The National Kidney Federation is unique because, although there are a large number of kidney charities, the NKF is the national kidney charity actually run by kidney patients for kidney patients.
Most renal units have a Kidney Patient Association (KPA) specifically attached to that unit, however, in January 1979 these independent charities realised that they needed a national organisation to fight their cause as renal provision was in dire difficulties, overstretched, and under resourced. If ever there was a case of post code provision, renal disease was it! Currently there are 49 KPAs and they come together as the controlling Council of the National Kidney Federation, the KPAs are both the ears and the eyes of the NKF and its controlling force. Patients are the Officers of the NKF, the Executive Committee of the NKF and some of the workforce of the NKF. Apart from nine members of staff, all other personnel are either kidney patients or carers of kidney patients.
Unlike other kidney charities, the NKF has only two roles, campaigning for improvements to renal provision and treatment, and national patient support services.
Campaigning
The NKF lobbied for, and got, an All Party Parliamentary Kidney Group of over 60 MPs and Lords established in Parliament and they feed that group on a day to day basis with the information needed to keep renal disease in front of the nose of Government.
They maintain a continuous dialogue with Ministers and the Department Of Health. They attend all of the main Political Party Conferences, and they joined with others under the BMA umbrella to be founder members of the Transplant Partnership.
When the Government announced that 34,000 renal patients were too small a group to warrant a National Service Framework the NKF took action. They formed with others a new charity The Kidney Alliance, and then worked with other members of it to create a Dialysis version of a National Service Framework (NSF) of their own. Then, they launched this document within the House of Commons in front of the very Ministers who had rejected the idea of an NSF. The Government took only 4 weeks from that day, to reverse their decision and announce a Renal NSF of their own. Quite a victory for any group, let alone a group of very ill patients! Part 1 of the Renal NSF was published by the Department of Health on 14 January 2004 with part 2 following in February 2005. The NKF provided considerable support and input to the Department of health during the preparation of these two vital documents.
Patient Support Services
The NKF provides and maintains a website which has rapidly become the hub of the renal community. This website is vast, and viewed by more than 1,000,000 patients, carers, renal professionals, doctors and nurses worldwide every year. The site is even more incredible when it is realised that like the NKF itself, the website was built by kidney patients. If the subject is renal, the answer is on this fantastic website. Above all the website has brought patients real information about their condition, and it has put patients in touch with each other. It has given kidney consultants, doctors and nurses a chance to talk with each other, and with patients, about issues and concerns that before the website they may have been completely unaware of.
For those that do not have access to computers, the NKF runs a FREE National Kidney Patient's HELPLINE
0800 169 09 36
Which takes about 200 calls a week from patients, carers and healthcare professionals, and the NKF distributes its own magazine, Kidney Life completely free of charge four times a year.
Whether you are an individual facing a Kidney Biopsy and just want one leaflet, or a Renal Unit requiring three thousand leaflets on anaemia, the solution is simple. You ring the Helpline and say what you need, then the information is downloaded into a set format, printed out, and put in the post that very same day. Thousands of different leaflets are possible, from travel insurance and holidays, to dialysis, transplantation and living donors.
Click here to see the Policy Statements of the NKF.
Once a year the NKF holds its own national patients' event to which more than 250 renal patients attend over a two day period. This is a very special occasion and one that takes much organisation. However, it is very successful and it provides a platform for the NKF to listen to patients, and for patients to tell the NKF where the shortcomings are in renal provision. Frequently, Government ministers and healthcare professionals are on hand to hear for themselves the issues, but above all it is an opportunity for a thorough exchange of views.
The NKF raises money directly from the public and is also supported in its work by the renal industries surrounding and supporting care of the disease. It exists solely because of the generosity of those sponsors and supporters, however money is always tight, and much more could be done with greater sponsorship.
Plans for the Future
The NKF wants to forge closer relationships with other kidney charities to ensure that resource is used effectively and that different groups dont keep reinventing the same wheel. A large number of kidney patients come from ethnic backgrounds and this presents separate difficulties which have to be faced, translation of leaflets, involvement in the patient organisations, shortages of donor organs, cultural views toward transplantation.
The Kidney Patient Associations (KPAs) themselves need strengthening and in the coming years the NKF intends to focus on providing real help to these groups of patients who are struggling to maintain their local service within their own units.
In Europe the Renal Patients organisation is called the European Kidney Patients Federation (EKPF), and the NKF is already a full and active member taking the fight for better treatment and resource both to the European Parliament and to individual countries as necessary and bringing back to the UK the successful ideas practiced abroad.
The National Kidney Federation is constantly aware that the earlier renal disease can be detected and treated the better the outcome for the patient. Much effort is to be put in, to try to identify these groups at high risk who are unaware of the danger to their health and the possibility of their entering End Stage Renal Failure.
Whilst there clearly have been many advances in renal care since the foundation of the NKF in 1979, it remains true that the period started with a shortage of renal provision and resource and ends in exactly the same plight. The NKF hopes passionately that over the coming years we will see real strides being made in adequate provision of health care to the current 61,000 end stage renal failure patients in the UK.
Read a copy of our Memorandum and Articles of Association here
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