› Forums › General Melanoma Community › To work or not to work?
- This topic has 54 replies, 10 voices, and was last updated 10 years, 10 months ago by ReginaTink.
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- February 21, 2014 at 2:18 am
I am wondering when others have decided not to continue at their job.
I am currently on medical leave (public school teacher) and have previously taken short leaves for surgery or treatment. I have been stage iv since 2001 with 7 years NED following a vaccine. Dealing with tumors (mostly subs) for past three years. Most recent tumor in cavity where uterus was removed in2012 due to tumor. AntiPD1 , yervoy and radiation in 2013. Tumor stopped bleeding and shrank by a cm and stable between Dec scan and recent.
So, does one return to work when tumor stable or not since who knows how long that will last? If it ends up being a good seven years ahead I will want to be working. But if it reoccurs I will not want to leave a class mid year.
What have others chosen? I know it is a personal choice but I am curios how others live along this path.
- Replies
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- February 21, 2014 at 12:12 pm
While there are many considerations and different strokes for different folks, I find work (full time) to be a welcome and pleasant distraction from my stage IV melanoma. Of course, if things were to take a turn for the worse, I'd have to re-evaluate.
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- February 21, 2014 at 12:12 pm
While there are many considerations and different strokes for different folks, I find work (full time) to be a welcome and pleasant distraction from my stage IV melanoma. Of course, if things were to take a turn for the worse, I'd have to re-evaluate.
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- February 21, 2014 at 12:12 pm
While there are many considerations and different strokes for different folks, I find work (full time) to be a welcome and pleasant distraction from my stage IV melanoma. Of course, if things were to take a turn for the worse, I'd have to re-evaluate.
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- February 21, 2014 at 12:54 pm
Personally, I need to work – not only to support my family, but as Mat noted above I need the distraction. From your comments, it seems like you want to work so I say just do it. The last thing any of us should be doing is living in fear such that it prevents us from doing the things we want to do because of the "what ifs."
Kevin
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- February 21, 2014 at 12:54 pm
Personally, I need to work – not only to support my family, but as Mat noted above I need the distraction. From your comments, it seems like you want to work so I say just do it. The last thing any of us should be doing is living in fear such that it prevents us from doing the things we want to do because of the "what ifs."
Kevin
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- February 21, 2014 at 12:54 pm
Personally, I need to work – not only to support my family, but as Mat noted above I need the distraction. From your comments, it seems like you want to work so I say just do it. The last thing any of us should be doing is living in fear such that it prevents us from doing the things we want to do because of the "what ifs."
Kevin
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- February 21, 2014 at 2:37 pm
You're right, it is ultimately your decision and what is going to help you the most. As others have said, working can be a great distraction, but not everyone wants or can handle that. I also understand not wanting to start something and then having to leave part way through- doing that (or even the thought of doing that, which for myself I veiw as "quitting" and that's something I just don't do) gives me ulcers nearly as bad as dealing with this stupid disease. I still struggle with the same question though, each time I have to start a new therapy. I know I should be a bit braver, but I hate having to leave things unfinished, contracts unfulfilled, etc.
If I could be working, I think I would. The difficulty for me is the type of work I do requires some significant physical ability. Additionally, I was diagnosed half way through my internship (a 1 year non-renewable contract) in 2011. I decided when I returned home not to go searching for work because I was starting interferon. I wanted to see how I would handle it before I made any promises to employers. Turns out I would not have been much use anyway. After that I took a couple months off to regain my physical strenght (and get married), then was looking for work again when I progressed to stage IV. I chose IL-2 first, which had me in and out of the hospital and with so many doctors appointments there was no way anyone in their right mind would hire me, then right after I finished that I progressed again and it was on to WBR and Yervoy. That doesn't appear to have worked and with new brain mets discovered in Dec I've been disqualified (for now) from clinical trials so I'm on the BRAF/MEK combo.
All of my very frequent relapses are not intended to scare you into not working, my situation is different- I didn't work because I didn't have a job to start with and was never really stable enough to get employment in my field (and laughably am "overqualified", love that term, for lower paying jobs). I never understood that- who cares if I'm overqualified, if I can do the job and am willing to do the job for the advertised pay, why can't I be considered? Anyway, I digress… Luckily my husband's salary and help from family has kept us afloat. My husband works for a University, which happens to be the same University I got my degrees at so I have been fortunate that former professors know me well and throw me little temporary easy jobs now and then that I can fit in between everythng else.
One of these jobs was to create a 3 week summer school course for high school students, which allowed me to mostly work from home at my own pace. It ran for the first time last summer, while I was getting WBR and Yervoy. It ran from 9am-4:30pm Mon-Fri and I was responsible for aprox 1/3 of the lecture material as well as all of the grading and writing exams. I was able to be there every day, do all of my lectures and all of the grading while recieving those treatments, and have some confidence that I could work comfortably with the combo I'm on now. My very round about point I guess is that even if you don't stay stable, the newer treatments are much easier and most people can work while they're recieving them, if they want to. So even if you progress, you likely wouldn't have to leave part way through the year, though you may have to miss occasional days for infusions, scans, or checkups.
Think about what makes you happy- if you enjoy your job or would welcome a distraction, go for it. You can't live your life always asking "what if?". At some point we need to throw caution to the wind and give it a shot. If it works, great, if not, it will be dissapointing, but not the end of the world (no matter how much our brains tell us it might be).
