DrLisk Posted March 1, 2016 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
Dallas Denny Posted March 2, 2016 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
jms Posted March 2, 2016 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
CHfather Posted March 2, 2016 Posted March 2, 2016 Welcome! I look forward to your participation here! Thank you for coming here. Quote
Bejeeber Posted March 2, 2016 Posted March 2, 2016 WHAT THEY SAID. A boon for us to have a neurologist CH'er in attendance! Quote
surgeonasim Posted March 4, 2016 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
sierra Posted April 12, 2016 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
Lallangoti Posted April 12, 2016 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
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