› Forums › General Melanoma Community › Biochemotherapy, 3 rounds total, stage 3B, when did you loose your hair?
- This topic has 27 replies, 8 voices, and was last updated 11 years, 2 months ago by mdsoza.
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- July 13, 2013 at 4:15 pm
Hello all, I am melissa and I am stage 3B, headed into the hospital on Monday for round 2 of 3 of biochemotherapy and I am wondering for those who have been through biochemotherapy, when did you loose your hair? ( interferon Alpha 2b low dose, continuous Interleukin-2, vinblastine, cisplatin and dacarbazine is the cocktail I am in for) I have a wig picked out but i dont want to buy it until i have to. is there anyone who didnt loose their hair at all? Thanks ๐
Hello all, I am melissa and I am stage 3B, headed into the hospital on Monday for round 2 of 3 of biochemotherapy and I am wondering for those who have been through biochemotherapy, when did you loose your hair? ( interferon Alpha 2b low dose, continuous Interleukin-2, vinblastine, cisplatin and dacarbazine is the cocktail I am in for) I have a wig picked out but i dont want to buy it until i have to. is there anyone who didnt loose their hair at all? Thanks ๐
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- July 13, 2013 at 4:22 pm
I did the same cocktail as you, minus the interferon. I only lost about a third of my hair. I would check with your local American Cancer Society – I did lose my hair on Zelboraf and got a free wig there. -
- July 13, 2013 at 4:22 pm
I did the same cocktail as you, minus the interferon. I only lost about a third of my hair. I would check with your local American Cancer Society – I did lose my hair on Zelboraf and got a free wig there. -
- July 13, 2013 at 4:22 pm
I did the same cocktail as you, minus the interferon. I only lost about a third of my hair. I would check with your local American Cancer Society – I did lose my hair on Zelboraf and got a free wig there. -
- July 13, 2013 at 4:38 pm
Brian,
i am currently NED and I am being treated at the Huntsman Cancer Institute in salt lake city utah. It is a pretty aggressive treatment plan but I personally couldnt live with a 60% chance of survival in 5 years and not do anything about it, I have been told by my doctors (Dr Antebaka and Dr Khong) that this is being looked at as a cure for me ๐ Good luck to you and let me know if you need any more information.
Melissa
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- July 13, 2013 at 11:06 pm
My daughter did this treatment. She lost most of her hair throughout the 3 sessions. It started falling out a day before she went back in for her second course. We got a wig for her before her third course and she started wearing it a week or two after she finished the treatment. She started with really thick hair though. Not everyone looses their hair but if you are going to it should start soon. It took a couple of months after the end of the treatment for her hair to start growing back in. -
- July 13, 2013 at 11:06 pm
My daughter did this treatment. She lost most of her hair throughout the 3 sessions. It started falling out a day before she went back in for her second course. We got a wig for her before her third course and she started wearing it a week or two after she finished the treatment. She started with really thick hair though. Not everyone looses their hair but if you are going to it should start soon. It took a couple of months after the end of the treatment for her hair to start growing back in. -
- July 13, 2013 at 11:06 pm
My daughter did this treatment. She lost most of her hair throughout the 3 sessions. It started falling out a day before she went back in for her second course. We got a wig for her before her third course and she started wearing it a week or two after she finished the treatment. She started with really thick hair though. Not everyone looses their hair but if you are going to it should start soon. It took a couple of months after the end of the treatment for her hair to start growing back in. -
- July 13, 2013 at 11:32 pm
I definitely think you are doing the right thing. I was Stage IIIB NED back in October 2011. I briefly looked at the biochemo options but the statistics back then just didn't seem to justify the toxcities. I think the cocktails they have today are a lot more sophisticated and definitely worth giving a try. Back in Oct 11 I opted for about the only thing available which was the IPI vs. Interferon trial. I ended up in the interferon arm and completed the one year of interferon. Unfortunately I progressed to stage IV a few months ago. After surgery I'm now back to NED and about to enroll in a MAGE vaccine clinical trial in Moffitt. Best of luck to you Melissa.
Brian
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- July 14, 2013 at 3:35 pm
I am doing the very same cocktail right now. Round two, day three. I am stage four, mets mostly in bones. I am concerned about sentence I read regarding treatment causing increased pain in tumors at first. Anybody else run into this? Tuesday will be four weeks in hospital, brought here by terrible pain to start with.
