Tonsil Cancer - Whirlwind Week

Hi All 

Firstly Hats Off to the NHS in Wales, they have been super amazing since my diagnosis on New Years Eve. Thank you all 

The title of the post is Whirlwind Week and this is why:

New Years Eve I have a phone call from ENT confirming tonsil cancer.  Very apologetic confirmed over the phone.  Wants me in for a biopsy.   Later the same day I get calls from ward team and covid test centre booking appointments.

Monday 4th January i have a covid test at 9.30am. Results back same day, negative for Covid19.  On route to test centre call from pre assessment team asking me to go in straight after my covid test for my biopsy pre assessment.   Forgot to mention biopsy booked for 7th January. 

Tuesday 5th January have an ultrasound at 9.30am and an MRI ar 11.00am.  The ultrasound was an external ultrasound of my neck. They decided to take two needle biopsies of lymph nodes which took some doing as the nodes were so solid they couldn't get needle in... Thank goodness for local anesthetic :)

From ultrasound they decided to send me for a 3d scan of my jaw.  This was done primarily in case I need any teeth removed pre radiotherapy treatment.  Apparently radiotherapy can cause your back teeth to crumble.  Don't panic not everyone has this done.  i believe it totally depends on size, position of tumour and the amount of radiotherapy you need.

After the jaw scan I went straight for my MRI.  Think I  had two 10 minute sessions,  the second 10 with dye injected into my blood.  I had also had this done for a CT scan on 18th December.

Wednesday 6th January day off.  Which I used to eat as many nice things as possible :)

Thursday 7th January 07.30am its minus 4 degrees c and I'm back at the hospital with my overnight bag ready for another biopsy, I was told to expect to be in hospital overnight.  Due to covid we have to wait at the entrance.  Just 3 of us, asked lots of covid related questions and temperature checked before being escorted to the clean ward.

The ENT surgeon comes to see me to explain the procedure.  Remember everyone is different.   So for me they are going to remove the good tonsil and send it for tests.  What? Not the bad tonsil?  The reason for this is because when you have cancer in one tonsil it is pretty much a done deal that you will get itin the other.   Also by leaving the cancerous tonsil in it allows for more treatment options.  If they cut it out there will only be one treatment path.

During the tonsillectomy they also took biopsies of my bad tonsil and my tongue.   After the op ENT told me that it would take about 7 days for the results so they expect to be calling my Wife and I in a week on Wednesday. 

I was allowed to go home as long as I had eaten something, drunk something and had a pee.  I was home by 7pm the same day.

Sunday 10th January its 6am and I am sat in bed writing this post.  Next to me is a glass of water which I sip all night, my 6am pills and a lip balm.  My bottom lip took a battering during surgery and is very swollen and sore.   The cancerous side of my throat and shoulder is still painful and the right side is even more painful from the tonsillectomy.  Even my lymph nodes seem to be complaining  :)

But you know what, I don't feel sorry for myself,  I don't feel sad.  I'm going to lose weight, but hey I'm 5ft 6inch and 13 and a half stone (male) i could do with shedding a few pounds ;) 

I know this is just the start of a long hard journey,  but I'm ready... bring it on I say!

Parents
  • Hi

    I think you are quite amazing. I am going to have a busy few days from tomorrow. I have also been lucky to have an efficient hospital so far. Christmas eve noticed my lump by tuesday had got bigger so went to doctors. 4th January at ENT had nasalendoscopy to find enlarged abnormla tonisl one side hard mass, non painful. Ultrasoiund booked for thursday 14th with aspiration then got cancellation for MRI tomorrow 12th then today get telephone call asking me to have a preoperative appointment for biopsy and panoscopy? not entirely sure on this one but think it is some sort of chest endoscopy., Not worried about MRI have had a few of thiose before, bit worried about aspiration and will be worried when i get date for biopsy. I am supposing that if anything shows on aspiration I may get a call to go in and discuss or wait for biopsy?? consultant said I could get call at any stage. Was not told about the other tonsil possibly getting cancer perhaps each hospital is also different. Let us know how you are getting on,. 

