I didn’t have the stoma because, as the surgeon put it, “your bowel wall is like sandpaper and to remove all the seeding I’d have to take your whole bowel out” - that was in January 2017 and I’m still doing fine 😁👍
I can remember my recovery from surgery. Yes, it was painful and slow, but now it’s just a memory - and yours will be too, eventually.
There are plenty on this site who will let you know how they coped with their stoma, I just want to say that better days are ahead for you so follow the advice and try to move even though it hurts.
Try a rolled up towel pressed to your belly when you roll out of bed as that helps with the muscle pain - and although I’m not sure if the same applies with a stoma, if they offer Laxatives TAKE THEM, constipation can increase your pain BIG time!
The chemo is to mop up and it’s impossible to say how you will react to it as everyone is different. You aren’t likely to get all the possible side-effects but are likely to get some, so take whatever help is available.
I found it helpful to ask for copies of all my tests and scan reports as it made me feel in control.
Pack a bag for your chemo day, with a book/Kindle/tablet, favourite food & drink, a rug, even fluffy slippers. I used it as a ‘pamper day’ - and try to get a lift to & from, just in case you’re not up to driving home.
You may be given an option to have a PICC line or port. I had a PICC line and it made chemo so much easier than them having to find a vein every time, so I would advise it, I assume a port also has advantages.
Good Luck 🍀and Congratulations 🍾🥂for getting this far on your journey.
Just finished my last round of chemo and it was a little rough I do admit. Asked my team and they said it was like going thru it the first time. The only issue had was my neuropathy, which was happy for which was the only thing.
Hi Margaret, delighted to hear you are over the op & doing ok. It will take time, but you will be amazed how quick you recover when you get home. You won't be allowed hoover,iron or lift anything heavy for 6 weeks & force yourself to get outside & walk a little more each day. I also have a stoma since my op in feb 2019 & gynaecologist said he won't reverse it till I have recovered fully. I had a few accidents with it when I came home first & it took awhile for me to have the confidence to go out to a coffee shop or to a restaurant but I got there. Just a tip I found the drainable one- piece stoma bags were much better as the skin barrier never comes away like the two -piece bags so no accidents & you will have to adjust your diet too to see what upsets your stomach or not. When you are going for your chemo bring your little bag with a supply of bags just in case because it's usually a long day & if you need to change it I am sure there will be a curtain around your chair for privacy. I also brought a spray deodorant with me 😂 You will get used to the stoma & look back in a couple of months & wonder what you were worrying about . I think Ovacome had information recently on stoma's maybe you could contact them or if you have anymore questions just ask me I will be happy to help. Good luck with your recovery & chemo & let me know how your getting on. Xx🌸
I have just had my last post op chemo. The debulking was pretty much as you describe with the exception of having to leave behind some in 4 locations. Despite initially being relieved I didn't have a stoma or an illyostomey only to be told they had to leave seeding on large and small bowel and rectum and also nodules on diaphram. My reaction to such a long anaesthetic wasn't good. I have come to terms with this and will have 18 treatments of Avastin hopefully starting soon. Had scan on Monday so hoping for the best from this. My advice for your remaining chemos would be to really rest up. I have experienced severe fatigue which I didn't pre surgery. I was advised this is the accumlative affect of chemo and so just go with the rest your body needs..fine line with the activity you need alongside the rest you need. Other advice I was given was to take the anti sickness tablets as a matter of course rather than waiting to feel sick. Have done that since 1st chemo and haven't had any nausea. (It was a chemo nurse that advised me to do that!). Good luck.
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