Good luck
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- February 21, 2014 at 2:37 pm
You're right, it is ultimately your decision and what is going to help you the most. As others have said, working can be a great distraction, but not everyone wants or can handle that. I also understand not wanting to start something and then having to leave part way through- doing that (or even the thought of doing that, which for myself I veiw as "quitting" and that's something I just don't do) gives me ulcers nearly as bad as dealing with this stupid disease. I still struggle with the same question though, each time I have to start a new therapy. I know I should be a bit braver, but I hate having to leave things unfinished, contracts unfulfilled, etc.
If I could be working, I think I would. The difficulty for me is the type of work I do requires some significant physical ability. Additionally, I was diagnosed half way through my internship (a 1 year non-renewable contract) in 2011. I decided when I returned home not to go searching for work because I was starting interferon. I wanted to see how I would handle it before I made any promises to employers. Turns out I would not have been much use anyway. After that I took a couple months off to regain my physical strenght (and get married), then was looking for work again when I progressed to stage IV. I chose IL-2 first, which had me in and out of the hospital and with so many doctors appointments there was no way anyone in their right mind would hire me, then right after I finished that I progressed again and it was on to WBR and Yervoy. That doesn't appear to have worked and with new brain mets discovered in Dec I've been disqualified (for now) from clinical trials so I'm on the BRAF/MEK combo.
All of my very frequent relapses are not intended to scare you into not working, my situation is different- I didn't work because I didn't have a job to start with and was never really stable enough to get employment in my field (and laughably am "overqualified", love that term, for lower paying jobs). I never understood that- who cares if I'm overqualified, if I can do the job and am willing to do the job for the advertised pay, why can't I be considered? Anyway, I digress… Luckily my husband's salary and help from family has kept us afloat. My husband works for a University, which happens to be the same University I got my degrees at so I have been fortunate that former professors know me well and throw me little temporary easy jobs now and then that I can fit in between everythng else.
One of these jobs was to create a 3 week summer school course for high school students, which allowed me to mostly work from home at my own pace. It ran for the first time last summer, while I was getting WBR and Yervoy. It ran from 9am-4:30pm Mon-Fri and I was responsible for aprox 1/3 of the lecture material as well as all of the grading and writing exams. I was able to be there every day, do all of my lectures and all of the grading while recieving those treatments, and have some confidence that I could work comfortably with the combo I'm on now. My very round about point I guess is that even if you don't stay stable, the newer treatments are much easier and most people can work while they're recieving them, if they want to. So even if you progress, you likely wouldn't have to leave part way through the year, though you may have to miss occasional days for infusions, scans, or checkups.
Think about what makes you happy- if you enjoy your job or would welcome a distraction, go for it. You can't live your life always asking "what if?". At some point we need to throw caution to the wind and give it a shot. If it works, great, if not, it will be dissapointing, but not the end of the world (no matter how much our brains tell us it might be).
Good luck
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- February 21, 2014 at 2:37 pm
You're right, it is ultimately your decision and what is going to help you the most. As others have said, working can be a great distraction, but not everyone wants or can handle that. I also understand not wanting to start something and then having to leave part way through- doing that (or even the thought of doing that, which for myself I veiw as "quitting" and that's something I just don't do) gives me ulcers nearly as bad as dealing with this stupid disease. I still struggle with the same question though, each time I have to start a new therapy. I know I should be a bit braver, but I hate having to leave things unfinished, contracts unfulfilled, etc.
If I could be working, I think I would. The difficulty for me is the type of work I do requires some significant physical ability. Additionally, I was diagnosed half way through my internship (a 1 year non-renewable contract) in 2011. I decided when I returned home not to go searching for work because I was starting interferon. I wanted to see how I would handle it before I made any promises to employers. Turns out I would not have been much use anyway. After that I took a couple months off to regain my physical strenght (and get married), then was looking for work again when I progressed to stage IV. I chose IL-2 first, which had me in and out of the hospital and with so many doctors appointments there was no way anyone in their right mind would hire me, then right after I finished that I progressed again and it was on to WBR and Yervoy. That doesn't appear to have worked and with new brain mets discovered in Dec I've been disqualified (for now) from clinical trials so I'm on the BRAF/MEK combo.
All of my very frequent relapses are not intended to scare you into not working, my situation is different- I didn't work because I didn't have a job to start with and was never really stable enough to get employment in my field (and laughably am "overqualified", love that term, for lower paying jobs). I never understood that- who cares if I'm overqualified, if I can do the job and am willing to do the job for the advertised pay, why can't I be considered? Anyway, I digress… Luckily my husband's salary and help from family has kept us afloat. My husband works for a University, which happens to be the same University I got my degrees at so I have been fortunate that former professors know me well and throw me little temporary easy jobs now and then that I can fit in between everythng else.
One of these jobs was to create a 3 week summer school course for high school students, which allowed me to mostly work from home at my own pace. It ran for the first time last summer, while I was getting WBR and Yervoy. It ran from 9am-4:30pm Mon-Fri and I was responsible for aprox 1/3 of the lecture material as well as all of the grading and writing exams. I was able to be there every day, do all of my lectures and all of the grading while recieving those treatments, and have some confidence that I could work comfortably with the combo I'm on now. My very round about point I guess is that even if you don't stay stable, the newer treatments are much easier and most people can work while they're recieving them, if they want to. So even if you progress, you likely wouldn't have to leave part way through the year, though you may have to miss occasional days for infusions, scans, or checkups.
