Meet others living with Head & Neck Cancer: Introduce yourself
Welcome to the Head and Neck Cancer group.
This is a welcoming, safe place where you can meet other people who are living with head and neck cancer. Let’s learn from each other and share experiences from diagnosis through treatment and coping with symptoms and recovery challenges.
As you know, head and neck cancer is the general term for a broad group of cancers that begin in the head and neck region. This include oropharyngeal cancer, hypopharyngeal cancer, laryngeal cancer, lip and oral cavity cancer, nasopharyngeal cancer, paranasal sinus and nasal cavity cancer, salivary gland cancer, squamous cell neck cancer or ameloblastoma.
Let’s get to know one another. Why not start by introducing yourself? What type of cancer have you been diagnosed with?
Interested in more discussions like this? Go to the Head & Neck Cancer Support Group.
Good morning, so sorry for your diagnosis. I have HPV16.
It was on the back of my tongue with cancer in both lymph nodes. My treatments were done at the same time.
5 chemo and 35 radiation treatments.
Unfortunately I had a feeding tube for 4 months and did not work. The side effects were worse than I was told. It wasn’t until I was experiencing the side effect that the Dr would say “yea that can happen.”
Side effects, over abundance of saliva in the beginning. Causes choking. Then suddenly you dry up. NO saliva, swallowing is a struggle. Drink something besides just water for hydration. Sorry this isn’t the news you wanted. If I can give you any other tips, please reach out.
God Bless
Thank you for replying. I had my tonsils removed in march of 21. When they diagnosed me with this they took a look back at my pathology report for tonsils, and it was clear. before this surgery i had 3 large lumps in my neck. The removed one fully and i do believe the other 2 are in there still. I will ask my doctors about what you suggest, ty. I am just hoping that the cancer hasnt spread to my cervix, or maybe it came from there, i have no idea. Im thinking my radiology appointment is going to talk about my treatment options. And i really hope i find out more answers. I have to wait until 4-10 for those appointments and the wait is driving me insane.
Again, ty for replying and I wish you the best of luck with your treatment plan. I will send good vibes your way as I dont believe in a higher power. Thank you.
I havent talked to my oncologist or radiation oncologist yet. That is on 4-10. But I will be weighing out all options. I hope I dont need another surgery. I hate what the anesthesia does to me its so embarrassing. Some people are happy and giddy. I am a hysterical basket case and cry very loudly.
Thanks. From what I read
It seems like there is one
specialist for inner cheek
and a different specialist for the lip. I would rather start with a specialist because I do not trust pcp
for this, but thanks for responding. I hope this site has some people with similar conditions.
I am very sorry to hear about your new possible illness. But much of what you read is dated and you really don't know the history of these patients. A lot has progressed with HPV. There is a protocol that is in place that is very successful I hear. I'm not a doctor but a cancer patient myself with HPV negative. Everyone I talk to that has successful outcomes are all HPV positive. Stay cool and dont read online too much. Best of success.
I had rare angiosarcoma 10 years ago in the skin on my cheek treated with surgical removal and radiation. It has reoccurred adjacent to old site but closer to eye and nose. They could not get clear margin close to my eye. I will have surgery to remove that tissue but no reradiation.( Concern for blindness,no clear margin). I was wondering if anyone has had adjunct therapies anywhere since radiation is off the table. The Sarcoma clinic I go to is not offering it in my situation.
I am 6 yrs, as of 23 March 2017, out from HPV p16 H&N cancer from an unknown site. But they thought it was under-my tongue and gave 35 radiation treatments that focused on that area. They found the cancer cells in 2 of 41 removed lymph nodes BUT apparently no cancer cells got out of those 2 nodes. Hence, I have no experience with the movement of cancer cells to other parts of my body as of my last checkup. I go in every 6 months. My response is regarding your question on whether scar tissue can have an affect on your swallowing? The answer is YES! I just had a swallow test and it was determined that the scar tissue caused by the intense radiation treatment affected the valve that opens and closes when I eat anything. It prevents food from going down the wrong hole to the lungs. Thus, eating is task but must done or use a feeding tube. I did that for 4 months but won't do again, unless needed. Sorry to say, you will need to learn how to swallow again with this permanent issue. Once you do that, life gets easier. God Bless!
Will you please tell me how I identify or go to the latest posts?
Right now I'm on an iPhone I could go to the computer, but typically I use the phone . Thank you, best
@westand731, You can view the messages in chronological order (Oldest to Newest) or you can choose to see the most recent messages first by selecting Newest to Oldest. The default order is Oldest to Newest. To see recent posts, you can skip to the last page of a discussion or change the sort to Newest to Oldest.
Learn more here:
- [TIP] Customize the Order You View Posts - See New Posts First https://connect.mayoclinic.org/discussion/new-customize-the-order-you-view-posts-see-new-posts-first/
@rubagaddal, any update about the cyst discovered on the left jaw and lung nodules? How are you doing?
@shielashepperd, I hope your voice continues to get stronger. Are you working with a speech pathologist?
@apple32, what a relief that early treatments have already relieved your husband's pain. Has he started radiation now?