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.
I appreciate you sharing more information, @ryanmary3341. I can understand that the surgery was difficult. How long were you hospitalized after the surgery? Do you have any blood sugar problems?
You mentioned that the tumor (or cyst) was precancerous. Did the biopsy give a name to the tumor?
I was hospitalized for 12 days. I do have a blood sugar problems. I understand it common with my condition. If they did give a name to my tumor, I do not remember. If it is important, I will investigate.
Hello @ryanmary3341
I just wondered about the name of the tumor because I feel it is important for each patient to be educated about their health. Also, we may have other members on Connect who have had the same type of tumor/cyst and we can introduce you to them for further support and information.
By understanding your health condition better you are able to advocate for yourself. This type of knowledge is generally empowering to patients.
If you are interested in finding out what type of tumor you have you can read the biopsy report. If your doctor or hospital has a patient portal, you can read and print the report and that will give you all the information about the biopsy results. Otherwise, if you want to know more about the tumor, you can call the doctor's office and have them mail you a copy of the biopsy report.
Yes, you are right, blood sugar problems are common with any disorder of the pancreas, especially if there is surgery on the pancreas.
Does your blood sugar high or low? How do you manage your blood sugar problems? Do you take meds?
The pancreatic tumor is pre-dominantly a intraductal papillary mucinous neoplasm with high-grade dysplasia with faci of invasive colloid carcinoma.
Hello Again: We are at MGH in Boston and they have told us that his cancer is confined to the pancreas but it is not operable at this time. They have communicated hope that the chemo Folfiorinox will be approximately 4 mos and then radiation another 6 weeks, hopefully followed by surgery at the end of the year. The goal is to get the tumor to come away from the blood vessel so they can operate. I have read in the Mayo lit that PET imaging is important in guiding the therapies. I know they don't use PET at many other places. How important is it? Anne
Hello @annebauer19
You ask a good question. As you know, on Mayo Connect we are not medical professionals, but patients who share their experiences. I'd like to tag some of those members in Connect to see if they have some information about your question. I'd like to tag @marvinjsturing
and @ryanmary3341
There is also a discussion about the PET scan in Connect's pancreatic cancer discussion, here is the link, https://connect.mayoclinic.org/discussion/pet-results-pre-potential-whipple-treatments/.
Perhaps your husband's oncologist or radiologist could help you with this? It wouldn't hurt to ask the question.
@annebauer19 @hopeful33250 My experience began 7 years ago. My oncologist wanted to do CT scans after my Whipple. CT scans work better when contrast is used. My chemo damaged my kidneys and my body cannot handle the contrast. I had PET scans for 5 years because instead of contrast they use a radioactive sugar which my kidneys can handle. Since my cancer came back a year and a half ago, I have been going back to Mayo every 3 months for a PET/MRI scan.
My chemo started yesterday, and so far no side effects. I will undergo 6 cycles(6) months of therapy, 3weeks on one week off for total of 6 months. I was doagnosis with EPI first and my gastro Dr. sent my to get further testing witch showed a 3cm cyst on my panceras and then he sent me to a surgical onocologist who reccomended the whipple surgery.
Hello again: thanks for the comments about PET scans. My husband has started chemo this week so we are just learning the rhythm of the 2 week cycles. So far his biggest complaint is stomach pain which comes and goes. It's not clear if it's related to the tumor. Docs seem to be unsure. Has anyone experienced this and found something that helps?? I am trying to keep up his spirits and mine. This pain seems to drain him.
Pain is draining - for both of you I might add. Has he been able to talked to the oncologist or symptom management nurse about the pain? They should be able to give him something to ease the pain.
Does this affect his appétit?