Think about what makes you happy- if you enjoy your job or would welcome a distraction, go for it. You can't live your life always asking "what if?". At some point we need to throw caution to the wind and give it a shot. If it works, great, if not, it will be dissapointing, but not the end of the world (no matter how much our brains tell us it might be).
Good luck
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- February 21, 2014 at 7:53 pm
Hey Maureen,
It is a lot to think about isn't it? Like the other posters noted…it is a very personal question with no right or wrong answers. I think you have to weigh what you feel is the best way to spend your time. After all…that's what life is, isn't it? Spending our time…somehow….for however long we are here. Then, there are the other issues…How do you feel? Are you physically and mentally strong enough to do your job? Can you get off when you need to for never ending doc appointments and treatments? And…esp in your case….are you ok with leaving your job should you have to do that after your return? I know that as a teacher, that could be pretty tricky for you. Anyhow…I've had to face all these questions myself. I took 6 months off work as a pediatric nurse practitioner to have lung surgery and my brain zapped. Thankfully my bosses were cool with that and allowed me to return when I was ready. My schedule was already set at: 3, 12 hour shifts a week. That allowed me to join an anti-PD1 trial in Tampa, to which I traveled from Chattanoogs every other week for 6 months and then every 3 months for 2 additional years. Had my work schedule not allowed the trip then I would not have been able to work. I guess I figure, if being an NP and taking care of kids is what I do and part of who I am, then…I want to keep doing it…at least for now. Recently someone posted a link to an op ed in the New York Times ("How long have I got left?" By Paul Kalanithi). It was written by a surgeon who returned to work after having been off for about 8 months after his diagnosis and treatment of metastatic cancer. He shares his thoughts, that given your question, you might find interesting.
I wish you the best with whatever you decide. I'm sure you will decide what is best for you!
Celeste
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- February 21, 2014 at 7:53 pm
Hey Maureen,
It is a lot to think about isn't it? Like the other posters noted…it is a very personal question with no right or wrong answers. I think you have to weigh what you feel is the best way to spend your time. After all…that's what life is, isn't it? Spending our time…somehow….for however long we are here. Then, there are the other issues…How do you feel? Are you physically and mentally strong enough to do your job? Can you get off when you need to for never ending doc appointments and treatments? And…esp in your case….are you ok with leaving your job should you have to do that after your return? I know that as a teacher, that could be pretty tricky for you. Anyhow…I've had to face all these questions myself. I took 6 months off work as a pediatric nurse practitioner to have lung surgery and my brain zapped. Thankfully my bosses were cool with that and allowed me to return when I was ready. My schedule was already set at: 3, 12 hour shifts a week. That allowed me to join an anti-PD1 trial in Tampa, to which I traveled from Chattanoogs every other week for 6 months and then every 3 months for 2 additional years. Had my work schedule not allowed the trip then I would not have been able to work. I guess I figure, if being an NP and taking care of kids is what I do and part of who I am, then…I want to keep doing it…at least for now. Recently someone posted a link to an op ed in the New York Times ("How long have I got left?" By Paul Kalanithi). It was written by a surgeon who returned to work after having been off for about 8 months after his diagnosis and treatment of metastatic cancer. He shares his thoughts, that given your question, you might find interesting.
I wish you the best with whatever you decide. I'm sure you will decide what is best for you!
Celeste
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- February 21, 2014 at 7:53 pm
Hey Maureen,
It is a lot to think about isn't it? Like the other posters noted…it is a very personal question with no right or wrong answers. I think you have to weigh what you feel is the best way to spend your time. After all…that's what life is, isn't it? Spending our time…somehow….for however long we are here. Then, there are the other issues…How do you feel? Are you physically and mentally strong enough to do your job? Can you get off when you need to for never ending doc appointments and treatments? And…esp in your case….are you ok with leaving your job should you have to do that after your return? I know that as a teacher, that could be pretty tricky for you. Anyhow…I've had to face all these questions myself. I took 6 months off work as a pediatric nurse practitioner to have lung surgery and my brain zapped. Thankfully my bosses were cool with that and allowed me to return when I was ready. My schedule was already set at: 3, 12 hour shifts a week. That allowed me to join an anti-PD1 trial in Tampa, to which I traveled from Chattanoogs every other week for 6 months and then every 3 months for 2 additional years. Had my work schedule not allowed the trip then I would not have been able to work. I guess I figure, if being an NP and taking care of kids is what I do and part of who I am, then…I want to keep doing it…at least for now. Recently someone posted a link to an op ed in the New York Times ("How long have I got left?" By Paul Kalanithi). It was written by a surgeon who returned to work after having been off for about 8 months after his diagnosis and treatment of metastatic cancer. He shares his thoughts, that given your question, you might find interesting.
I wish you the best with whatever you decide. I'm sure you will decide what is best for you!
