Talking Frankly about Living with Advanced Cancer

kathleekin, What you say is so True! Remember the old poster in the 60's and 70's, "Stop and Smell the Roses"! We all need to stop and enjoy!
That is what is so Wonderful about Mayo Connect! People on here are so compasionate and kind! We may be suffering some other Malady, but we Stop for a Moment and give our encouragement to others!
I start my mourning off when I come in my office and read the night before postings! Then end my day to sit down and read what has been posted during the day!
The Kindness and Thoughtfulness that eveyone gives to others is a Testament how Wonderful people can be and how lucky we all are to be conected!
Thanks,
Sundance(RB)

@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.

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!

@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

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.

@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

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

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!