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 am a 92 yr. Old woman and was diagnosed with Stage 4 pancreatic cancer 4 months ago, with a prognosis of 6 months to a year left. I chose not to have chemo because of my age. I do not want to go through the pain and suffering of chemo to get an extra 3 months, if I am lucky. Nor do I want to put my family through that. A CAT scan last week showed that the tumor had doubled in size and is wrapping around the artery to my left kidney and spleen. I have lived a good and long life and want to leave this earth with dignity. I am going to have a Neurolytic Celiac Plexus Block this week to hopefully relieve some of the pain and discomfort I am starting to have. Have any of you had this procedure, which is done with an endoscopy? I will let you know hos the Celiac Block goes.👍

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@sonomaga

I am a 92 yr. Old woman and was diagnosed with Stage 4 pancreatic cancer 4 months ago, with a prognosis of 6 months to a year left. I chose not to have chemo because of my age. I do not want to go through the pain and suffering of chemo to get an extra 3 months, if I am lucky. Nor do I want to put my family through that. A CAT scan last week showed that the tumor had doubled in size and is wrapping around the artery to my left kidney and spleen. I have lived a good and long life and want to leave this earth with dignity. I am going to have a Neurolytic Celiac Plexus Block this week to hopefully relieve some of the pain and discomfort I am starting to have. Have any of you had this procedure, which is done with an endoscopy? I will let you know hos the Celiac Block goes.👍

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I am 75 and was diagnosed with stage 4 pancreatic cancer in September 2024. I had the block in Octotober and they said it may wear off. So far so good. It took that terrible back pain away and I also wear a 12mg Fentanyl patch. I was on chemos gemsar and abraxane. They took me off the abraxane because of the awful after effects. They gave me a brake from gemsar because my Magnesium was very low, my glucose was 231 and my platelets were 58. The low for platelets is 150. I finally went back to chemo last Thursday, with a lower dose of chemo and have this week off but they want me to come in to check on my platelets. My Tumor was 7.2 cm and shrank .67 inches since October but my cancer is wrapped around the celiac axis and the body plus the tail. Onc. said I am inoperable and will not survive this disease but will not tell me how long I have. Good luck to you and I appreciate your decision not to have chemo because it wreaks havic with your body.

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@56pan

https://ascopubs.org/doi/10.1200/JCO.20.01399
I spent some time reading up on chemotherapy induced neuropathy last night and over the past few days. This, in my opinion, is the best article I found. Bears out my belief that the only thing that helps is getting off chemo and plenty of time. I'll find out on July 17 after an MRI if I'm a candidate for SBRT for the two tumors I have that have been reduced due to the chemo. Liver and pancreas. If that procedure works and my oncologist takes me off chemo, I'll pass on the results here. I started on Folfirinox and am now on Gemcitibine/Abraxane. The Abraxane has made my neuropathy much worse.

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Yep. I was on the gemcitabine/abraxane for my last three chemo treatments and they did a number on me and my neuropathy. It got quickly worse during and after my treatments which were scheduled every three weeks apart. I’ve now been off all chemo for about seven weeks now and can report that I’m feeling a small amount of improvement but not enough to say I’m comfortable yet by any means. Taking 1800 units of gabapentin daily but I’m not sure it really does anything. Time will probably be the best healing process for it.

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@kakalena

My oncologist recommended B complex, which I was already taking. He also said Alpha lipoic acid, and L-Glutamine might help. I am on gem-brax and just had my 8th treatment which is when my neuropathy in feet started., so am taking all of the above, plus Epson salt foot soak really helped. As of today. 3 days later, no pain or tingling.

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Can u share dosage on each? Husband is really struggling with the neuropathy.

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Might have sent a partial list for dosing. Here's the whole thing again. B- Complex no dosage given, but be sure it is ""super" B-complex or it won't have B-12 in it.
L-Glutamine 2,000 MG. 2 x a day.
Alpha Lipoic acid 600 MG. a day.
The Super B complex you can get from a drug store. Alpha Lipolic drug store or Health Food store, L- Glutamine in capsule form (specified) Health Food Sore only. At least in my rural area. Hope it helps.

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@suelannon

My husband had Distal Surgery last July 2024 and could not eat. He had lost over 40 lbs and still losing. Someone at work mentioned RSO to me so I asked Oncologist and she said she was
a big fan. He started taking that and it was amazing. He has gained back 30 lbs so far.

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Wow that’s great to hear. Did he get it from a dispensary?

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