Celeste
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- February 22, 2014 at 1:13 am
I really know how you feel!! I am in a dilemma myself considering going back to work or not. I know I had good reason to be off work when I was on interferon which I was able to tolerate for 12 treatments. I returned to work when feeling better and I felt maybe this much interferon nipped this nasty disease by the bud after I had a radical lymphectomy with one node revealing metatasis. Low and behold when I had a pet scan, it spread to other lymph nodes between my trachea and esophagus. I am now on a clinical trial with yervoy and not knowing what side effects I would have I decided to go on special leave. I will be going for my third treatment next week and actually having few side effects. I decided to wait until my treatments are completed and after I receive results from my pet scan April 9th because I too did not want to start working and then find out I have to go through another course of action. I think what type of job has a lot with deciding to stay home or not. I probably would be at work if I had a job where I was just in one place. I am a caseworker and I travel every other day to different places, like personal care homes, hospitals, nursing facilities and homes in the community. I just did not want to over exert myself and be stressed to keep up with my job. April 9th will be a big day for me and I will just have to wait and see. If you want to connect with me through my e-mail you can regarding your decision. It is hard to keep a continuous monolog in this site, I've found. my e-mail is [email protected]
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- February 22, 2014 at 1:13 am
I really know how you feel!! I am in a dilemma myself considering going back to work or not. I know I had good reason to be off work when I was on interferon which I was able to tolerate for 12 treatments. I returned to work when feeling better and I felt maybe this much interferon nipped this nasty disease by the bud after I had a radical lymphectomy with one node revealing metatasis. Low and behold when I had a pet scan, it spread to other lymph nodes between my trachea and esophagus. I am now on a clinical trial with yervoy and not knowing what side effects I would have I decided to go on special leave. I will be going for my third treatment next week and actually having few side effects. I decided to wait until my treatments are completed and after I receive results from my pet scan April 9th because I too did not want to start working and then find out I have to go through another course of action. I think what type of job has a lot with deciding to stay home or not. I probably would be at work if I had a job where I was just in one place. I am a caseworker and I travel every other day to different places, like personal care homes, hospitals, nursing facilities and homes in the community. I just did not want to over exert myself and be stressed to keep up with my job. April 9th will be a big day for me and I will just have to wait and see. If you want to connect with me through my e-mail you can regarding your decision. It is hard to keep a continuous monolog in this site, I've found. my e-mail is [email protected]
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- February 22, 2014 at 1:13 am
I really know how you feel!! I am in a dilemma myself considering going back to work or not. I know I had good reason to be off work when I was on interferon which I was able to tolerate for 12 treatments. I returned to work when feeling better and I felt maybe this much interferon nipped this nasty disease by the bud after I had a radical lymphectomy with one node revealing metatasis. Low and behold when I had a pet scan, it spread to other lymph nodes between my trachea and esophagus. I am now on a clinical trial with yervoy and not knowing what side effects I would have I decided to go on special leave. I will be going for my third treatment next week and actually having few side effects. I decided to wait until my treatments are completed and after I receive results from my pet scan April 9th because I too did not want to start working and then find out I have to go through another course of action. I think what type of job has a lot with deciding to stay home or not. I probably would be at work if I had a job where I was just in one place. I am a caseworker and I travel every other day to different places, like personal care homes, hospitals, nursing facilities and homes in the community. I just did not want to over exert myself and be stressed to keep up with my job. April 9th will be a big day for me and I will just have to wait and see. If you want to connect with me through my e-mail you can regarding your decision. It is hard to keep a continuous monolog in this site, I've found. my e-mail is [email protected]
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- February 22, 2014 at 4:31 am
Thank you all for responding. I appreciate the varied viewpoints. All things I am thinking about. What especially resonates is " …that's what life is…spending our time". How do we choose to spend it… regardless of cancer? I suppose that is really what I struggle with, not wanting to waste my time and not certain how it is best spent. Daily.
Thanks .
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- February 22, 2014 at 4:31 am
Thank you all for responding. I appreciate the varied viewpoints. All things I am thinking about. What especially resonates is " …that's what life is…spending our time". How do we choose to spend it… regardless of cancer? I suppose that is really what I struggle with, not wanting to waste my time and not certain how it is best spent. Daily.
Thanks .
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- February 22, 2014 at 4:31 am
Thank you all for responding. I appreciate the varied viewpoints. All things I am thinking about. What especially resonates is " …that's what life is…spending our time". How do we choose to spend it… regardless of cancer? I suppose that is really what I struggle with, not wanting to waste my time and not certain how it is best spent. Daily.
Thanks .
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- February 22, 2014 at 3:07 pm
I have found that it has been nice to cook more for my husband and now concentrating on crocheting for my granddaughter who will be one in March. I have been going to physical therapy 3x per week except on my treatment weeks and I have been in touch with my co-workers. When there is snow and bad weather, I thank God that I am not working at this time. I am not a person to be non-productive and I really try to keep busy. What is screwing me up is sleeping in and getting up in varied times because I am so used to getting up early at the same time. I am sticking to this melanoma site at this time for good updates but I have been a difficult time opening the chat line. I have thought of getting more involved with my church which I should look at as my next project because I feel I need to be out with people more. I really have to push myself to do anything periodically; and I do find myself just laying on the couch and watching a lot of TV. In other words I can be all over the map in determining what to do on a daily basis. We are all in this together and it is good that we can find support.
