US military obviously agrees with BAF with regard to acupuncture's effectiveness in pain relief as its Warrior Transition Unit Clinics treat large numbers of soldiers injured in combat with Battlefield Acupuncture for pain relief. The World Health Organisation states that low back pain is the leading cause of activity limitation and work absence throughout much of the world, so if you haven't suffered from it yet, the odds are that you will. Do you want to be deprived of an effective treatment within the NHS and have to rely on anti-inflammatory drugs with their known side effects? -- If not please sign the petition and support patient choice.

The government want to change the way disabled people can appeal rejections and claim their benefits. The main change is holding the appeals over the telephone, on a webcam or even by reading submitted paperwork. The other worrying change is replacing a judge with a clerk or solicitor with no experience in disability law. Moving the process out of the courts to a decision made by a clerk or retired lawyer is dangerous as they don't have experience making fair decisions in this area. The clerk would also be given performance indicators likely to contain targets for how many people should be rejected. This makes the process more biased against the disabled person. If the changes go through, disabled people would only have their case heard through a virtual court or by submitting evidence on paper. This makes it much harder for disabled people to give detailed and persuasive evidence and for the clerk, to see how their disability affects their ability to work. When assessments for benefits are wrong, disabled peoples’ lives are turned upside-down. It put my family through months of stress and uncertainty. I was assessed as being fit to work although my condition means I can’t stand without help. But thanks to the appeals process in court, I won back benefits that were vital for my family’s survival. If I had gone through the new process I might not have got the benefits I am entitled to and rely on. For many disabled people receiving benefits can be a matter of life or death. The appeals process currently works for lots of people - these changes will prevent disabled people like me from fairly challenging assessments about a person’s ability to work. I count myself as lucky - I won my appeal and now as a family, we’ve managed to keep our heads above water financially. I worry about everyone else that might be wrongly assessed though, and what the proposed changes will mean for them. Everyone deserves a fair, legal hearing. The government are currently consulting on the changes so it's important we make our voices heard.

My mother died on 6th October of cancer. Instead of spending her last weeks in a hospice where her pain and nausea could be controlled and she could spend her days in peace she was in a crowded, noisy, stressful hospital ward being served unsuitable food she couldn't eat without vomiting and suffering pain. Last year MPs rejected the Assisted Dying Bill saying end of life care provision was good. They were wrong. Despite great compassion from the ward staff, my mother's last week was not a peaceful one because the local hospices are overstretched and could not offer her a bed in time. For the last seven weeks of her life she could not sleep because of the nightly shouting of patients who should have been in psychiatric or dimensia specialist care. This is not acceptable in the fifth richest country in the world. I ask MPs and the Departmenr of Health: is this how you would want to spend your last days?

There are many in our community who have trouble walking or cannot walk at all and there are many places in Middlesbrough that do not cater enough for a wheelchair users needs. Please make Middlesbrough more wheelchair friendly so that those who are wheelchair bound have more freedom and independence! We need more ramps, lifts and easier access from street to building for these people, so this means in some cases we need bigger doors! Please sign and make this happen!