Throat Cancer in cartilage of Epiglottis

Diagnosis given and MDT appointment same day, stage is T3, radiotherapy will not work as it does not get into the cartilage and would only give 40% chance of cure, so my only option is surgery.    If they have to remove too much I will be on permanent feeding tubes and possible voice box removal but this is worse case scenario.  Speech therapist has to teach me how to swallow properly as this will likely cause aspiration of the lungs and I will get multiple chest infections.  Pretty scary stuff.  Possible radiotherapy after the op has healed to ensure all is gone but have to take it one day at a time.

Has anyone else got experience of cancer in this area.  I have read some of the blogs on radiotherapy but was not prepared for this.

Surgery is planned for next Thursday 23rd May.

Parents
  • Well today is my 61st Birthday and I have had so many flowers had to go out and buy new vases.  Had a lovely Steak dinner and a couple of glasses of Champagne.  Really glad that my surgery was delayed until next week now it has given me a chance to come to terms with things and to enjoy my birthday.  Keep fighting wherever you are and whatever stage you are at.  Some days like today i keep expecting Jeremy Beadle to leap out of the bushes and tell me its all a joke as I dont feel ill, how can i have cancer?  Then I read about Dog the Bounty Hunters wife who started off with Stage 3 throat cancer 2 years ago and who died yesterday, then it hits me that this is serious.  Excuse ramblings probably champagne talking.

     

    Best Regards

    Mo xx

  • Hi Mo happy birthday try and keep,a positive mental attitude I can’t help yiu with surgery as I onky hadn’t radiotherapy n chemotherapy but hang on in there

     

    hazel,x

  • Thanks Hazel

    There is no only about Radiotherapy, I think that scares me more than surgery as might have to have some afterwards.  It all depends on the histology am having Trans Oral Resection with frozen section, which means they will send bits down to path lab before completing surgery to check if they have it all.  Feel like a bit of a trekky going into the unknown as I have no idea if I will be able to eat afterwards or alternative feeding as consultant put it and worse case scenario Stoma, so it really is a bit of a mystery till they start cutting but surgery gives me 60% chance of a cure whereas Radio and chemo combined only gives me 40% so have opted for the higher odds.  But it does all seem a bit surreal, guess you all felt that way before treatment began.  I know it wont be easy but I also want this cancer out of me.

    Have a lovely evening at least the sun is shining.

    Love Mo xx

     

  • Mo I missed your birthday sorry . I hope you had a happy one . All the very best for your treatment . Hugs Ginny x x

  • Thank you Ginny

    Its been a nice day.  Been keeping my self busy as Surgery is now on the 3rd next Weds so been trying to not overthink things and just going with the flow.

    How is your husband now, is he starting to feel a bit better after his treatment, I have been thinking of you as reading all the threads it gets worse before it gets better once the radio finishes.  Best wishes to you both.

     

    Love Mo xx

  • Hi Mo we are all different but the same I was freaked in case of surgery but ok with radiotherapy knee the after effects would be bad just didn’t realise how much I would miss saliva we all tske it fir granted until u don’t gave any n trying to explain it to anyone I get blank stares. But the cancers gone yep it has but the after effects are still there cx re alternative feeding how about think tomorrow s world good old Raymond Baxter always envisioned us popping a pull instead of food n cooking so you may be ahead of the trend. Hope that made u laughs. Ps I likened my dark period to Apollo 13 and being sling shotted  round the back of the moon. 

    Keep in touch please let us know how u get on 

    h d

  • Actually feeling angry and upset.  Just got home from hospital after so called surgery.....  Story is we were told to be at hospital 7.15am yesterday morning, around 8.30 we were called to a room to see the anaethatist, who was fine with everything.  Then about an hour later two surgeons I have never met turned up, they wanted to put a camera up my nose as not been looked at for a couple of months.  Said nothing much had changed but i would be better off going for radiotherapy and said the odds were 50/50 for either but invasive surgery we could not come back from.  But having looked at all these things with original surgeon I decided to go ahead with surgery.  Was told it would be long and i would have a feed tube when i woke up and all the things that could go wrong with breathing etc.  Surgery was delayed and i eventually walked to teh theatre about 1.30 yesterday afternoon, imagine my surprise when at 2.30 i noticed the clock in the recovery room.  No one came to see me and explain anything, was kept in overnight but slight sore throat less pain than after the biopsy was all i had.  Saw another different doctor this morning and asked him what had happened as no frozen sections were done.  He did not want to talk to me just said they had removed the lesion and sent it for histology.  This is not the op that i understood i was having so now I have no idea if by some miracle they have removed the cancer or if I now have to undergo radiotherapy as well or what is happening but have an appointment for 2 weeks time yet to arrive.  I am now so upset as i dont have a clue what is going on, the treatment plan was ignored and i know i still have the cancer there is no way they have removed it with this small op.  Sorry for long rant but want to write it all down so there is a record.

