Dr Tarvez Tucker at UK Medical Center in Lexington KY
Question:
Boy!! Where do we get these "healers". My son is an auto technician with Chevrolet. He’s got his degree in automotive tech and continues with his education as cars get more complex. HIS doctor told him… "You’re pretty smart for a mechanic." Needless to say he’s still doc shopping. Do you think ASHM could make the Best Seller List if we compiled anecdotal accounts of our worst office visits? Chrissy, you can be the first to submit your loser! Liz
– Hide quoted text — Show quoted text -I live in Elizabethtown KY. About 20 miles from Ft Knox. It’s about 1hr or just a little more to Bowling Green. It would be a dream come true.(iv infusion) I have been without any meds other than triptans for like 50 days now. My longtime neuro closed his office practice in DEC but continued to fill scripts till Jan. (this is such a long story, stop if you need too) My Dad is an investigator for the state medical licensenure (sp) board in Western KY. So, i asked him to check out the three docs in our town. Two have current litigation pending (no details) and the third (who I went to see) had a case for patient abuse (physical) dismissed against him. Great choices I know. Well, Dr Oropilla did nothing but YELL about my previous doc. They had been neighbors and didn’t get along. No, he never worked with him, and did not know how his treatment plans worked. He also told me that he would never prescribe butabital and he had no clue why anyone would. He did not understand why I rotated my triptans between migraines. He told me that the ocipital nerve blocks that I have had in the past (and worked great) were inefectual for my "type" of migraine and he would not give me an order for any. Then he ended the hour long torture by telling me that If i were to seek treatment at the hospital for my migraines, then I would be labeled a drug user. What an asshole. The only question he did answer, was to tell me that he did not suffer from migraines. I pretty much need you to walk in my shoes to understand me…know what I mean? And while I am on a roll, he told me I was fat…not overweight…fat. OMG…It must have just snuck up on me while I was waiting in your make shift office. I thought that was the final cherry on my little rude sundae. Chris
Response:
I live in Elizabethtown KY. About 20 miles from Ft Knox. It’s about 1hr or just a little more to Bowling Green. It would be a dream come true.(iv infusion) I have been without any meds other than triptans for like 50 days now. My longtime neuro closed his office practice in DEC but continued to fill scripts till Jan. (this is such a long story, stop if you need too) My Dad is an investigator for the state medical licensenure (sp) board in Western KY. So, i asked him to check out the three docs in our town. Two have current litigation pending (no details) and the third (who I went to see) had a case for patient abuse (physical) dismissed against him. Great choices I know. Well, Dr Oropilla did nothing but YELL about my previous doc. They had been neighbors and didn’t get along. No, he never worked with him, and did not know how his treatment plans worked. He also told me that he would never prescribe butabital and he had no clue why anyone would. He did not understand why I rotated my triptans between migraines. He told me that the ocipital nerve blocks that I have had in the past (and worked great) were inefectual for my "type" of migraine and he would not give me an order for any. Then he ended the hour long torture by telling me that If i were to seek treatment at the hospital for my migraines, then I would be labeled a drug user. What an asshole. The only question he did answer, was to tell me that he did not suffer from migraines. I pretty much need you to walk in my shoes to understand me…know what I mean? And while I am on a roll, he told me I was fat…not overweight…fat. OMG…It must have just snuck up on me while I was waiting in your make shift office. I thought that was the final cherry on my little rude sundae. Chris
Response:
I will let you all know. My appt is 02MAY05. I am seeing her because my "new" neuro refused to treat me. He told me has has no success with patients like "me". Whatever that meant. He told me to try Lexington. It just sucks because its 80 miles from my house.
I’d go if it weren’t a bizillion miles from my house. I’m north of Toronto. She sounds like a dream come true. IV infusion suite so you don’t have to go to the ER? FINALLY someone who understands…sorry you’re so far away too. I will keep you informed. There is so little in the way of good treatment centers in KY (that I am aware of).
