I have two sons who both live with Duchenne Muscular Dystrophy. We are grateful for the NHS and have always received fantastic care any time we have needed it. There is just one problem, most of the Nurses we have encountered in both Paediatric and Adult Departments have little experience in Moving and Handling patients who require hoisting. This is due to a comparatively small number of patients requiring this, however for those patients who do, this is essential. Nurses really ought to receive moving and handling training, including with slings and hoists, and should have access to refresher courses at least once a year, to ensure that every patient receives the best care possible. Every patient deserves the best care, and when Nursing Staff have little or no experience this can result in injury to the patient and themselves.

The NHS was founded as a two pronged system. There was the NHS - The national Health Service, and there was the NHS - The Natural Health Service. The second NHS is far less well known but equally important. The idea behind the movement was to give all people access to the natural landscape around us for the benefits it gives to us mentally and physically. This was important as people has just returned from second world war - people had died for this land and they deserve access to it. The move to give people access to our natural landscape was blocked by the House Of Lords (as you can imagine they don't want people snooping around there land). The point here is that the NHS was founded under the principle that we would have access to landscape and people. Today, social and nature prescription is on the rise but still has little to no space in the public sphere as a genuine way for us to tackle our health crisis. We need it as a part of our preventative and ongoing care for people with issues from mental health to physical ailments. It's cheaper than medecine and strengthens community bonds and resilience.

Targets, (whether or not they are achieved by the NHS), help us to judge the performance of the NHS over time.

A family doctor, who knows your medical history, is vital to our health and well being and should be available for all of us. Our GP practices are under more pressure than ever before. There is a national shortage of GPs and central government is undermining and failing to support surgeries which are led by GP partners - instead they are encouraging the privatisation of GP surgeries leading to disastrous consequences for patient care. Companies such as Virgin, Boots and US company Operose are buying up GP practices when the GPs eventually give up due to underfunding. The private Companies may even get more funding than the GPs were given in some cases. Patients then find that they are unable to get appointments and the same level of care they received before. One practice in Kent, bought up in 2016, went from outstanding, when run by GPs, to inadequate in the 18 months after it was bought up by a private firm. Other GP surgeries have been highlighted on Panorama, showing how the private companies make more money by employing fewer GPs ( perhaps as little as 1 per practice) and making up the needs with less highly trained and much less well paid physician associates who need support, which they may or may not get, from a GP so they don't make mistakes with diagnosis or patient care. The government is encouraging a two tier system to develop. In the near future, if this trend is not reversed, only rich people with access to private health care will be able to get reliable health care when they need it. My own GPs have criticised the political decisions being made which are making it so difficult for the doctors - they say this started in the Thatcher years but every government since has contributed to the problem. One of them described it as "heartbreaking" because the poor will not be able to get adequate care and many may die unnecessarily. The service is at breaking point already. Almost all the appointments at my surgery are now telephone only and this can lead to mistakes being made. I would like to see these decisions reversed by the government and I call on the Health Secretary to take urgent action. It is completely inappropriate for private companies to be running GP surgeries for big profit while neglecting patient care. Central government should be adequately supporting GP led and run partnerships- they are the ones who know how to do the job properly and they are invested in the work. Big business just doesn't care. It's profits before people. If we all petition the Government on this issue, they have to take notice as privatisation of the NHS through the back door is an election loser. I want this to be debated in the House of Commons. This is a national issue which affects all of us.

Since the summer I have been making contact with my local GP to book an appointment to have my current coil (expiring in November) replaced. I was made aware by female family/friends that I should make contact with my GP as far in advance as possible as the waiting list for the coil is extremely long. After calling my GP in the summer I was told that I had made contact too early and I should call again one/two months in advance to book in. I followed these instructions and was eventually added to the coil waiting list in September. After chasing up my case in October and then again in early November I was informed by the administrator in charge of the 'Coil waiting list' on both occasions that she could still not offer me an appointment as there are still no slots available. I raised my concern about the fact my coil is now expiring in a matter of weeks and as a result I wouldn't be protected from getting pregnant unless my husband and I use condoms. The clinician advised that there is nothing she could do about getting me an appointment any earlier as the waiting list is very long and there are only two practitioners who take appointments for the coil. I asked if she could give me any sort of time frame as to how long I would have to continue with my expired coil and she couldn't give me an answer. In an attempt to be proactive, I made contact with my local Sexual Health Clinic to enquire if I could make an appointment with them to have my coil removed. They informed me that this is not a service they offer anymore and I needed to make an appointment with my GP. I have since researched the 'NHS coil waiting list' and found that it can be as long as 6 months to a year women have to wait to have their coil removed. More clinicians in GP practice need to become qualified to take appointments relating to the coil. The 'NHS coil waiting list' is an issue directly related to female empowerment. The current system within the NHS is completely ineffective and has personally left me feeling completely out of control of my own body. Choosing the correct method of contraception is an extremely important issue that every woman in the UK goes through at some point during their life. As a married woman in my late 20's, I am settled with a long term partner but not yet ready to start a family. The coil is the correct method of contraception for me at this stage of my life, however I am unable to access it. Furthermore I have a coil that will be expiring imminently and I am unable to book an appointment to have it removed in time, and there is absolutely no time scale that can be provided by my GP as to when I will get an appointment. Women in the UK should not have to wait for this ridiculous amount of time to gain access to contraception. Not only is the process of trying to get an appointment for the coil emotionally draining and exasperating, it is unbelievable that we are in 2022 and women in this country are left to feel completely out of control in matters to do with their own body.

