Online Chordoma Support Group
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.
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
Contact with support group
Please contact the Chordoma support group here:
Originally Posted by peg1974
We have been trying to contact you but email is bouncing.
The online Chordoma Support Group
The Chordoma support group has moved to
Hello ! My name is Betsy and I am a 7 year clival chordoma survivor! I had 3 resections (brain surgeries) and completed Proton Beam Radiation in 2005. I am looking for others who have walked the walk so to speak that I can communicate with.