How I survived, researched, and overcame Trigeminal Neuralgia

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I'm going to tell my story so it will be kind of long, but has a great end ing..promise;-). In 2011, at age 29, I noticed a sharp pain when I brushed my teeth. At the time, like many others, I assumed it was dental related. I went to the dentist and they found nothing wrong. As the weeks went on, the pain started happening when I talked, brushed, washed my face, clenched my teeth, slept, smiled, if the wind blew hard, etc. It was the WORST pain of my life. It felt like an electric shock going off in my the left side of my face by my jaw. Sometimes the pain would be just a quick stab, and other times the pain would vibrate through my face and all I could do was stop all motion and wait until it passed. I would even wake up out of my sleep sometimes from the pain if I accidentally turned on my left side. The pain would last for weeks then go away for a week and I thought it was over. BIG MISTAKE! It came back with a vengeance.

After many painful days and nights, I started looking up my symptoms on the internet (yeah for Google) and the same diagnosis kept coming up..Trigeminal Neuralgia. I was confused because although my symptoms matched, it said that this disease usually showed itself in older individuals and I was only 29. I made an appointment with my physician and after cruelly poking my facing with his finger after I told him my symptoms, he confirmed that although it was rare for my age, I had TN. He prescribed me a steroid prescription and sent me on my way. No further explanation. If I had not already researched this, I would have been lost. So I took the pills, and besides making me gain a couple pounds, the pain remained. By now, I had researched so much about TN, I felt like an expert. I called my physician and asked to be referred to a Neurologist.

Long story short on this part, Before the Neurologist saw me , he sent me to get MRI which was clean so no MS and he spent all of three minutes seeing me, told me I had TN, gave me a prescription for TEGRETOL, and sent me on my way. No further explanation about my disease. He failed to tell me that the Tegretol would make me CRAZY!!!!!!!!! I am a teacher and the Tegretol had me so nuts, some days I couldn't even function. I have a 2 1/2 yr old and between the Tegretol and pain, I'm sure I was a pain for my child.

The Tegretol did help a little but I could not see myself having to live the rest of my life on Tegretol. It would have been HELL!!! I had already researched Gamma Ray treatment and surgery to cut skull open and put something in between nerve and blood vessel. Both did not appeal to me.

THIS IS WHEN IT GETS GOOD!!! I live in Alabama (US) and one day when I was researching, I saw that a Neurosurgeon in Birmingham, AL, Dr. Swaid N. Swaid does something called CYBERKNIFE TREATMENT. CYBERKNIFE is a non invasive radio surgery that is used to treat everything from cancerous and non cancerous tumors and TRIGEMINAL NEURALGIA!!! It beams a high dose of radiation to the area that precisely goes to the spot needed. I felt like this was my only hope. I called to make an appointment and luckily, a referral was not needed since my Dr. and Neurologist were of no help. I went to see Dr. Swaid the next month and he was the first Dr. to sit down and explain exactly what I had and the treatment options. Because of my age, he thought the brain surgery was better but I told him that I would rather do the Cyberknife. The brain surgery, besides be invasive, would make me have to take 2-3 weeks to recuperate while Cyberknife, I would go into treatment 1-5 times, depending on my xray of my nerves and lay on the table for 45 minutes and left the robot do it's thing and get up and be just fine. No pain, no cutting!

Made my appointment for Cyberknife, went in to talk to Radiologist who told me Cyberknife was just as good as the invasive method. He actually drew me a picture to describe what was going on in my face and told me that I was suffering from Trigeminal Neuralgia in my 3rd trigeminal nerve (the one by the lower jawline). After they looked at my

Xray, they decided I only needed one treatment. They made a mold of my face that is like a net they had to put on my face to keep me prefectly still. I laid on the table, listened to the music of my choice, and listened to the robotic arm buzz over my face for @ 40 minutes. Got up and was on my way. I was warned that the results would not be

immediate. The radiation slowly kills the nerve that is being affected. But month after month, sure enough, the pain became less and less. I went to see Dr. Swaid every 3 month for the next 9 months. He said by the 6th month, if the pain was gone, most likely it would be gone forever. The only side effect I have is that sometimes when I chew on that side of my face, because the nerve was killed, I get a little painless tightening in my jaw (like lock jaw) for a few seconds. I laugh because I'll take that anyday over TN and it only happens usually when I chew something really tough on that side

I have been pain free for about a year now but I'll never forget the worst part of my life. I encourage anyone dealing with TN TO DO YOUR RESEARCH and do what is best for you. If you have a Hospital that offers Cyberknife in your area, I encourage you to look into it. Never give up hope that you can't overcome this and know that there are others that have had to deal with this too....You DO NOT have to settle for taking medication for this disease for the rest of your life! RESEARCH, RESEARCH RESEARCH. God Bless!!!

