Trigeminal Neuralgia Testimonial after DTR 

I'm so happy for Kevin no one deserves such pain

Hey good idea next time. What did that doctor do to help you. Dont have to give the exact just a idea of what was done

I am suffering with Trigeminal Neuralgia. as of now I could hardly talk, it causes me a real pain. I am from the Philippines.

I started to think my jaw misalignment was ths reason for TN. Since I never had a concussion and I dont have MS, as stated the biggest reasons for the condition to come upon patients. I then felt as if my epilepsy started it, but my neurologist had told me no it doesnt. But about 2 years ago I started to think about my teeth being misbalanced, since now I literally have a slight lisp. Never had that before, I seriously feel this is the cause of it but I would like to know the correlation of that to the nerves in my brain. I have had an MRI, 2 actually, that showed no type of artery touching the nerve. So I was told that I wouldn't be a candidate for the MVD surgery. As I bite down on like a sandwich or pizza, the bite isnt effective to rip it off for me to chew, so usually I tear it with my fingers.

I AM SUFFERING WITH TN. I KNOW HOW YOU FEEL I JUST GOT DIAGNOSED I GOT FROM A DENTIST THAT DID NOT WHAT THEY WERE DOING I HAD IT FOR 19 YEARS BUT I DID NOT KNOW WHAT IT WAS UNTIL I SEEN A VIDEO ON RU-vid IT THE TEN WORST PAIN TO MEN

How can Canadians get help in Canada is there anyone here doing this treatment? 😢

How do you know when this will help TN? I just got diagnosed with TN, and it is more mild for now, but slowly gets worse and worse. I got an MRI showing I have an artery on both sides of my head touching my trigeminal nerves, which seems to be the classic cause, but I’m wondering if correcting my bite would actually help me. I did have TMJ pain last year or so that I got the bite testing done for, and was about to schedule to get it corrected, but then was told the cost and cancelled. Now I have TN pain this year after having a baby and don’t want to take anticonvulsants for it until my baby is weaned, so I’m suffering through the pain a few more months. Maybe it isn’t necessary though, and I should reconsider fixing my bite? I had had braces before like 15yrs ago, but my teeth have slightly moved. Could that slight change cause all this pain?

Dear Dr. Sutter, i am from Cyprus, my sister who has been enduring severe chronic facial pain for the past three years. Despite numerous medical consultations and even an MVD surgery in Germany, her discomfort persists, significantly impacting her quality of life. She's a single mother with an autistic child, and the ongoing pain has taken a toll on her mental and physical health. Having come across your expertise in Disclusion Time Reduction (DTR) therapy, I am keen on exploring this as a potential solution to alleviate her suffering. She is unable to travel that far in her condition, i cannot find this method here , what can we do ?

Rhonda Long. I got your notification but cannot respond for whatever reason

Hi I’m currently in the uk and would like to book an appointment to come to the US and visit yourself. I’ve watched quite a few videos that you’ve posted and feel like you could definitely help me, Please could you point me in the right direction to get into contact with yourself? Thanks Dr!

Can you tell me what the cost of this treatment is? I have dental insurance but not aware if it will cover the costs. Please advise.

Hi Dr, what exactly is DTR treatment? Is it a splint? What do you think about getting jaw expansion first with soemthing like MSE expander and then using DTR therapy? I have a narrow jaw which makes me clench at night due to airway blockage so would widening arch need to be done first? Thank you !

Can you help with atypical trigeminal neuralgia? I have constant pain in many of my gums.

Does having the treatments stop the "I have an artery on both sides of my head touching my trigeminal nerves" from touching?

Do you have any recommendations for a dentist in chicago Illinois who does DTR?

I'm moving to Canada.

Is this TN1 or atypical?

M suffering from menier's disease Is there any hope in India?