I had a cancer of the tongue in 2011, which I am now free from, but the treatment has effected my swallowing and ended up with aspiration pneumonia last December. I’m now having to live with a peg. Has anyone else suffered similarly or is now living with the side effects and how do you manage living with a peg?
Hi and welcome to the Online Community, although I am so sorry to see you having to find us.
A cancer journey, even years on can have long lasting effects and as a result can bring a lot of stress but talking with people who are on the same journey can help a lot and will reduce the whirlwind wind that is rushing in your head.
As my cancer journey was rather different you may like to follow this link to our Head and neck cancer Forum where you will connect with people who understand the journey you are on and have experience of living with a PEG.
Follow the link and join the group by hitting the ‘Join the Group’ tab just under the main group name. At this point go to the right on the group home page and select how you want to receive email notifications when someone answers your posts.
The best way to get support is to go to the 'Start a Discussion' tab just under the main group name. Set up your own Discussion and Introduce yourself to the group - you could just copy an paste what you have in this first post.
You may find our various Macmillan Support Line Services to be helpful - call them on 0808 808 00 00 This free service covers Emotional Support, Practical Information. Clinical Information, Financial Support and Work Guidance mostly open 8.00 to 8.00 but check the link.
We also have our ‘Ask an Expert’section where you can post questions to our mostly Volunteer Experts but please allow 2 working days to get a reply.
Talking to people face to face can help a lot so check to see if you have any Local Macmillan Support Groups in your area or a Maggie’s Centre as these folks are amazing.
When you feel up to it think about putting some information in your profile. This really helps others when answering. It also means that you don't have to keep repeating yourself.
To do this click on YOUR username, look to the left and select 'Edit Profile'. Put as much or as little in your profile and you can amend it at any time - you can see members profiles by hitting our forum names.
All the best.
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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