Finding a great Neurologist


Research, Research, Research…..

Over the last 7 years it took me 3 tries to find the right neurologist. Sometimes it takes a few tries, and takes a few months to feel them out. But when you realize they are not helping you or hearing you, it time to move on or find a new neurologist. The biggest thing is find the right doctor that fits your personality, your needs and fits your family’s needs too.

You can actually do a lot of research online. I found the neurologist that I have now by doing a lot of research online and looking at reviews. There is a lot of websites that  have reviews on doctors. Of course there will be those few bad reviews but if a doctor has mostly bad reviews then it’s probably best to look at a different doctor.

The last neurologist I had was referred by my primary doctor and after a year of struggling with her and the clinic I decided to find a different neurologist. So not all referrals mean they will be great neurologists, not to say they might be.

Once you have the appointment with your neurologist, make sure to ask questions. You can never ask enough questions. If you have a doctor that’s not talkative and doesn’t say much and just want’s to give you a bunch of medication with out even talking to you, that’s probably not the right doctor, I had a few doctors like this, it was extremely frustrating. I would be in with the doctor for 5 minutes and all i came out with was new medications.

Finding the right doctor can be tricky but within a month or two you should know if it’s the right fit. The neurologist I have now, I loved him straight away, i’ve been seeing him for over a year now. He was the only doctor that has told me about upcoming treatments they are developing, like they are coming out with an injection you can take that will prevent migraines for up to 6 months to a year. It hasn’t come out yet but he always keeps me updated.  He lets me talk and then he tells me what he thinks, and then decides with me. When I have problems at home he responds the same day and even calls me himself, not his nurse call me like I’ve had with previous doctors.

When your having severe migraines or even bad headaches the best thing to do is get in the care of a really good neurologist. The first thing they will do is order a CT scan or MRI if you haven’t had one done recently. When you do see a new doctor it’s always best to get your records transferred so they can see the whole picture, and you don’t have to explain from the beginning.  Now it’s not as hard as it was years ago because they have this electronic system called “Care everywhere” which most hospitals and clinics have, you just have to give them permission.  So when I transferred doctors it was easy.

So when finding a neurologist my tips are: 

  • Research
  • Try get a referral from your primary care doctor, although it’s not always needed. 
  • Consider the experience of the neurologist 
  • Review patient survey reviews online for the doctor you are seeing
  • Quality of the hospital or clinic the neurologist is located at
  • Check your insurance, you don’t what any surprises 
  • The style of the doctor (i.e Communication etc.)
  • A doctor that respects your values, religious decisions etc.
  • Decide if gender is an issue (Ex. Some people prefer a female doctor if they are female etc.


So in conclusion, finding the right neurologist for you is very important and is the best way to start getting you feeling comfortable. They can prescribe a lot of different medications that can prevent migraines and headaches and medications that you can take when you get the migraines that can make the pain and nausea bearable. So when you suffer from these chronic migraines it’s very important to be in the care of a great neurologist. 

If you can’t see a neurologist due to insurance cost, try to see a primary care doctor because they can sometimes prescribe some medications to help for nausea and may be able to help you with other medications with your migraines especially if they know about your insurance problems. 

One last thing I want to add is, for those of you who don’t have insurance and can’t afford to see a neurologist but are really suffering. There are programs at a lot of hospitals for people who don’t have insurance or people who don’t have much insurance coverage. They go based of your income and expenses. They will cover 20 %, 50% or 100% of your bill based off your income. So if you think you can’t afford it, just call the hospital or clinic up and ask if they have this. A lot of private clinics don’t offer this, but all the main hospitals seem to in my experience. I have Medicaid now, but a few years back this was the only way I was able to get care was with these programs. 


If you have any questions please comment below or contact me. 


Thanks for reading 



*Disclaimer* I am not a doctor or health care professional, I’m just sharing and writing about my personal experiences and offering advice.




Published by

Lisa Wilson

I’m 33 years old and have been suffering from Chronic Migraines for 7 years. I have had migraines all my life, the first one was when I was in 4th grade, and as I got older they got worse. My migraines turned into chronic migraines 7 years ago and have become so debilitating that I can no longer work or have much of a social life. Bright lights and fluorescent lights are a major trigger, so I have to wear dark sunglasses most of the time. Because of that, I can no longer work, go shopping or be outside for a long time. Over the last 7 years I’ve learned how to live with this disease. Many people don’t understand the pain & sickness because Chronic Migraines are a silent disease. I get migraines 3-4 times a day, I loose my vision, and get very nauseous and confused. The only thing I can do when this happens is take my medications and sleep. I’ve been trying to get disability for 7 years now & had no luck. The problem with this illness is because you can’t see it like a broken arm or leg etc. Everyone thinks it’s not a big deal. Unless you have experienced this, many will never understand. To be honest, I wouldn’t want them to. This disease is a nightmare and wouldn’t want anyone else to go through this. I have suffered so long and am still suffering, that I have depression now. After 7 years I have learned a lot of information and tricks, and that’s what I want to share. My goal is to help others get through this day by day, because I understand what your going through. I understand the excruciating pain, the times where you don’t want to move your head because it feels like a cement block. I understand all the times people have passed you off because they think your exaggerating or being lazy. I understand all those times the doctors have just given up on you. I have had countless tears over the last 7 years. I have a great family and I try and get by with what I have and that’s what’s important. If I could I would start a charity or organization for people with Chronic Migraines so we wouldn’t have to rely on the government when we simply cannot work because the moment we start a job within 10 min we would have a migraine. I sympathize with all of you. I have been through it all. I’ve tried many treatments and medications and tried many natural ways to help. I’ve learned a lot over the last 7 years and I want to share and help others in need as much as I can. I want to share what has worked and what hasn’t, Tricks that make the headaches and migraines get better, and information on migraines and the different types of migraines. My mission is I want to help others that suffer like I do. If I help 1 person that will be enough for me. God Bless

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