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.

@kathyheidt

Thank you for your comments. I just met with msk in nyc and they said radiation chemo instead of surgery I have squamous cell carcinoma in maxillary sinus. But it is in the bone. Will radiation get it out of bone. He said flap surgery very invasive and no guarantees

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Please get a second opinion. I had cancer SCC of maxillary sinus. Surgery was the only option. ( maxillectomy) ) Followed then by radiation. No chemo. Tumor size 2 with no metastasize ( initially) This was almost 4 years ago. Radiation was a fail because the cancer recurred in a couple of lymph nodes in the neck. Long term side effects from radiation continue to be challenging.

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Thank you I have got one opinion from nyu saying a flap then chemo/ radiation and the other at msk saying no surgery bc flap so radical and for combo radiation and chemo.
So confused. Now want to reach out to me Anderson which is suppose to be specialists.

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@judyrichter

William, thank you for the welcome. I began part of my story in 2002, when my dentist noticed “something” . Well after a biopsy they discovered cancer. Never smoked a day in my life, but there it was, second hand smoke cancer. After removing most of my left jawbone, I was considered “cancer free.” Yea, right! Went to my dentist, oncologist, and oral surgeon every two months or so, regularly. Thru the years they removed many suspicious spots. Twenty years later, my oral surgeon, on word from oncologist, did another biopsy on my right side. Did not show any signs of cancer. However my surgeon notice the left side of my cheek to be suspicious and did a biopsy. Stage IVa soft tissue cancer, fast moving new type of cancer. My surgeon, referred me to a younger surgeon, new oncologist, new plan. My doctors said I need newer, younger, specialist. Well, I got them. Lucky enough to live close enough to the Sammons Cancer in Dallas. Am going there now. Have had surgery, 32 rounds of radiation (horrible), and over 50 chemos. While under going radiation and chemo, the cancer come back in my head. They had warned us it could. My Oncologist began chemo, chemo and Key Truda. Key Truda was every third week. Now present day, I told my doctor I wanted to stop my chemo. He said after two clear scans I could and continue with Key Truda every 3 weeks. He said they didn’t know if it was the chemo or Key Truda that said bye to cancer. So right now, I’ve had my first scan since being off. Chemo and it still “cancer free”. I will continue as is until…. Just glad to finally find people like me. Fighting to live.

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Hi Judy, I add my welcome. You may also wish to share your Keytruda journey with fellow members in this related discussion:
- Keytruda for Head & Neck cancers
https://connect.mayoclinic.org/discussion/keytruda/

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@kathyheidt

I have been diagnosed with squamous cell carcinoma in my maxillary sinus. Can you please connect me with others or advice
Thank you

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Hi Kathy, I'd like to add my welcome. Here is a list of discussions where members are talking about sinus cancer:
https://connect.mayoclinic.org/group/head-neck-cancer/?search=sinus&index=discussions
Click the link and post a comment in any relevant discussion to connect with others like you. 🙂

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@nnurse

Please get a second opinion. I had cancer SCC of maxillary sinus. Surgery was the only option. ( maxillectomy) ) Followed then by radiation. No chemo. Tumor size 2 with no metastasize ( initially) This was almost 4 years ago. Radiation was a fail because the cancer recurred in a couple of lymph nodes in the neck. Long term side effects from radiation continue to be challenging.

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Thank you are you doing chemo now

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My husband has been diagnosed with stage 4 tonsil cancer. He has metastasis to lymph nodes and bones. Surgery is out and radiation is out. He is going to start a clinical trial in a couple of weeks.

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@handyman69

My husband has been diagnosed with stage 4 tonsil cancer. He has metastasis to lymph nodes and bones. Surgery is out and radiation is out. He is going to start a clinical trial in a couple of weeks.

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Hi @handyman69 and welcome. Stage 4 tonsil cancer? Fine one day and the next not so much or were the symptoms being ignored until they could no longer be ignored? I don't mean to sound harsh but there has to be more to this story. Do you have a question or something to share about this clinical trial? I would imagine it is going to be strong Chemo for quite some time as by stage four, it has metastasized to the point where surgery and radiation would be everywhere and not feasible. Hopefully there has been an analysis of the type such as HPV16+ which can significantly change the type of Chemo required. Good luck and good healing.

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@hrhwilliam

Hi @handyman69 and welcome. Stage 4 tonsil cancer? Fine one day and the next not so much or were the symptoms being ignored until they could no longer be ignored? I don't mean to sound harsh but there has to be more to this story. Do you have a question or something to share about this clinical trial? I would imagine it is going to be strong Chemo for quite some time as by stage four, it has metastasized to the point where surgery and radiation would be everywhere and not feasible. Hopefully there has been an analysis of the type such as HPV16+ which can significantly change the type of Chemo required. Good luck and good healing.

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Hello, I just had a sore throat that didn’t get better after two courses of antibiotics. Then went to ENT doctor and was told had tonsil cancer. This was in Georgia came down to Mayo Clinic for biopsy , ct scan and pet scan. I noticed swollen lymph node and had sore throat. I have no other pain. No bone pain. I am 69 and otherwise healthy and active. It is HPV +16. The clinical trial is immunotherapy. I guess my question was is anyone else with stage 4 tonsil cancer and how are there treatments going.
Thank you for your reply.

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@handyman69

Hello, I just had a sore throat that didn’t get better after two courses of antibiotics. Then went to ENT doctor and was told had tonsil cancer. This was in Georgia came down to Mayo Clinic for biopsy , ct scan and pet scan. I noticed swollen lymph node and had sore throat. I have no other pain. No bone pain. I am 69 and otherwise healthy and active. It is HPV +16. The clinical trial is immunotherapy. I guess my question was is anyone else with stage 4 tonsil cancer and how are there treatments going.
Thank you for your reply.

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So basically you had stage four with limited symptoms, which is rare but does happen. At least being HPV+16 is Chemo treatable and even with drugs like Keytruda which has been listed for several years now with excellent results.
Do you have a backup plan if the clinical trial has you on placebo or simply fails? Stage four, or for that matter practically any stage of cancer is not something most folks would want to experiment with because in the end, the cancer will kill you if not stopped. Is the clinical trial at Mayo Jacksonville?

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The clinical trial is at Mayo in Jacksonville. The trial is a drug that is like Keytruda plus two other drugs. At the least you get the one drug and you may get one or both of the other. If it doesn’t work for you or you decide to stop you can go to the standard of care chemo and immunotherapy but if they don’t work you can’t back track and get on the trial. You are scanned every eight weeks. So we decided to try the trial first.

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