Hi Salival I think I was meant to read your post today as I sit in the cafe at Austin Hospital having a well deserved coffee. I have just been to the Olivia Newton John Centre and has what I thought we be a breeze, a face mask made, mouth plaque and ct and mri scan. I’ll back track - I was diagnosed with TC in February and went into hospital for 10 days having it removed and my lymph nodes as well as a skin graft. I was also diagnosed with 2 melanomas at the same time of diagnoses so I asked if they could do that surgery at the same time which they did. I too noticed a raised bit at the base of my tonque in October last year and it spread quickly that I got it check out then which the local Dr said was probably just a blocked saliva duct and it should just heal on its own. Well of course it didn’t and I saw another Dr in Jan and he quickly sent me to the Austin which diagnosed TC squamous cell T2. They went in just over 5 mm and although I was given the all clear through my body of “cancer clear”.... such a wonderful sound to hear, they said the margin was borderline clear/close, meaning there could be microscopic cancer cells there which doesn’t get picked up in surgery. So radiation was a surety and just a few days ago they suggested a small bout of chemo as well. I have a small group of very supportive friends and two daughters in their twenties that have left home but are my world…as well as my 6 week old grandson whom is my little angel. Anyway, sorry I’ve gone off track. I hear the side effects to R, which I start on 26 April (later than expected as I had to have a rotten tooth pulled out) is the first two weeks of tiredness, then likely a burning on one side of your neck as the radiation leaves your body (like sunburn but it will peel off), possibly burn sensation in that side of mouth as well. Taste my go but comes back, saliva production is effected too. Anyway, I will see and keep u posted. I was told that the day after my surgery I would be “unintelligible” but I was pleasantly surprised and my normal voice is back, I just have a bit of a dropped lip. If you need anymore help or questions please feel free and I’m glad I have found a site specific to Head and Neck Cancer. Hugs 🤗to everyone on here. lyndy 🌸
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