Hello from the Tarheel State. I am a 61 year old, soon to be 62, nurse who has practiced nursing for 35 years. In 1990 I was found to have leukoplakia under my tounge. The ENT I chose told me it was precancerous and I allowed him to perform laser surgery to remove the troublesome spots. From 1990 until 2003 I had 2 operations to remove the leukoplakia then in April 2007 I have an area to appear in between my gum and right cheek. Upon biopsy it was revealed to be a papllioma. Along with the papllioma I also had lekoplakiia on the back of the gum. My ENT this time was a very young doctor who assured me he would get it all when he operated. As I lay in the pre op area I again asked him to be sure to get IT all. In the recovery room I awoke to find he had removed the growth but not the leukoplakia. He assured me that I DID not want that on my return visit and that leukoplakia once thought to turn into cancer was no longer a risk.
In December of 2007 I developed what I thought was an absessed tooth where the leukoplakia had been left to grow. My gum became very sore and not wanting to believe what I feared and after numerous attempts to find someone to help me I found a very rude oral surgeon who after 4 weeks of waiting by his office performed a biopsy. I did not like the surgeon and because of his curt, rude attitude where he tole me no doctor in our area took BCBS I went online and found oral surgeons in Chapel Hill who DID take my insurance. Not wanting to go back to the rude surgeon I had my family MD send a referral down to Chapel Hill and I was quickly seen there before the oral surgeon here even got the results. Being somewhat naive, I had no idea that the biopsy was sent to UNC dental school until I was there one week later. They informed me that the biopsy was in the system and that the pathologist could get my results. My hubby had to run out to the car to check on our pouch and while he was out in the parking deck the kind doctor came in to give me the news. At first I did not want him to tell me but I figured the ENT knew best and that I would not have cancer as he assured me I can't explain the pain, fear and horror when I was told it was squamous cell carcinoma. But thank God for those wonderful dental school employees. They took charge, stayed with me until my hubby returned from the parking deck, helped to provide us with emotional support and from that time until this past September they became just a few of my heroes. They took care of making my appointment with Dr. Couch at UNC all I had to do was show up. The rest of my journey from Feb 11 until I walked out of UNC hospital under my own power March 31, 2008 was nothing less than a miracle. I will not take up more time to describe all the ups and downs of the journey but suffice to say after sitting in the surgical suite for 5 hours on 3/6 and waiting only to be told I would have to come back on 3/13 as they did not have a bed in ICU for me and having to come back to Winston-Salem to return a week later is just one of the detours. I survived the 12 hour surgery with the fibula free flap,( thansk Dr. Halvorson for such a great job grin) PEG tube placement and trach, trach removed before I left the hospital 3/21 and came home to recouperate and with the help of my wonderful husband, change dressing, tube feed myself and even was allowed to remove my own PEG when I could finally eat. Albeit I am thankful that the surgery went so well and my oncologist and the tumor board did not feel chemo or radiation was necesaary at that time it now frightens me to hear some of the stories here. I am 12 months, 23 days post op and returned to work full time on May 5 of last year without restrictions and now walking 120 minutes a day. I have been truly blessed and feel that when she told me this was cureable I am taking her word for it. Without the prayers and encouragement by friends, family and the many churches who prayed for me I do feel I am cancer free and will stay that way. The lymphedema and swelling as well as having to "smush" up all my food is a small price to pay. Optimism is my friend. Thank you for allowing me to vent about my journey. smile


T2N1M0 Stage IV SSC right lower alveolar ridge with fibula free flap, Peg, trach, selective neck dissection,one node positive. No Chemo or radiation.Surgery 3/08.Cancer free for 2 years as of March 13.

Hope is a good thing, maybe the best of things and no good thing ever dies.