Online Chordoma Support Group

[AnnCan]

http://groups.msn.com/Chordoma

This is an online support group for people affected by clival, spinal or sacral chordoma, a rare tumour occuring in about one in two million population.

[peg1974]

Hi my name is peggy and i have a nine year old son with chordoma and im want some advice on what it is and how can it be cured

[AnnCan]

Hi my name is peggy and i have a nine year old son with chordoma and im want some advice on what it is and how can it be cured

Please contact the Chordoma support group here:

http://groups.msn.com/chordoma

or here:

chordomamanagers@gmail.com

We have been trying to contact you but email is bouncing.

[AnnCan]

The Chordoma support group has moved to

www.chordomasupport.org