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- February 22, 2014 at 3:07 pm
I have found that it has been nice to cook more for my husband and now concentrating on crocheting for my granddaughter who will be one in March. I have been going to physical therapy 3x per week except on my treatment weeks and I have been in touch with my co-workers. When there is snow and bad weather, I thank God that I am not working at this time. I am not a person to be non-productive and I really try to keep busy. What is screwing me up is sleeping in and getting up in varied times because I am so used to getting up early at the same time. I am sticking to this melanoma site at this time for good updates but I have been a difficult time opening the chat line. I have thought of getting more involved with my church which I should look at as my next project because I feel I need to be out with people more. I really have to push myself to do anything periodically; and I do find myself just laying on the couch and watching a lot of TV. In other words I can be all over the map in determining what to do on a daily basis. We are all in this together and it is good that we can find support.
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- February 22, 2014 at 3:07 pm
I have found that it has been nice to cook more for my husband and now concentrating on crocheting for my granddaughter who will be one in March. I have been going to physical therapy 3x per week except on my treatment weeks and I have been in touch with my co-workers. When there is snow and bad weather, I thank God that I am not working at this time. I am not a person to be non-productive and I really try to keep busy. What is screwing me up is sleeping in and getting up in varied times because I am so used to getting up early at the same time. I am sticking to this melanoma site at this time for good updates but I have been a difficult time opening the chat line. I have thought of getting more involved with my church which I should look at as my next project because I feel I need to be out with people more. I really have to push myself to do anything periodically; and I do find myself just laying on the couch and watching a lot of TV. In other words I can be all over the map in determining what to do on a daily basis. We are all in this together and it is good that we can find support.
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- February 23, 2014 at 1:29 am
Here is the deal with me.
DX'D 1987 Stage III Melanoma
Following surgery, I went back to work.
Nine years later, I was DX'D Stage IV.
Back and forth between treatments and surgeries. My work resume became quite sketchy.
I soon realized that "jobs" were not in my future. So I once again struck out on my own…..and started a business, based upon my own merits……………..not my health.
I have never looked back, and I will be damned if I apolgize for my health to ANY employer ever again.
I still work, still have melanoma; but it is on My terms.
1987-2014=27 years MY way.
…and melanoma can STILL kiss my shiny white butt.
Yeah, it was and IS personal.
Charlie S
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- February 23, 2014 at 1:29 am
Here is the deal with me.
DX'D 1987 Stage III Melanoma
Following surgery, I went back to work.
Nine years later, I was DX'D Stage IV.
Back and forth between treatments and surgeries. My work resume became quite sketchy.
I soon realized that "jobs" were not in my future. So I once again struck out on my own…..and started a business, based upon my own merits……………..not my health.
I have never looked back, and I will be damned if I apolgize for my health to ANY employer ever again.
I still work, still have melanoma; but it is on My terms.
1987-2014=27 years MY way.
…and melanoma can STILL kiss my shiny white butt.
Yeah, it was and IS personal.
Charlie S
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- February 23, 2014 at 1:29 am
Here is the deal with me.
DX'D 1987 Stage III Melanoma
Following surgery, I went back to work.
Nine years later, I was DX'D Stage IV.
Back and forth between treatments and surgeries. My work resume became quite sketchy.
I soon realized that "jobs" were not in my future. So I once again struck out on my own…..and started a business, based upon my own merits……………..not my health.
I have never looked back, and I will be damned if I apolgize for my health to ANY employer ever again.
I still work, still have melanoma; but it is on My terms.
1987-2014=27 years MY way.
…and melanoma can STILL kiss my shiny white butt.
Yeah, it was and IS personal.
Charlie S
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- February 25, 2014 at 2:34 pm
That is great that you can be your own employer. It all depends on what my PET scan results will be April 9th if I go back to work. I hate to give up my skills that took a long time to develop and the feeling of accomplishment of what I do. I may just have to bite the bullet at one point and go on disability, even if I have to also work part time. It is stress enough wondering if this treatment is going to work and now I am just taking care of myself. ReginaTink
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- February 25, 2014 at 2:34 pm
That is great that you can be your own employer. It all depends on what my PET scan results will be April 9th if I go back to work. I hate to give up my skills that took a long time to develop and the feeling of accomplishment of what I do. I may just have to bite the bullet at one point and go on disability, even if I have to also work part time. It is stress enough wondering if this treatment is going to work and now I am just taking care of myself. ReginaTink
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- February 25, 2014 at 2:34 pm
That is great that you can be your own employer. It all depends on what my PET scan results will be April 9th if I go back to work. I hate to give up my skills that took a long time to develop and the feeling of accomplishment of what I do. I may just have to bite the bullet at one point and go on disability, even if I have to also work part time. It is stress enough wondering if this treatment is going to work and now I am just taking care of myself. ReginaTink
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- February 23, 2014 at 7:04 am
It's a difficult choice to make.
When I was first diagnosed in 1989 as a stage I at age 24, I couldn't imagine not working.
But time and perspective changes so when I was diagnosed again in 2005 as a stage IV, I really started to question whether or not I wanted to fight cancer and work full-time as a high school English teacher and coach.
I did return to work after successful surgeries and chemotherapy but cut back on my extra jobs- no more coaching. But when another brain lesion appeared in 2007 and I had to undergo a craniotomy, I knew that that was the sign that I needed to confidently say, No more.
