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CHORDOMA
CHORDOMA SUPPORT GROUP An independent, international, online, support group for all those affected by Chordoma
to offer each other friendship, support and information.
More about Us * Active since 2001 * Contact us at this email
 Please use only the New Posts message board .
You may add to an older thread on another board but, please, start new threads on the New Posts list. This is because we are backing up all the threads since 2001, one at a time, (!) and it's going to take a while.
We are up to July 2007. We have been told that the MSN Groups service will close in February 2009. We have another server and will be updating you soon on the transfer progress. | This is an independent, international, online, support group for all those affected by Chordoma.
There is no charge for the use of this website and we do not fundraise for the site. This is a peer group, who focus on day to day management of the disease and treatments.
This site cannot replace professional, medical advice. We welcome patients, caregivers, family and friends. More | Trouble accessing this site? Contact us for help here. |
Important Announcement
