Woobyjay Posted June 11, 2020 Share Posted June 11, 2020 Hey guys I live in CT. Just wondering if any cluster warriors live in ct or in the tri-state area? Quote Link to comment Share on other sites More sharing options...
Desperately Seeking Relief Posted June 11, 2020 Share Posted June 11, 2020 I am in CT. Just joined today. Suffering since 2011. Quote Link to comment Share on other sites More sharing options...
kat_92 Posted June 11, 2020 Share Posted June 11, 2020 @Desperately Seeking Relief Welcome to the forum! Quote Link to comment Share on other sites More sharing options...
Desperately Seeking Relief Posted June 11, 2020 Share Posted June 11, 2020 Thank you. Im hoping to find some relief. Something my drs at Yale havent been able to do in nearly 10yrs. Quote Link to comment Share on other sites More sharing options...
FunTimes Posted June 11, 2020 Share Posted June 11, 2020 Something to look into: https://clinicaltrials.gov/ct2/show/NCT02981173?cond=Cluster+Headache&cntry=US&draw=2&rank=6 1 Quote Link to comment Share on other sites More sharing options...
Dallas Denny Posted June 11, 2020 Share Posted June 11, 2020 @Woobyjay @Desperately Seeking Relief if ya'll maintain a presence on Facebook shoot me a PM and I can put you in touch with several clusterhead friends who live in NY, NH, and Mass.....can't recall any that are in Connecticut but the folks I know usually have at least one meet n greet a year for clusterheads in the new England area! Clusterbusters actually had a cocktail party in the works in NYC but I'm fairly certain that was postponed or canx due to covid. DD Quote Link to comment Share on other sites More sharing options...
jon019 Posted June 11, 2020 Share Posted June 11, 2020 6 hours ago, FunTimes said: Something to look into: https://clinicaltrials.gov/ct2/show/NCT02981173?cond=Cluster+Headache&cntry=US&draw=2&rank=6 YEAH!!!!...and this is at Yale 1 Quote Link to comment Share on other sites More sharing options...
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