  • Hi Elona

    Welcome to the whirlwind!  I am glad that I am not the only one :happy:

    Thinking of you at your MRI, I too have had a few...  The noise just strangly brings back memories of the 90s raves :laugh:

    Sounds like we are going through pretty much the same at pretty much the same stage.  And luckily both with very efficiant Hospitals.

    I originally went to the doctors back in May 2020 with an enlarged tonsil that had a couple of white patches.  Because it was the early days of Covid and it was a throat issue I had to see a locum in the surgery car park.  She said there was nothing wrong, but may have a bit of thrush.  She subscribed Thrush treatments and away I went...  Obviously the treatments didn't work :laugh:

    I didn't know I was having the good tonsil (only the good one, with biopsy of cancerous one and tounge biopsy) removed until the day of the op.  Didn't even know I was down for a tonsillectomy until I was at my pre assessment.  The Nurse could find no info on the system...  As it turns out there were two perfectly good reasons.  I saw the dental surgeon (One of my MDT members) at my ultrasound and he told me that they were a victim of their own efficiency and that the op could change right up to the moment before I have the anesthetic.  Hence lack of info.  I don't mind, I'm just so impressed with everything.

    What is an aspiration?

    Let me try and put your mind at rest about the biopsy.  I had a fine needle biopsy which was done under local anesthetic.  This was a biopsy of the lymph nodes taken through the side of my neck. I could feel them pushing around, but no pain.  After the anesthetis wore off it was a bit uncomfortable for a day at the most.

    Under general anesthetic I had a deep tonsil and tounge biopsy.  This was at the same time as having the right (good) tonsil removed.  All the staff were brilliant, the surgeons came and saw me pre and post op explaining everything.   Ooh and the bed was soooo comfortable.  I was left with no pain or discomfort from the tongue and deep tonsil biopsy as far as I know.  This may be due to the overall pain and discomfort from the tonsillectomy disguising anything from the biopsies.

    All of my appointments were made via phonecalls or I was sent for a test whilst at the hospital having something else done.  

    How am I getting on?  The throat is still sore from the op, but the pain is very managable.  It's a great excuse to eat icecream  :wink:  I wont lie there are moments of Ahhhrrrggggg!  But they do not last long.  Earache now in both ears Boooo!   I have been living with an invisible condition, for a few years, that causes a lot of unnecessary pain daily.  So me and pain are good ole friends, he is annoying but without him I wouldn't be here (I have no idea why I made my pain male) The trick with pain is to find other, better, happier things to occupy your mind.  Hence I've written so much here, whilst writing this my pain is dampened.

    Keep in touch, as we are in such a similar position.  It'll be interesting to see how our treatment paths differ or assimilate.  It'll also be a good and informative read for others who pass by.

    Take care, be strong

  • Hi Elona

    Thank you very much for your thoughts for tomorrow, it means a lot :happy:

    Whilst waiting for this page to load, took me three attempts to find cancer chat today.  Loading page was all about donations, so I clicked on the home page and no sign of the cancer chat link.  I then clicked on the Cancer UK logo, and hey presto!  Here I am.

    Anyway where was I?  Ah yes, whilst waiting for chat to load I was thinking how to start my reply to you...  I know I will be a gentleman and ask how the devil you are, but alas you have already answered this today.  Now you have thrown me and I have to think of something else :laugh:

    I am so glad that you managed to get a better nights sleep, sleep is so important.  It's not simply for how long, but more importantly the quality of the sleep.  It does make it so much harder when not only suffering pain and discomfort, but at this time it is difficult to stop your mind whiring away.