Good luck Chris. Where are you? I have great-nieces and nephews in the Bowling Green area. (Smith’s Grove.) Dana
Response:
I will let you all know. My appt is 02MAY05. I am seeing her because my "new" neuro refused to treat me. He told me has has no success with patients like "me". Whatever that meant. He told me to try Lexington. It just sucks because its 80 miles from my house. I will keep you informed. There is so little in the way of good treatment centers in KY (that I am aware of). Thanks, Chris
Response:
Has anyone see this doctor or have any information about her? Thanks, Chris
Response:
Has anyone see this doctor or have any information about her? Thanks, Chris
Found this: http://www.uky.edu/PR/News/050421_headache_center.htm Sounds promising for those who live in that area, especially the fact that they’ll even give you a treatment that would normally involve the ER. ~Sage —-== Posted via Newsfeeds.Com – Unlimited-Uncensored-Secure Usenet News==—- http://www.newsfeeds.com The #1 Newsgroup Service in the World! 120,000+ Newsgroups —-= East and West-Coast Server Farms – Total Privacy via Encryption =—-
Response:
– Hide quoted text — Show quoted text – Has anyone see this doctor or have any information about her? Thanks, Chris Found this: http://www.uky.edu/PR/News/050421_headache_center.htm Sounds promising for those who live in that area, especially the fact that they’ll even give you a treatment that would normally involve the ER. ~Sage
I just went to the site, read the stuff and saw the picture. I swear she was at UCSF under Vicious Lord Raskin while i was seeing him. He used to allow certain students in on his appts, and i swear she was one of them. I remember the faces of the students cuz i was always so relieved to see that they were there. He was always gracious and courteous while they were observing. He also allowed them to ask me questions (i’d told him that was hunky-dory) and he also allowed them to scope my eyes (apparently there is scar tissue behind my left from the surgery.) Anywho, i would favor her for having studied neuro at UCSF….she will know more than the average bear about migraine and the meds to try. Good luck, Chris! And PLEASE, let us know how your appt. went!!!! Deep peace, Lavon
Response:
I will let you all know. My appt is 02MAY05. I am seeing her because my "new" neuro refused to treat me. He told me has has no success with patients like "me". Whatever that meant. He told me to try Lexington. It just sucks because its 80 miles from my house. I will keep you informed. There is so little in the way of good treatment centers in KY (that I am aware of). Thanks, Chris
OH NO Chrissy, How awful! I can relate to that. My old neuro. after many unsucessful attempts at treating me told me that he was afraid he was going to have to send me on my way. He was a little bit of a jerk about it. He then felt bad for me, and so then he did my paperwork for me to get disability {the drs. portion of} , we had to get the rest of it done,of course. I’m what they call "a difficult patient to treat" So you are probably one as well. He problably didnt mean it to come out the wrong way, then again I could be wrong. As there are many drs./specialists out there that dont know their’ @ss from a hole in the ground. I sure hope you get treated the best as possible in the future. BTW FWIW My neuro I currently see is 3 hours away from me. sigh. MM {Migraine Momma}
Response:
GREAT! Thank you for the update, Chris!!! I think hope of that kind is worth much more than monetary value…. deep peace, Lavon
– Hide quoted text — Show quoted text – Just wanted to update on my visit to Dr. Tucker and the UK Headache Clinic in Lexington. I had no idea what "clinic" meant in this particular setting. Apparently it meant that everyone showed up at one time and you were seen in the order in which you signed in. We got there about 10:30 (appt was at 11am, person who made the appt told me to be there by 10:30 to fill out paperwork) and saw the Dr at 1pm. I saw the nurse first, Nadine. She was great. Asked detailed questions about my migraines, any meds that I had taken, which ones worked and the ones that didn’t. Dr. Tucker was fab. Very interested in my migraines and how they started, what the trigers were, what was I doing to control them. She gave me Celebrex, Amitriptyline, Clonzapam, and Maxalt. I had good success with Vioxx in the past so the thought the