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.

@optimist1591

Hello. A recent MRI showed "T2 bright lesions" in my pancreas with "no obvious connection to the pancreatic duct." I know this is not cancer...for now. Protocol states follow-up MRI in six months. As a two-time cancer survivor (breast cancer 1998 and thyroid 2008), my sense is that six months is too long to wait. I am following up with my primary care and obtaining other medical opinions. Am I over-reacting? I would appreciate feedback from anyone who has been here. Thank you.

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@optimist1591 , I can't say much about the protocols specifically, but if you are considered a HRI (High-Risk Individual) there's usually a separate category in the flow chart.

Most of the HRI assessments include genetic testing for inherited mutations and discovery of close blood relatives with cancer history. Since you've already had two types of cancer, I suspect you'd fall into a higher-risk category that justifies more frequent testing.

Sometimes they interweave different types of tests (EUS, MRI/MRCP, PET) in shorter intervals to get different views and check for rapid changes, then back off to less frequent monitoring if all appears stable.

But with your history, I would err on the side of caution... Seek out a second opinion, second imaging appointment, and start getting fairly regular blood tests for CA19-9 and CEA to get a baseline of those. They're not gold-standard indicators on their own, but it's easier to know if they're increasing when you have a healthy reference to compare them to. Get a germline (hereditary) genetic test like Invitae if you haven't already.

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Hello. A recent MRI showed "T2 bright lesions" in my pancreas with "no obvious connection to the pancreatic duct." I know this is not cancer...for now. Protocol states follow-up MRI in six months. As a two-time cancer survivor (breast cancer 1998 and thyroid 2008), my sense is that six months is too long to wait. I am following up with my primary care and obtaining other medical opinions. Am I over-reacting? I would appreciate feedback from anyone who has been here. Thank you.

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Thank you so much for your information and your reply. They did move his scan up from mid May to next week, so we will see what that says. Until then we are trying to remain positive or at least neutral and not totally freak out about the very dramatic increase in that value. I always seem to prepare a little space in my mind for the worst news just so I can better handle it when it comes. I know that is probably not the most hopeful or positive way to approach this but maybe it is just a coping mechanism for me. Not sure. Regardless, thank you for your reply and prayers for all facing this journey,

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@clschreiner

Good afternoon,
My husband has Stage IV pancreatic cancer that has metastasized to the liver, perineum, and possibly a couple lymph nodes. He had a stent placed this week to help with a blocked kidney ureter and then had his 13th round of chemo yesterday. Because he is on a trial they do extensive labs every 2 weeks. Two weeks ago his CA19.9 was rising but not drastically. It was at 2,819 on the 25th of March and his labs yesterday report a CA19.9 of ">34,000. The office did confirm for me that this is not a typo and moved his scan up from May to two weeks from now. Has anyone else had a drastic jump like this? His CEA is also rising slowly, it is at 3.8 now I believe. When he was diagnosed in August of 2023 the highest CA19.9 he ever had was just over 10,000. I am slightly panicking at this new lab value. Any experience or insight on this that can be shared would be appreciated.
Thank you in advance.

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@clschreiner, that must be very scary for you both. You are not alone. There are other members talking about dramatic increases in CA 19-9. You may wish to join these discussions:
- CA-19 has elevated even more
https://connect.mayoclinic.org/discussion/ca-19-has-elevated-even-more/
- CA 19-9 and pancreatic cancer: What do the numbers mean?
https://connect.mayoclinic.org/discussion/ca-19-9/
See all: https://connect.mayoclinic.org/group/pancreatic-cancer/?search=Ca+19#discussion-listview

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Good afternoon,
My husband has Stage IV pancreatic cancer that has metastasized to the liver, perineum, and possibly a couple lymph nodes. He had a stent placed this week to help with a blocked kidney ureter and then had his 13th round of chemo yesterday. Because he is on a trial they do extensive labs every 2 weeks. Two weeks ago his CA19.9 was rising but not drastically. It was at 2,819 on the 25th of March and his labs yesterday report a CA19.9 of ">34,000. The office did confirm for me that this is not a typo and moved his scan up from May to two weeks from now. Has anyone else had a drastic jump like this? His CEA is also rising slowly, it is at 3.8 now I believe. When he was diagnosed in August of 2023 the highest CA19.9 he ever had was just over 10,000. I am slightly panicking at this new lab value. Any experience or insight on this that can be shared would be appreciated.
Thank you in advance.

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Hi thank you for the reply and tagging others. His Surgery is scheduled for this Friday. Due to a new group of doctors haven’t gotten a clear update oneverything yet. as soon as I know more I will post it. Don’t have a twitter account tho.
burksgrl

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@burksgrl

Hi joining on behalf of relative dx pancreatic cancer 12/2019. completed radiation and chemotherapy. had gb stent placed at the time, and replaced recently. now admitted to hosp after vomiting large amt old blood. followed by two episodes BRB vomiting requiring 2 units. Ca 19 has been normal thruout (?). has had multiple CT’s and a pet scan showing no new mass.
Now planning a minimally invasive duodenal bypass surgery. no peritoneal lesions noted after laparoscopic exam (large amount of scat tissue) and washings submitted for pathology
(negative). currently on tpn and npo.
The main concern right now is to avoid a repeat gi bleed .
platelets 130 and stable. Hgb 8.6
any experience with this type of gi surgery? They are hoping to avoid open laparotomy.
Thank you for any help.

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Welcome, @burksgrl. I'm tagging a few members like @mamarina @faithann64 @lfitz @k13 and @hopeful33250 who are familiar with GI issues after pancreatic cancer treatment and may have experience to share about bypass surgery for a blocked duodenum.

You may also be interested in this related discussion:
- Anyone have experience with total parenteral nutrition with PC?
https://connect.mayoclinic.org/discussion/anyone-have-experience-with-total-parenteral-nutrition-with-pc/
How soon is the surgery planned for?

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Hi joining on behalf of relative dx pancreatic cancer 12/2019. completed radiation and chemotherapy. had gb stent placed at the time, and replaced recently. now admitted to hosp after vomiting large amt old blood. followed by two episodes BRB vomiting requiring 2 units. Ca 19 has been normal thruout (?). has had multiple CT’s and a pet scan showing no new mass.
Now planning a minimally invasive duodenal bypass surgery. no peritoneal lesions noted after laparoscopic exam (large amount of scat tissue) and washings submitted for pathology
(negative). currently on tpn and npo.
The main concern right now is to avoid a repeat gi bleed .
platelets 130 and stable. Hgb 8.6
any experience with this type of gi surgery? They are hoping to avoid open laparotomy.
Thank you for any help.

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@colleenyoung

Welcome, @pfrances. to help you on your pursuit to monitor the pancreatic dilation, here are a few discussions that may be helpful.
- Dilated pancreatic duct: What to do?
https://connect.mayoclinic.org/discussion/4mm-dilated-duct-pancreas/
- Sphincter of Oddi Dysfunction: What helps you?
https://connect.mayoclinic.org/discussion/i-have-sphincter-of-oddi-dysfuncfion-it-causes-severe-upper-abdominal-pain/
See more discussions using the group search: https://connect.mayoclinic.org/group/pancreatic-cancer/?search=dialation&index=discussions

How often are you being monitored?

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Thank you so much Colleen! I will check out those resources.

Next MRI is 3 months.

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@dksissy10

Diagnosed 1/16/24

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Welcome, @dksissy10. I see you were diagnosed only a few short monght ago. I look forward to learning more about you. What stage of pancreatic cancer do you have? What treatment options are available to you? How are you doing?

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