    Its wonderful that you are getting some sun over there in the East, the sunshine simply makes life Oh so much brighter, its healthy too.  We're in our rainy season at the moment, really looking forward to the sun making an appearance so we can get out into the garden.  We didn't get much time to enjoy it last year as by the time we had finished it the summer was all but over.  Lisa's already purchased some lights to go out there when the weather turns.   We're very luck too as we live in a protected dark skies area so on clear summer nights we get amazing views of the Milky Way and meteor showers and the like.

    Our thread was mentioned by one of the moderators to a newly diagnosed person on chat.  I will go over and invite them as I expect they have looked at out thread but they may feel that they can not join in as we have been going for some time now.

    I took your advice on the title for the blog.  I have renamed it Neck Cancer Journeys.   I've been channeling my depleting energy at that.  Its all ready to go live, but I messed up a bit.  It costs £8.50 a month to publish with many benefits such as web address, anylitics etc, a couple of days after opening my account with the provider I was offerd £4.50 a month, but I had to take the offer within 24 hours.  I wasn't 100% sure at the time and I hate feeling pressured so I decided that I would rather the £8.50 a month and be sure...  Hope you're keeping up with this...  Anyway I wanted to pay monthly, which I found turns out to be £11.00 a month which also does not include any of the benefits, on top of that I would still have to pay for a web address.  Ahhhrg!  So now I have to find £102 for the annual subscription (£8.50pm) if I want to go live now.  Although I really wanted to go live pre treatment I have decided to hold out for another £4.50 offer from the provider, which they are sure to do it's just a matter of when.  Nothing is ever easy is it.

    Thinking that when I add a few more parts to it, especially the forum I will need a hand running it if you are up for that.  I can add you as an administrator.  Have a think.

    I love the sound of your wallpaper.  I keep looking for a feature wall where we could have something like that.  You must be so happy with your bathroom kitchen.  I have no idea why I thought it was your bathroom the other day.  To be fair some days I forget my own name :laugh:

    I really think that you should be getting the jab, though as you said it may not be the best time with your body fighting so much at the moment.  Unpaid carers should be somewhere near the top of the list.  It just sounds mad in my head that they're not.

    Here's hoping that the sun keeps shinning and that your sleep keeps improving.  Ready to fight the good fight.

    Right time to try and eat a roast with my remaining teeth :laugh:

    Stay strong

    Al

     

  • Hi AL

    I would be honoured to be an administrator if you are happy. Do you want contributions to monthly? you can personally email me and i can set up DD. 

    Sounds like you have been working hard on it. Fantastic work but dont over do it. 

    Enjoy those roast veggies. we had borsch. very good proper russian recipe. Came from a holiday hubby and i loved and a place we would go back too if it was at all possible. 

    love the fact you have protected skies so can see everything that goes on above our heads - must be amazing with a glass of wine on a clear night. 

    sleep well

  • Hi Elona.

    12 Hours Earlier...  Well chemo bag is packed, tablet loaded with a couple of films and games (downloaded incase of poor WiFi) and fully charged.  Spare reading glasses, headphones, fruit pastels, meds, tissues and a bit of cash.  My radiochemo suit is washed,  aired and ready to wear...  Whats a radiochemo suit? I hear you ask.  A nice new comfy tracksuit with no metal in it, comfy for the 6hrs of chemo, no metal zips etc so I can keep my dignity through radiotherapy :laugh:

    Alarm set for 6am so I can leave at 7:20 and be on the ward by 8:30am.

    Present Time...  It's 10am and I am sat in a big comfy chair having the first part of my chemo which involves a kidney flush for an hour.  The flush is administered via a drip which is attached to a cannula in my hand.  I have had a plethora of pills which include anti sickness and ones to make me wee... cos I need that.  I have to ask to go to the loo, not done that since infants, as although the machine is mobile it is plugged into the mains. 

    Even though I left home at 7:20am I didn't arrive until 9am!  10 miles of zero to 10mph on the duel carriageway.   Fortunately my nurse and many others here were caught in the same jam. So I don't feel so bad now.  I will update on the progress. 

