My Nonprofit Reviews
Review for Chordoma Foundation, Durham, NC, USA
I've been diagnosed with sacral chordoma in august. My doctor got me in contact with CF The Netherlands. Soon i took part in the facebook-group of Chordoma Survivors. In the early days after diagnosis, CF provided me with a lot of really very essential information. It helped me to make the right choices considering treatment. CF provides me with a whole support system: it gives me medical and practical information, but also gives me emotional support! It would have been a great difference if I had to go through this alone!!!