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.

@saltis

Hi friends,
Everybody tells me that I look fablous & not at all sick. Nobody ever told me that I look fab when it was important & I wasn't sick. 22 years of cancer & now for the last 3 years stage 4 & it has spread to my chest, too. Hopefully I would start my new treatment on Tuesday and by then I hope to be able to breath as before, normally. My new chemo is based on pills Capecitabin, 8 ones everyday in two weeks time & then a rest week & then I would continue two other weeks.
Sometimes I feel that my oncolog is a bit intimated by me and blurbs out words or phrases that are not so diplomatic but he is a human being and my fablousness puts him in disadvantage, lol! Like while treating my lung problem I started to notice that my right breast which was operated and a fourth of it was taken away is losing it's form and now is stuck like a clump on my chest and is a very little thing. Anyway he has never seen anything like it and then he tells me that I have lived quite a long time with my cancers and must expect organ failures in future. I asked him is there anything I can do?
He told me No, just don't expect too much! You mean no biggest lottery Prize? Between us I still feel that I am lucky and I have my family & friends around me. When I can breath I feel lucky & everything would work out for the best somehow.
Take care folk and enjoy your day, night ...

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shortshot80) hello everyone. Friday Jan. 12, I went to my oncologist. My cat scan has helped and I can breath better. But my blood count was low so had to have a blood transfusion. They started the transfusion around 1:30pm and it wasn't cone till 7:pm. Two units. Yesterday I just rested watch tv an rested some more. Today is not so good. Could not sleep bat 2am just simi slept. Tried to get up and was so dizzy I sat down. Then after a few minutes got up and got a cup of coffee, and then started to shake. In typing this I shake and hit too many letters. Wrong ones at that. Don't know what to do about that. Hopefully it will it will get better. Nancy

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@saltis

Hi friends,
Everybody tells me that I look fablous & not at all sick. Nobody ever told me that I look fab when it was important & I wasn't sick. 22 years of cancer & now for the last 3 years stage 4 & it has spread to my chest, too. Hopefully I would start my new treatment on Tuesday and by then I hope to be able to breath as before, normally. My new chemo is based on pills Capecitabin, 8 ones everyday in two weeks time & then a rest week & then I would continue two other weeks.
Sometimes I feel that my oncolog is a bit intimated by me and blurbs out words or phrases that are not so diplomatic but he is a human being and my fablousness puts him in disadvantage, lol! Like while treating my lung problem I started to notice that my right breast which was operated and a fourth of it was taken away is losing it's form and now is stuck like a clump on my chest and is a very little thing. Anyway he has never seen anything like it and then he tells me that I have lived quite a long time with my cancers and must expect organ failures in future. I asked him is there anything I can do?
He told me No, just don't expect too much! You mean no biggest lottery Prize? Between us I still feel that I am lucky and I have my family & friends around me. When I can breath I feel lucky & everything would work out for the best somehow.
Take care folk and enjoy your day, night ...

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Hi Nancy, @shortshot80

You will have great fun!! The birthday party especially sounds good. I like the "cookie" book idea, that is a winner!

Teresa

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@saltis

Hi friends,
Everybody tells me that I look fablous & not at all sick. Nobody ever told me that I look fab when it was important & I wasn't sick. 22 years of cancer & now for the last 3 years stage 4 & it has spread to my chest, too. Hopefully I would start my new treatment on Tuesday and by then I hope to be able to breath as before, normally. My new chemo is based on pills Capecitabin, 8 ones everyday in two weeks time & then a rest week & then I would continue two other weeks.
Sometimes I feel that my oncolog is a bit intimated by me and blurbs out words or phrases that are not so diplomatic but he is a human being and my fablousness puts him in disadvantage, lol! Like while treating my lung problem I started to notice that my right breast which was operated and a fourth of it was taken away is losing it's form and now is stuck like a clump on my chest and is a very little thing. Anyway he has never seen anything like it and then he tells me that I have lived quite a long time with my cancers and must expect organ failures in future. I asked him is there anything I can do?
He told me No, just don't expect too much! You mean no biggest lottery Prize? Between us I still feel that I am lucky and I have my family & friends around me. When I can breath I feel lucky & everything would work out for the best somehow.
Take care folk and enjoy your day, night ...