This new hospital is urgently needed to bring our NHS facilities into the 21st century and to provide top quality care. In the meantime many people will continue to suffer and lives will continue to be unnecessarily lost. Staff morale is at an all time low because of this.

I was diagnosed with Bowel cancer aged 37 after being misdiagnosed with diverticulitis. Misdiagnosis is common in people under 50 because they are considered too young to have Bowel cancer and red flags are ignored. There is no age limit to Bowel cancer. There are approximately 42,886 cases of Bowel Cancer each year. Bowel Cancer has a 54% survival rate, if caught early enough. There is no action you can take to prevent bowel cancer, it is considered “The smoking old man’s meat eating cancer” which is simply not the case for everybody. My doctors have not been able to identify a single reason why I have this cancer and I don’t fit the bill at all. It is possible it has been present for years even though I am “too young” to have it. My blood loss and pain was thought to be a gynaecological issue and I was diagnosed with a Anaemia. Even a perforated bowel didn’t seem to ring alarm bells. Cancer was not a consideration. We now know I was losing blood via stools, without realising and a tumour had perforated my bowel, eventually causing excruciating pain. Screening could have detected this and I may not have had to have part of my colon removed in emergency surgery and have to live with a stoma. I want it made possible to stop this cancer in its tracks before it gets to my stage or further for anybody else. After all, if Bowel cancer develops it can also spread to lymph nodes then onto other organs which can be even more devastating. Let’s try to prevent more Bowel cancer related deaths in the future by screening adults aged over 30 annually and allowing anyone over 18 to opt in as well. Feel free to follow my journey on Instagram @paloma_the_stoma22

Many people on low incomes will lose their lives through hypothermia, as they will not be able to afford heating. Many more older people will just try and wrap up warm instead of putting the heating on because they can't afford the gas, or electric. Many disabled people on low incomes will have to choose between heating or food. This is corporate murder. The outcome of this is a massive rise in the death rate this winter. I myself am looking at a winter of severe pain with little to no heating each day. My mother is likely to just not turn the heating on and wrap up as warm as possible as she is of the wartime generation. I fear that she will not survive the next winter. Many of her generation, and their children on low incomes (state pensions) will likely do the same as they will not be able to afford heating this winter. Please do not start up a similar petition as it will weaken this petition. Instead share this one so as many people can sign it, and it gets brought before the house of commons.

Covid is still here it hasn't gone away, we need to protect The disabled,vunerable, elderly and keep them safe. The government has the right to change the law back to make face masks mandatory again in Hospitals and Doctors Surgery’s, so they are safe and secure places to go when we need treatment. Please sign my petition.

Other people should join this petition to tell those organisations, the government and the NHS that it could be doing better and 2030 is just not good enough. There is no reasonable explanation why HIV cannot be stopped sooner and why are these organisations. like THT, the Elton John AIDS foundation decided to sit on their hands and fail over the decades to democratise HIV sector and push for better representation of HIV+ people directly to have a say in their own NHS care - why has been left to a doctors union to saturate the commissioning of HIV services and wield to much power over the sector. It is important to stop the silent complicity that is threatened by adverse public contract outcomes by the people who set the specifications for HIV treatment and also have a hand in the awarding of contracts to HIV charities and sit on the boards and trustees for the same charities. It is important to stop excluding HIV+ people as they have limited say and input into a sector that claims to be representing their needs but is constantly prioritising the funding applications for public contracts.

I have, I believe, suffered with POTS since I was 16/17 years old. The symptoms I developed at 16/17 years old have got worse over the years. I was told repeatedly it was all anxiety related. I was even wrongly diagnosed with BPD, mainly because I always argued my case around my physical health problems which were denied. I was repeatedly admitted to hospital and not listened to. Finally I was diagnosed with POTS in November 2021, before this symptoms such as breathlessness on walking from one room to another and passing out when standing up were put down as anxiety. I have heard repeated stories from around the world of people suffering endlessly because sufferers of POTS are not taken seriously! This needs to stop NOW.

Start action now with poverty and the energy crisis at all time low the working class cannot afford private. Do we want a nation with related health conditions brought on by poor dental hygiene are we still looking at the poor, rich divide. We pride ourselves on our NHS services envied by the world over yet the government are destroying the very establishment which makes us who we are. Invest now, action now, no more excuses. Sign the petition get it in front of the people we voted to represent us and we want answers and a solution not for 10 or 20 years down the line we need action now with a worldwide recruitment campaign and investment in this country to equip our own residents with knowledge and the expertise to work and invest in the country they live in.