MoxieGirl Posted February 14, 2013 Share Posted February 14, 2013 Does anyone use Twitter? If so, there are several people commenting on cluster headaches there, an one person has set up a @clusterheads - called ClusterMeetingPlace, and reposts a lot of cluster related tweets. Some hash-tags that are starting to pop up: #clusterheads #clusterheadache @UKcluster (Cluster Headaches UK) MG Quote Link to comment Share on other sites More sharing options...
MoxieGirl Posted February 14, 2013 Author Share Posted February 14, 2013 Also, just found this FaceBook group.. https://www.facebook.com/groups/CHSupport/ Quote Link to comment Share on other sites More sharing options...
ClusterHeadSurvivor Posted February 15, 2013 Share Posted February 15, 2013 i know the girl who started the FB support group. I dont have FB. Dont want it. Too bad. Sounds awesome Quote Link to comment Share on other sites More sharing options...
Vickle Posted February 15, 2013 Share Posted February 15, 2013 I'm on twitter. Thanks for posting. VictoriaHames1 on twitter Quote Link to comment Share on other sites More sharing options...
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