People are finding it hard to make ends meet and some times have to choose between eating and having medication. People with Parkinson's, asthma and other life changing illnesses are finding this difficult to deal with. Ministers claim that it is not possible for England to abolish the charges because it would leave the NHS with debts of £450million a year. However The BMA chairman Dr Hamish Meldrum said that the Government should abolish charges and that many of the exemptions were unfair Still England is the only one paying . Read this for more information http://www.dailymail.co.uk/health/article-1372063/Prescriptions-From-today-English-pay-prescriptions-thats-April-Fools-joke.html#ixzz2vlx3a4IH

Currently Mental health patients can have to wait for more than a year for treatment or therapy and are not guaranteed the most appropriate therapy for their condition. I feel this unacceptable and a wait that can be too long for people that are in very difficult and what can be dangerous circumstances. Shorter waiting lists will help reduce the impact on other departments and teams within the NHS that deal with patients in crisis, often reoccurring due to lack of support and treatment. Surely a prevention of the crisis is better than having to deal with the crisis? Link to Early day motion 1063: http://www.parliament.uk/edm/2013-14/1063 For more information: http://www.bacp.co.uk/policy/edm1063/

We are supposed to live in a caring country where our health needs are looked after, irrespective of our financial position, free of charge from the cradle to the grave. Perusing the internet for nursing care for elderly people will uncover many examples of people not receiving the funding from the NHS for their health care that they have every legal right to expect. Many people have had to resort to expensive court action to force the National Health Service to fulfill its statutory obligations. This is not acceptable and is a national disgrace which needs to be addressed at the earliest opportunity. Please have a look at this useful website, it is crammed full of information and can provide help. http://www.caretobedifferent.co.uk/

We have a brand new, gleaming hospital which people cannot reach because it is not on a bus route. Many of the services based there: physiotherapy, falls prevention, community dieticians, are geared towards people who are frail and cannot walk long distances. 500m might not seem a long distance for most people, but on a zimmer frame or crutches it is forever. Parts of the hospital are empty because local GPs do not want to move to a building which their patients cannot access. The plans for this building always included a bus stop, but what we need now is a bus which will actually stop outside the hospital door. There is a cross party consensus that this needs to happen urgently. Please add your voice so the Mayor of London understands how important this is. Thanks.

I am disabled and it caused me a great deal of unnecessary stress and physical discomfort to have to go though a very complex form answering the same questions again and again when the DWP have already had the reasons for my claim. All they need to do is ask a patients GP or consultant to do a simple patient report that can be printed out from their computer to answer all the questions that are required. I am one of millions of people who have to do this and I am sure there are worse people than myself who will find this both distressing and painful. The reason l say distressing is because you realize what you are living and trying to cope with everyday. I was in so much physical pain after filling in this form again l was sobbing with the pain. Doctors don't put patients on morphine with a cocktail of painkillers for nothing. It is just common sense and it is about time someone said enough is enough. We are claiming DLA/PIP because we need to not because we want to.

The closure of respite care and transfers for after care from hospital to Winifred Kettle home in Westhoughton is very important to our community Many people have used the facilities of this wonderful care home over many years. The services of dedicated staff from cleaners, domestics, carers and managers is exemplary. We all may need the services in the future. The elderly population is increasing, but more homes are closing. Many carers are elderly themselves and circumstances do not allow them to look after loved ones. We must rally round together to put pressure on Bolton councillors to change their minds.

Children with ASD usually suffer with anxiety, but this can be increased massively due to not handling or coping with the children correctly. Increased anxiety in ASD children can then cause a "meltdown" or tantrum to occur which can last a long period of time and the effects of this usually result in the said child being excluded from School as they are now labeled violent and a Health & Safety risk. We are increasingly hearing of children being labeled and treated as "Naughty" by teachers simply because they do not have the ability to recognise or understand ASD and the impact that this has on the child. This is not the child’s fault but the way the situation is handled. We are seeing and hearing of an increasing number of children being penalised by mainstream schools for having a disability. They do not receive the correct level of help and support whilst in school due to the lack of teacher training. If all teachers received the appropriate level of training and support then all parties involved and most importantly the child, would benefit. Children are often left demoralised and anxious and feel picked on by their teachers. This is due to their teachers not getting the required training to help them cope more effectively with the challenging concept of handling these unique personalities. More importantly, parents are left fighting for understanding and help against budget cuts and the bureaucracy of Government departments and LEAs. Whilst this continues both the child and parents feel bullied by the LEA's and the Government’s lack of understanding of ASD which results in stress for parents and children and the officials getting defensive instead of dealing with what should be the common goal… the child’s welfare and education. This then causes years of struggles between the parents, schools and LEA's to try and get the correct level of support for the children themselves with the children and parents often made to feel like criminals. If a child has a physical disability such as being in a wheel chair, provisions are made for their disability to ensure they receive the appropriate level of education and core skills that can only be learned as a child. Why should it be any different for a disability that you can’t see? Why should it take so long for the professionals we trust our children with each day to recognise and understand the educational and developmental requirements of our beloved children? This shameful treatment of our ASD children who have to fight for the right to be understood, to have someone who understands what they are going through and is able to nurture not misunderstand when they are going through difficult stressful times that create sometimes violent outbursts. This can be changed by the government and LEAs who set the curriculum and have both the means and the power to ensure all children no matter whether black or white, physically disabled, able bodied or indeed mentally disabled, have the appropriately trained teachers and staff to help them develop to the best they can be. Give these children a chance by giving teachers the appropriate training to recognise, understand and help these children. They are neither naughty nor stupid, they are simply misunderstood. Help our teachers to help our children! This is appalling treatment of our children. Please help to put an end to it.

