People are suffering and not enough is being done done. Even the GP's who work in this field and they are few and far between, still dont fully understand it. They need to speak to health professionals who suffer with the conditions http://m.wikihow.com/Live-With-Chronic-Fatigue-or-M.E

Trans fatty acids (produced industrially as hydrogenated oils) are estimated to KILL 7,000 people in the UK every year. All responsible bodies in the UK, and many countries in europe and states of the USA have already banned them. Doctors, NICE (the National Institute for Health and Care Excellence), and main articles in the Guardian, the Telegraph, the Daily Mail all agree: there is no reason to have these in our food. Many supermarkets have also eliminated them - in their own brand products at least - including Sainsburys, Marks and Spencer, Waitrose, Tesco and the Co-op. But other food sources use them, with no required information to customers and no control over their use. The American Medical Association has stated that there is no safe limit. NICE has called for their ban. These fats have no food value, but increase LDL (bad) cholesterol and reduce HDL (good) cholesterol, and even a 2% amount in the diet is reported to double the risk of coronary heart disease. There is no need for this junk in our food other than for the convenience of the food industry (it prolongs shelf life and is a cheap way of solidifying oil in fast foods). Recently Andrew Lansley has stated that the average UK citizen only consumes under 1% in the diet (though this is still a significant increase in risk), and voluntary codes of conduct are sufficient. The food manufacturers make an identical case. But the average is not the point: better off older people - customers of M&S, Waitrose, and other supermarkets - consume very little. But younger people who naturally use fast food outlets often consume considerably more than that average. They are in general unaware of the risks and, being young, sometimes don't think too much about what will happen in 20, 30 years. Older people have a duty to care on their behalf. One other point. Some supporters think such a ban is against the freedom of people to choose what they eat. But this is a poor argument at best. Trans fat was banned from Denmark 9 years ago, and there is no noticeable change in the taste or quality of food, nor any desire to reverse that change. This is such an easy policy change, and so absolutely beneficial. Just do it! References: https://en.wikipedia.org/wiki/Trans_fat http://www.dailymail.co.uk/news/article-1291041/They-kill-7-000-people-year-trans-fats-wont-banned.html http://www.belfasttelegraph.co.uk/life/food-drink/why-are-toxic-trans-fats-in-food-still-legal-in-the-uk-28656231.html http://www.theguardian.com/world/2013/nov/07/fda-ban-trans-fats-health http://www.theguardian.com/society/2010/jan/18/trans-fats-ban-comment

At the moment LDN is not widely available on the NHS to MS sufferers in the UK but in other parts of the World,like the USA it has been available for years. Lots of MS sufferers who've had to buy it on private prescription say that it has rid them of symptoms which even high dose toxic drugs did not. It has also been for use in many other conditions, http://www.lowdosenaltrexone.org/index.htm#How_does_LDN_work_ but it seems that this is not widely known to most sufferers. At the moment most Doctors do not prescribe it or know of it's uses for other conditions and sufferers have to buy it privately. It is a cheaper Drug to buy than most other MS Drugs I've heard but yet it's not viable for Drug Companies to endorse it at such low doses (profit wise) and therefore tests have not been untaken on a large scale to make NICE approve of its use for this purpose

Why should a resident of doncaster recieving treatment by doncaster nhs have to go to leeds nhs to qualify for funded treatment? This is creating all sorts of problems and issue for this lady she is 69 years old and as had a horrendous experience with her treatment as it is and to cap it all doncaster n.h.s. will not fund her home care. This is terrible and unfair. Sign this petition if you agree and want to do something about this.

The NHS was giving to the people of the UK it belongs to us and not the private proffiteers, We all pay for NHS in our taxes and local charity collettions for the local NHS Hospitals for things that they need like CAT scans. I like many others are not prepared to see it sold off bit by bit. The idea at the moment is to get people interested in saving the NHS nationally and the only way left now is a masive march in London on a mid week day.

