A Life Well Lived

Posted by Denise @denisestlouie, Oct 4 10:16am

I'm a financial advisor by profession. I have spent my life planning for the future and teaching people how to use their resources to accomplish what they are planning. Most of the time they have wanted to educate their kids and to retire financially comfortably. Along the way we usually have to make adjustments to that plan because life went in another direction.

I'm no exception. During my life I've had to change my hopes for the future many times. I've started over in both marriage and career more than once. I struggled with infertility when having a family was important to me. Every time I came through those experiences feeling like I live a charmed life, because I was standing in a good place. A place that I was able to piece together that was comfortable and I had all I needed and often times more.

I had an awesome plan before cancer. I own my own practice. That means I could work as much as I wanted for as long as I wanted. I was planning on working into my 70s. I enjoy my clients and I enjoy the income. My ultimate goal was to make my daughter a very wealthy woman when I die at a very old age.

I expected to live long. I'm from a long lived family. My fear was that I would live to long and run out of resources. Then came the cancer diagnosis. That was shocking enough, but then I learn that my cancer cell line is rare, aggressive, resistant to treatment and comes with a poor prognosis. How do I put the pieces together after that?

The diagnosis is less than 4 months. It's been a whirlwind of activity. Most of my education about my situation has been through research I do myself and then asking the providers their opinion on what I learned. The Doctors and Nurses Practitioners are limited in the time they have with me. Their objected is to assess my well bing and they don't have time to go into the kind of detail that a person like me wants to know.

Four months is enough time though to realize all hope is not lost. I do have the opportunity to do things thing that will help me rid my body of cancer.

I'm adjusting my plan once again. I want to live long and I don't want to be distraught if learn that I won't. That's a tricky plan to put together. Be where:

"The best-laid plans of mice and men oft' go awry …and leave us nothing but grief and pain, For promised joy!” Robert Burns

The moral of that poem for me today is that I need to see the joy of everyday and know that my plan my never come to fruition, not for the lack of planning but because life has a way of doing its own thing.

I have decided to make cancer life style changes the focus of my plan and to make that an enjoyable pursuit. I already made many of those changes before the knowledge of cancer so I'm well on my way.

Yesterday I told my trainer I wanted to be a bodybuilder and showed him a video of a 72 year old woman bodybuilder. I'm also well in my way for that as well. I have lost 40 pounds over the past 2 years and I'm very lean. I'm also muscler.

I'm going to keep working but with a different mind set. I need to work because I love the interaction I have with my clients. The income is very good and it will allow me to spoil myself, my daughter and the man I love. I'm a financial planner. I have purchased the products that will make my daughter wealthy even if I don't become a very old lady. I don't have to keep up with the Jones and I never did, usually.

I've got this! No matter what life brings me I'm going to be able to adjust my plan. Living long isn't as important as a life well lived.

To all of you who are in a journey similar to mine, you have the ability to have a life well lived. Godspeed to you.

Picture is from last night. A witches walk with my sister and soulmate.

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

Your strength is awesome, you give encouragement to so many. I'm not sure how you cope with the four month part, how is it possible to wrap your head around that. I'm not good putting the words to paper but I had to respond to your post above. You said there is still options and I hope they can slow things down for you. For me, they can "control" it. I'm 19 months in and doing okay. I wish the best for you on your journey and hoping it is a long one. Best to all.

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@stevecando54

Your strength is awesome, you give encouragement to so many. I'm not sure how you cope with the four month part, how is it possible to wrap your head around that. I'm not good putting the words to paper but I had to respond to your post above. You said there is still options and I hope they can slow things down for you. For me, they can "control" it. I'm 19 months in and doing okay. I wish the best for you on your journey and hoping it is a long one. Best to all.

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Steve I hope you have many more joy filled days.

Thank you for your kind words.

Denise

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Thank you for sharing your story so beautifully. I am hoping to see another update from you long after 4 months. Wishing you all the best in your journey. You are an inspiration.

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Denise,

You so eloquently express many of my thoughts about cancer and how it has changed your/my outlook on life, after other experiences have changed it before. I have “no evidence of disease” NED, for now, although my family history keeps me alert and wary of formulaic reassurances.

I have not been an excellent manager of money, although I have tried. I admire you for this! My daughter’s peace of mind and adequate welfare are two of my highest priorities to work toward as I prepare for my eventual end of life, whenever it will take place. Like you, some of my best strategies involve extending a quality life as long as possible.

