NORTHWEST NEUROLOGY

After a year with this place, they mess up appointments and are full of attitude towards their patients! My last straw was when they refused to let my husband join me like he had ALWAYS done. Their excuse was because he's not vaccinated, yet they jam pack the tiny waiting room... Let's use some common sense people!!
Dec 20th, 2021

If you’re looking for billing nightmares, then this is the group for you. They use their own labs without checking with you or your insurance company to see if they are covered. They then send you to collections without first calling you to help rectify your billing issues. Their credit collection company (Merchants) calls you up asking you for personal information without even identifying who they are first. I paid my bill directly with Northwest Neurology and still have creditors calling. Never again!
Nov 16th, 2021

I have doctor Gordon as my neurologist and he’s the best he’s very nice and respectful take Care well good of me
Aug 14th, 2021

I worked at northwest neurology for 3 weeks and they let me go because they were too lazy to train me. It was run terrible. They sent me to 3 different locations to work and each time no one knew what to do for me so I sat there. Do not work there. It is awful. Rude people in the office. I was in disbelief how they talked to their patients. Sandy is a terrible manager. She lied straight to my face about asking for a work pamphlet just to find out the next day she never had one for me.
Jan 8th, 2021

Katsamakis fired me in January. I have had MS since 1977. I could not afford health insurance (pre-existing condition) until the ACA in 2014, when I started seeing Dr. Katsamakis. Though I had many symptoms, I was basically strong and fairly able. With insurance I thought I would finally be able to get some of the big, expensive drugs that others spoke of — but no. Katsamakis told me that they would not help and only prescribed minor "picker uppers" and nothing more. In 2015 (by Katsamakis recommendation) I got major neurosurgery fusing 7 vertebrae in my neck, which only made me considerably worse. By now, I can barely sit up, I can't walk and need an electric cart to move. When last I saw him in January to ask if there might be anything new to help me, he became very agitated, snide and abusive -- yelling at me to get out and not come back, even yelling at the office staff to never accept another appointment from me while I sobbed. (The office staff was quite nice.)I realized that when challenged, you find out that he really doesn't know anything. I learned more from a couple of MS exercise classes at Neuro Balance than I learned in six years of seeing this egomaniac. And now we are all in lockdown, I have no neurologist and needless to say, I'm very discouraged. If I could give him negative stars, I would.
Dec 27th, 2020