And so I went on disability retirement. In that time I have had 3 grandchildren arrive, been able to help a sister diagnosed with MS, and had peace-filled days with my husband and family. I have also been NED since deciding to live a life with less stress. Sometimes I feel guilty and think I should be working, but I know what I've been through and I know I can't go back.
I am beyond grateful that I have the choice when so many others don't.
Best to you as you make this tough decision.
Best of health to you as well.
Karen
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- February 23, 2014 at 7:04 am
It's a difficult choice to make.
When I was first diagnosed in 1989 as a stage I at age 24, I couldn't imagine not working.
But time and perspective changes so when I was diagnosed again in 2005 as a stage IV, I really started to question whether or not I wanted to fight cancer and work full-time as a high school English teacher and coach.
I did return to work after successful surgeries and chemotherapy but cut back on my extra jobs- no more coaching. But when another brain lesion appeared in 2007 and I had to undergo a craniotomy, I knew that that was the sign that I needed to confidently say, No more.
And so I went on disability retirement. In that time I have had 3 grandchildren arrive, been able to help a sister diagnosed with MS, and had peace-filled days with my husband and family. I have also been NED since deciding to live a life with less stress. Sometimes I feel guilty and think I should be working, but I know what I've been through and I know I can't go back.
I am beyond grateful that I have the choice when so many others don't.
Best to you as you make this tough decision.
Best of health to you as well.
Karen
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- February 23, 2014 at 7:04 am
It's a difficult choice to make.
When I was first diagnosed in 1989 as a stage I at age 24, I couldn't imagine not working.
But time and perspective changes so when I was diagnosed again in 2005 as a stage IV, I really started to question whether or not I wanted to fight cancer and work full-time as a high school English teacher and coach.
I did return to work after successful surgeries and chemotherapy but cut back on my extra jobs- no more coaching. But when another brain lesion appeared in 2007 and I had to undergo a craniotomy, I knew that that was the sign that I needed to confidently say, No more.
And so I went on disability retirement. In that time I have had 3 grandchildren arrive, been able to help a sister diagnosed with MS, and had peace-filled days with my husband and family. I have also been NED since deciding to live a life with less stress. Sometimes I feel guilty and think I should be working, but I know what I've been through and I know I can't go back.
I am beyond grateful that I have the choice when so many others don't.
Best to you as you make this tough decision.
Best of health to you as well.
Karen
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- February 25, 2014 at 3:08 pm
Thanks so much for your response. I have stage IV cancer after 4 wide excisions since 2009 and recent spread of cancer in lymph nodes between esophagus and trachea. I am now being treated with Yervoy and will have my 3rd treatment tomorrow. This is a very difficult decision to make and I keep on hanging on to hope to go back to the routine I had with working. It depends on the next PET SCAN if I should bite the bullet and go into full retirement or not. I will then look into disability which will help me out financially. I thank God that my husband has insurance. I know it was a good decision to go on special leave this time because I can not afford to have more stress that I already have. I have heard that stress does aggravate cancer so we should not feel guilty of any decisions we have made. Please keep in touch.
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- February 26, 2014 at 4:42 pm
I'm glad you have options and a husband who has insurance.
I don't know what state you work in but here in Ohio our disability retirement offers insurance which is expensive but worth it if you want to keep it as a backup (plus I know once I stop it, nobody is going to sell me individual life insurance).
Also, don't know how many years you've been working. I had 14 yrs and was pleasantly surprised that my pay loss wasn't as bad as I thought it would be (most state education sites have calculators so you can see what you will be making).
You probably have had your PET scan by now. I hope that it was good news.
Please contact me if you have any other questions or concerns. I know that I went thru a mourning period when I retired under disability, but I was also relieved of so much worry. Eventually I came to accept it and enjoy not having the indecision and stress anymore.
Best to you,
Karen
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- February 26, 2014 at 4:59 pm
Additionally after reading "Anonymous's" post, I second his point that as a stage IV you'll get quickly through the application process. By the time my sick leave ran out, disability was all ready to start the very next month.
As for the effects of stress, I absolutely believe that for me it affected my disease. All 3 diagnosises came during some of the most stressful times in my life. I also realized after returning to work for those two years as a stage IV that I spent most of my days wishing I was any place but a classroom. I loved my job, but as Anonymous cited, my profession and any gains I made from it are not going to be important at the end of my life. It all comes down to God, family….life as it should be!
I prioritized my values and found that my work did not make the list 🙂
Karen
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- February 26, 2014 at 4:59 pm
Additionally after reading "Anonymous's" post, I second his point that as a stage IV you'll get quickly through the application process. By the time my sick leave ran out, disability was all ready to start the very next month.
As for the effects of stress, I absolutely believe that for me it affected my disease. All 3 diagnosises came during some of the most stressful times in my life. I also realized after returning to work for those two years as a stage IV that I spent most of my days wishing I was any place but a classroom. I loved my job, but as Anonymous cited, my profession and any gains I made from it are not going to be important at the end of my life. It all comes down to God, family….life as it should be!
I prioritized my values and found that my work did not make the list 🙂
Karen
-
- February 26, 2014 at 4:59 pm
Additionally after reading "Anonymous's" post, I second his point that as a stage IV you'll get quickly through the application process. By the time my sick leave ran out, disability was all ready to start the very next month.
