› Forums › General Melanoma Community › yervoy side effects and work schedule
- This topic has 33 replies, 11 voices, and was last updated 11 years, 6 months ago by HopefulOne.
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- November 26, 2012 at 11:48 pm
I am currently on zelboraf but I'm considering switching to yervoy. Is there anyone who has continued to work full time while on yervoy or are the side effects too much? Right nowIi am working two 12 hour days a week. I'm wondering if i can continue this if i go to yervoy infusions.
I am currently on zelboraf but I'm considering switching to yervoy. Is there anyone who has continued to work full time while on yervoy or are the side effects too much? Right nowIi am working two 12 hour days a week. I'm wondering if i can continue this if i go to yervoy infusions.
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- November 27, 2012 at 11:29 am
I was on the MDX-010 trial (Yevoy) and worked full time throughout. I experienced some side effects and was placed on high dose steroids and still managed to work full time. Everyone is different of course, but there have been many of us on the bulletin board that worked full time during the treatment. Best of luck to you…
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- November 27, 2012 at 11:29 am
I was on the MDX-010 trial (Yevoy) and worked full time throughout. I experienced some side effects and was placed on high dose steroids and still managed to work full time. Everyone is different of course, but there have been many of us on the bulletin board that worked full time during the treatment. Best of luck to you…
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- November 27, 2012 at 11:29 am
I was on the MDX-010 trial (Yevoy) and worked full time throughout. I experienced some side effects and was placed on high dose steroids and still managed to work full time. Everyone is different of course, but there have been many of us on the bulletin board that worked full time during the treatment. Best of luck to you…
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- November 27, 2012 at 1:29 pm
I have done two rounds of IPI and have continued my current work schedule. For me that is 3 1/2 days a week. This treatment for me was easier than interferon and way easier than being in the hospital for biochemo.Good luck to you,
Julie in Las Vegas
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- November 27, 2012 at 1:29 pm
I have done two rounds of IPI and have continued my current work schedule. For me that is 3 1/2 days a week. This treatment for me was easier than interferon and way easier than being in the hospital for biochemo.Good luck to you,
Julie in Las Vegas
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- November 27, 2012 at 1:29 pm
I have done two rounds of IPI and have continued my current work schedule. For me that is 3 1/2 days a week. This treatment for me was easier than interferon and way easier than being in the hospital for biochemo.Good luck to you,
Julie in Las Vegas
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- November 27, 2012 at 3:36 pm
I was able to complete Yervoy (4 treatments) and work my regular schedule of 40 hrs a week, and I also have a 1 hr commute to and from work. I would only take time off on the day of the infusion. The worst side effects I had was the bad rash and the itching, mainly on my upper body and both sides of my face.
Rosa
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- November 28, 2012 at 4:03 pm
I just finished my 4th dose of ipi yesterday and have been working full time. well… other than the 5 weeks I took off for a small bowel resection to remove a tumor… 🙂 I work 5 days a week (and have about 2 hours of commuting round trip).
Hang in there! So far no major side effects for me. but then again… just finished #4 yesterday.
Erin
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- November 29, 2012 at 9:08 am
hey did you take zelboraf prior to taking yervoy? just wondering. I have been taking zelboraf for 14 months and now it seems like one of my tumors is slowly growing the other 4 are no longer visible on ct. My dr wants me to switch to yervoy if this one coninue to grow. I'm hoping to continue to work if I switch. Are you having good results from the Yervoy?
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- November 29, 2012 at 9:08 am
hey did you take zelboraf prior to taking yervoy? just wondering. I have been taking zelboraf for 14 months and now it seems like one of my tumors is slowly growing the other 4 are no longer visible on ct. My dr wants me to switch to yervoy if this one coninue to grow. I'm hoping to continue to work if I switch. Are you having good results from the Yervoy?
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- November 29, 2012 at 9:08 am
hey did you take zelboraf prior to taking yervoy? just wondering. I have been taking zelboraf for 14 months and now it seems like one of my tumors is slowly growing the other 4 are no longer visible on ct. My dr wants me to switch to yervoy if this one coninue to grow. I'm hoping to continue to work if I switch. Are you having good results from the Yervoy?
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- December 11, 2012 at 4:47 pm
wondered how things are going now after your last infusion. My husband is having his last infusion as I type this. Has been going pretty well.. some joint pain controlled by meds and rash.. all doable in hopes of good overall results. He's still working too. Best wishes for you and great results!
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- December 11, 2012 at 4:47 pm
wondered how things are going now after your last infusion. My husband is having his last infusion as I type this. Has been going pretty well.. some joint pain controlled by meds and rash.. all doable in hopes of good overall results. He's still working too. Best wishes for you and great results!
