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.
@gmaryanne,
Thank you for your reply. We are at a major medical center, midwest. When I clicked to find providers of excellence from your post, I was surprised to find they werent on it! but another local hospital is! Soninlaw is now 4 1/2 years out from diagnosis and chemo radiation . Now having GI bleeding issues due to radiation damage, apparently.
There are a lot of major medical centers, but not many pancan centers of excellence.
It is extremely important to go where the best are!
@drhmch, I'm sorry to hear that chemo has been a challenge with unanticipated complications. For some patients, surgery is not possible and some patients choose not to have surgery due to the reasons you've stated.
I think you might appreciate joining this related discussion in the pancreatic cancer support group:
- Decided not to have surgery. What’s next?
https://connect.mayoclinic.org/discussion/whats-next-5/
I find a fairly quick response through the messages in the app. Usually 24-48 hours.
When they were first diagnosing my husband's cancer, we contacted Cleveland Clinic for a virtual second opinion. Very disappointed with that as they simply repeated what the oncologist said here... and they both misdiagnosed the primary so it set us back months of wrong treatments. I was told afterwards that we (non medical people) could have requested additional tests, etc. But we went for the virtual second opinion believing that the oncologist there would order any relevant tests, and he didn't. His words gave us false hope that we were on the right tract. If we did it again we would ask many more questions.
Oh very interesting! We just submitted a request to Mayo fora second opinion. Wonder if that will be the same?
I sure hope not…..
In my husband's case all the reports kept coming back saying "consistent with lung cancer" so apparently no one checked to see if it could have been something else. A CA19-9 blood test would have shown easily that it was pancreatic cancer. Or a biopsy on the spot in the pancreas. But until we switched oncologists, those were not done and we had no reason/knowledge to request them. I don't have any experience with Mayo but would hope they are more on top of these things. Good luck to you!
One of the basics - and cheap - is CA 19-9 blood test.
Any competent medical facility, or even a family doctor should be knowledgeable enough to insist on this.
Hi @breemichelle26, I believe your question is for @marciak9. I'm tagging her to make sure she sees it.
Hello!
They haven’t done a scan yet. I go to Mayo on the 16th and they might have news. I’m scheduled for a PET on the 17th here. I just had my 6th treatment.