As for the effects of stress, I absolutely believe that for me it affected my disease. All 3 diagnosises came during some of the most stressful times in my life. I also realized after returning to work for those two years as a stage IV that I spent most of my days wishing I was any place but a classroom. I loved my job, but as Anonymous cited, my profession and any gains I made from it are not going to be important at the end of my life. It all comes down to God, family….life as it should be!
I prioritized my values and found that my work did not make the list 🙂
Karen
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- March 2, 2014 at 3:19 pm
My Pet Scan is April 9th and I'm informing the people who I work with that this will be my deciding factor. This indecision period is hectic in my life right now. Especially now with getting more side effects with this treatment which is daily stomach upset. I am glad you have found the place in your life of not having to make this decision. I quess I am hoping for the best to go back to that routine and prove to everyone that I am still able to work. I need to do much praying about this and learn to take more care about myself. Thanks for your words of widom. Regina
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- March 2, 2014 at 3:19 pm
My Pet Scan is April 9th and I'm informing the people who I work with that this will be my deciding factor. This indecision period is hectic in my life right now. Especially now with getting more side effects with this treatment which is daily stomach upset. I am glad you have found the place in your life of not having to make this decision. I quess I am hoping for the best to go back to that routine and prove to everyone that I am still able to work. I need to do much praying about this and learn to take more care about myself. Thanks for your words of widom. Regina
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- March 2, 2014 at 3:19 pm
My Pet Scan is April 9th and I'm informing the people who I work with that this will be my deciding factor. This indecision period is hectic in my life right now. Especially now with getting more side effects with this treatment which is daily stomach upset. I am glad you have found the place in your life of not having to make this decision. I quess I am hoping for the best to go back to that routine and prove to everyone that I am still able to work. I need to do much praying about this and learn to take more care about myself. Thanks for your words of widom. Regina
-
- February 26, 2014 at 4:42 pm
I'm glad you have options and a husband who has insurance.
I don't know what state you work in but here in Ohio our disability retirement offers insurance which is expensive but worth it if you want to keep it as a backup (plus I know once I stop it, nobody is going to sell me individual life insurance).
Also, don't know how many years you've been working. I had 14 yrs and was pleasantly surprised that my pay loss wasn't as bad as I thought it would be (most state education sites have calculators so you can see what you will be making).
You probably have had your PET scan by now. I hope that it was good news.
Please contact me if you have any other questions or concerns. I know that I went thru a mourning period when I retired under disability, but I was also relieved of so much worry. Eventually I came to accept it and enjoy not having the indecision and stress anymore.
Best to you,
Karen
-
- February 26, 2014 at 4:42 pm
I'm glad you have options and a husband who has insurance.
I don't know what state you work in but here in Ohio our disability retirement offers insurance which is expensive but worth it if you want to keep it as a backup (plus I know once I stop it, nobody is going to sell me individual life insurance).
Also, don't know how many years you've been working. I had 14 yrs and was pleasantly surprised that my pay loss wasn't as bad as I thought it would be (most state education sites have calculators so you can see what you will be making).
You probably have had your PET scan by now. I hope that it was good news.
Please contact me if you have any other questions or concerns. I know that I went thru a mourning period when I retired under disability, but I was also relieved of so much worry. Eventually I came to accept it and enjoy not having the indecision and stress anymore.
Best to you,
Karen
-
- February 25, 2014 at 3:08 pm
Thanks so much for your response. I have stage IV cancer after 4 wide excisions since 2009 and recent spread of cancer in lymph nodes between esophagus and trachea. I am now being treated with Yervoy and will have my 3rd treatment tomorrow. This is a very difficult decision to make and I keep on hanging on to hope to go back to the routine I had with working. It depends on the next PET SCAN if I should bite the bullet and go into full retirement or not. I will then look into disability which will help me out financially. I thank God that my husband has insurance. I know it was a good decision to go on special leave this time because I can not afford to have more stress that I already have. I have heard that stress does aggravate cancer so we should not feel guilty of any decisions we have made. Please keep in touch.
-
- February 25, 2014 at 3:08 pm
Thanks so much for your response. I have stage IV cancer after 4 wide excisions since 2009 and recent spread of cancer in lymph nodes between esophagus and trachea. I am now being treated with Yervoy and will have my 3rd treatment tomorrow. This is a very difficult decision to make and I keep on hanging on to hope to go back to the routine I had with working. It depends on the next PET SCAN if I should bite the bullet and go into full retirement or not. I will then look into disability which will help me out financially. I thank God that my husband has insurance. I know it was a good decision to go on special leave this time because I can not afford to have more stress that I already have. I have heard that stress does aggravate cancer so we should not feel guilty of any decisions we have made. Please keep in touch.
-
- February 24, 2014 at 1:20 am
This is an interesting topic and one that I am grappling with as well. Given that you are stage IV you will be fast tracked for Social Security Disability and will likely see automatic approval within a few weeks. That really isn't enough money to cover bills in most areas of the USA but helps. The next question is do you have private or group disability indurance as well? Ask yourself if you automobile insurance and you were in an accident that caused some extensive and expensive damage to you car would even consider not putting a claim in. You absolutely should consult a reputable disability attorney for advice on how to proceed. If you have medical issues resulting from the disease or from the treatment then you have a decision to make regarding your direction. I had primary sites on my skin that metastized to my lung which was surgically resected and then to my brain. The brain tumor was treated with SRS but I had a reoccurance at the same spot 18 mos later and had surgical resection and SRS again. Physically feel fine currently but attention, focus and memory issues, some rage moments, etc. Clearly not the same person I was prior to this and clearly not able to do my same level of output as before. Although I remain optimistic I can beat this I am not foolish enough to think that truly has a high probability long term. On my deathbed I am confident I won't be thinking about how many more deals I did, how many more late night business dinners I hosted and how much I made. I do however think I'll reflect back on the quality time I spent with my beautiful bride, my 15 year old son and 13 year old daughter. If you have a honest claim, the economics work and you can afford not to work it comes down to a personal decision. If you have real health issues impacting your ability to perform at work there shouldn't be any guilt about making the decision not to do it if that's your inclination. You can always go back to work, you can't go back to living if you are dead.