    Thank you for accepting to help administrate the blog,  it will be a big help.   And thank you very much for your offer to help with the costs,  for now I will decline.  I have plans to make it self sufficient over time.   As soon as I work out how to add you I will.   

    Right really need a wee...

  • Well my first visit to the facilities was a mission, got myself into a right jumble with all the tubes and wires :laugh:

    I have been promoted though, I can now unplug myself without the need for assistance....

  • Another vist to the facilities,  the kidney flush is definitely working :laugh:

    Flush is finished.  They have swapped the bag for the actual chemo, cisplatin (not sure of the spelling)... This bit lasts for two hours, so headphones in and film on.

    Al

  • ... watched around 20 mins of my first film when my nurse came around with a chemo card.  I have to carry it 24/7 in case of emergency. Back to film... 5 mins later nurse is back with home meds.  Back to film... few mins later tea lady arrives,  I opt for coffee and biscuits.   Back to film.... not 5 minutes later sandwich trolley turns up, I go for chicken mayo.  

    Just put my headphones in....  Gotta weeeeeee!

    Hopefully that's it now and l can finish my film.

    How's your day going?

    Al

  • Well so'n'so's law i fell asleep before the end of the film.  And chemo waa soon finished.  Went a lot quicker than I had imagined it would. 

    Straight to radiotherapy,  load more gumph for the folder lol  only in there about 20 mins, machine hardly makes a noise and they had some good tunes playing.  Mask is now a bit more snug due to hardening.

    On way home now for a much needed cuppa.  Heres hoping the journey back is better than the one here...  Thank you for sending your sunshine over by the way....  its a joy to see that rare ball of flame.

     

    Al

  • Thanks for the invite guys.

    So you've read my post previously I guess.

    I had my meeting today at the hospital. I'm not going to lie my emotions are very much all over the place. 

    So I'm stage III and HPV+. However I've had the affected Lymph nodes and surrounding tissue already removed leaving what they're saying a T2 sized primary in my tonsil. (The nodes were my primary symptom)

    Told ill be starting Chemo/Radio in about 3 weeks. With 1 dose on Day 1 and another in week 3.

    I'm working atm to control emotions. Been prescribed some Sertraline which has helped I think and possibly not in others as I think my levels of Seretonin are all over the place!

    Been tough on my partner as well. Been blessed with having lots of people around me.

    One spark of good news was that my teeth were fine and don't need any work. 

    Told a number of factors will hopefully go in my favour with age and HPV Status. 

    Strange thing is I'm so wanting to survive this for the sake of my family but with everything coming its so hard to visualise. 

    Being in the Ambulance Service for 13 years I developed coping mechanisms after stuff I've dealt with but those mechanisms become totally useless when it's you who's ill.

    Ready for a night's sleep I think. 

    Sam

  • hahaha love your notes i am living your day!!! 

    glad you got some sun makes all feel better! 

    well it was my birthday today - getting older by the minute but despite this insisted i still had to do my one job a day so out came the extendable paint roller and calico dulux to paint the spare room wall. now bearing in mind it is a single bedroom should have been easy but when the handle kept sliding the roller towards my hand or flipped it over to one side so i was painting another section of wall you can imagine the swearing ...... 

    anyway since i have all day to do my one jobs it didnt matter and it now looks good - consequently the roller has been thrown out the window! 

    tried a chocolate muffin for tea as a kind of birthday cake and nbearly choked on it decided not a good one for the throat. shame was looking forward to a decent amount of chocolate. oh ice cream came will let you know what the piggie tastes like .. 

    hope your not too tired after your adventure today 

    take csre

     

  • Hi Sam

    really nice for you to join our talk. We aim to discuss everything so other people can read and know what to expect and hope., 

    it is a very worrying time for all and there is so much information to take in and tests to do etc you have hardly time to gather your thoughts. My friend Al will tell you that. 

