Talking Frankly about Living with Advanced Cancer

Are you living with advanced cancer (sometimes referred to as stage 4 or metastatic cancer)?
This discussion is a safe space where you can connect with others to talk about the realities of living with limited time. It's not easy to find people who understand what it is like. For many reasons, you may not feel comfortable talking about your thoughts and emotions with friends or family. Perhaps you are alone. Even if you are surrounded by people who support you, you may experience intense loneliness.

Connect is a place where honest conversation can safely take place. You can speak frankly and be heard without judgement. I invite you to share your reality facing death and living now.

Interested in more discussions like this? Go to the Cancer Support Group.

Profile picture for Teresa, Volunteer Mentor @hopeful33250

I'm glad that you posted this discussion, Colleen. As I've had three surgeries for neuroendocrine tumors, a rare form of cancer, I've found myself wanting to look positively at the future, but with a cautious-eye on the reality of three occurrences. While I keep active, and I volunteer, work and maintain friendships, the reality of cancer is always there. I find myself still searching for answers and still trying to live a normal life. It really is a different reality from my life prior to cancer.

I would love to hear from others who are living with this dilemma. How are you balancing the different feelings of optimism and the reality of a cancer diagnosis?

Teresa

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Living with cancer is definitely different than before. In October we discovered a melanoma on my back and that my prostate cancer was back and had metastasized to 4 other areas of the bone. I am 70 and had thought that I was in control of my life, as much as you can be, including a successful business career. We still own one business that we have had for 35 years and I am the president. I only say this because I never realized what the mental trauma could be when you realize this can kill you? I was definitely no longer the one in control of my body! I was lucky that when they removed the melanoma and also lymph nodes from my arm pit and the margins came back clean so at least for now we don't have that hanging over us. I have always been an optimist, so keep that in mind but I do realize all of us have a death sentence. We don't get out of this alive. That was an important concept for me to come to grips with. What is really important, if you can, remember that you are still alive and how you live the rest of your life is up to you. Live for the people who love you. I have a great wife of 45 years, a son and his family, my daughter and so many more who I love dearly. I plan on doing everything I can to make the rest of my life what I want it to be. Medicine is always advancing and new treatments may be out there. I could beat cancer or I could die from it down the road or in an accident this morning riding my bike for exercise. We just never know. So fight with the tools you have, make sure, if you can, that you do your best to live the best life you can based on what is important to you. I of course know every day that I have this cancer and it sucks but I am fighting it every day as well. If your doctor doesn't have more ideas don't be afraid to reach out to another clinic or doctor. The Mayo Clinic seems to be a really good option. As a final thought I had a customer years ago who was in his 80's and he had beat eight different forms or recurrences of cancer. He was a true role model of how to live your life.

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Profile picture for leannn @leannn

@sundance6 Oh that's a great idea. Please do. I have to admit, I'm new at this (new thread, etc.) so I'd be happy for you to take the lead. lol

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I certainly encourage anyone to start a new discussion about pets or perhaps you'd like to join this one:
- What Pets Can Do: Health and Healing https://connect.mayoclinic.org/discussion/what-pets-can-do-health-and-healing/

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Profile picture for fmh1 @fmh1

Colleen, thanks for serving as moderator! I have an idea to share with you and seek your ideas as well.

At 62, I am living with stage 4 prostate cancer, currently on hormone therapy (Eligard every three months), and am an insulin-dependent diabetic (30 years) with advanced coronary disease (super high CAC), but you'd never know it to look at me and my 40+ hour work schedule! I was treated four years ago with combination therapy, external beam + brachytherapy, but it did not stop the cancer progression. I can handle the side effects of hormone therapy except for one, the increased blood sugar, which is dramatically higher. Because of this, I am actively seeking second opinions from Mayo and MD Anderson regarding alternatives to hormone therapy after chemo ( I had 6 treatments of taxotere, ending on 7/11/19).

