erinreznik

Hi! I was recently diagnosed (after quite a journey to get to a diagnosis) with paroxysmal hemicrania. I learned about this group from NPR and became excited to hear there is a group for people who have pain similar to mine. I know paroxysmal hemicrania but I was wondering if ClusterBusters could be a resource. Any thoughts on if I belong here? Any one else who is non-CH but in a similar situation still get resources from this group? thank you! erin