National Society for Phenylketonuria
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What is PKU
What is the NSPKU
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Welcome to the NSPKU web site.

IMPORTANT NOTICE

We have experience unauthorised changes to our website including additions of links at the bottom of some of our pages.  These links selling drugs have been added without our consent and may cause harm to your computer.  Please ignore them.

In order to correct this, we are having to restore this website from a backup and so you may experience difficulties during this time.  We apologise for the inconvenience.  If you cannot find the information you require, please telephone our helpline on 0208 364 3010

Please follow the links at the side and the top of these pages to navigate around the web site or use the quick links below to find the most popular items.

Quick links

bullet Introduction - what is PKU
bulletNews
bulletHelp page
bulletDietary information booklets
bulletThe Management of PKU booklet
bulletNews and Views - our quarterly magazine - Issue 124 is now available to download
bulletEvents - Find presentations and abstracts from the recent conference here
bulletHow to join the NSPKU - download membership forms and gift aid forms
bulletContact us

What is the National Society for Phenylketonuria (NSPKU)?

The NSPKU exists to help and support people with PKU, their families and carers. It was formed in 1973, see history.

The NSPKU actively promotes the care and treatment for those with PKU and works closely with medical professionals in the UK.

It organises conferences and others throughout the UK, publishes a wide range of publications (including food lists) for parents, those with PKU and medical professionals.

Events - the NSPKU organises conferences and study days. Local support groups also hold study days and other events.

The NSPKU also sponsors medical research into PKU.

If you are a new parent of a baby that has just been diagnosed with PKU, we suggest that you follow the link to the What is PKU page before exploring the rest of the site.

What's New?

bullet2009 Conference and Family Weekend Announced
bulletFAQ page now available
bulletHelp page now available
bulletEmail mailing list now available;
bulletOnline donations now available;
bulletDon't forget to check out our news page from time to time;

Please Note

The treatment of PKU varies for each individual.  No patient should alter their own treatment as a result of anything written in this web site without first consulting their doctor or dietitian.

The NSPKU cannot be held responsible for the content of any external links.

The content of this web site are NSPKU copyright.  If you wish to reproduce anything from this site, please read our copyright notice.

This site contains a few photographs mainly of past events.  If you appear in one of these and object, please contact the webmaster advising which picture you would like removed.

Please contact the webmaster if you find any errors or faulty links.

Contact Information

 
Telephone
0208 364 3010 Helpline 
          0207 099 7431 Recorded information line 
Text
07983 688 664
Fax
0845 004 8341
Postal address
NSPKU, PO Box 26642, London, N14 4ZF.
Electronic mail
General Information: info@nspku.org
Publications: publications@nspku.org
Merchandise: mechandise@nspku.org
Webmaster: webmaster@nspku.org
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[ Home ] News ] What is PKU ] What is the NSPKU ] Publications ] Merchandise ] Events ] Help ] Links ] Contact ] Donate ]

Send mail to webmaster@nspku.org with questions or comments about this web site.
Copyright © 2004-2008 National Society for Phenylketonuria Charity number 273670.
Last modified: 16 July, 2008