I have got through 30 sessions with the bloody mask - I wobbled a few times but kept going forward.
Now to recuperation and getting back to full health
'It's a marathon not a sprint'
Thanks for all your support guys
Thanks Dani
I suppose because they say I prob not need a feeding tube due to the radiotherapy to the one side it gives you a false sense of security. It may only be the one side but all these niggles on top of the tonsillectomy and neck dissection are beginning to build up now .
Allana
Hi Allana
I have been using Manuka Honey (from Aldi) in hot water every day whilst having radiation. So far I have not had any ulcers. My mouth still feels manky but I can still swallow.
I am no expert or medically qualified but the honey drink is quite soothing.
Don’t worry too much. If you get into trouble eating you can have an NG tube. I had one for eight weeks. They aren’t pretty but they do the job and come out quickly when not needed any more. Mine wasnt uncomfortable at all.
Dani
Base of tongue cancer. T2N0M0 6 weeks Radiotherapy finished January 2019
I wrote a blog about my cancer. just click on the link below
Hi ALana Par fir the course sadly. Tell team on Monday I was given gelclair to help with the ulcers I had them full length of my tongue. Sadly it’s part of the treatment. Always happens on a
weekend as well. Remember on a Friday make sure you’ve enough medication I went downhill more ir less at end of week 3 my ng tube was my lifesaver. Hugs.
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
Hey Hazel
yip, I’ve been reading all your blogs so although I’m kinda prepared I suppose you are always thinking maybe I will miss that stage:
it’s not bad just now so I suppose I’m taking all your advice and trying for damage limitation .
Allana
Hi please do not struggle your husband means well I’m sure but it’s your cancer and your body. If you need the feeding tube you need it. I credit mine with me having a fairly quick recovery. Until you cant swallow something as simple as a sip of water it’s hard to comprehend. I hope you don’t need it but don’t struggle please. Treatment s hard enough. A few do manage but they are the minority.
hugs Hazel. X
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
Thank you for reading my blog I had only minimal radiotherapy to my non cancer side but end if week 3 I couldn’t maintain hydration or nutrition The thing with n g tube they tend to be out quicker than feeding tube in tummy.
we’re all here to help.
glad blog helping keep referring to it just rennet we are all different.
Hazel x
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
I know there is no malice and I understand the thinking behind ‘radiation to one side so the other side should be fine to allow you to swallow ‘ BUT it was only one tonsil out and only one side with neck dissection and I lost the ability to swallow . Only for a short time to be fair .
im still at work at the moment but realising that its all changing and as you all say on here . Need to listen more to our bodies and stop trying to plough on x
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