Celebrex would be a good alternative. She asked me about the Topamax. I explained that I was up to 400 mg a day and that it just stopped working, and that I couldn’t deal with the tingling and my hair falling out. She asked me if i wanted to try Botox. She said to call her back in ten days to see if the ins co would pay for it. It’s 800 bucks. She did write me an order for the occipital nerve blocks. That worked wonders for me in the past. She asked me to wait though until she found out about the Botox. All in all a good visit. I don’t think I would ever use the infusion treatment they offer. It was 170 miles round trip for me to go up there. I could never drive that far with a raging migraine. She understood that. FWIW, I would drive up there again to see her. Chris
Response:
Just wanted to update on my visit to Dr. Tucker and the UK Headache Clinic in Lexington. I had no idea what "clinic" meant in this particular setting. Apparently it meant that everyone showed up at one time and you were seen in the order in which you signed in. We got there about 10:30 (appt was at 11am, person who made the appt told me to be there by 10:30 to fill out paperwork) and saw the Dr at 1pm. I saw the nurse first, Nadine. She was great. Asked detailed questions about my migraines, any meds that I had taken, which ones worked and the ones that didn’t. Dr. Tucker was fab. Very interested in my migraines and how they started, what the trigers were, what was I doing to control them. She gave me Celebrex, Amitriptyline, Clonzapam, and Maxalt. I had good success with Vioxx in the past so the thought the Celebrex would be a good alternative. She asked me about the Topamax. I explained that I was up to 400 mg a day and that it just stopped working, and that I couldn’t deal with the tingling and my hair falling out. She asked me if i wanted to try Botox. She said to call her back in ten days to see if the ins co would pay for it. It’s 800 bucks. She did write me an order for the occipital nerve blocks. That worked wonders for me in the past. She asked me to wait though until she found out about the Botox. All in all a good visit. I don’t think I would ever use the infusion treatment they offer. It was 170 miles round trip for me to go up there. I could never drive that far with a raging migraine. She understood that. FWIW, I would drive up there again to see her. Chris
Response:
Wow Chris. Sounds like a great place. I found a press release about her and the clinic on the web. Wish I lived closer. Keep us abreast of your progress. Joy
) http://www.uky.edu/PR/News/050421_headache_center.htm – Hide quoted text — Show quoted text – GREAT! Thank you for the update, Chris!!! I think hope of that kind is worth much more than monetary value…. deep peace, Lavon Just wanted to update on my visit to Dr. Tucker and the UK Headache Clinic in Lexington. I had no idea what "clinic" meant in this particular setting. Apparently it meant that everyone showed up at one time and you were seen in the order in which you signed in. We got there about 10:30 (appt was at 11am, person who made the appt told me to be there by 10:30 to fill out paperwork) and saw the Dr at 1pm. I saw the nurse first, Nadine. She was great. Asked detailed questions about my migraines, any meds that I had taken, which ones worked and the ones that didn’t. Dr. Tucker was fab. Very interested in my migraines and how they started, what the trigers were, what was I doing to control them. She gave me Celebrex, Amitriptyline, Clonzapam, and Maxalt. I had good success with Vioxx in the past so the thought the Celebrex would be a good alternative. She asked me about the Topamax. I explained that I was up to 400 mg a day and that it just stopped working, and that I couldn’t deal with the tingling and my hair falling out. She asked me if i wanted to try Botox. She said to call her back in ten days to see if the ins co would pay for it. It’s 800 bucks. She did write me an order for the occipital nerve blocks. That worked wonders for me in the past. She asked me to wait though until she found out about the Botox. All in all a good visit. I don’t think I would ever use the infusion treatment they offer. It was 170 miles round trip for me to go up there. I could never drive that far with a raging migraine. She understood that. FWIW, I would drive up there again to see her. Chris
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