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.

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

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?

My son was diagnosed with Autism around 5 years ago, but not in Sefton. His diagnosis was received through one, locally commissioned NHS Trust, and looking back, the pathway to diagnosis was founded on clear, pre-determined steps that every child in the area followed. This process was well defined and simple, whilst meeting all clinical guidelines; resulting in my son receiving a diagnosis of autism within 6 months of referral. In comparison, my daughter is currently on the Autism Assessment Pathway in Sefton. As a parent, it quickly becomes clear that this process is inefficient, not fit for purpose, and very much based on an ad hoc, undefined approach. Across Sefton, it is well known that the result of this approach, is an average timespan of 4 years to diagnose a school aged child with autism, from the time of referral. Every step on the pathway, requires separate referrals, and it has been evidenced that overall, the waiting times for each appointment, are massively outside clinical guidelines. The results of this are catastrophic for everyone involved: The child who doesn't understand their own difficulties for example, and who is left untreated; the family who desperately need help to support their child and maintain equilibrium in the home; and interestingly, with the current system being so inefficient and time consuming, the financial implications and waste of public funds must be severe! In fact, the consequences of ignoring this cannot be underestimated, with further health issues arising, specifically from the stress and strain placed on children and families who are left powerless. Put simply, this MUST change with immediate effect, and Sefton's Autism Pathway brought in line with clinical guidelines at least. Simple, clearly defined steps, coming from a single referral for assessment, must be identified and put into practice. It is obvious to say, that decisions must now be made, that prioritise the health and wellbeing of children and families across Sefton. However, a clearer, unified pathway, would also bring the additional benefit, of a more cost effective approach that protects public funds.

Dropped kerbs make a huge difference to my life and those of other disabled individuals where they are available but this availability is patchy at best with individual roads often having them only in some spots but not in others rendering overall access little better than if there were none at all. Dropped kerbs affect individuals who use crutches or walking sticks or frames or wheelchairs or mobility scooters and also affect parents with prams too so they matter to a considerable section of the community. Dropped kerbs need to be protected from careless parking by means of double yellow lines or they may be rendered useless even where they are otherwise available and these need to be rigidly enforced too. This amenity is particularly important in relation to buildings where disabled access is a necessity yet, taking my local hospital as an example, outside that complex there is no dropped kerb and an over eight inch drop to the road from the pavement. This is a far from uncommon experience and highlights the need for fresh action to put these matters right. Disabled people struggle enough to get around as it is without making this any more difficult thanks to the patchy and ill thought through provision of dropped kerbs that we currently have. Central government action and matching funding is needed as well as local government action to put the work into place.

people who have cystic fibrosis suffer their whole (short life span ) lifetime, in and out of hospital frequently at more cost to NHS maybe with correct meds and funding their lifetime would be more bearable