Hi, just thought I'd say hello. I'm also struggling but not on the scale you are experiencing. I'm 66 and I have a form of skin cancer/melonoma which was in three places on my scalp. This resulted in 80% of my scalp being removed and it now looks like a crater. I can't go out or won't go out, I feel like a freak and I am so angry myself that within a few months it's all change. I now feel a bit of a cheat having listened to your problems and I do wish you well.
Hello and welcome from me. Sorry you have had to come on here, but we all understand what you are going through. I know my wife took my diagnosis far worse than I did and I probably did not make things easier for her, but we got through it.
I am sure Macmillan can offer you some emotional support and a charity called The Swallows run by a fellow H&N cancer survivor and his wife would be an excellent first point of contact to help you through this. I don't think I am allowed to post a link, but Google "The Swallows". For me it comes first in the Google search results page.
Hi Shanna welcome from me Peter has given excellent advise Chris and his wife Sharon run an excellent service.Please give them a call. Cancer treatment to head and neck is pretty brutal my oncologist said he would take a year out of my life but he would cure me he did both. It’s often harder for our other half’s ,we are the ones who are centre of attention my husband just got on with it. But I did try to make sur he was ok we did have a few words during the recovery period and we don’t have words !!
https://theswallows.org.uk/
This is the link ,with them being a registered charity we can put link in PFJTHS fingers x I’m sure ??
Hope this helps 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 to Peter and Hazel, I really want to apologise for posting my problems with melonoma/skin cancer, feel really bad to have entered the community. I've left the site and again apologies if any offence caused.
Thanks for the support, I mentioned to Peter I would look into it. Just needed to vent a bit. And good to share others experiences dealing with this type of cancer, you’re right, it’s brutal.
Hi Smarty. Don’t be silly cancer is cancer it’s not a competition. Yours sounds just as horrific. Please please don’t beat yourself up We are all one big family helping each other along the way.
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
Hi Smarty
No need to apologise and leave the forum. I am so sorry to hear of your struggles and what you are going through. We are a kind and friendly group here. we all understand how after treatments can make us feel and the difficulties they cause us. We are here because we want to listen, share and help each other.
Nicky x
Smarty, if you do read this... there is no need to apologise. We all have difficult emotional aspects to our cancers and part of the godsend that is this group is the ability to offload and gain support from others who understand.
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
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