I just found this group and have already found some comfort reading through some of the posts!
My husband, 60 years, and I are Danish citizens, living in Italy since year 2000. Around Christmas my husband had some small issues eating, so he saw our doctor who referred him to a gastroskopi. The biopsi showed cancer! We were referred to a PET-scan, which showed cancer in the stomach.
During all our time in Italy we have been covered by private health insurance, and have used the Swiss health system, which is also where my husband is being treated now. However, this has caused even more concern as we also had to decide where/which country (Italy/Switzerland/Denmark) to seek treatment, and we have been in total shock from the diagnosis! It is only now I can manage to try to seek information.
You all seem to know your exact diagnosis, and I feel so stupid, because we know very little! Until now we have felt so overwhelmed that we have not had any questions, just waited for more bad news.
During the labaropskopi the surgent took biopsi of 2 lymph nodes which showed cancer, so we were told that for now surgery is not an option. The oncologist has not mentioned cancer in any other organs, and we have not asked! For now and for the next 2-3 months my husband will have chemo and immune therapy every 2 weeks, he just finished 2nd treatment. Then a scan, which will hopefully show that the cancer has stopped growing or even diminished in the lymph nodes. If so surgery will become an option. The oncologist told us the surgery will be complicated, and will have to be performed by specialists in Milano, because they don’t have the necessary knowhow in Switzerland.
So we are hoping the treatments will have an effect, so surgery will be possible! Reading here has comforted me regarding surgery, and especially how you cope afterwards!
However, for now I dare not hope! The oncologist was fairly optimistic the treatments would work, because the lymph nodes were still small. Also if the treatment works my husband would feel an improvement when eating, and already after 1st round he has less trouble eating.
For now I have no questions for this forum - I still don’t know what to ask, and I am not sure I want to hear any answers! The whole situation just feels so unreal - we are still waiting to wake up from this nightmare! We have been preparing for the worst possible outcome, but reading here gives me some hope, thank you! Tina
Hi so sorry to hear of your husband’s diagnosis… you’ve come to the right place to have a chat… when you are ready to ask questions, hopefully someone here can give you the answers…
I was diagnosed in November 2021 with stage 4 signet ring and had my stomach removed a year ago… I had 8 rounds of chemotherapy in total called FLOT… touch wood I’ve been ok and I am getting my life back to normal…
Take care
Michele
Ahhh, so sorry you find your self here Carate I know only to well what it feels like not knowing much at all and everything seems to take time. My husband had his stomach out in Jan and he’s doing absolutely fine at the moment.
As Vespa says when you’re ready to ask us a question I’m sure someone will be around to help you. Hope you get to know something soon xx
Hi
Welcome to our group! This must be such an uncertain time for you! The only good thing is you have access to different medical opinions in different countries! But that brings its own challenges.
I have heard of others in this group who have travelled abroad for treatment not available in the UK.
I think it’s more difficult to get a second opinion here!
Chemo can be very effective and immunotherapy is such a breakthrough in cancer treatment!
I do hope that you get good news and that surgery becomes an option!
Do use this group for support, there are lovely people who understand and can support you!
Jac
On Thursday we had an appointment with the oncologist to hear more about how many rounds of treatment and when to expect a scan. The cancer is stage 4 and has spread to the peritoneum. They are planning for 6 rounds of treatment, then a scan and depending on the result maybe an operation. My husband is experiencing very few side effects, is eating much better and his mood has improved tremendously, which is all good, of course, but also has caused me to forget that we don’t know until the scan IF the cancer is responding to the treatment!
I am feeling so depressed and lonely - I know I should try to stay positive, but I am so scared!Reading all your stories here, and all your kind support and encouraging words to me and everybody else, made me hopeful that we will manage to beat the cancer, but right now I dare not hope! How does anybody manage to cope with all this uncertainty?
My husband’s heart is stressed by the 5fluorouracile, so next time they will give him another drug, just as efficient, which might cause diarrea. Hopefully he will not be too affected, but after 3 rounds of chemo/immune-therapy we were starting to feel that we knew what to expect. Now it is back to starting point. And we don’t know if it will help!
So again no question - only the big ones - how do you all manage? How do you manage to stay positive? How do you manage to offer support and encouragement to other people? How do you manage all the waiting? How do you manage all the uncertainty?
Morning My husband too has had total gastrectomy and begins final chemo on Tuesday. Hes very low mentally as hes so used to being busy all day but is constantly tired (to be expected) I was wondering if you could give me any advice re his diet Did you find a good book to help you? We actually live in France and my language skills are not brilliant and although we see a nutritionist they dont seem to offer any practical ideas? At the moment hes being fed at night from a feeding tube Oh and he enjoys Jelly !! when I can find it in the supermarket!!! Bonne chance (Good luck) for continued recovery
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