What I can say to you, because I have become a bit of a rehab— gym “rat” since my diagnosis in order to improve my physical functioning and to manage pain, is that I see folks older than their 70’s who have used diet, exercise, enriched social connections and as much living, with joy, in the now, as possible to achieve that ongoing life well-lived in the face of life threatening injuries and illnesses. I watch Barb, who is in her very late 70’s, walk on a treadmill while lifting weights above her head that would slow or stop me if I was facing forward and standing still, and she does it while walking backwards(!). I see Carol, who shuffles into the gym supported by a walker with tennis balls fitted to the bottom to keep her from falling, then laboriously climbs onto a recumbent bicycle and pedals away for more and more minutes each day. She smiles when she has it in her, asks the rest of us how we’re feeling, tells us of the beauty she’s seen in nature that morning, and listens to others with care as she continues to pedal and pedal. Bill walks in the salt-water pool each day after parking his cane, tells a few well-timed silly jokes and sings, beautifully, taking requests. Denise, whose spine was surgically fused, is able to move in that pool, and laughs with us at Bill’s quips while encouraging others. Jeff, far my senior, hogs a corner of the gym early each morning to re-condition his knees and back and minimize vertigo in spite of severe lung problems secondary to a cancer about which I don’t have specific details. Except, he’s away these next few weeks, co-leading a bicycle tour of Italy, focused on eating amazing food in each province. I could go on and on. At times, it feels to me as if each of my lifetime friends outside the gym have simultaneously faced such challenging experiences that I am the only one with anything to give, and I start to feel overwhelmed and alone as I try to be there for them now. But I’ve got my elders at the gym. At 63 I’m the baby. So much lightness and fun is possible there. This is why, as much as all the other benefits, I spend more and more time there. We laugh, play, encourage and occasionally share some suffering or discouragement. My outlook is uplifted and I leave feeling fed with loving connection.

For myself, on my own, I get outside in the early mornings to listen to the birds’ dawn chorus and to take in the light, either from early morning sun or from stars as we shift toward winter. I take moments to breath in as fully as possible and to breath out slowly and as fully as possible to release tension. Singing, badly, as loud as I feel like it when I’m alone in my car helps with this, too. I try to limit my time sitting by getting up every hour in the workday to walk a bit and stretch. I do my best to reach out to others, spreading further what I have received.

I try to limit pain, which helps me to have less fear. I find that my tendency when pain occurs is to freeze with worry, not knowing what might make it worse. Inevitably, though, it is getting unstuck from the freeze that seems to alleviate some of the pain, allowing me to move more and feel more hopeful.

I think one of the things that makes the emotions that accompany a cancer diagnosis of any severity more difficult to bear is the shock we experience on hearing it. This group, reading the experiences and strategies and hope of others here, like you, as much as anything else, helps me to recognize how shocked I have felt; how difficult it suddenly became to sleep, how tense and hyper-alert, jittery, suddenly hot or cold, or empty and hollow I have felt in my gut. As recognition and this (truly) blessed sense that I am not alone…I have all of you as sisters on this part of my journey, allows me to turn toward my experiences and to just be with the energy of that built-in alarm system that we all have. I can shake, shudder, shiver as it all moves through. After that, my fear, rage and sadness are somehow easier to bear without me becoming overwhelmed.

I am deeply grateful to you, Denise, and all others here who voice, in writing, your experiences and feelings and thoughts as you face what’s so for each of you. I hope something of my shared experiences gives someone a tiny bit more comfort, or hope about some aspect of what they hold.

I wish you the very best with your missions of continuing to live a life well-lived and leaving your daughter with a richness that includes safety and resources for comfort, but also the knowledge of ways you have made her well-lived life a priority for you. She is much blessed.

With deep gratitude,

Gynosaur

REPLY
@gynosaur42

Denise,

You so eloquently express many of my thoughts about cancer and how it has changed your/my outlook on life, after other experiences have changed it before. I have “no evidence of disease” NED, for now, although my family history keeps me alert and wary of formulaic reassurances.

I have not been an excellent manager of money, although I have tried. I admire you for this! My daughter’s peace of mind and adequate welfare are two of my highest priorities to work toward as I prepare for my eventual end of life, whenever it will take place. Like you, some of my best strategies involve extending a quality life as long as possible.

