Adenoid Cystic Carcinoma
It it is hard to believe that it has been 3 years since I finished my rads, and so far am cancer free. I thank the Lord for his goodness. My energy has returned mostly. My tastebuds are 90%, things tend to not be as flavorful, and I don't eat many crackers, chips, since they are so dry - sort of like eating sawdust. And I still have a very dry mouth especially when I wake up in the morning. you do get used to it, and it seems somewhat normal.
I will have a CT scan next month, and see my oncologist, and ENT every 3-4 months, with @ 3 ct scans per year.
I am writing this to give others hope about this type of cancer. I rarely get on this site, but was on it a lot when I was going through the rads, and was always looking for anything positive to give me hope and encouragement. HOpefully this will help and encourage someone else.
Comments
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Hello !
Thank you for your encouraging post ! I too was dx'd with adenoid cystic carcinoma. There are a few others that have posted and been through surgery and rads and doing well also ! It is so important to pass on the good news that this type of dx isn't all doom and gloom ! Wishing you all the best, and please continue to post so others know this is doable ! Katie
Also very important to pass along about the rechecks (scans) for our dx. A bit different then for other dx's. I'm sure you know about this site, but when I get a chance I like to pass the information along for others. www.accrf.org and www.accoi.org fabulous information on what this dx is and doctor lists and tx's ect.
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