In a nutshell, i view prostate cancer like this: metastatic prostate cancer is like a car driving around with living people/cancer cells, driving away from the prostate and dropping off the cancer cells in various locations (bones, liver, kidneys) as it travels around your body on the bloodstream highway. However, for men, the car needs gas, and that gas is testosterone; by cutting off the gas supply, or minimizing its fuel, it cannot travel as far or as fast throughout the body. While the car is the vehicle that carries the cancer cells all over the body, the cancer cells/passengers themselves, per the work of Dr. Thomas Seyfried, Cancer As A Metabolic Disease, cannot survive without glucose/sugar and glutamine in the blood. Dr. Seyfried's simplified theory is to cut off the food supply --- glucose and glutamine --- to the cancer cells, and over time they cannot survive or thrives, regardless of whether or not the car still has fuel/testosterone to carry them around the body. They will simply die off over time without glucose/glutamine. Admittedly, Dr. Seyfried's theory is still under clinical investigation, but it holds great promise for cancer patients.

Here is the dilemma for insulin-dependent diabetics on hormone therapy: while the drug drops testosterone/fuel for the spread of cancer to nearly zero, it dramatically increases blood sugar, the fuel for the cancer cells that are still alive, food for metabolism/replication. What is the potential implication of this? Existing cancer cells will get more than enough fuel to survive and thrive, though spreading more slowly without testosterone. My cancer doctor's advice was this: consult with your endocrinologist and adjust your insulin. I did that, and my insulin requirements increased to an insanely high amount to get my blood sugar even close to normal (80-110).

This is why I am seeking a second opinion from either Mayo or MD Anderson. Your thoughts appreciated as well!

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Hi @fmh1, such a good topic of discussion "Dealing with diabetes and cancer". I bet that you are not the only member here on Connect who is managing both conditions. I might suggest that you start a new discussion in the Cancer group about it. In these instruction, you can find out how to start a new discussion: https://connect.mayoclinic.org/get-started-on-connect/

As for clinical advice regarding glucose and glutamine, that is out of my pay grade. It is certainly well worth clinical investigation. Do you know of any current clinical trials? You may wish to contact Mayo's research department:
Cancer-related clinical studies questions
Phone: 855-776-0015 (toll-free)

Did your endocrinologist explain why and increased amount of insulin was required? What changed?

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Profile picture for kathleenkin @kathleenkin

I will continue to pray for you that you can enjoy each minute of every day

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@kathleenkin Thank you!

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Each day is a gift. Tear that wrapping paper off and grab that gift! Sing, dance, breathe, smile, love, and dream - yes dream. Now go out and make that dream come true! Enjoy your life.

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Profile picture for Ginger, Volunteer Mentor @gingerw

@leannn @IndianaScott @kathleenkin @hannahkeels @naturegirl5
I want to thank all who posted in this thread since @leannn's original post. You have given me much to think about. I have dealt with a rollercoaster of issues including an ultra-rare kidney disorder with no treatment nor cure. In October this year I was diagnosed with smoldering multiple myeloma. Now I face the quarterly testing of waiting-for-the-other-shoe-to-drop to see if the MM will morph into active status. But you have shown me the positivity of living each day for now. Thank you.
Ginger

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I will continue to pray for you that you can enjoy each minute of every day

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Profile picture for odette @odette

Dear naturegirl5, I wrote to you when you first joined the group. I'm glad to see that you are doing well. Like you, I don't post very often. However, I noticed your comment about your worries regarding a recurrence or secondary cancer. I would imagine all of us share those concerns, perhaps for a lifetime. Although I would say, as time goes on it does seem less burdensome emotionally on a daily basis. Most of us experience anxiety prior to an appointment. I had one in October and my blood pressure was sky high when normally it is quite low (they have me monitor it at home). I'm always completely elated when it is all over and my husband and I celebrate. Then I turn my attention to my life, my loved ones, and dear friends (I don't have a pet as I travel too much, but I had dogs for years). I'm certain your appointment will go well in February, but I truly understand your feelings. Be well.