What I can say to you, because I have become a bit of a rehab— gym “rat” since my diagnosis in order to improve my physical functioning and to manage pain, is that I see folks older than their 70’s who have used diet, exercise, enriched social connections and as much living, with joy, in the now, as possible to achieve that ongoing life well-lived in the face of life threatening injuries and illnesses. I watch Barb, who is in her very late 70’s, walk on a treadmill while lifting weights above her head that would slow or stop me if I was facing forward and standing still, and she does it while walking backwards(!). I see Carol, who shuffles into the gym supported by a walker with tennis balls fitted to the bottom to keep her from falling, then laboriously climbs onto a recumbent bicycle and pedals away for more and more minutes each day. She smiles when she has it in her, asks the rest of us how we’re feeling, tells us of the beauty she’s seen in nature that morning, and listens to others with care as she continues to pedal and pedal. Bill walks in the salt-water pool each day after parking his cane, tells a few well-timed silly jokes and sings, beautifully, taking requests. Denise, whose spine was surgically fused, is able to move in that pool, and laughs with us at Bill’s quips while encouraging others. Jeff, far my senior, hogs a corner of the gym early each morning to re-condition his knees and back and minimize vertigo in spite of severe lung problems secondary to a cancer about which I don’t have specific details. Except, he’s away these next few weeks, co-leading a bicycle tour of Italy, focused on eating amazing food in each province. I could go on and on. At times, it feels to me as if each of my lifetime friends outside the gym have simultaneously faced such challenging experiences that I am the only one with anything to give, and I start to feel overwhelmed and alone as I try to be there for them now. But I’ve got my elders at the gym. At 63 I’m the baby. So much lightness and fun is possible there. This is why, as much as all the other benefits, I spend more and more time there. We laugh, play, encourage and occasionally share some suffering or discouragement. My outlook is uplifted and I leave feeling fed with loving connection.

For myself, on my own, I get outside in the early mornings to listen to the birds’ dawn chorus and to take in the light, either from early morning sun or from stars as we shift toward winter. I take moments to breath in as fully as possible and to breath out slowly and as fully as possible to release tension. Singing, badly, as loud as I feel like it when I’m alone in my car helps with this, too. I try to limit my time sitting by getting up every hour in the workday to walk a bit and stretch. I do my best to reach out to others, spreading further what I have received.

I try to limit pain, which helps me to have less fear. I find that my tendency when pain occurs is to freeze with worry, not knowing what might make it worse. Inevitably, though, it is getting unstuck from the freeze that seems to alleviate some of the pain, allowing me to move more and feel more hopeful.

I think one of the things that makes the emotions that accompany a cancer diagnosis of any severity more difficult to bear is the shock we experience on hearing it. This group, reading the experiences and strategies and hope of others here, like you, as much as anything else, helps me to recognize how shocked I have felt; how difficult it suddenly became to sleep, how tense and hyper-alert, jittery, suddenly hot or cold, or empty and hollow I have felt in my gut. As recognition and this (truly) blessed sense that I am not alone…I have all of you as sisters on this part of my journey, allows me to turn toward my experiences and to just be with the energy of that built-in alarm system that we all have. I can shake, shudder, shiver as it all moves through. After that, my fear, rage and sadness are somehow easier to bear without me becoming overwhelmed.

I am deeply grateful to you, Denise, and all others here who voice, in writing, your experiences and feelings and thoughts as you face what’s so for each of you. I hope something of my shared experiences gives someone a tiny bit more comfort, or hope about some aspect of what they hold.

I wish you the very best with your missions of continuing to live a life well-lived and leaving your daughter with a richness that includes safety and resources for comfort, but also the knowledge of ways you have made her well-lived life a priority for you. She is much blessed.

With deep gratitude,

Gynosaur

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Thank you both for sharing your stories here. As someone who is dealing with a rarer form of an aggressive blood cancer, your journeys and your gratitude for life leaves me humbled and more inspired to make the most of each day and to face the continuing treatments with hope. I do believe we are all amazing beings with so much courage and strength. But it is good to be reminded by the examples set by others (loved reading about all of the amazing gym companions Gynosaur). Thank you again for sharing your stories. Best of luck to you both in your healing journeys.

