Hey everyone my names jenny and my dad was diagnosed with tongue cancer squamous cell cancer on the 15th march 2021. He had a biopsy, CT scan and MRI to see if had spread where? Thankfully it hadnt but the consultant was concerned about a growth in the side of my dads neck. So sadly after dad was examined all round hes head and neck we were told he had a very aggressive Tongue Cancer and it was at stage 4 already. Dad had been having a bad " toothache" and was never one for drs or dentists hospitals definitely no! But didnt ever imagine it could be that but I put on a brave face for my dad to be strong but inside my heart was breaking. Theres only me and dad he has no family as he didnt have a very good childhood and is separated from my mom so theres only been me who's been by hes side all these years. So the clinical plan was that dad have hes PEG fitted and then RADIO for a week then 2 weeks break then another week but when dad went for hes Mould fitting for radiotherapy the nurses and drs noticed how much weight my dear dad had lost and how malnourished hed gone and living alone cos hes very independent I never knew so they said dad needed this PEG asap! He needed to be strong for the radio as it's very aggressive. So moving on a couple of weeks dad is now in the hospital been there a week now as hes blood pressure was so low and he wasnt having enough fluids so he was dehydrated so hes had the PEG fitted a few days now and had feeding bags and the drs have said how better he looks. I have PEG TRAINING with the dietician on friday with dad so I can see how its managed so I can make sure that dad can manage it too. A care package is in place for when hes back home hell have the district nurses and carers go in and as I'm a carer for my hubby I can also go down as much as I can to help dad aswell. It's been such a sudden and heartbreaking journey so far and as I'm new to this group I just want to say what inspirations you all are! You all sound so brave and reading your journeys of you and your loved ones breaks my heart but stay strong and love to you all thankyou so much x
Hi Jen Louise
thank you for sharing your dear dads story.Cancer is so cruel try and stay strong and good luck with the peg training. I had n g tube my husband did all the feeding and cleaning for me it took all the pressure off me. Good that you’ve got carers going in to relieve the pressure off you.
keep in touch when you can.
Hazel
Hazel aka RadioactiveRaz
My blog is www.radioactiveraz.wordpress.com HPV 16+ tonsil cancer Now 6 years post treatment. 35 radiotherapy 2 chemo T2N2NM.Happily getting on with living always happy to help
2 videos I’ve been involved with raising awareness of HNC and HPV cancers
Hi Jen Louise and thank you for posting your loving and thoughtful message.
You sound like a lovely daughter to be supporting your dad through this very difficult time.
I hope you can both weather the treatment and that it buys you some time together.
It won’t be easy but please come and share your worries if you are able. There are plenty of shoulders to lean on anytime
Best wishes
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
Thankyou so much for your lovely message it means such a lot to know I have people to talk to so you stay strong take care x
Hi Jen Louise and welcome to the forum.
I didn't have a PEG when I was having treatment but I was the carer for my father in law who did have a PEG so I understand the training side of things from your point of view.
Well done for being such a wonderful support for your dad. Make sure you have the direct number of his Specialist Nurse so you can make contact if you need to. It will probably be on his paperwork but if not, you should be able to get it on Friday.
All the best for Friday and any questions or support required you know we're here to help as much as we can.
Linda x
Hey Linda its jen I justed to let you know how I got on friday with my PEG TRAINING for my dad. Well I thought it would be a simple demonstration with my dad having a little tube in hes belly and I just attach the feeding syringe to hes tube and feed him boy was I wrong!! Lol no it was much more complicated cos u see my daughters dad sadly passed away 5 years ago with throat cancer he was only 49, we had been separated before my daughter was born but she grew up with him so it rocked her world but she has a wonderful stepmom who has now become one of my best friends and shes been helping me with so much advice and support throughout my dads cancer so I told her when i got back from the hospital and she said the PEG my daughters dad had was so much different to my dads. But it's under the NUTRICIA HOMEWARD SERVICE. And the tube is attached to this purple little machine and you have put in the dose and how many mls dad has to have and he'll be having a litre a day of liquid feed , 84mls an hour but it was really interesting and terrifying at the same time like how about if I dont get it right or how about if an alarm goes off on it?? All these questions but it's a lot simpler the dietitian said then it looks so I'm just relieved my dad will have the nurses go in to do the feeds for him as I'd hate to get it wrong. But I asked how he felt about it and he said typical dad oh it's ok I dont feel anything bless him he is sooo much calmer and braver then I am and hes the one who has to go through all this but yea I just wanted to let u know so sorry I've offloaded a bit! But how are you sweet? Hope everything's ok and I hope you dont mind me asking but is your dear father in law still with you? Talk soon take care x
Hi Jen Louise,
Sure Linda will be along shortly, just wanted to say well done on your peg training, I'm sure you will get into the swing of it no problem.
You sound like you are doing an amazing job looking after not only your dear dad but also your husband. Please make sure you look after yourself too and take time out for a little treat here and there,
Julie xx
Hey julie thankyou so much for lovely message yes it's been very exhausting looking after the 2 men in my life! Lol but we have lots of support from my hubbys sister shes been amazing honestly I think shes kept me going to be honest julie but I think my dad will feel more happier once hes home from the hospital so hes in hes own surroundings. But I'll keep you and all the lovely kind people on here updated on my dads progress. Sending lots of hugs take care sweet xx
Hi Jenny
Your dad's PEG sounds VERY different to the one my father in law had. If I understand youir post correctly, the nurses are going to do all the feeds? Sounds like your dad is in the right place at the moment to build him up and then a good support package in place for when he goes home.
Sadly my father in law died. He was 93 and underwent huge surgery in the belief it would get rid of the tumour but sadly it had wrapped itself around his carotid artery and he was too weak to go through radiotherapy. He too was extremely calm through everything.
I'm so pleased you've got some support around you with people who understand.
Good luck and take care.
Linda x
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007