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.
marcia,
Where are you being treated?
In many cases, stopping chemo based on a standards of care approach, might be the wrong thing to do ... could you provide more info?
I'm also considered inoperable due to blood vessel involvement. I've also been told I don't qualify for radiation due to flat lesions in my abdomen that the radiation wouldn't hit. But I'm still doing chemo--round 19 will be Tuesday. FWIW, at my appointment last Friday, my NP said she has several patients who are into their second year of chemo. My oncologist and I agree that I'll keep going on chemo until I decide to stop and/or the meds are less effective. I'm on modified Folfiri (we dropped oxaliplatin after round 8) at 60 percent of typical dose. Why did you decide to stop chemo? Can you restart? It's not the funnest thing (is that a word? ha!), but if it works and holds the cancer at bay, it might be worth resuming it.
I’m being treated at Mayo in Rochester. The tumor was shrunken and considered dead. My CA19-9 is 10. They consider me no evidence of disease.
I also have sarcoidosis in my lungs that was under control. Now it might be triggered or the cancer is metastasizing. I see my pulmonary dr on Tuesday.
The drs originally ordered 12 rounds of chemo. They’ve never spoken of continuing. They seem to think I’m in remission
Hoping Stave IV Survivor will jump in to comment.
I am not a medical professional, but I continue to read of folks who stopped chemo, were declared in remission and then there was indication, again. I don't understand it, but many have discussed the sometimes advisability of continuing chemo. So confusing.
Thank you, but the spread to my lungs occurred before my chemo treatments. My January CBC, CMP and CA19-9 were all good 🙂 so I am still on my "break" from chemo.
Couldn't agree more
Hi @rayb2024, what did you learn at the second opinion appointment? What treatment is suggested for you? How are you doing?
Hi Diane that is such good news 😊keep strong girl you have this!
My scenario is similar diagnosed in ER after 7 months of pain ! What is your chemo med regimen?
Every other week for chemo. On #11. After another ct scan will most likely start radiation. Wishing you luck, keep strong.