Hi everyone, my husband had his staging lap on the 6th Dec, we never see the surgeon after so I'm guessing it goes to the MDT meeting, hopefully get to know by the end of next week. 
Today we received a pamphlet about the procedure, it really scared me.

What other tests will he have to have, he's had CT, PET plus staging lap. Does he have to have a fitness test or things like that.
If you remember it was found through his yearly CT scan for his kidney cancer, also at the same time they found he has Non Hoskins Lymphnoma.

Its good to talk to anyone who's been through it and come out the other side.

Im getting ahead now but the cooking when he comes home is reall worrying me, in fact I'm so so scared xxx

Thanks Milly, I'm still scared but the infos very helpful. Xx

Hi y'all. 
I am barely breathing here watching the football! Wow.c'mon the Dutchmen (:

SueCC- Of course you are scared, bit strange it you weren't- the emotions experienced through the whole thing were crazy . The full spectrum - anger, joy, optimism, pessimism, tears, laughter. Don't worry about feeling what you do, just go with it, it is okay.

Glad the lap is done. Another item- ticked off, We didn't see the consultant until MDT D day. That's when you get the verdict , if you like. They'll tell you the clinical staging and what they can do about it.

it truly is a surreal time, but here we still are having gone through the mill and out the other side. Look back on it and still can't belive it was all real! I struggle sometimes to remember what exactly happened in what order.
The fitness test is what they do pre op, if surgery is part of the plan- but you'll find out more on MDT appointment. If questions pop into your head- as they do, frequently- then jot them down to ask- as you'll come out of there saying " I wish I'd asked that" 

I totally agree with Millie in that we certainly do get it (: and about google and the net in general- what a horror show- doesn't reflect on the reality at all.

When is your MDT?
Always keeping that faith

Hilts

Hi [@Hilts]‍ , husband was cheering on the Duchmen as well but not to be.

The MDT meeting is Monday evening so hope to here middle of the week, but on the letter I had to take from the hospital staging lap to his doctor it says "proceed to total Gastrectomy " so that to me says take his stomach out, am I on the right track there?
Does everyone have in a letter with all the things that can go wrong it name quite a few, like having to have a feeding tube for ever, lots,of awful things also with a 50-60% 5 year survival rate. It makes you sit up,and think, I don't think he can have chemo with having one kidney and lymphoma pluss his age 79.

Anyhow thanks for answering me, Take care x

Aha, Sue CC

I did make me 'smile' rather when you mentioned the 'surgical risks'letter !! I remember it well- a total horror show. A 20% risk of death and other happy facts. Yes, unpleasant to say the least. Informed consent has its downsides!!
BUT our view was and probably still is " what choice did we really have" at 56years at diagnosis- in order to give best chance for getting above that age we or rather he had to undergo surgery. If he was say 90 we might not have made the same choices- if that makes sense.

Blimey though, that letter being delivered by your good self to the GP , was a tad 'insensitive' by the hospital
But if total gastrectomy is what is planned, that is removal of stomach- same ,sort of ,as oesophagectomy ,as the stomach becomes the new / replacement oesophagus during op. He will be able to eat again, but will have feeding tube for a bit like all of us on here. It wasn't so bad, husband managed it all himself and it did take the pressure off having to eat.

I would say though , if it had spread all over the place, they would not even being considering surgery, so a plus in a strange sort of way. 
Do ask the MDT , but they are likely to tell you anyway,  about any chemo or radiotherapy . Because the whole thing is so specialised toward the individual, maybe some patients just don't need the chemo for whatever reason. I think it would be fair to say all of us on here, that despite having the same condition have had differences in treatment for one reason or another, but ask them.

As for the Dutchmen, what a fantastic fight back, just watched Morocco pull it off - wow, some achievement. I won't be watching later, my nerves won't take it! Husband will be down the pub- sipping a few pints!!! He has just stuffed himself- without a stomach with steak and chips! I give up!
all faith keeping 

hilts 

Morning Sue,

You are on the right track there ! Total Gastrectomy is whole stomach removal, which is the procedure I had ... so if you or your Husband have any specific questions, concerns or need help with anything - feel free to ask.

I was in for 9 days post surgery, fed intravenously via nutrition drip bags overnight for 6 days whilst nil by mouth while the join inside healed and then transitioned onto normal food and discharged. 
 

There's a lot of information shared earlier on through this thread of foods I was eating when I first got out which might be helpful to you to read back through to understand Total Gastrectomy journey etc.
 

A run across the rooftops of my journey etc is on my profile if you click on it and if you want to know anything else, happy to help out.

[@Hilts]‍ you make me laugh about your husband stuffing him self before the pub. Gives us hope.

[@Redski]‍ thank you so much, I'd got into kinda of thinking Ivor Lewis was the operation every one had no matter what was coming out! then realised that couldn't be. So what I've read on here most people seem to have had the Ivor Lewis, Does that still include the stomach or part of it and the Oesophagus coming out or does it depend where the cancer is in it.?

As I said if my husband can have the operation its his stomach that'll be coming out. I'd be interested to know how long your operation lasted for. He was told he won't be having Chemo I don't know why maybe as he's 79 and only has one kidney also Lymphoma (found same time as stomach cancer) but I will ask when we get his results.

Its the MDT meeting tonight and I really hope we get his results this week.

I read all your posts this afternoon Redski and the kids meals sound interesting , I'll look into that. That's one thing that's scares me the food, will I get it right, I've read about Dumping syndrome and it sounds so very frightening. 
Do any nurses come and see you when you're home? I think I know the answer to that though, 

Really nice to know you're there, could I message you if need be Redski?
Thanks everyone for all the answers you give so very helpful at a very stressful time xx

I think the surgical procedure varies by tumour location, size and also the surgeon doing the operation.

My surgeon does robotic keyhole but in my case he decided to do the old fashioned, open procedure and was weighing up between the Ivor Lewis and a Total Gastrectomy and in the end for went for removing the whole thing,

Ivor Lewis removes most of the stomach, but leaves a small portion of it behind to serve as a pouch / pseudo stomach.

My op was 8 hours on the table, but that included live histology in the lab, to check for clear margins (think dry rot removal on wood!)

Don't be frightened, its OK ... and if you need anything else - just ask, plenty of experts with bags of experience between DoogGreg, Hilts, Milly, Andi and the gang.

Hi Redski, Sue and all,

As we all say everyone is individual. My husband had Ivor Lewis but initially part by keyhole on abdomen and open at the back. He had half his oesophagus removed and a third of his stomach with everything moved up. Surgeon said his remaining 2/3 of stomach is now located near his second button on his shirt! He is able to eat/drink pretty much anything now fingers crossed just a bit less. 

Sue we chose to have an electric bed as we had originally ordered a new normal bed before diagnosis. He has found this brilliant. You can get wedge pillows which he has for going away both solid and inflatable. You get VAT off bed due to medical reasons. 

keeping the faith for everyone 

Milly