Hi all,as they say it helps to talk,so here I am “talking” …..so it’s now day 8 after my husband’s first cycle of intense chemotherapy and it’s as every bit as awful as I thought it would be!! I have now been signed off work with anxiety and stress,it definitely helps not going in as they all know my husband and people on my post round do too so I was constantly telling everyone how he is feeling,which was fine because people care and they are going to ask but it was very hard!! So now I’m at home and in between trying to help him in any way that I can I’m thinking!! I became overly positive when I saw his eye becoming less “bulgy” and puffy as early as day 2!! I questioned myself as to wether it actually was or if it was just because I wanted it so badly,but others say it has too and he said it feels less swollen and less pressure,so like i said this has made me SUPER positive BUT now I’ve started thinking again “so what now” if it’s shrinking but won’t actually go completely is this our life now? His consultant still hasn’t said what happens long term if it does (which we think it is) shrink it,so much time to think,it consumes you doesn’t it!! I’m trying to get him to eat,he tries but everything taste so bad he says and his mouth is sore with ulcers,I’ve got him swooshing the mouthwash to try and help,this morning he said his head hurts less but his back is really painful,he can’t get comfortable,he feels generally rough but I do think he is improving a little day by day.It’s literally a living nightmare,the constant thinking what the future holds,I just want my hubby better,I think the journey is going to be extremely rocky but we will hopefully get back to a happy pain free place.If you are still with me,I thank you for “listening “ it certainly helps to get it out
best wishes to you all xxx
Hi Anxious71, The only thing I could say is, if he is feeling things are getting slightly better, and you can see things are improving, that's a very good sign. As for his pain, if you keep his team updated on it, they may be able to up his pain killers. I really do hope you get your hubby better and get back to a pain free place. We are all still here for you, anytime you need to talk we will listen, so post as often as you want. All the best to you both.
Regards Ray.
Hi. Best advice take it one day at a time baby Steps. Try not to think too far in advance you can’t influence anything the chemos will do its job. You’re there like my husband was for me to pick me up and keep life on track.
I found it easier to move into spare bedroom then I wasn’t disturbing John plus I had my own space if I wanted to cry into my pillow ( which I did do ) I could do it without upsetting him any more than he was. Plus I could get up and take a sneaky sip of morphine as treatment progressed without him knowing.
It helps to talk so rant away in here. Remember treatments brutal but it has to be to get rid if the cancer. Just keep doing what you’re doing.
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
You can’t help but think sometimes … might help to write things down… one it takes longer than thinking, too, you can see if you’ve already thought it! You can add positives, not just worries. Or just continue to post here. Do a blog!
from what I can tell you are doing a fantastic job supporting your husband, but I think slow down on expectations … I myself am having to do this. Live for today, what you achieve today and small term goals. Continue to help food, mouth ulcer wise … and try not to think about the future, although that is probably easier said than done. It will be what it will be, but by god there’s some good medicines and treatments about nowadays, so stay positive even if you’re not sure why. I am an eternal optimist and very rarely let myself go down the what if it hasn’t gone route, soI’m very lucky and realise that is easier said than done.
keep up your anazing support and keep the faith! Xx
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