Ampullary Cancer

Hi. My Husband was diagnosed with Ampullary cancer last August..I would like to ask if anyone on here has or know someone who has the same and what your/their experiences are.His diagnosis came with a 6 to 12 month life expectancy. We got to the 8/9 months and it has now spread to his liver, stomach and pancreas.He only has palliative care as any operation was ruled out due to a life changing stroke in 2006.Chemo was also not an option as only a 1 in 5 chance of any major difference and would have made him very very poorly..

Parents
  • Hi, my husband was diagnosed in July 2018, by August he had the Whipple procedure. Horrendous operation with complications following this. The following March he had 6 months of chemotherapy followed by 6 months of recovery. In this time we were able to get out and about a bit however he was always exhausted. He started chemo again this March as it has spread to lungs, neck, aorta and other areas. With COVID this was then put on hold til June, after a spell in hospital through infection, he has only had another 2 rounds. He is receiving palliative care and we have no idea what the future holds. He is currently in hospital again with an infection. We just want him to have some quality of life, be able to get out and enjoy life, for however long that may be. I must say, the living in limbo and not knowing timescales is the most frustrating thing. Sending positive thoughts your way.

Reply
  • Hi, my husband was diagnosed in July 2018, by August he had the Whipple procedure. Horrendous operation with complications following this. The following March he had 6 months of chemotherapy followed by 6 months of recovery. In this time we were able to get out and about a bit however he was always exhausted. He started chemo again this March as it has spread to lungs, neck, aorta and other areas. With COVID this was then put on hold til June, after a spell in hospital through infection, he has only had another 2 rounds. He is receiving palliative care and we have no idea what the future holds. He is currently in hospital again with an infection. We just want him to have some quality of life, be able to get out and enjoy life, for however long that may be. I must say, the living in limbo and not knowing timescales is the most frustrating thing. Sending positive thoughts your way.

Children
  • Hi,So sorry to hear about your husband.Sadly my hubby passed away on the 8th of november 19. He was given 6 to 12 months but fought for 15..He was unable to have any treatment at all due to a life changing stroke, only a 1 in 5 chance of any recovery. Ampullary Cancer is very difficult to treat.In his last couple of months it had spread very quickly..He was 66.

    Thinking of you both,I empathise with you, take each day as it comes and support each other, do what you can  and when you can..If I can be of any support, please dont hesitate to contact me.Wishing to all the very best and look after yourself too.. x

  • I wanted to add my rather more positive experience. I was a grad student in the US and was 44 (very young) and relatively healthy (overweight, but nothing else). I had itching and nausea and eventually was jaundiced. I was tested for hepatitis, and when that was negative, I was quickly diagnosed with ampullary adenocarcinoma. I had a temporary stent to relieve the bile buildup.  I had the Whipple procedure a couple of months later. Horrible operation with a long recovery time, and I had another spell in hospital for an infection. But they decided no further treatment was necessary, so no chemo or radiotherapy. 

    Three years later I was diagnosed with diabetes, I think because of the removal of part of my pancreas, but I'm fine taking insulin. It's been 15 years since I was diagnosed. 

    I think my good outcome was probably due to my age and general health, including the factor of doctors taking my symptoms more seriously, so early diagnosis.  Also, having an experienced surgeon, because this is a rare cancer, and Whipple isn't done much. I lived in a major city, so there were experienced surgeons there. 

     

     

  • Thank you for kind words. I'm sorry to hear you lost your husband, I feel I have been grieving for months now. The disease has progressed as in he was given a time of 2-3 months in November 20. He is at home and doing ok, unable to get out and about but we are taking it a day at a time and seeing family as much as we can. 
    take care.

  • My Mum is in hospital today (Whipple Surgery) she was diagnosed with Ampullary Cancer in mid-February 2021 after turning yellow and complaining about stomach pain / dark urine. She’s been ill for some time now with stomach pain and fatigue, the doctors started giving her B12 Injections in 2019, and she’s also had polys in and around the bile duct. We have been told the tumour is approximately 5-6mm and hasn’t spread to the other organs. They will be taking the lymph nodes out during surgery to check for cancer cells. Mum is 71 and relatively fit, she’s been coping very well and didn’t want to talk much about the Whipple Surgery, I on the other hand have been researching since she was diagnosed and it’s been absolutely terrifying. It’s so refreshing to hear your story Harpy61. I’m personally finding this experience emotionally painful! So many things can go wrong and even though I’m 100% an optimist it’s difficult to comprehend this surgery in detail.       

  • Hi Brooksy41,

    I feel for you & your Mother. I had the same diagnosis & had the Whipples Procedure on 22nd December 2020. It is a severe op & I had a four week hospital stay due to complications, however, I'm still alive & returned to work a couple of weeks ago. Also, to add, I had three lymph nodes removed & they also found a tumour on my right kidney which was also removed.  

    Eating post op is a real challenge but it does get easier over time. 

    Keep the faith & just take each day as it comes. Thinking of you both & sending my warmest wishes. 

  • Hello

    I hope you don't mind but I have sent you a friend request.

    Thankyou 

  • Hello DGDigital. 

    I'm so sorry to bother you but could I message you?

    I sent you a friend request a few weeks ago. 

    Thankyou 

  • Hey Fallmare, 

    I've now accepted your friend request & replied to another one of your posts. :)

  • Hello, 

    It has been really useful to read the comments on this thread. 

    On Wednesday I had an Endoscopy and they found a tumour around the Ampullary. I am having a CT scan on Monday morning so I am pleased that they have rushed this through. Of course I have no idea what the result is going to be but I am obviously a little apprehensive. They have pushed it to a panel that are going to look at in on Monday afternoon. 

    The only symptoms I have at this stage is constantly feeling fatigued, abdominal discomfort and my toilet visits have gone from once a day to 4/5 times a day. I go most days now with feeling sick at some point and this puts me off eating, but I have had no weight loss, in fact ive been putting it on with my stomach increasing in size. I dont overley eat and never have done, and mainly just one meal in the eveing and nothing much in the day. 

    Its not making much sence to me if im honest.

    Kindest regards

    Ian  

     

  • Hey, Ian,

    Thanks for sharing a piece of your heart & journey with us all. It's one heck of a roller-coaster-ride, eh?! 

    I can relate to you symptoms, I'd sleep the clock round on a day off. I couldn't eat either due to nausea, & weight loss was the result. I also experienced bloating, so perhaps that's how it is for you too. 

    I had three different diagonosis: first one was pancreatic cancer, second it was duodenal cancer & final one was, ampullary adenocarcinoma. 

    I asked if that was their final answer, or if they wanted to phone a friend. (fun) ;) 

    To be fair, I'll take the third & final one over the first one. 

    I wish you well & sending you my warmest wishes. 

    If you do happen to reply I'll get an email notification, though you don't have to do anything. 

    We're here if you need us for support. 

    DG :)