rsd-crps.co.uk Report : Visit Site

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home | what is rsd? | about rsd uk | support | information | news & activities | feedback | site map rsd uk this website is dedicated to the rsd uk which is now closed. service reduction program changes in the delivery of services at rsd uk are to be made from 1st april 2007. following consultations with the trustees, directors, major stake holders and the charity commission a program of reduction leading to service closure is being planned. the timescale to closure will be approximately 10 months and will coincide with the termination of internet services provided to rsd uk, including the domain name, email and all internet services including the forums. the helpline service will also be ended. the reasons for this decision are many and varied. rsd uk has been in existence in one form or another since sept 2000 and has made significant progress in raising awareness of the condition and educating medical professionals. all this has culminated in the release of the new book, “insights into pain & suffering”, which we will continue to sell until stocks run out. this will also mean that the rsd uk conference held in 2005 was the last one to be organized by rsd uk and that the proposed 2010 conference will not now go ahead. in january 2008 the charity will begin its final closure process and any remaining funds in the bank account will go to the bath institute for rheumatic diseases. rsd uk has been more than a full time job for those involved in the day to day running and we have made many friends during this time. the directors and trustees wish you all well and pray for continued research into the condition. rsd uk is a voluntary non-profit making charity which was set up to give support to those concerned with reflex sympathetic dystrophy/complex regional pain syndrome, often abbrevieated to rsd, crps type i or crps type ii. you may also have been given the diagnosis of sudecks atrophy, causalgia, allodynia, hand shoulder syndrome and many more. there are three working groups within rsd uk and these are a support group where members can share experiences, fears and good/bad days and ask questions; this is free to join an education & information service to share knowledge with medical professionals or lay people who haven't yet had experience of or knowledge about rsd/crps an awareness group that campaigns peacefully, working with medical professionals and other organisations to raise awareness of rsd/crps and related pain issues reflex sympathetic dystrophy (complex regional pain syndrome) is a multi-symptom, multi-system syndrome usually affecting one or more extremities, but may affect any part of the body. although it was clearly described well over 100 years ago by drs. mitchell, moorehouse and keen, it remains very poorly understood and is often unrecognised. rsd/crps is a disabling condition with simultaneous involvement of nerve, skin, muscle, blood vessels and bone, a patient does not need all symptoms to be present for a diganosis to be made. many medical professionals haven't encountered rsd/crps yet, and the chances are that if you are a patient you will meet one such doctor. we try to help people understand that if a doctor does not know about rsd/crps that does not make him/her a bad doctor - it merely means he hasn't yet had experience in this area. hopefully with work from all those within the rsd uk alliance and other organisations rsd/crps will soon be a well recognised condition, giving patients the understanding and care they are entitled to. we have literature available for interested persons and an annual conference aimed at professionals and patients which helps work towards a better understanding of the condition. we are keen to work with other organisations for the benefit of rsd/crps patients and to date these include doctors (gp's, consultants etc) and other medical professionals occupational therapists and physiotherapists researchers (salford and bath) arc (arthritis research campaign) & dipex skip (supporting kids in pain) & rsd alert gold bullion ms national uk pain clinics medtronic we hope you find the information or support you are looking for. please help our ongoing awareness campaign by forwarding this page to all your contacts, thank you. information if you would like a patient information booklet posting , please email (uk residents only) for all other information please email full contact details may be found on the contact page. a history of the rsd uk 2010 2010 applies to the name rsd the logo and all graphics on this site, they must not be re-produced without written permission from the author

URL analysis for rsd-crps.co.uk

http://www.rsd-crps.co.uk/rsduk.htm
http://www.rsd-crps.co.uk/news.htm
http://www.rsd-crps.co.uk/support.htm
http://www.rsd-crps.co.uk/home.htm
http://www.rsd-crps.co.uk/info.htm
http://www.rsd-crps.co.uk/rsd.htm
medtronic.co.uk
arc.org.uk
dataprotection.gov.uk
bullionbypost.co.uk

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the WHOIS query quota for 2600:3c03:0000:0000:f03c:91ff:feae:779d has been exceeded
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WHOIS lookup made at 16:04:56 17-Oct-2017

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  REFERRER http://www.nominet.org.uk

  REGISTRAR Nominet UK

SERVERS

  SERVER co.uk.whois-servers.net

  ARGS rsd-crps.co.uk

  PORT 43

  TYPE domain

DISCLAIMER
This WHOIS information is provided for free by Nominet UK the central registry
for .uk domain names. This information and the .uk WHOIS are:
Copyright Nominet UK 1996 - 2017.
You may not access the .uk WHOIS or use any data from it except as permitted
by the terms of use available in full at http://www.nominet.uk/whoisterms,
which includes restrictions on: (A) use of the data for advertising, or its
repackaging, recompilation, redistribution or reuse (B) obscuring, removing
or hiding any or all of this notice and (C) exceeding query rate or volume
limits. The data is provided on an 'as-is' basis and may lag behind the
register. Access may be withdrawn or restricted at any time.

  REGISTERED no

DOMAIN

  NAME rsd-crps.co.uk

NSERVER

  FS9.CHURCHFARMHOUSEMUSEUM.CO.UK 88.208.194.135

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