    it is also really interesting comparing strategies for treatment in each case and this will help other people too. 

    there are several things but i think the important thing is hope never give up on hope. As you said age is on your side and also being HPV+ (having better success rate). Make sure you get plenty of rest so you dont get too axious. Mind you if you canget over operations like you have then you must be pretty good already. I also get very anxious when i have any tests and my blood pressure rises lol. 

    involve your partner as much as possible he will need your support as much as you will need his, even though it is you having the treatment bleieve me it affects partners as much in every aspect. having the love there will help. 

    whatever support we can give you we will gladly. 

    rest easy 

     

Reply
  • Hi Sam

    really nice for you to join our talk. We aim to discuss everything so other people can read and know what to expect and hope., 

    it is a very worrying time for all and there is so much information to take in and tests to do etc you have hardly time to gather your thoughts. My friend Al will tell you that. 

    it is also really interesting comparing strategies for treatment in each case and this will help other people too. 

    there are several things but i think the important thing is hope never give up on hope. As you said age is on your side and also being HPV+ (having better success rate). Make sure you get plenty of rest so you dont get too axious. Mind you if you canget over operations like you have then you must be pretty good already. I also get very anxious when i have any tests and my blood pressure rises lol. 

    involve your partner as much as possible he will need your support as much as you will need his, even though it is you having the treatment bleieve me it affects partners as much in every aspect. having the love there will help. 

    whatever support we can give you we will gladly. 

    rest easy 

     

Children
  • Hi Guys

    Hope your both doing ok. 

    Had my covid jab today arm feeling little heavy and am feeling tired but otherwise fine. Glad i have managed to get it. Hubby was having hius so as care etc etc managed to have a spare and gave it to me. 

    Al - hope your not too tired after your first chemo and radiotherapy. I hope your feeling ok. 

    Sam hope your ok.

    Hoping my results have come through and are being discussed as its wednesday and MSD discussion day. - fingers crossed am getting fed up feeling like this now. 

    keeping occupied as usual but also getting fed up have decided am c... at skirting boards !!! will take ages to get done. bummer. 

    take care 

  • BLOG UPDATE: 

    I forgot to add this morning that I was gutted that I missed another 24hr offer for 50% off for the year.  But all is not lost... I  sent them an email explaining the importance of getting the blog live and they have sent a promo code which lasts 7 days, so blog should be live by this weekend yay!

    They also had a quick peek at the set up of the pages so far and gave it the thumbs up.... now that's service for you.

    Al

    Al

  • Any news yet?  

    Just remember we're here for you

    Al

  • Hi Al

    well no news is good news isnt it and I have not had any phone call so hoping that is the case. Beginning to think i am going to be like this for ever lol. 

    Piggy paradise ice cream is lovely but not as good as the cookie dough. It has tiny chocolate pig faces in a vanilla and mashmellow ice cream with some toffee every now and then also. worth a try! 

    Hubby got me a pyrex chicken dish he had been looking a pottery chicken pots but resulted with this and it is brilliant I put carrots, potatoes underneath and the chicken and veg came out really succulent i felt happy having an almost roast for the first time in ages. 

    so pleased your blog is positive and going live - what a phrase isnt it hubbby said that started coming in just before he left his job. cant wait to see it! 

    glad your feeling ok have been thinking of you and wondering thank you for your long message detailing everything and reply to Sam. so important to get it all written down or people just get a basic idea of things. You often hear things but never exactly what happens and thats why your blog is so important. I am not surprised you were tired the last few days they often say it takes it all out of you. heres looking up to the future. 

    I also love art and often do paintings with acrylics but mitre carpentry is a definate no go area have finished the room just needs painting but will avoid the skirting if i can - unfortunately there is still some to do in the living room oh well will leave it for last lol. 

    tomorrow have decided to have a day of and just do a little wall painting, more gentle and easy. Fingers crossed get phone call tomorrow. That is I am presuming the results came back and the meeeting did go ahead? they never tell you its a guessing game. 