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- December 11, 2012 at 4:47 pm
wondered how things are going now after your last infusion. My husband is having his last infusion as I type this. Has been going pretty well.. some joint pain controlled by meds and rash.. all doable in hopes of good overall results. He's still working too. Best wishes for you and great results!
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- November 28, 2012 at 4:03 pm
I just finished my 4th dose of ipi yesterday and have been working full time. well… other than the 5 weeks I took off for a small bowel resection to remove a tumor… 🙂 I work 5 days a week (and have about 2 hours of commuting round trip).
Hang in there! So far no major side effects for me. but then again… just finished #4 yesterday.
Erin
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- November 28, 2012 at 4:03 pm
I just finished my 4th dose of ipi yesterday and have been working full time. well… other than the 5 weeks I took off for a small bowel resection to remove a tumor… 🙂 I work 5 days a week (and have about 2 hours of commuting round trip).
Hang in there! So far no major side effects for me. but then again… just finished #4 yesterday.
Erin
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- November 27, 2012 at 3:36 pm
I was able to complete Yervoy (4 treatments) and work my regular schedule of 40 hrs a week, and I also have a 1 hr commute to and from work. I would only take time off on the day of the infusion. The worst side effects I had was the bad rash and the itching, mainly on my upper body and both sides of my face.
Rosa
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- November 27, 2012 at 3:36 pm
I was able to complete Yervoy (4 treatments) and work my regular schedule of 40 hrs a week, and I also have a 1 hr commute to and from work. I would only take time off on the day of the infusion. The worst side effects I had was the bad rash and the itching, mainly on my upper body and both sides of my face.
Rosa
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- December 1, 2012 at 4:22 pm
I was on Yervoy before the drug was approved, so I wound up getting 4 cycles of treatment (16 infusions). My doctor said that he thought I might have gotten more ippi than anyone else in the world. That being said, I felt completely fine the entire time I took the drug and I worked the entire time. The only side effects I experienced were crazily itchy legs (like, tear off your skin itchy). Not pleasant, but nothing that would have stopped me from working or leading a totally normal life. Best of luck!
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- December 1, 2012 at 4:22 pm
I was on Yervoy before the drug was approved, so I wound up getting 4 cycles of treatment (16 infusions). My doctor said that he thought I might have gotten more ippi than anyone else in the world. That being said, I felt completely fine the entire time I took the drug and I worked the entire time. The only side effects I experienced were crazily itchy legs (like, tear off your skin itchy). Not pleasant, but nothing that would have stopped me from working or leading a totally normal life. Best of luck!
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- December 1, 2012 at 4:22 pm
I was on Yervoy before the drug was approved, so I wound up getting 4 cycles of treatment (16 infusions). My doctor said that he thought I might have gotten more ippi than anyone else in the world. That being said, I felt completely fine the entire time I took the drug and I worked the entire time. The only side effects I experienced were crazily itchy legs (like, tear off your skin itchy). Not pleasant, but nothing that would have stopped me from working or leading a totally normal life. Best of luck!
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- January 19, 2013 at 10:16 pm
Hi-
i was diagnosed with metastatic melanoma in 2009. I did IL-2 (utterly vile, laid me out flat, and I got no benefit at all.) I've also done a number of clinical trials without much effect until I did BRAF, which gave me some shrinkage and then stability for nearly 15 months. I had a number of side effects, including joint pain, itching and fatigue, so I ended up on a low dose. I got some good reduction, but it stalled. I did Ipi this fall. I worked fulltime through all four infusions, but felt progressively more fatigued after each, and immediately after the fourth infusion had major nausea. From that point, I had terrible diarrhea, and ended up being one of that very small percentage of people who get ulcerative colitis from Yervoy. It was a bad scene, I ended up in the hospital for two weeks, and they nearly had to perform surgery on my colon. A combination of Remicade and Prednisone eventually handled the issue. After discharge from the hospital, they started reducing the steroid dose, and the symptoms came right back. So I'm still taking a lot of steroids, and I've started a Remicade infusion protocol. After the next infusion we'll try reducing the Prednisone again, and see of the Remicade infusions will keep the nasty at bay. BUT, I had a PET/CT this week, and low and behold, I got a really good result from the Yervoy. I had a lot of lymph node activity that is now completely gone, and my primary tumors have shrunk considerably. And the positive effects may still be happening. Given this result, I would make the decision to to Yervoy even if I knew I would be an unlucky recipient of major side effects. If I start getting regrowth, my next stop is PD-1.
