DrLisk Posted March 1, 2016 Share Posted March 1, 2016 I am a neurologist in Pasadena, CA and am a cluster headahce sufferer myself. I am new to the group but wanted to say hello. I will be at the conference in Austin. I am currently enrolling my clinic in a cluster headache trial. We have not had a site visit or review of the protocl yet but are waiting to see if our site gets added into the clinical trial. Quote Link to comment Share on other sites More sharing options...
Dallas Denny Posted March 2, 2016 Share Posted March 2, 2016 Welcome to the community Doc! I was diagnosed in Dallas by a neurologist that was also a CH'er! I'll look forward to meeting you in Austin! Dallas Denny Quote Link to comment Share on other sites More sharing options...
jms Posted March 2, 2016 Share Posted March 2, 2016 Welcome - of course no one is actually glad to welcome one who is unfortunately affected by CH, but this is the place to come to where people understand. I hope your clinic makes the enrollment in a CH trial. This forum has been a great resource for information on CH and hopefully will lead to the ultimate goal - a cure! Quote Link to comment Share on other sites More sharing options...
CHfather Posted March 2, 2016 Share Posted March 2, 2016 Welcome! I look forward to your participation here! Thank you for coming here. Quote Link to comment Share on other sites More sharing options...
spiny Posted March 2, 2016 Share Posted March 2, 2016 Great to have you here DrLisk. Quote Link to comment Share on other sites More sharing options...
Bejeeber Posted March 2, 2016 Share Posted March 2, 2016 WHAT THEY SAID. A boon for us to have a neurologist CH'er in attendance! Quote Link to comment Share on other sites More sharing options...
surgeonasim Posted March 4, 2016 Share Posted March 4, 2016 Yes Jeebs . I suddenly feel sooo guilty... Never happy to hear aoout anyone's pain...but for all CHers' sake. I hope and pray Dr Lisk finds a cure for himself and us all. Welcome to the forum Doc. You are going to be fine. Quote Link to comment Share on other sites More sharing options...
sierra Posted April 12, 2016 Share Posted April 12, 2016 Welcome Doc, I would not wish this condition on anyone, but I do wish there were more neuro's who were as interested as you are in finding new or alternate ways to treat CH. I have been to four different neuro's in the Detroit area and none of them were any help. The more Doctors we can get to attend, the better, try and bring some of your fellow neuro's. Quote Link to comment Share on other sites More sharing options...
Lallangoti Posted April 12, 2016 Share Posted April 12, 2016 I am a neurologist in Pasadena, CA and am a cluster headahce sufferer myself. I am new to the group but wanted to say hello. I will be at the conference in Austin. I am currently enrolling my clinic in a cluster headache trial. We have not had a site visit or review of the protocl yet but are waiting to see if our site gets added into the clinical trial. What is the nature of the trial? Quote Link to comment Share on other sites More sharing options...
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