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I share your diagnosis of stage 3, for me C and type high grade serous and I can attest to being terrified of chemo back in 2017 when I was diagnosed and my treatment plan was confirmed; Surgery \hop first followed by six cycles of chemo.and other than a glitch on the first infusion, I really coasted through. But if you type in the key words into the "search bar" at the top right of your screen it will pull up discussions and comments on the topic that might be interesting. Just remember that chemo is customised and our own responses to it differ. But also remember the staff in the chemo room will try their best to make the experience as easy as possible for you. Make sure you communicate how you;re feeling and don't try to be a martyr. The can't fix any discomfort , if you have any, if they don't know it' happening.
Hopefully your cancer centre offers some kin of preparation program...a tour of the chemo room and overview. And do research he topic on the OCC website, along with ordering the booklet By Your Side from them. It's a very helpful guide through primary treatment.
Wishing you all the best and do keep us posted on your progress along with reaching out any time we can be of help.
Yes I must say I have been worried.
i have been told it can be tough but it’s my hope
I recall last year a considerable amount of chat amongst the community on preparing for chemo...what to take, wear etc. Those may be hard to find since there's lots of posts on the general subject of chemo but if you go to the 'search' box on the upper right and type in key words like: chemo, prepare, what to bring, they might pull up the relevant discussions. Other than that I can offer a few tips:
These are basics. Ask the nurses for any suggestions, especially anything they recommend to counter neuropathy. Some gals swore by loose socks and having cold packs on or under their feet the whole time. But yes, you can get up and move around, go to the washroom etc. while in treatment. My chemo room wouldn't allow you to leave it's confines so visits to the coffee kiosk or shop etc. wasn't viable for me. My first chemo was pre Covid so it was nice that my husband could come along and sit with me. I did miss that later on, and so did he. Perhaps that restriction on visitors will change at some point.
- Ask but generally yes you can eat while getting treatment. I used to pack a large bottle of spring water to stay hydrated (water at the hospital tastes awful), depending on what time my chemo something for lunch or snacks. Hate to admit it but there as always a Kit Kat in my bag. Don't pack anything that's strong smelling though. Others in treatment may find that offensive.
- Wear loose, comfortable clothing. Layering is good so you can adjust to the temperature in the chemo room. I usually wore track pants, a T, and a loose track suit top. The nurses are good to bring you a warm blanket if it's exceptionally cool.
- A good book to read, or notebook, or anything to pass the time.
- I usually feel just fine after treatment, but about half way home fatigue hits me. So I make sure my husband or someone is available to pick me up and drive me home.
Again good luck and continue to reach out as other questions arise. And don't worry too much. Most of us found it much easier than we expected and if there is any discomfort or issues the chemo staff are well trained to jump in an make things more comfortable for you. Just ensure you keep them informed on how you're feeling.