Melanoma is a difficult road to travel, but there is a lot of optimism these days, the science is moving at lightening speed. The succession of trials has kept me going much longer than first expected – here I am at the three year mark, still working, still living a very full life. Hang in there, and embrace trials – I'm convinced that the various trials back to back cumulatively, has brought me this far – and new things keep coming along at a good pace. Whether one has cancer or doesn't have cancer, no one knows what the future holds, and every day is a blessing.
C in SB
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- July 21, 2013 at 4:35 pm
Hi C in SB,
Just wanted to say I love your positive energy in spite of all you've been through. Keep fighting! Best to you.
Kimberly
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- July 21, 2013 at 4:35 pm
Hi C in SB,
Just wanted to say I love your positive energy in spite of all you've been through. Keep fighting! Best to you.
Kimberly
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- July 21, 2013 at 4:35 pm
Hi C in SB,
Just wanted to say I love your positive energy in spite of all you've been through. Keep fighting! Best to you.
Kimberly
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- January 19, 2013 at 10:16 pm
Hi-
i was diagnosed with metastatic melanoma in 2009. I did IL-2 (utterly vile, laid me out flat, and I got no benefit at all.) I've also done a number of clinical trials without much effect until I did BRAF, which gave me some shrinkage and then stability for nearly 15 months. I had a number of side effects, including joint pain, itching and fatigue, so I ended up on a low dose. I got some good reduction, but it stalled. I did Ipi this fall. I worked fulltime through all four infusions, but felt progressively more fatigued after each, and immediately after the fourth infusion had major nausea. From that point, I had terrible diarrhea, and ended up being one of that very small percentage of people who get ulcerative colitis from Yervoy. It was a bad scene, I ended up in the hospital for two weeks, and they nearly had to perform surgery on my colon. A combination of Remicade and Prednisone eventually handled the issue. After discharge from the hospital, they started reducing the steroid dose, and the symptoms came right back. So I'm still taking a lot of steroids, and I've started a Remicade infusion protocol. After the next infusion we'll try reducing the Prednisone again, and see of the Remicade infusions will keep the nasty at bay. BUT, I had a PET/CT this week, and low and behold, I got a really good result from the Yervoy. I had a lot of lymph node activity that is now completely gone, and my primary tumors have shrunk considerably. And the positive effects may still be happening. Given this result, I would make the decision to to Yervoy even if I knew I would be an unlucky recipient of major side effects. If I start getting regrowth, my next stop is PD-1.
Melanoma is a difficult road to travel, but there is a lot of optimism these days, the science is moving at lightening speed. The succession of trials has kept me going much longer than first expected – here I am at the three year mark, still working, still living a very full life. Hang in there, and embrace trials – I'm convinced that the various trials back to back cumulatively, has brought me this far – and new things keep coming along at a good pace. Whether one has cancer or doesn't have cancer, no one knows what the future holds, and every day is a blessing.
C in SB
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- January 19, 2013 at 10:16 pm
Hi-
i was diagnosed with metastatic melanoma in 2009. I did IL-2 (utterly vile, laid me out flat, and I got no benefit at all.) I've also done a number of clinical trials without much effect until I did BRAF, which gave me some shrinkage and then stability for nearly 15 months. I had a number of side effects, including joint pain, itching and fatigue, so I ended up on a low dose. I got some good reduction, but it stalled. I did Ipi this fall. I worked fulltime through all four infusions, but felt progressively more fatigued after each, and immediately after the fourth infusion had major nausea. From that point, I had terrible diarrhea, and ended up being one of that very small percentage of people who get ulcerative colitis from Yervoy. It was a bad scene, I ended up in the hospital for two weeks, and they nearly had to perform surgery on my colon. A combination of Remicade and Prednisone eventually handled the issue. After discharge from the hospital, they started reducing the steroid dose, and the symptoms came right back. So I'm still taking a lot of steroids, and I've started a Remicade infusion protocol. After the next infusion we'll try reducing the Prednisone again, and see of the Remicade infusions will keep the nasty at bay. BUT, I had a PET/CT this week, and low and behold, I got a really good result from the Yervoy. I had a lot of lymph node activity that is now completely gone, and my primary tumors have shrunk considerably. And the positive effects may still be happening. Given this result, I would make the decision to to Yervoy even if I knew I would be an unlucky recipient of major side effects. If I start getting regrowth, my next stop is PD-1.
Melanoma is a difficult road to travel, but there is a lot of optimism these days, the science is moving at lightening speed. The succession of trials has kept me going much longer than first expected – here I am at the three year mark, still working, still living a very full life. Hang in there, and embrace trials – I'm convinced that the various trials back to back cumulatively, has brought me this far – and new things keep coming along at a good pace. Whether one has cancer or doesn't have cancer, no one knows what the future holds, and every day is a blessing.
C in SB
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