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  • Posted

    I had a pain that I thought was my tooth but it turned out to be nothing wrong, then the pain got worse in my face , again I thought it was a tooth. I decided to go to my primary Doctor to see if he knew what was going on. They sent me to have an MRI and it showed that something was going on with my nerve. I suffered for 4 months before they knew it was TN and it was the worse pain ever, I cried all the time because I felt like I was being shocked and it was really painful. So the Doctor referred me to a Doctor at John's Hopkins Hospital in BALTIMORE Maryland and he is the best ( Dr. Lim) . So far I have been pain free for about 18 months now and I thank God and my Doctors for everything that they have done for me.

  • Posted

    i went slow like down a bit once every few weeks. i cant remember exactly but it went faster than I thought it would. to be safe, I would just reversed the process. like if you went up 100ml one everyweek or so just reverse it.

    • Posted

      that should say"once" every week or so, not "one"

  • Posted

    Hi there and thanks for sharing your experience which pretty much mirrors my own. I was diagnosed about three years ago with symptoms that almost exactly mirror your own, luckily for me my GP was pretty switched on and after going down the dental route i too was prescribed tegratol and it was a life saver. Unfortunately as the condition progressed i had to up the dose incrementally from 500 mg a day to 600 mg a day and it turned me into a zombie that could easily sleep for 14 hours a day and left me completely unable to work. I live in western australia and unfortunately it took me two and a half years before I managed to get the Cyber Knife treatment. I'm currently 55 and like you I wasn't keen on the MVD option and I also became an armchair expert on my condition thanks to google. I had my procedure last december and my experience was identical to yours. Initially I was very disappointed since for several months my pain was as bad if not worse than it had been before, especially as I was trying to wean myself off the dreaded tegratol. I was warned that this procedure could result in facial numbness of varying degrees in about thirty percent of patients but I had none, then four months later I started to experience some facial tingling not unlike that you experience as novocane wears off after a trip to the dentist. At this point I stopped taking Tegratol and have been completely pain free for about six weeks. Now it is possible that that I have merely gone into a period of remission but I'm feeling very hopeful. I can recommend this treatment and if you are unlucky enough to have an unsuccessful outcome you always have MVD to fall back on. This is the WORST condition known to mankind and I'm so grateful that I live in a time where there are drugs and treatments available because without them I would have reached for the shotgun without a shadow of a doubt. Good luck and bottomless empathy to my fellow sufferers, stay safe...

    • Posted

      Hi. My pain came back in 2020 and I took alot of meds that did not work well. I ended up having MVD in April and have been pain free since with just numbness on that side of my face.

  • Posted

    Hello!

    Thank you for sharing your journey. I was recently diagnised with TN after sufferring for 3 months.

    your story helps in deciding my treatment plan.

    Was there any diet plan or excercise that helped? Please let me know if there are any home remedies that helped.

    Thank you

    • Posted

      Hi. My pain came back in 2020 and I took alot of meds that did not work well. I ended up having MVD in April and have been pain free since with just numbness on that side of my face.

  • Edited

    Hiya I am at the begining of my TN journey after earned also a fibro diagnosis after Whipalash 2 years ago. I agree the drugs just mess so much with your life and I want to avoid any surgery or beams. I am still learning about what this may mean for my future but so far the MRIs came normal so no MS (thank you).

    On treatment has anyone tried medical CBD or Cannabis from a private GP, there lots here in the UK, but I am more interested if anyone had any feedback in using these treatments I am on a low dose of amitriptyline (an antidepressent that works on nerve pain for the Fibro) because otherwise I am a zomby and with the TN Diagnosis I will be offered many of the drugs mentioned before which have horrible side effects.

    • Edited

      Hi. My pain came back in 2020 and I took alot of meds that did not work well. I ended up having MVD in April and have been pain free since with just numbness on that side of my face.

    • Posted

      wow you had a long time pain-free from Cyberknife, about 9 years or so? Where did you have the MVD surgury done? I am looking into this. i am in beginning of this process, getting the MRI today!

  • Posted

    how are you doing after all these years after Cyberknife? i have had this pain for a week and its the most horrible pain, i am already looking into treatment. my pain is constant, it doesn't go away 😦

    • Posted

      Hi. My pain came back in 2020 and I took alot of meds that did not work well. I ended up having MVD in April and have been pain free since with just numbness on that side of my face.

  • Posted

    thank you! you gave me hope. im 39 and was given diagnosis of TN yesterday by my doctor. as i started reading and researching i got more and more depressed. why would someone young and healthy have it for no reason? ots so debilitating and the last thing i want to do is take medication, as its so damaging to liver, kidneys, hair, nails etc but no other pain relief works. its a trap tht appeared out of nowhere

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