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Hi Teresa, (shortshot80) I really like color, It raises my personal feelings a whole lot. Today I am going to make some whit fudge with cranberries in it. I have a "tea" to go to tomorrow and am supposed to bring a finger food. Also I received a call from my Pastor's daughter who will be 11 tomorrow, to come to her birthday party and her dad will pick me up. That really pleased me. I haven't been to a kid's BD party in years. I went through my cook books and picked out a "cookie" book which is old, printed in 1986 and another cook book which also is old 1960, has several riseipe's and I put a note in and requested that she read the book to her little brothers. Ssounds like I will have some fun both on Saturday & Sunday. Nancy

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@saltis

Hi friends,
Everybody tells me that I look fablous & not at all sick. Nobody ever told me that I look fab when it was important & I wasn't sick. 22 years of cancer & now for the last 3 years stage 4 & it has spread to my chest, too. Hopefully I would start my new treatment on Tuesday and by then I hope to be able to breath as before, normally. My new chemo is based on pills Capecitabin, 8 ones everyday in two weeks time & then a rest week & then I would continue two other weeks.
Sometimes I feel that my oncolog is a bit intimated by me and blurbs out words or phrases that are not so diplomatic but he is a human being and my fablousness puts him in disadvantage, lol! Like while treating my lung problem I started to notice that my right breast which was operated and a fourth of it was taken away is losing it's form and now is stuck like a clump on my chest and is a very little thing. Anyway he has never seen anything like it and then he tells me that I have lived quite a long time with my cancers and must expect organ failures in future. I asked him is there anything I can do?
He told me No, just don't expect too much! You mean no biggest lottery Prize? Between us I still feel that I am lucky and I have my family & friends around me. When I can breath I feel lucky & everything would work out for the best somehow.
Take care folk and enjoy your day, night ...

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Hi Nancy, @shortshot80

Thanks for checking in, I'm so pleased to hear about your hats and the cribbage board! Bazaars can be such fun - especially when you are able to find things that you really like. It feels good to have lots of color, doesn't it?

I hope you are able to take it easy for the next day of so. It sounds like you could use a rest.

Teresa

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@saltis

Hi friends,
Everybody tells me that I look fablous & not at all sick. Nobody ever told me that I look fab when it was important & I wasn't sick. 22 years of cancer & now for the last 3 years stage 4 & it has spread to my chest, too. Hopefully I would start my new treatment on Tuesday and by then I hope to be able to breath as before, normally. My new chemo is based on pills Capecitabin, 8 ones everyday in two weeks time & then a rest week & then I would continue two other weeks.
Sometimes I feel that my oncolog is a bit intimated by me and blurbs out words or phrases that are not so diplomatic but he is a human being and my fablousness puts him in disadvantage, lol! Like while treating my lung problem I started to notice that my right breast which was operated and a fourth of it was taken away is losing it's form and now is stuck like a clump on my chest and is a very little thing. Anyway he has never seen anything like it and then he tells me that I have lived quite a long time with my cancers and must expect organ failures in future. I asked him is there anything I can do?
He told me No, just don't expect too much! You mean no biggest lottery Prize? Between us I still feel that I am lucky and I have my family & friends around me. When I can breath I feel lucky & everything would work out for the best somehow.
Take care folk and enjoy your day, night ...

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December 6th Shortshot80, haven't beenhere for several days so thought I would catch up. Things have been going good, (tired) but good. There were several Christmas Bazaars held in the area last Saturday. Bob jr droe me around. First one I bought a Cribbage board for Bob sr., and then I found a bunch of hats. Knitted/crochet. All colors, well I found one had that was multi colored. Best siven dollars I've spent in a long time. It will match anything and everything I wear. Anyway I went to chemo yesterday 65 miles) and everyone really liked my hat. Wore it again this morning to primary doc for a change in meds. He liked it to with remark "what a hat!. Last night I did not sleep very good, don't know why but...woke up several times and got up at 4;30 and poured myself a cup of coffee. and a small donut to have with my medicine. Then today was doctor, wash clothes and fold them. Then a nap. Now to fix something for dinner.Busy couple of days. Have a great rest of your day. Nancy

