Pancreatic Cancer Group: Introduce yourself and connect with others
Welcome to the Pancreatic Cancer group on Mayo Clinic Connect.
This is a welcoming, safe place where you can meet people living with pancreatic cancer or caring for someone with pancreatic cancer. Let’s learn from each other and share stories about living well with cancer, coping with the challenges and offering tips.
I’m Colleen, and I’m the moderator of this group, and Community Director of Connect. Chances are you’ll to be greeted by fellow members and volunteer patient Mentors, when you post to this group. Learn more about Moderators and Volunteer Mentors on Connect.
We look forward to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Pull up a chair. Let's start with introductions.
When were you diagnosed with pancreatic cancer? What treatments have you had? How are you doing?
Interested in more discussions like this? Go to the Pancreatic Cancer Support Group.
Hi @barbchar63, welcome to Mayo Clinic Connect. You've had quite the journey. While @marvinjsturing doesn't have kidney cancer that has metastacized to the pancreas, he does know the feeling of cancer returning.
You may also be interested in this discussion with Marvin, @luckyone4321 @kjrita and others
- Total Pancreatectomy https://connect.mayoclinic.org/discussion/total-pancreatectomy/
Hi, I'm @mscarano and was diagnosed with pancreatic cancer in October 2019. However, biopsy was not conclusion. I went to Memorial Sloan Kettering and they recommend surgery to remove the tumor (stage 2?). However, after opening me up they decided is was wrapped around veins more complex then they thought and did not remove the tumor (but biopsy from surgery confirmed carcinoma. I then went on 4 months chemo and 4 weeks radiation. Current diagnosis is slight shrinkage but too risky to do surgery. More treatment does not increase chance for survival. Now in wait and see mode to see if tumor has been killed. Next scan is December.
I have decided to get a second opinion from Dr. Mark Trudy, which is currently being triaged. My one question to the group is my consistent "bowel purge events". I can't seem to go more than 10 days without the event, which is emptying my bowels totally, but not diarrhea, but sometimes a little at the end. I have increased my enzymes to 4 pills (36,000) at breakfast and lunch, 5 for dinner and 2 for snacks. I lost about 55 lbs from my normal weight but over the past few months have stabilized around 137 lbs (6 ft tall), work my way up to about 144 before having the "purge" event and then back to 137 lbs. I also salivate into a cup when having the purge event most times. All doctors say is to work on better managing enzymes, but this cycle has been going on for months.
That's ii for now.
Hi @mscarano and welcome to the pancreatic cancer support group on Mayo Clinic Connect. I think you might also be interested in this discussion regarding stage 2 and treatment with Dr. Truty:
- Need advice: Stage 2 pancreatic cancer https://connect.mayoclinic.org/discussion/need-advice-2/
In these discussions, members, like @dakotarunner @fassbinder @kjrita @mayojoe7 @marvinjsturing @lml @susan2018 are talking about getting the right amount of enzymes for digestion and loose bowels
- How are others with pancreatic cancers managing diarrhea? https://connect.mayoclinic.org/discussion/managing-diarrhea/
- Pancreatic enzyme replacement https://connect.mayoclinic.org/discussion/pancreatic-enzyme-replacement/
What advice do you doctors give you about managing enzymes?
Thanks for the info. Will check it out. Doctors just stated need to better manage my enzymes but not easy. They did recommend increasing, which I did.
This is very interesting. Do you happen to know how to locate a surgeon who does arterial resection? Anyone?
I am curious of what Dr. Trudy has to say. Please share when you know. Thank you!
Still waiting on a formal response. They want to do more diagnostics but have yet to discuss with any doctor. Will contact surgery unit next week as that is my point of contact.
The Mayo Clinic in Jacksonville has two surgeons with arterial resection experience. One of them was scheduled to perform this on me in 2018 but my cancer miraculously broke up between the date of scheduling the surgery and actual surgery which was whipple procedure. I am now a 27 month survivor. Local oncologists and surgeons had told me to go home and get my affairs in order. Fortunately, I was able to locate the Mayo site explaining how the arterial resection is performed. I think they have at least one qualified surgeon at Rochester. I do not know about Phoenix.
Have diagnostic tests scheduled in Rochester on Oct 27 and Dr. Truty appt on Oct 28 to determine best path forward. Coming from New Jersey so first time traveling out of state (flying) since COVID-19,
Hello @mscarano,
I appreciate your posting about your appointments at Mayo Clinic. Wishing you safe travels there and back home.
I would love to hear an update about your experience at Mayo and any information you learned from your appointments. Will you post again?