This is Important because Cannabis is proven to help as a medicinal natural option while people have certain illnesses such as cancer and MS. We would be able to produce no polluting bio-degradable plastic. The oil crisis the world is facing would no longer be part of britains troubles as hemp oil could be used from the stem of the cannabis plant. There is a possibility that there would be less deforestation(which doesn't really apply to uk but it's worth a point) as we could produce hemp paper, And we wouldn't need wood to burn as we would have the hemp oil. According to a recent source Cannabis has been statistically found to cure 7 out of 10 cancer patients. Whereas Chemotherapy has been statistically found to have killed 7 out of 10 cancer patients. As to how true this is i do not no. I hope you will take the time to read through this and make action, not just for the stereotypical stoners that some of the public seem so afraid of, But for the welfare,healthcare, and wealth of the United Kingdom. Thank You.

Pauls Campaign aims to raise awareness of Sarcoma on two fronts, public awareness and with those of influence. Sarcoma:'the Forgotten cancer' Sarcomas are rare cancers that develop in the supporting or connective tissues of the body such as muscle, bone, nerves, cartilage, blood vessels and fat. There are around 3800 new cases of sarcoma diagnosed each year in the UK. 100 people a year are diagnosed in Northern Ireland. Sarcomas account for about 11% of childhood cancers and about 14% of cancers in teenagers. There is a huge need for research into sarcoma, research is lagging behind that of other cancers. Sarcoma is hard to diagnose, hard to detect and hard to treat. Biopsy is the only diagnostic tool and surgery often the only curative treatment. Many Sarcomas resist current cancer treatments, Sarcoma destroys so many lives before they ever have the time to blossom. visit us at https://www.facebook.com/pages/Pauls-Campaign/1395524224058670 www.paulscampaign.com @paulscampaign (twitter)

Increasing research and global experience in both Nuclear Energy and Fracking highlights the profound danger of these energy sources to all Sentient Beings and the precious Earth that supports us. New Nuclear and the proposed storage of nuclear waste on threatened coastal sights is a potential environmental catastrophe of horrifying proportion; is a threat to human health and the Earth; has a huge funding legacy that will continue to increase all our energy bills for years to come; and is totally unnecessary in the light of viable, safer and more economic green alternatives. Fracking has profound implications environmentally for the safety of water supplies,the poisoning of land, air quality, atmospheric carbon levels and the potential to cause earthquake. There are now safe, economic and green alternatives which must be supported by Government alongside an energy conservation programme. If we are concerned with the future of our children, and care for the Earth that so lovingly supports us all, we will act now and encourage a potential Prime Minister to review energy policies. What we do unto this Earth we do unto ourselves. Thank you.

We as a local support group from South Tyneside have been campaigning since 2006, because a Diabetes pandemic has been predicted by professionals and we need to be prepared for this. As it stands Diabetes sufferers have to attend regular check ups e.g. Eye and Foot screening, Blood tests, podiatry and annual reviews at GP's surgery or hospital, at the moment these appointments are held at various locations and ideally would be much better to be done under one roof especially for the elderly or children who need public transport to attend each of these very important services.

This is a totally unnecessary decision and shows the Government does not value hard working nurses and health care support workers and are relying on their good nature and dedication to just accept it. A recent pay review body recommendation to increase MP’s salaries was accepted but then it was MP’s voting for their own pay increase! Please sign up to our petition so the Government knows how bitter a pill they are trying to make us swallow.

We call upon the National Assembly for Wales to urge the Welsh Government to ensure that a dedicated Consultant/Clinic and medical support team for Myalgic Encephalomyelitis (M.E.), Chronic Fatigue Syndrome & Fibromyalgia sufferers is set up in South East Wales. I request that this petition be treated as an official voice of M.E. sufferers, their families, carers and interested parties. Currently, sufferers of the above ailments are not being supported, with a few exceptions, by the medical profession. They are unable to work but the government bodies assessing them do not appear to understand their problems. This is the basis for this petition.

As I suffered Polio at the age of 2yrs back in 1953 I had no ideal that it would return and bite for a second time in later life, my Dr has not got a clue about it and I have given him leaflets etc telling him but all he says is do more walking, I wish that I could its not through lack of trying my one good leg is worn out and needs a new knee while my other shorter leg has no joint movement and lack of muscle owing to the Polio all them years ago,