Thyroid Cancer During Covid-19

Hello, I would like to tell my story of how I came to be diagnosed, this may help somebody who is starting the process of investigations.

October 2019

I went to the doctor as has symptoms of an ear infection... given antibiotics, beconase nasal spray and hayfever tablets to try and unclog my ear tube. All was fine and asked to come back if not cleared by end of Jan 2020... fast forward Jan came and went still not cleared. Forgot to go back due to working and Covid-19 happening at work (HR).

March 2020

I eventually phoned GP to go and see him but due to restrictions I could only talk on the phone. He referred me under the two week rule as suspected tumor blockingbthe tube. 

April 2020

I had my appointment with the cancer ENT consultant on the 1st April, the weekend before I felt a lump on my neck... very small one and wouldn't of noticed it without prodding around. I had a camera up my nose to check for anything but luckily nothing was found for the fluid blockage. Surgery will be needed if it doesn't clear, consultant felt my neck and recommended a scan to get it checked out. Given a prescription of nasal drops... also had a pre existing hearing loss in other ear which turns out is otosclerosis... surgery to make it better. Went home and waited for the scan.

One week later I get the appointment and 6 days later I went for my scan, all looked fine to start with but then I get told I have an abnormal looking node and a nodule on my thyroid. My original node that was poking out looks fine but the other node was a concern. I had a FNA biopsy done, two samples taken, (only felt the anesthetic injections). Told 2 weeks for the results. Following week had call to say samples was inconclusive as was much debris. Got another appointment 1week later to repeat it, had it done with another 3 samples taken - again didn't hurt ( tender and sore for 2 days after). Missed the call 9 days after as phone was playing up. Called secretary to find out if results were back, told I would get a call, I received an appointment letter the next day to come in on 12th May.

May 2020

Arrived for the appointment with the consultant and another lady sat in the room (Macmillan nurse - didn'tknow who she was until got told i had cancer and i was alone for this appointment due to covid-19). I was told that there was cancer cells in my lymph nodes (where they biopsied) and i have papillary thyroid cancer! Shocked but somewhat had an idea it was bad.

Have a lovely Macmillan nurse and support worker who have been lovely and waiting for my surgery to remove my whole thyroid and cancerous lymph nodes and expect to have radioactive iodine treatment after. It is treatable which is great and reassure that type of cancer is the best form of cancer to have as it is very treatable and no chemo involved. Yay get to keep my hair.

 

I can tell you that waiting was the worst part and now I know I feel a slight form of relief but having the cancer is still lingering. Telling my boys was okay as i avoided the c as ncer word but telling other members of my family has been the hardest.

 

You are never alone in this and you will always be supported. If you have any question please feel free to ask. :). Covid 19 has not impacted my cancer diagnosis or treatment so far so please don't be afraid of getting the results.

  • Hi there,

    im sorry to hear of your diagnosis but happy to hear that it is treatable. Your message was very reassuring to anyone who is waiting for results.

    I have been to the GP today after 10 months of unexplained ear pain. No infection has been detected so I have today been referred to ENT.

    Can I ask if your ear pain was constant and was it only one ear that was affected? Also, did you have any throat or neck pain?

    I am dreading my appointment but I guess it's time to get some idea of what's going on.

    I wish you well in your journey x

  • Hi Casca29,

     

    I am sorry to hear that you are getting referred, but I wish you all the best with the results.

    My symptoms was just a full feeling in my ear and hearing loss, I didn't have any pain with it. I actually still have it and they don't know what is causing it still. Will have to be surgically drained if the nasal drops do not work. It only affected one of my ears, one thing I should say is my ear problem is not relating to my cancer.

     

    Please don't be scared of finding out the problem but one bit of advice I can give you is please don't google search... it literally made me worry and get thoughts into my head and think the worst. I know my outcome was the worst situation but it doesn't mean that yours will be the same :).

     

    I had no symptoms relating to cancer at all  it was by pure luck that I had something else that was checked that led me to the ENT department in the first place.

     

    Please let me know how you get on with the appointment. My fingers are crossed for you x

  • Thank you so much for your reply. 
    Thank goodness you had the ear problem and you are now on the way to getting treatment for your thyroid. 
     

    I admit that I am terrible for googling my symptoms and have diagnosed myself with all sorts! 
    I think because I have the one sided throat pain too that I am terrified of the outcome. The GP didn't seem to think that it would be anything serious because it has been going on for so long but said I would have to get it investigated to rule out anything going on in my throat.

    Good luck with the rest of your journey. You sound like a very positive person and it would be lovely to hear how you get on.

     

  • I think I was very lucky, must have a guardian angel :).

    I wish you the best of luck for your appointment when you have it and please let me know how you get on. Thank you for the kind words and i will be updating post op and post treatment. I will find out more on how aggressive and if it has traveled further than expected from the results from the removal of thyroid and affected nodes in my neck.

     

    Positivity is key in this situation and without it you are only convincing yourself to fail. If you have anymore questions please let me know x

  • Hi Amy,

    I have just read your post and I am sorry you are going threw this, but too like me I am going threw the exact same thing, recently just had total thyroidectomy and neck dissection (papillary thyroid cancer) , and I will be receiving radioactive iodine treatment in about 4-6 weeks wich I am terrified of having, just wanted to no how it all went, I don't think I am prepared for this part, and that c word always manages to pop up everyday which is a nightmare as you could imagine!! I thought I would give u a lil message basically to speak to you about it really as I hardly no anyone who's been threw this :/.

     

    Would love to hear back from you thankyou. 

    -Georgia xxxx

  • Hi lovely  thank you for commenting .

     

    I want to say I am sorry you are going though this too! You are over the worst part (surgery) for me that was awful as my parathyroid glands were damaged and my nerve was bruised so I have had loss of muscle and weakness in my right shoulder. Physio helped and it is getting better slowly. 

     

    I also had neck dissection and had 41 lymph nodes removed, 8 of those were cancerous so I am glad to get rid. Radioiodine ablation was a breeze for me, it is more scary as a thought than in reality. No side effects other than salivary glands swelled up, that was only for a day I had this issue. It is more boring than anything having to be in a room for 1 day and night. Not seeing my kids for 5 days after. 

     

    Had a scan the following Monday (had treatment on Wednesday) which took over an hour to have done so be prepared for it, laying still with ADHD was extremely annoying. Then having regular blood tests to get levothyroxine level right, still on going as still not right from May. 

     

    Don't be scared or nervous about the treatment as honestly it was nice to have something done that didn't cause me discomfort or pain, the nurses will be great while you are there. It will be 9 months after your treatment before you find out if it worked.

     

    If you have any questions please just ask. Good luck lovely xx

  • Hello Amy, 

     

    Thankyou for your reply this has settled my nerves alot. 1of my parathyroid glands had to be removed but 3 of them remain, currently on calcium to stabilise that.yes my nerves are bruised too and my shoulder if sore and numb along with my ear wich feels so wierd haha!! Also have a droopy eye too urgghh! Wich is normal as the surgeon explained because of the bruised nerves. 

     

    Once again thankyou for commenting back to me I think I can possibly remain alot calmer now and prepare myself for this treatment and yes your right the worst part is over now (surgery that was the big part)

     

    I appreciate you telling me this it has calmed me down alot (I'm a big worrier I worry about the weather haha) nice to no I am not on my own dealing with this, I hope everything went well for you, I will keep posted after the treatment. 

     

    Thankyou again xxxx