    Hubby is suffering from the covid jab today has a sore arm and headache, thankfully I am fine body obviously thinks it is trivial. 

    had a lovely surprise today a bird table hand made hubby bought for me is placed outside my bedroom window so if i get too tired hopefully can attract some birds and watch them. 

    waiting for the ring...

     

     

  • Hi Elona 

    Hopefully not too much of a wait for your results, to me that was still the worst time so far.  I know how you're feeling.

    I really fancy some cookie dough ice cream right now, thank you for that lol.

    Just had last radiotherapy for the week, now sat in another part of hospital waiting to have my bloods.

     

    Home now, cookie dough purchased on return journey :happy:

    Al

  • Good Morning Elona.

    Just a couple of lines to wish you well for the day.  

    And to let you know I ate half the tub of cookie dough ice cream last night, which I  may remind you that its your fault i purchased haha!  so there shouldn't be any problems with me weighing in at my 80kgs on Monday. 

    Thinking of you both

    Al

  • hahaha that cookie dough ice cream is a goodie! happy to contribute towards the weight control lol. 

    mnaged to go all night without getting up for more pain relief yay! but i need a dentist to file a tooth down think they moved my jaw when they took my tonisl out and it is rubbing - hate dentisit will put of for as long as possible - that is if i have dentist any more lol. mine throws you out if you dont go reguarly and i didn not go last year. oops! 

    sun is shinning on the frost we had last night so planning the job of the day might be a bit of skirting painting. quite tired today though so we will see might just move some things around. at the moment i am sitting in bed with a cuppa lol 

    i read your reply to Sam you are a very amazing person and ia m in or being an artist of that callaber must have been quite something but to loose it must have really weighed on you then to regain your self is something to be very proud of. most people would only aspire to be as good as you - i certainly would i love painitng animals and am not bad but wow would love to see your work some day, can you adapt your condition to doing a different style painting? or is it still little painful. 

    now if i was you savour the cookie dough and order some more! 

  • Hello Elona 

    How are you?  Any news yet?  How's the tooth?  You should be OK  most dentists stopped seeing patients back in March 2020. Mine was one of them.

    Sun shone all weekend here,  out in the Garden in February here... Unheard of!  Gave the garden gate two coats, not real energy though, sadly steroid infused lol.

    Just finished my second chemo and 6th radio today and not feeling too bad yay.

    Sunny here tomorrow  hope its sunny with you too

    Be Strong

    Al

  • Hi Al

    sounds like you are doing really well - keep it up! 

    congratulations on the two coats of paint - i only managed one on the skirting boards today. tooth is feeling bit better today think it is a wisdom tooth that need sorting but have bought a file so am going to see if i can file the tip tiomorrow lol anything to avoid dentist lol 

    no news yet so figure they cannot have got results back - susoect then they must be trying to culture something. 

    am finding that somethings get stuck in throat - hubby knows this feeling well he had a stricture and had to have his throat enlarged monthly for nearly 2 years. hoping this does not sty like this. taste is still not 100~% either. otherwise today is much like another ! the list of jobs are getting longer and longer! my pond decided to break - the hose pipe to the pump and i could not mend so have ordered some parts but may have to find someone to help me. grr 

    anyway take care

     

  • yes sunny here it is good to see the sun but boy bitterly cold brr couldnt face being outside for long. quick throw food at animals and run inside lol. feels like winter again. 

    did manange five minutes yesterday to sut a salvia in the front garden and plant some galanthus and primula in a basket on a fence to brighten the place up a bit. 

    hubbby got me the new bird table and i was watching a blackbird and starling on it - so pleased to see it being used especially as we have crows, rooks, jackdaws that could scare of the smaller birds. 

    happiness keeps you positive x