GP surgeries could lose up to 15 per cent of their income from April if some services they currently offer such as spirometry, ECG and 24-hour blood pressure are given to private providers. This financial loss could harm the overall work of the surgeries, while patients would have to travel further to access the privatised services. The threat of privatisation of LES services arises from the Government's unleashing of competition law on the NHS. But Stockport CCG should stand up to the pressure, as some other CCGs have done - we need to tell them this urgently, at their February 12 meeting.

Horizontal hydraulic fracturing, ‘fracking’, is a way of extracting oil and/or gas. Water, sand and toxic chemicals are injected at high pressure into underground rocks to shatter them. This releases the gas/oil which can be collected. Investing in carbon-intensive fossil fuels is a distraction from the need to decarbonise our electricity supply. And it's hazardous. Studies show that fracking pollutes water supplies (with arsenic and lead), causes earthquakes, and spoils local communities. And there are nightmare stories coming form the States. Like in the town of Dimock, PA, residents have reported their water turning so brown that it stains crockery. Their water was later found to contain methane, and a host of toxic chemicals. But it gets worse. "My son had sores up and down his legs from the water." " My daughter... would have to get out the of the shower and lay on the floor." Those are the words from Greg Saunter, a local resident, whose water supply was shut off for his own good. He cannot shower in his own home. Or drink water out of his taps. Fracking has ruined his life. It cannot happen here. We call on the council to preserve the quality of life of its residents, and reject all planning applications for fracking.

My Mum who has rapidly progressing Alzheimer’s disease uses the centre. It is a local lifeline for many local residents, as a caring unit which understands her condition and provides a friendly and stimulating environment, and for the carers such as myself to get some much needed respite. The proposal is to move the Patey clients to the Royal Albert Day Centre in the centre of Portsmouth which would be extremely detrimental for the majority of them. They are a close knit group of individuals who thrive on the familiarity and security of both their number and setting. The skilled carers provide stimulating activities which maintain their clients' skills, helping them to feel valued and promoting independence. The move to the much larger Royal Albert Centre and much longer journey would be frightening and hasten the progress of their disease as the unfamiliarity will cause confusion. Portsmouth City Council's own Dementia Action Plan 2013/14 states: “Objective one of the Portsmouth Joint Health and Wellbeing Strategy is to enhance the quality of life for people with dementia” “2142 residents will have some form of dementia · 55% (1178) will be mild, 32%(685) will be moderate, 13% (279) will be severe” “Portsmouth aspires to be a dementia friendly city where people with dementia will be treated with respect and feel included in our local communities.” “There will need to be a shift away from acute care towards primary and community based service provision, including rehabilitation and reablement.” “Support for carers is key” By closing the Patey Centre there will be just 60 spaces for the 2142 sufferers of alzheimers and dementia in the whole of Portsmouth. Portsmouth NEEDS more spaces not less. The Council claim this is a cost cutting measure however this is only true in the short term. Longer term there will be: growing costs of caring for increasing numbers of isolated dementia sufferers in their homes for whom there are no day care spaces; an increased need for residential care as overwhelmed carers without specialist day care respite will reach breaking point faster; and additional costs transporting people to the Royal Albert. The Council's intention is to sell the land the Patey Centre is on to help fund a residential home for people with alzheimers in the north of the city, why doesn't this incorporate the Patey Centre? The 2142 sufferers of alzheimers and dementia in Portsmouth are vulnerable people, many with carers such as myself who are stretched to breaking point. Their needs are being ignored and their excellent day centre is being lost. Please don't close the Patey Centre in Cosham, without providing alternative specialist day care for people with alzheimers and dementia in the north of Portsmouth, put the needs of the people of Portsmouth first.

I've heard that Hywel Dda health board are to downgrade Bronglais. They'll stabilize patients in Bronglais, then fly them down to Carmarthen

Recently, Jeremy Hunt lost his appeal against closing Lewisham Accident and Emergency. The law that protected it would be removed if Clause 118 passes. The Clause will allow the government to close or downgrade any hospital in the country, with barely any consultation of local people, if there is a Trust in financial difficulties anywhere nearby. They will be able to appoint an administrator to one Trust who will be able to take decisions to fast-track the closure of hospitals in another area - no matter how successful or popular those hospitals are - using the 'unsustainable provider' legislation that was designed only for insolvent Trusts. If it becomes law, this Clause means that *no* hospital will be safe, no matter how successful. Check out this link http://www.opendemocracy.net/ournhs/stop-hospital-closure-clause for more information. We will update you on further campaign actions you can get involved in. Please share on Twitter and Facebook.