    Mo xx

  • Hi Mo you have every right to feel angry i think I would  have refused to to leave hospital without someone giving me an answer. Have you tried speaking to original consultants secretary and getting at least a phone consultantation booked in. ? I know you were freaked out at the thought of radiotherapy look if I can do it anyone can will always be on site to talk you through  it  send me a friend request if you want to be a bit more private in the meantime don’t let it fester away inside if you try and remain positive 

    Hazel x

  • Thanks Hazel I rang the cancer nurse this morning and she went off to chase down the consultant.  It seems that they decided frozen section wasnt needed and depending on the histology of what they removed i might have to have some radiotherapy.  So I have to wait 2 weeks to find out what the next step is.  Consultant did apologise through her to me as it was not explained and hoped i was coping with the pain and able to eat and drink, which i am although must say quite a bit swollen today, dont feel like much at all and sore just natural swallowing.  So its not quite dancing in the street news but better than I expected although seems likely I will be having some Radio which i absolutely fear, its the thought of being tied down I am going to panic because of something that happened when i was young.

    Lots of Love Mo xx

Reply
  • Thanks Hazel I rang the cancer nurse this morning and she went off to chase down the consultant.  It seems that they decided frozen section wasnt needed and depending on the histology of what they removed i might have to have some radiotherapy.  So I have to wait 2 weeks to find out what the next step is.  Consultant did apologise through her to me as it was not explained and hoped i was coping with the pain and able to eat and drink, which i am although must say quite a bit swollen today, dont feel like much at all and sore just natural swallowing.  So its not quite dancing in the street news but better than I expected although seems likely I will be having some Radio which i absolutely fear, its the thought of being tied down I am going to panic because of something that happened when i was young.

    Lots of Love Mo xx

Children
  • Hi mo I will get u through this number one nothing to panic about. 

    If u have radiotherapy ask if they will put eye holes in your mask it really helps and staff don’t always think to ask 

    number 2 it’s rare for you to be on the table much longer than 12-15 mins 

    so I am sure you have a favourite walk fav place to go ? Fav film or similar practice now lying down in bed in sofa outside shut your eyes set s timer for 15 mins and take your self mentally there  I did with bike rides I included coffee stops loo breaks anything . Surprising some days I didn’t even get half way n the staff were coming in to get me out  

    3 ask if they have CD player maker uo a playlist or take I pod in u can’t hsbe ear buds in but maybe music on your phone  

    I varied ftom queen to spring stem ABBA to Elton John stagg used to love guessing which ones I was having that day  st the end I left the CD s for them  

    the mask personalise it mine had a name I walked in every day said good morning to her n told her the next few mins she was helping safe my life  

    please don’t fret  

    why do u say something when u were young ? Are u h p v positive if do remember 84 % of the world is 

    hope this helps keep in touch try to eat soft things poached eggs on mashed avocado are goid

    h x

     

     

  • Hi Hazel had follow up with Oncology today and surprise surprise as I thought they did not get it all.  At least the surgeon had a one on one with me and discussed what he has done and why.  So next step is that he is going to go again with another Trans Oral Laser Resection and remove a bit more as there were still some rogue cells to close to the edges.  Bet I dont get out of a second op as well as this first one but lets give it a go.  He said we could do this several times but once we play the Radiotherapy card there is no where else to go but complete voice box removal and Stoma so best to conservatively cut and keep a close eye on me, throw Radiotherapy at it if it comes back and take it from there.  Hope he is right I dont like the thought of it wandering around in case of mets.  Anyway he said 2 - 3 weeks and to ring and pester if not heard in 2 weeks a new date so here we go again.