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- February 24, 2014 at 1:20 am
This is an interesting topic and one that I am grappling with as well. Given that you are stage IV you will be fast tracked for Social Security Disability and will likely see automatic approval within a few weeks. That really isn't enough money to cover bills in most areas of the USA but helps. The next question is do you have private or group disability indurance as well? Ask yourself if you automobile insurance and you were in an accident that caused some extensive and expensive damage to you car would even consider not putting a claim in. You absolutely should consult a reputable disability attorney for advice on how to proceed. If you have medical issues resulting from the disease or from the treatment then you have a decision to make regarding your direction. I had primary sites on my skin that metastized to my lung which was surgically resected and then to my brain. The brain tumor was treated with SRS but I had a reoccurance at the same spot 18 mos later and had surgical resection and SRS again. Physically feel fine currently but attention, focus and memory issues, some rage moments, etc. Clearly not the same person I was prior to this and clearly not able to do my same level of output as before. Although I remain optimistic I can beat this I am not foolish enough to think that truly has a high probability long term. On my deathbed I am confident I won't be thinking about how many more deals I did, how many more late night business dinners I hosted and how much I made. I do however think I'll reflect back on the quality time I spent with my beautiful bride, my 15 year old son and 13 year old daughter. If you have a honest claim, the economics work and you can afford not to work it comes down to a personal decision. If you have real health issues impacting your ability to perform at work there shouldn't be any guilt about making the decision not to do it if that's your inclination. You can always go back to work, you can't go back to living if you are dead.
-
- February 24, 2014 at 1:20 am
This is an interesting topic and one that I am grappling with as well. Given that you are stage IV you will be fast tracked for Social Security Disability and will likely see automatic approval within a few weeks. That really isn't enough money to cover bills in most areas of the USA but helps. The next question is do you have private or group disability indurance as well? Ask yourself if you automobile insurance and you were in an accident that caused some extensive and expensive damage to you car would even consider not putting a claim in. You absolutely should consult a reputable disability attorney for advice on how to proceed. If you have medical issues resulting from the disease or from the treatment then you have a decision to make regarding your direction. I had primary sites on my skin that metastized to my lung which was surgically resected and then to my brain. The brain tumor was treated with SRS but I had a reoccurance at the same spot 18 mos later and had surgical resection and SRS again. Physically feel fine currently but attention, focus and memory issues, some rage moments, etc. Clearly not the same person I was prior to this and clearly not able to do my same level of output as before. Although I remain optimistic I can beat this I am not foolish enough to think that truly has a high probability long term. On my deathbed I am confident I won't be thinking about how many more deals I did, how many more late night business dinners I hosted and how much I made. I do however think I'll reflect back on the quality time I spent with my beautiful bride, my 15 year old son and 13 year old daughter. If you have a honest claim, the economics work and you can afford not to work it comes down to a personal decision. If you have real health issues impacting your ability to perform at work there shouldn't be any guilt about making the decision not to do it if that's your inclination. You can always go back to work, you can't go back to living if you are dead.
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- February 25, 2014 at 2:43 pm
It is good to know about the disability part and everything at this point depends on my Pet Scan results on April 9th. It is so hard to be in limbo and determining what direction to take. I will need to go on my husband's insurance soon because of being on leave for so long. All I know at this time, I am taking care of myself right now because it is stress enough going through the treatments and wondering if it is working. My focus and attention has also been compromised, so I know what you mean. I'm getting ready for my next treatment which is tomorrow, a nervous wreck and hoping my IV goes in easy this time. ReginaTink.
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- February 25, 2014 at 2:43 pm
It is good to know about the disability part and everything at this point depends on my Pet Scan results on April 9th. It is so hard to be in limbo and determining what direction to take. I will need to go on my husband's insurance soon because of being on leave for so long. All I know at this time, I am taking care of myself right now because it is stress enough going through the treatments and wondering if it is working. My focus and attention has also been compromised, so I know what you mean. I'm getting ready for my next treatment which is tomorrow, a nervous wreck and hoping my IV goes in easy this time. ReginaTink.
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- February 25, 2014 at 2:43 pm
It is good to know about the disability part and everything at this point depends on my Pet Scan results on April 9th. It is so hard to be in limbo and determining what direction to take. I will need to go on my husband's insurance soon because of being on leave for so long. All I know at this time, I am taking care of myself right now because it is stress enough going through the treatments and wondering if it is working. My focus and attention has also been compromised, so I know what you mean. I'm getting ready for my next treatment which is tomorrow, a nervous wreck and hoping my IV goes in easy this time. ReginaTink.
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