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.
Has your PC been staged?
Where is it specifically located? This is important ... it sounds as if, given the biliary stent, that it is pressing on the bile duct?
You should review this - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469083/ - and as many more recent papers and analyses, as possible.
What are your CA 19-9 cancer marker numbers?
My sense is that you may not have read enough to ask the questions - and, demand answers. And, since you are at a local hospital, you may be getting a standards of care approach. This is, in my mind, NOT sufficient for pancreatic cancer.
I can only say - if it were me, I would be on the phone with Anderson, Mayo, Kettering, etc - TOMORROW - and immediately travel to your choice - frankly, whoever can see you IMMEDIATELY. Please don't wait!
This is exactly what I went through last October. My oncologist recommended 12 rounds of chemo. Then the surgeon at Mayo wants 3weeks of radiation. Then the Whipple. But I guess every person has a different diagnosis. My tumor is on the head of my pancreas and is sitting on a major blood vessel so they really want to shrink the tumor as much as possible before surgery. The surgeon says once you do the Whipple there’s no do over. He’s got to make sure he gets it all with good margins.
I wish you the best. The whipple scares me to death but maybe it’s the only hope. Curious if you could share any information about a Mayo Clinic whipple. Would it be done laparoscopically and perhaps even robotically? What did they tell you about surgical complications and what a post whipple surgery recovery/life would be like. Thanks.
Would like to know too . Following ♥️🙏
My surgeon says not laparoscopic or robotic. He said he will do it the old fashioned way. A cut from the bottom of my ribs to my belly button! I have heard they can do it laparoscopic but my surgeon won’t. It could be because my tumor is sitting on a major blood vessel.
marviak9,
The usual reason for not doing Whipples laparoscopically is the lack of training of the surgical team, and the lack of sufficiently advanced surgical theater and equipment.
While the survival rates are close to the same, reportedly, the post operative infection rates are better with laparoscopic approach.
Please consider going to a major pancreatic cancer center.
I had an open Whipple surgery 12 weeks ago and am finally able to say that I feel pretty good. The road to recovery was slow for the first 5 weeks and then things gradually started getting better from week to week. Going in to it, I was most concerned about recovering my appetite and not losing weight post-surgery. Fortunately, I was able to eat fairly well one week after surgery and never had any major gastrointestinal issues. The main issue was pain and discomfort from the incision and itchy sensitive skin around the incision. It just took time for this to heal.
I had my surgery done at Johns Hopkins and my surgeon has considerable experience doing robotic Whipple procedures. I was expecting/hoping for a robotic surgery, but plans changed at the last minute due to some unexpected pancreatitis-related issues I had leading up to the surgery. My tumor was also in close proximity to blood vessels, which complicated things. Having been through an open surgery and the experience of dealing with the incision, I feel that recovery from a robotic procedure has got to be a lot easier to deal with. But whether this is an option will depend on where you are and your specific circumstances.
mmatunis,
A very good point - there are medical reasons, as you noted, to not perform Whipple laparoscopically, and given your experience was at JH, I would be comfortable with that decision.
Thank you for your advice. I am going to Mayo in Rochester and am very confident with my providers. Yesterday they found a small (7mm) lesion on my kidney so they will do a biopsy on that next week.
What kind of radiation protocol? Ask about Magnetic Resonance guided Adaptive Radiation Therapy. This is a „curative“ protocol and involves about 5 high-Dose radiation, every other day. Nothing else that I know of is „curative“