     

    Best Wishes Mo xx

     

  • Hi Mo

    thank you for updating like you say u know your body and I agree once the radiotherapy card as come into play it can’t be repeated. In my case as one if lymph nodes was too close to spine to operate in comfort we had to take the chemo radiotherapy road. Kerp on top of appointment don’t slip through the net. Keep positive they know what they are doing

    take care keep in touch

    hazel xx 

  • Hi All

    Had my second laser surgery and did not get away with it so well this time.  Am on thickened liquids at the moment due to ammount they had to remove from Epiglottis.  Good news is this time they did the frozen section and have got it all.  Bad news is they also found a small lesion on my voice box this time so need to wait untill meeting in two weeks to see what the score is with that.  Admit i am struggling a bit this time, throat is so swollen breathing is affected and i cant stop coughing which is making it sore.  managed a small bowl of ready brek before discharge yesterday and had a little mash with cheese today but not really interested in food.  Hospital was awful again they didnt give me any pain killers because i could not swallow them, they didnt give me the nebulisers recovery asked them to guess its cos they are under so much pressure.  Got to see GP as i am iron deficient and this is not urgent to them so try to get an appointment, impossible.  Feeling a bit down and fed up with it at the moment.  Still sure i will bounce back.

     

    BR All Mo xx

     

  • Hi Mo

    thats a *** re nebuliser I know you can buy them from Lloyd’s chemist but there’s are about£70 I git a small hand held off amazon for £25 but bybtime it came if u ordered it today probably be too late. Have you tried swishing round your mouth dissolvable aspirin if you can use it indound it numbed everything a little . Plus try some protein drinks we have a hime bargains that are selling some atb£1 a bottle. Do hope your m d t meeting in 2 weeks turns out to be ok good that they’ve even got it all from epiglottis.a few nights ago I couldn’t see into back of my throat first time in a year and my clacker or proper name uvulva the dangly bit has dissolved due to radiotherapy would have been nice if someone’s had told me. Have found out my dry throat is caused by that as it produces lots if thin saliva umm ain’t going to come back now so just git to learn to adapt. My acupuncture seems to have slightly improved my saliva round my cheeks . Agree the n h s does seem stretched at the min I have. Struggles to get an ENT consultant appaointment umm he wants to see me everyb6 weeks so what do I get offered 14 weeks ! so after lengthy phone call managed one at 8;weeks .

    keep in touch H 

  • Hi Hazel

     

    I know you have written blogs but I thought I would do one as I went along in regards to laser treatment as I couldnt find anything on this when it was planned for me.  Appreciate if you can take a quick look then it is there for anyone who might find this post in the future and hope it helps them.  Not sure if my battle is now complete, will find out more at next appointment.  Have been suffering a bit this time with terrible mucus, guess this is my body making it to protect me and have to have my thick coffee and water so cant wash it away.  Using rols of kitchen towel but you will know this with the damge the Radio did you.  Yes NHS is definitely struggling and i found on the surgical side it was awful.  Appointments meant to be 2 weeks are usually 6 and so forth.

     

    Anyway link is.  community.macmillan.org.uk/.../diagnosis-and-plan-for-surgery

    Cheers Mo xx

     

  • Hi Mo

    i will certainly enjoy tracing your blog and will put a link from mine in it as well.

    totally agree Re : n h s after care they are deffo struggling .

    Yes the mucus is your bodies way of protectingbthe delicate membranes in mouth and throat area even know if u swallow anything with an edge on the mucus thickens and coats everything so although it’s  no longer a man size packet of tissues every day it certainly isn’t at least one every 2 weeks !

     

    will get back to you after uve read your blog but onwards  And upward so hopefully from here !

    Keep in touch

    Hazel x

     

  • Good news from the Hospital today the second surgery got it all and I am now cancer free.  Obviously got to have all the follow up appointments just in case it raises its ugly head again but for now I am cured hooray.....

  • Hi welcome to the cancer free club yesterday I had my one year check up all looking good for me as well. You’ve had a rocky road now time to get back on track 

    onwards n upwards 

    hazel x

  • That's fantastic news Mo. I'm so pleased for you :)