Disclaimer
SWAN UK (Syndromes Without A Name) is a project run by Genetic Alliance UK offering support and information to families of children with undiagnosed genetic conditions.
This group is for social purposes and for families to share information, access mutual support and keep up to date with the development of the SWAN UK project.
To join SWAN UK please contact the project coordinator Lauren Roberts on 0207 704 3141 ext 110 or email SWAN@geneticalliance.org.uk.
The information presented on this site is for general use only and is not intended to provide personal medical advice or substitute for the advice of your physician. Medical information changes rapidly and whilst the Genetic Alliance UK make effort to update the content of the site, some information may be out of date. Remember to always seek the opinion of a medical doctor. There are a number of links from this website to sites maintained by other groups.
These links are provided purely to assist you, and in good faith. The presence of a link does not necessarily imply that the Genetic Alliance UK endorses or supports those other groups, nor does the absence of a group imply that the Genetic Alliance UK does not support it. The Genetic Alliance UK cannot be held responsible for any damage or loss caused by any inaccuracy in this site, or in linked sites/pages.
Please note that the views represented on this site do not necessarily reflect those of the Genetic Alliance UK. The Genetic Alliance UK website does not host or receive funding from advertising. Posts and comments made are monitored regularly but neither SWAN UK or Genetic Alliance UK can take responsibility for the content of comments made.
Posts and comments made are monitored regularly but neither SWAN UK or Genetic Alliance UK can take responsibility for the content of comments made.