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@vsinn2000

Allison,
I'm truly sorry that your concerns and questions weren't answered or addressed. Perhaps an appointment with both doctor and radiologist would give you the information you are looking for in a neutral setting? It sounds as though you are frustrated right now but have been with your doctor for a while. I'm new enough that I am not sure if each hospital has their own set up, or if a care team meeting would be a normal part of the process? I am still meeting all of mine to get treatment started but I believe I will ask if this would be possible if I had concern or an issue like this.
Vicky

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@vsinn2000 Yes, this next appointment will soon be over. I am glad that your tire blew before your trip and not during. I guess we have to be thankful for small blessings. 🙂

Teresa

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@vsinn2000

Allison,
I'm truly sorry that your concerns and questions weren't answered or addressed. Perhaps an appointment with both doctor and radiologist would give you the information you are looking for in a neutral setting? It sounds as though you are frustrated right now but have been with your doctor for a while. I'm new enough that I am not sure if each hospital has their own set up, or if a care team meeting would be a normal part of the process? I am still meeting all of mine to get treatment started but I believe I will ask if this would be possible if I had concern or an issue like this.
Vicky

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Teresa,
Thank you. It calms me reading your words. I have anti-anxiety meds, I suspect I need something stronger. I don't have a clue what to expect, so that ratchets it up almost beyond control immediately. Unfortunately. And just because Murphys law runs my life, we blew a tire yesterday so my husband is out trying to find a dealership that has my tires in stock. BUT at least we weren't going down the interstate when it went so that's a plus. So my day is already a mess with "the plan" changing from a morning to pack the car and get ready to a morning of chaos. I suppose if we are going to have a lufe changing medical condition we may as well have something we can learn from. I thank you for your morning prayers! They are much appreciated!
Updates later,
Vicky

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@vsinn2000

Allison,
I'm truly sorry that your concerns and questions weren't answered or addressed. Perhaps an appointment with both doctor and radiologist would give you the information you are looking for in a neutral setting? It sounds as though you are frustrated right now but have been with your doctor for a while. I'm new enough that I am not sure if each hospital has their own set up, or if a care team meeting would be a normal part of the process? I am still meeting all of mine to get treatment started but I believe I will ask if this would be possible if I had concern or an issue like this.
Vicky

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Oh, Vicky, @vsinn2000

I can certainly understand your anxiety and panic. I'm also the type of person who, if I know what to expect, it makes it easier to approach. Anticipation of an unknown event is probably far worse than the experience itself. (Does that help just a little?) Yes, keeping off the internet might be good plan for today.

Unfortunately, I don't know of anyone who has had any experience with this type of cancer or treatment. It is rather like the NETs that I have had - there is little information out there.

With that said, I pray that you will be able to experience some peace. Do you have any anti-anxiety meds to help you through this process tomorrow? Are you expecting any sedation for the procedure?

Keep in touch - I prayed for you first thing this morning when I woke up.

Teresa

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@allisonsnow

Just had my mid-way scans for my chemo and am trying to figure out what is going on. Was told if we saw no improvement they would not suggest the continuation of the gemzar and xeloda. What the scans showed was no shrinkage and many areas had some growth BUT Dr. said to continue chemo treatments. I have to take what he said as truth as he showed me only one scan and sped through the discussion. I was still in some shock and a lot of disappointment to take in all he said. He showed the most enthusiasim when I said I would take part in a study.
When I asked what the next step would be if we still saw no improvement and he said try a different chemo regiment though he didn't know what. I am not a guinea pig for random drugs with no track record !!! I have made it clear I chose quality of life overall. The Dr. seemed to think I was handling side effects very easily which is not the case it just looks that way. I constantly hear how good I look which is nice but people then take for granted I feel good which is far from the truth some of the side effects are quite nasty and I am afraid how long they will take to go away. I present myself well when I do go out and I just don't go put when I can't appear healthy.But anyway the Dr. didn't seem to want to pursue the severity of my side effects and as I said I was in a bit of shock and surprise. Sorry I am not usually so whinny but I am still deciding what to do. Thanks for listening

for those that don't know me ( I haven't been on in a while) I have metsastic Thymoma

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Hi Allison@allisonsnow

Yes, when we talk (or post) with others who "get it" it really does make a difference, doesn't it? You have helped many people through your posts. That is what makes Mayo Connect so great - we are equally supportive of each other when we need it.

Teresa

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that is a good suggestion !!!!

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