Tha staff here is absolutely wonderful. Very helpful, and take care of each other. Very well run,…read moreand Dr. Woodrow is marvelous.

Dr. Krivosheya and staff are excellent. Went there for a catscan for my head (checkup after…read morecondition from childhood). The care and compassion I was shown was VERY professional. The nurses put up with me and my sense of humor (lol) and all were very attentive to my needs.

Ridiculous wait times. Cancellations at the last minute. A…read moredoctor that does not like to be challenged.

Dr. McPherson is an amazing old-school doctor who truly cares about his patients and provides…read morethorough compassionate care. I'm very fortunate to have him as my Mom's neurologist. He was able to diagnose and treat a vestibular disorder that had gone undiagnosed for years. He looks at the big picture and is willing to address issues that wouldn't normally be part of his practice. We thought she had plantar fasciitis, but he quickly ruled that out and had her cut down on the folate in her supplements. Her foot pain is gone. My Dad passed away last week and now my Mom has pneumonia. Dr. McPherson has been a huge support. He went above and beyond to keep my Mom out of the hospital by immediately calling her GP and stressing that admittance to the hospital would be detrimental to her health with her vestibular disorder and trauma of my Dad's death. He has been in contact with me daily and provided instructions for the care of Mom's pneumonia. I'm happy that my Mom is much better thanks to Dr. McPherson. We were planning to have my Dad's memorial 6 weeks from now but Dr. McPherson suggested that this would be too hard on my Mom. This was invaluable advice that we needed at a very vulnerable time. Just talking to him was very comforting for us. Please PM me if you have any questions. This Doctor is the best!!

Way too busy, the doc I saw , saw 5 other people in the hour I was there. He seemed to not care…read moreabout any of my concerns other than I was a pain management patient and blamed everything I came in for on my pain meds even when I told him I had the problems 3 years prior to being on the meds.No bedside manner, seems to hate his job

Doctors too busy. Keep making you change to a different one. Rush you in and out. Takes forever to…read moreget an appointment.

As a patient, I don't feel like I'm listened to. I keep…read morebeing told I have rebound or medication overuse headaches, and I don't. Twice I was told to stop all abortive meds to break the cycle, and twice it didn't work. Migraines run in my family. My brother and many of my cousins on my dad's side have them. This office keeps pushing infusions on me that I've made quite clear I don't want. They cost me about $600 out of pocket with insurance and they work less than 24 hours. This office has under medicated me and caused me unnecessary pain and suffering. I'm in several chronic migraine support groups and most people are prescribed (9) 100 mg Imitrex per month, and their doctor "recommends" they be broken in half to make them last a month. Maximum 200 mg per day. Or they are prescribed different forms (nasal spray, injection) of the same medicine, or they are prescribed 2 different kinds of abortive medicine to make them last a month. I have been prescribed (9) 50 mg Imitrex a month w/max 100 mg per day. Taking no more than 2x a week as prescribed, but if I get 2 bad migraines in a week (from weather or if I get my period and then have migraines for more than 2 days in the same week) and I need (2) 50 mg per migraine, that's half my prescription gone in a week. Since I'm taking half of what is maximally allowed in a day, then no wonder I don't feel well and I'm running out before 30 days. Yet this office treats me like a drug seeker and sends the message that it's my fault I have migraines because I take too much medication. Whenever I brought up additional treatment options to this office (such as described above), I was told no and only offered infusions, which as I stated above is not a good option for me, physically or financially. At one of my exams Jennifer Woods made a "joke" about "bilateral daiths, you must have been desperate." Yes, I was, because this office hasn't helped me. I was completely dropped in the middle of treatment because they no longer took my insurance and will not accept cash. I was forced to get a new neurologist in Brecksville who I had to wait months to see. So yes, I got fed up with trying a bunch of different off-label meds that did nothing for me and pierced my ears. The piercings worked for about a year, but when I became chronic again and the new anti-CGRP drugs came back out, this was the only reason (other than insurance) I came back to this office. And other than changing my anti-depressant, this office still hasn't helped me. I ended up getting samples of anti-CGRP from my PCP. Jennifer Woods has a terrible bedside manner. Making fun of someone's migraine piercings to someone who is struggling daily is wrong. With the anti-CGRP I'm finally down to 2x a week for triptans (except for my period) and this office will not help me out with any sorts of changes to abortive medications. I own a small business and I have 2 children that I homeschool. I don't have time to be laying in bed in a dark room vomiting because this office wants to push infusions that cost 1000s of dollars instead of prescribing me abortive medications in a reasonable manner. As a patient, I feel this office has done nothing but try and make money off my migraines, not to actually manage my disease and lessen my symptoms so I can live my life to the fullest. I write this in the hope that someone will take the time to listen and perhaps the next patient can be spared some of what I've gone through the past 8 years. The staff (medical assistants, administrative, etc) has been incredible.