Brian,
I'm a data junkie.
I'm always thinking of stats, and how to best present the real picture.
Do you think it would be possible to somehow depict the location of the OCF members and caregivers? It may give a visual that could be especially useful when trying to show how many people are afflicted with head and neck cancer in the states and across the globe to PBS, doctors, all types of venues. I noticed as a caregiver from the Buckeye state, that there seems to be a lot of us here from Ohio. This info could even help bring awareness to our health care system to show where there is a greater need for CCC's around the world that specialize in head and neck cancers. Many people travel hours to get to their CCC's. It would be great to help get good treatment where it's needed.
Or at the least to show what a need there is for help with transportation to treatment.

Maybe the location of members could be pulled from the profiles to be compiled and then could be used to make graphs/maps, etc. It might be a visual that people could use when they are guest speakers, and so on.

What do you think?


Dad had oral lichens planus, and oral leukoplakia before T2 SCC,2 nodes.
DX10/23/03
IMRT 12/29/03.30 rad,3 boost.
Brachytherapy 3/8-3/11/04.
Recurrence Nov07 Stage IV.
4 Surgeries
No rads, no chemo
I have oral lichens planus,
thrush,leukoplakia 2/20/08
6/2/08 biopsies "inflammation"