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Hello Odette, Thank you for your warm response and encouraging comments. Yes, I recall your kind note when I joined the group. My partner (a pathologist) often tells me that the chance of recurrence is very minimal given the grade (FIGO 1) and stage (1a) and no signs anywhere else. That's the reality. But you know how that is - there is reality and then there is anxiety that often has a limited basis in reality. The worries come and go and I'm hopeful, as you wrote, that the anxiety will lessen over time. Like you, I don't dwell on the cancer (but it's often in the back of my mind) and focus on what is most important in life: my family, our animals (we have a geriatric dog who requires more sensitivity and supervision), close friends, and my rewarding part-time work as a psychologist. How are you doing, Odette?

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Profile picture for Ginger, Volunteer Mentor @gingerw

@leannn @IndianaScott @kathleenkin @hannahkeels @naturegirl5
I want to thank all who posted in this thread since @leannn's original post. You have given me much to think about. I have dealt with a rollercoaster of issues including an ultra-rare kidney disorder with no treatment nor cure. In October this year I was diagnosed with smoldering multiple myeloma. Now I face the quarterly testing of waiting-for-the-other-shoe-to-drop to see if the MM will morph into active status. But you have shown me the positivity of living each day for now. Thank you.
Ginger

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@IndianaScott @kathleenkin @hannahkeels @naturegirl5 @sundance6 @laihuaqing @gingerw @odette (Hope I didn't miss anyone) Absolutely! Thank you, everyone. Ginger said it well, you've all truly helped and encouraged me. Thank you! I know that I will think of all (Ginger, I'll be thinking of you and your quarterly testing!) and our stories hoping and praying in the days ahead. Sometimes I'm guilty of life getting busy and not even wanting to think of the word cancer. When that happens, I find myself not reading or posting. But I sure appreciate all your responses and see the power we have to uplift each other here. I will pay it forward one way or another. Blessings to all!

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Profile picture for Sundance(RB) @sundance6

He is so Cute! They are so understanding! They are here on earth to Help us make it through Life!
Sundance(RB)
PS we should all start a new thread! Post pictures of our animal spirits!

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@sundance6 Oh that's a great idea. Please do. I have to admit, I'm new at this (new thread, etc.) so I'd be happy for you to take the lead. lol

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Profile picture for Helen, Volunteer Mentor @naturegirl5

@leann @kathleenkin Thank you for posting the photos of your lovely dogs. I check into this discussion but have not posted in awhile and I was pleasantly surprised by the photos. Our companion animals are such a blessing. As soon as I sit down, one of the cats is on my lap and if we let the cats into the bedroom at night they would both sleep on or next to us (my partner says no animals in the bedroom).

I worry about recurrence or second cancers. I was diagnosed with endometrial cancer (endometrial adenocarcinoma FIGO Grade 1) in July, 2019) and went to Mayo Clinic in Rochester after I got the diagnosis from my local gynecologist. At Mayo, I had a radical hysterectomy with salpingo-oopherectomy and pathology after surgery showed that the adenocarcinoma was 1a with minimal invasion in the myometrium and no spread. So, I'm a cancer survivor. I'm due for my first 6 month follow-up in February, 2020 and I'll return to Mayo in Rochester for that appointment and all of my follow-up care.

I'm trying to think why I'm writing this now. Maybe it's the worry in the back of my mind that never completely leaves although is often suppressed in my day-to-day life. What else can I or any of us do but live with our lives that we share with our humans and companion animals? And some of us, like Marshall, get to share our gifts as therapy animals! And notice our blessings everyday.

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Dear naturegirl5, I wrote to you when you first joined the group. I'm glad to see that you are doing well. Like you, I don't post very often. However, I noticed your comment about your worries regarding a recurrence or secondary cancer. I would imagine all of us share those concerns, perhaps for a lifetime. Although I would say, as time goes on it does seem less burdensome emotionally on a daily basis. Most of us experience anxiety prior to an appointment. I had one in October and my blood pressure was sky high when normally it is quite low (they have me monitor it at home). I'm always completely elated when it is all over and my husband and I celebrate. Then I turn my attention to my life, my loved ones, and dear friends (I don't have a pet as I travel too much, but I had dogs for years). I'm certain your appointment will go well in February, but I truly understand your feelings. Be well.

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