My sincere appreciation to "all" of you for your best wishes, concerns, and prayers. Thank you.
I will try to answer all your questions. Yes, I have had head and neck CT scans, MRI's with and without dye, visited ENT, neurologists, orthodontist, endodentist, pain specialists, and all were suppose to be excellent in their field. I have been picked, poked, and maybe even skewered. :) After 2 or 3 months, the typical meds sent me to ER several times vomiting bile and dehydrated. I even visited a laser clinic for about 5 weeks to no avail.
A few months ago after visiting a reputable neurosurgeon, I was told he could not find a blood vessel pressing on a nerve. About 3 months later, it had become so bad that I had lost 95% of my ability to swallow anything and I was wasting away to skelton proportions. At this time, I KNEW somthing had to be done, as I know longer wanted to exhist this way.
Cleveland Clinic is about a 7 hr.drive, which is duable. I made an appointment with one of their neurologists. After my appointment he referred me to their pain clinic and that very day they discovered the spot (cancer) in my throat. They did this by a simple office exam. First they sprayed a numbing mist in both nostrils and put a scope through my nasal passage and looked down my throat. I could even see it myself as I asked to look at the monitor at the side of my chair.
By this time, I had almost completely stopped swallowing, including saliva, due to the pain. Also, my throat was sore and I had an extremely raspy voice. The typical symptoms of throat cancer. I was scheduled for a biopsy and immediately following, I, strangely, could swallow and eat or drink anything. Boy, did I eat. Two weeks following the biopsy, I had my surgery. This past week, I am slowly getting my strength back and eating again. I must still meet again with my head and neck surgeon ,Dr. Khan. Also, he wants me to meet with a couple other Drs. One does laser and one a radiologists. All lymph nodes were healthy but I made need a few cells lasered near the vocal cords which showed dysplasia. However I have to will wait until I meet with both Drs. Unbelieveably, the pain from the neuralgia stopped after the bioposy and has not returned as yet.
I cannot figure out for the life of me why I know longer have this bone jarring pain???
I have tried to give you a quick synoposis and answer your questions. If I have not answered your question, please let me know and I will do so. Thanks to all and keep me in your prayers, as I have you.