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!!!
26 likes, 244 replies
lisa07071 IsurvivedTN
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IsurvivedTN lisa07071
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jimmyk1595 lisa07071
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joe09732 jimmyk1595
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I am truely sorry for all the pain and suffering you have had to endure. Especially at such a young age. It's not fair. You are in my prayers.
lisa07071 IsurvivedTN
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lisa07071 jimmyk1595
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nurseAngela lisa07071
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lisa07071 nurseAngela
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tali. nurseAngela
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Hi Angela,
Can you please describe where exactly you feel pain? And for how long it lasts? Also, does "TN type 2" is a professional diagnose given by a doctor?
I am dealing with an insufferable pain for over 3 years (I’m 53 yo) visited our country top neurologists and neurosurgeon who couldn’t get to a precise diagnose. My symptoms are very similar to TN however it is not the classic case (according the Doctors and Professors). The pain is in the left side of my face and head. It’s like someone is stabbing, burning, electrocute me. It can last for hours and days. I mean, I’m always in pain, there’s no break and usually it’s an extreme one (it’s very unpredictable and random). The pains appears around my ear, eye, nose, upper mouth, upper and rear head and lower jaw (mandible). Cold or wind that hit my face would also cause pain. I’ve heard about MDV, Gamma knife and Cyber knife but I’m afraid that without an exact diagnose I won’t be able to go through one of them.
Looking forward to your reply, thank you!
nurseAngela tali.
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Am so sorry to hear as i know it is awful to be in chronic pain! I had surgery in 2005 as there was a large tumor wrapped all around my trigeminal nerve. The pain before surgery were just horrible headaches all the time but no nerve pain--after the surgery the right side of my face was numb to touch and has a constant burning sensation. my right eye also has a burning sensation. When i wake up i don't feel it but after a few hours it just starts to progress --the burning pain will also include pressure especially around my right eye. Feels like my eyeball is going to explode. I will also have a pressure sensation that again increases throughout the day. Only occasionally will i get the sharp stabbing electrical pain but it's very subtle compared to what most people deal with. I have tried all the meds.....Lyrica worked but the side effects were awful so i stopped after 6 weeks. Then when i stopped the pain was about 10 times worse for a few weeks as my body adjusted to not being on the med. It took awhile for me to figure out my triggers as mine weren't the classic ones. For whatever reason drinking ice cold water all the time helps. avoiding the sun and bright lights help. wind is awful! spicy foods trigger it! by the evening the pain is the worst and i can't wait to get into bed and put an ice pack on my face and go to sleep. stress makes my pain much worse so i try to keep that in mind. exercise is the only thing i've found that helps for whatever reason. pain is still there but much lower. from the research i've done the MDV could make me worse which is a frightening thought! i did find a specialist who did a sphenopalantine block which actually helped for a week. for some people it works longer. i've found most doctors don't really know too much about it. Not sure what area you live in but I'm in LA and there is one specialist here that i have not seen yet who has written articles and has been recommended by two different doctors. Steven B. Graff-Radford. Hope that helped! Your's sounds more like typical trigeminal neuralgia which MDV is much more successful in! Keep researching!
melinda10856 tali.
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howard10515 tali.
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Hi tali, yes, ATN/TN2 is a diagnosis that a doctor can say. It is harder to diagnose, though, since it can mimic some TMJ symptoms, some classic TN symptoms, and can be misdiagnosed as atypical facial pain. Many times there are no outward signs that show the cause. I have ATN which was caused by shingles inside the head. My pain is constant and is in pretty much the same areas as your's. MVDs, Gamma/Cyberknife, balloon decompression, etc. are surgeries that generally are not recommended because these can be more dangerous and painful in the long run. For me, the only solution was getting a neurostimulator. It works to relieve at least 75% - 80% pain relief. There many Facebook support groups for TN/ATN and I have one called TN, ATN, ON Sufferers Group. I would urge you to join it or any other support group.
Brendalr joe09732
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what is low level laser therapy? who does this and how can in find someone who does this?
reesee IsurvivedTN
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IsurvivedTN reesee
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Hauk IsurvivedTN
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