Update three weeks post op

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Hi there , im not on any pain killers as ive had no pain after two weeks being home my op was on the 24th of June,  I was in intensive care for nine days with pneumonia then on the ward for another three. Once I was home I was already drinking fluids and soups and had protein shakes in hospital which they said they would send me more , they come yestaday so was lucky to have my own protein at home to make my own shakes . Im eating small now have one weetabix with milk and a drizzle of honey ( helps me keep my bowels active) ive been have full fat greek yogurt with a drizzle of honey , ive had a kids mac and cheese ( but go slowly ,chew and soon as you feel a little bit  full stop. I ate a bit much first time and got the sweats for 10 min but it went off ) ready brek is easy to consume and last night I had one piece of small salmon ( used to eat the two in the packet) two and a half sprigs of steamed brocoli which I drizzled olive oil over and squeezed some lemon then seasoned with  salt and pepper was so nice .I find going for a small walk after eating the more whole foods help and chewing gum is helping me digest it quicker . Of a night ive woke up with acid creeping up even though ive propped my self right up but hospital said i can take lansoprazole before bed and in the morning and it really is helping me as sleep as been my main struggle but last night I had a good rest .I now have 8 boxes 4 chocolate 4 banana of the protein drinks they sent me yesterday,  57 sachets in each box , im in essex if anyone needs some or more I'll drop off for you all un opened , such a shame to waist guess I could ask the hospital if they want them back to give out . Take care everyone , your all in my thoughts xx stay posative ...tony x️ 

  • Hi Tony,

    Sounds like you’re doing really well for being only 3 weeks post surgery. Was it the Ivor Lewis op you had? Do you have the large wound on the right side of your chest or did you have the robotic procedure? From what you have said about your eating, I presume you didn’t have to have a feeding tube fitted. I hope your recovery continues as well as it has started. Best wishes, CB

    • Hi cool blue , yeah was the ivor Lewis op, I didn't need a feeding tube .im still coughing and stuffs slowly coming off my chest but had a xray last week and alls clear , they just said obviously they clapsed my lung then I got pneumonia so its normal to still be coughing and feel a bit of discomfort.  When I say discomfort if I take a big breath at the top of the  breath I get a minor pain top of my rib cage and I then cough , I had two courses of steroids in hospital but they assure me I dont need more , ive been walking loads took my son and father to the coast and on my father's fit bit we walked 17 miles in 3 days lol I really didn't mean to walk that far but mooching round shops differant beaches etc . They said I have 6 - 8 weeks post op before I start chemo again and ive just started to get some sort of hair style back lol never mind it will grow back again 
  • Antibiotics not steroids 

  • That’s brilliant. There’s certainly no way I was walking those sort of distances at your stage! I’m nearly 17 months post surgery and  could manage it ok now. I try to get out for at least one good walk a day plus some cycling and swimming. I have also set up a wee gym in our shed and do some resistance exercises two or three times a week. I can eat pretty much anything I want now (have to go easy with chocolate though) albeit in small portion sizes. Intermittent reflux is my biggest problem as it can knock me back for a few days after a bad episode. Fortunately these episodes are becoming less frequent and usually occur when I eat past my 8pm cut off time. I had an annoying cough too for about 6 weeks after my surgery. You’ll probably find the post-op chemo tougher than the pre-op. I did anyway. After 4 cycles at 100% pre-op I only managed 3 cycles at 75% strength post-op but my oncologist was okay with that as my pathology was pretty good. 

    • Ok , good to hear you are eating what you like and ive fancied chocolate but not gone there yet but like you said just smaller portions. I was a bit of a gannet I ate food fast and I could get through big portions,  now its practicing eating slowly and my eyes are defo bigger than my belly just need to know when to stop and and im learning thats before I feel full coz thats when it becomes uncomfortable etc so smaller slower is key . Yeah ive wondered what strengh second round of chemo will be ive got to go hospital 28th of July to see lab results of what they took , surgeon said it went really well but got to see how many lynth nodes they took . My mum had this cancer 7 years ago she struggled after having second chemo and they stopped had had same procedure as me etc but hers come back in covid as 3 brain tumers and they sent her home and we looked after her till she passed god bless her x she was 73 and hers was mor advanced than mine. I think she give me a nudge from up stairs as I wouldn't av known about this cancer or got checked out . I had that fear of thinking it can come back but got over that to the point of just stay positive no one knows what's round the corner ,every day is a blessing. 
  • Well done sounds like you’re doing great !!

  • Thank you Dibden doll Blush