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

    costs:  none for Social Security folks.

    Don't know about everyone else.

    Wish we all had universal health care like those on Social Security.

    Without that I would be in debt prison even though I worked like a dog all my life, but for myself for little or no benefits. 

    Did an 8 year stint as a public school teacher. That's how I got enough benefits to cover the TN surgeries.

    .

     

    • Posted

      Alicot,

      I don't know how old u r but it isn't social Security that gives money, its medicare.

      A lot of people don't know but medicare can begin as early as age 62. At age 65, social security will give extra money in order to pay medicare part B.

      If a person drew social security at 62 and went back to work that person at age 65 will still get 93.3 percent and a lot of people at age 66 still working will get 100percent.

      God bless,

      us and keep us and give us peace

    • Posted

      Lee12629,

      Elen, she had a young boy about ten years old on her program who had this awful TN, so age is but a number.

      Get as mmany opinions and suggestions on procedures that u can.

      ]rocedures all depend on how much experience neurosurgeon have.

      I will tell u to go see 1, ,2, ,3,,4, 5, 6 neurologist and neurosurgeon before you let anyone do anything to you .

      Make sure u ask doctors who perform other procedures how they r done.

      God bless

      us and keep us and give us peace

    • Posted

      Lee12629,

      Make appointment with a neurologist .

      Part of the presidents healthcare plan made all insurance so that u won't have to get a referrel from your primary care physician,

      But many want ur records from the last dictor who worked on u.

      So your previos doctor and tell them to send your information in a fax to whatever dr. You want to see.

      God bless

      us and keep us and give us peace

    • Posted

      Amen to that,we have a 6000 deductable before it pays for anything.
    • Posted

      I dont know anyone who can get medicare at 62. Its 65.
    • Posted

      Is it covered with Medicaid because I get ssi I have medicaid that's the only insurance I have and I can't afford to pay for it.

  • Posted

    IsurvivedTN,

    I was zo glade that Cyberknife worked for u.

    I wish I had known of this procedure b4 I had undergone MVD surgery.

    I hope everything stays positive for u, and all the others who have had other procedures done.

    God bless

    us and keep us and give us peace.

  • Posted

    I've had TN for almost 2 years now. This year I finally saw a pain management dr and all we've done was try different medications and none of them work. I'm only 20 and have had it before I even turned 19. Thank you for sharing your story, it really gives me hope.

    • Posted

      So young and with TN! I got it at age 60.  And like you none of the meds worked.  I did Radiofrequecy surgery..works well and is perhaps the least invasive. Check it out...
    • Posted

      Thank you! I'll definitely look into it.

  • Posted

    IsurvivedTN,

    Anything new in discovery for TN

    God bless

    us and keep us and give us peace

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