REPLY
@gynosaur42

Denise,

You so eloquently express many of my thoughts about cancer and how it has changed your/my outlook on life, after other experiences have changed it before. I have “no evidence of disease” NED, for now, although my family history keeps me alert and wary of formulaic reassurances.

I have not been an excellent manager of money, although I have tried. I admire you for this! My daughter’s peace of mind and adequate welfare are two of my highest priorities to work toward as I prepare for my eventual end of life, whenever it will take place. Like you, some of my best strategies involve extending a quality life as long as possible.

What I can say to you, because I have become a bit of a rehab— gym “rat” since my diagnosis in order to improve my physical functioning and to manage pain, is that I see folks older than their 70’s who have used diet, exercise, enriched social connections and as much living, with joy, in the now, as possible to achieve that ongoing life well-lived in the face of life threatening injuries and illnesses. I watch Barb, who is in her very late 70’s, walk on a treadmill while lifting weights above her head that would slow or stop me if I was facing forward and standing still, and she does it while walking backwards(!). I see Carol, who shuffles into the gym supported by a walker with tennis balls fitted to the bottom to keep her from falling, then laboriously climbs onto a recumbent bicycle and pedals away for more and more minutes each day. She smiles when she has it in her, asks the rest of us how we’re feeling, tells us of the beauty she’s seen in nature that morning, and listens to others with care as she continues to pedal and pedal. Bill walks in the salt-water pool each day after parking his cane, tells a few well-timed silly jokes and sings, beautifully, taking requests. Denise, whose spine was surgically fused, is able to move in that pool, and laughs with us at Bill’s quips while encouraging others. Jeff, far my senior, hogs a corner of the gym early each morning to re-condition his knees and back and minimize vertigo in spite of severe lung problems secondary to a cancer about which I don’t have specific details. Except, he’s away these next few weeks, co-leading a bicycle tour of Italy, focused on eating amazing food in each province. I could go on and on. At times, it feels to me as if each of my lifetime friends outside the gym have simultaneously faced such challenging experiences that I am the only one with anything to give, and I start to feel overwhelmed and alone as I try to be there for them now. But I’ve got my elders at the gym. At 63 I’m the baby. So much lightness and fun is possible there. This is why, as much as all the other benefits, I spend more and more time there. We laugh, play, encourage and occasionally share some suffering or discouragement. My outlook is uplifted and I leave feeling fed with loving connection.

For myself, on my own, I get outside in the early mornings to listen to the birds’ dawn chorus and to take in the light, either from early morning sun or from stars as we shift toward winter. I take moments to breath in as fully as possible and to breath out slowly and as fully as possible to release tension. Singing, badly, as loud as I feel like it when I’m alone in my car helps with this, too. I try to limit my time sitting by getting up every hour in the workday to walk a bit and stretch. I do my best to reach out to others, spreading further what I have received.

I try to limit pain, which helps me to have less fear. I find that my tendency when pain occurs is to freeze with worry, not knowing what might make it worse. Inevitably, though, it is getting unstuck from the freeze that seems to alleviate some of the pain, allowing me to move more and feel more hopeful.

I think one of the things that makes the emotions that accompany a cancer diagnosis of any severity more difficult to bear is the shock we experience on hearing it. This group, reading the experiences and strategies and hope of others here, like you, as much as anything else, helps me to recognize how shocked I have felt; how difficult it suddenly became to sleep, how tense and hyper-alert, jittery, suddenly hot or cold, or empty and hollow I have felt in my gut. As recognition and this (truly) blessed sense that I am not alone…I have all of you as sisters on this part of my journey, allows me to turn toward my experiences and to just be with the energy of that built-in alarm system that we all have. I can shake, shudder, shiver as it all moves through. After that, my fear, rage and sadness are somehow easier to bear without me becoming overwhelmed.

I am deeply grateful to you, Denise, and all others here who voice, in writing, your experiences and feelings and thoughts as you face what’s so for each of you. I hope something of my shared experiences gives someone a tiny bit more comfort, or hope about some aspect of what they hold.

I wish you the very best with your missions of continuing to live a life well-lived and leaving your daughter with a richness that includes safety and resources for comfort, but also the knowledge of ways you have made her well-lived life a priority for you. She is much blessed.

With deep gratitude,

Gynosaur

Jump to this post

Thank you, you said so many important things I had to read it again. The writing is one thing, but the responses are so valuable

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