Melissa, I hope you do incredibly well with treatment. -
- July 14, 2013 at 3:35 pm
I am doing the very same cocktail right now. Round two, day three. I am stage four, mets mostly in bones. I am concerned about sentence I read regarding treatment causing increased pain in tumors at first. Anybody else run into this? Tuesday will be four weeks in hospital, brought here by terrible pain to start with.
Melissa, I hope you do incredibly well with treatment.-
- July 13, 2013 at 11:32 pm
I definitely think you are doing the right thing. I was Stage IIIB NED back in October 2011. I briefly looked at the biochemo options but the statistics back then just didn't seem to justify the toxcities. I think the cocktails they have today are a lot more sophisticated and definitely worth giving a try. Back in Oct 11 I opted for about the only thing available which was the IPI vs. Interferon trial. I ended up in the interferon arm and completed the one year of interferon. Unfortunately I progressed to stage IV a few months ago. After surgery I'm now back to NED and about to enroll in a MAGE vaccine clinical trial in Moffitt. Best of luck to you Melissa.
Brian
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- July 13, 2013 at 11:32 pm
I definitely think you are doing the right thing. I was Stage IIIB NED back in October 2011. I briefly looked at the biochemo options but the statistics back then just didn't seem to justify the toxcities. I think the cocktails they have today are a lot more sophisticated and definitely worth giving a try. Back in Oct 11 I opted for about the only thing available which was the IPI vs. Interferon trial. I ended up in the interferon arm and completed the one year of interferon. Unfortunately I progressed to stage IV a few months ago. After surgery I'm now back to NED and about to enroll in a MAGE vaccine clinical trial in Moffitt. Best of luck to you Melissa.
Brian
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- July 14, 2013 at 3:35 pm
I am doing the very same cocktail right now. Round two, day three. I am stage four, mets mostly in bones. I am concerned about sentence I read regarding treatment causing increased pain in tumors at first. Anybody else run into this? Tuesday will be four weeks in hospital, brought here by terrible pain to start with.
Melissa, I hope you do incredibly well with treatment. -
- July 15, 2013 at 11:50 pm
Melissa I completed my 3rd round of biochemo in April. Had (2) tumors that were un operable. Both shrunk and we used surgery to get tumors out. I did not lose my hair. It thinned but did not lose it. Keep up the fight. I am glad I did the treatment hope it is the same for you.
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- July 15, 2013 at 11:50 pm
Melissa I completed my 3rd round of biochemo in April. Had (2) tumors that were un operable. Both shrunk and we used surgery to get tumors out. I did not lose my hair. It thinned but did not lose it. Keep up the fight. I am glad I did the treatment hope it is the same for you.
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- July 15, 2013 at 11:50 pm
Melissa I completed my 3rd round of biochemo in April. Had (2) tumors that were un operable. Both shrunk and we used surgery to get tumors out. I did not lose my hair. It thinned but did not lose it. Keep up the fight. I am glad I did the treatment hope it is the same for you.
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- October 12, 2013 at 9:52 am
Biochemotherapy remains a promising new treatment for metastatic melanoma.
Yes it is possible to stop hair loss… But it depend on your treatment… and your imunity system…
Ref: heavy duty racks
____________
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- October 12, 2013 at 9:52 am
Biochemotherapy remains a promising new treatment for metastatic melanoma.
Yes it is possible to stop hair loss… But it depend on your treatment… and your imunity system…
Ref: heavy duty racks
____________
-
- October 12, 2013 at 9:52 am
Biochemotherapy remains a promising new treatment for metastatic melanoma.
Yes it is possible to stop hair loss… But it depend on your treatment… and your imunity system…
Ref: heavy duty racks
____________
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- October 15, 2013 at 6:36 am
Hello Melissa,
You are really strong girl.. My one friend is suffering from cancer.. He is completed his 2rd round of biochemo treatment, But still he didn't loss his hair… So you don't woory about it… it's happened in rare cases…
Ref: payroll management software
______________________
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- October 15, 2013 at 6:36 am
Hello Melissa,
You are really strong girl.. My one friend is suffering from cancer.. He is completed his 2rd round of biochemo treatment, But still he didn't loss his hair… So you don't woory about it… it's happened in rare cases…
Ref: payroll management software
______________________
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- October 15, 2013 at 6:36 am
Hello Melissa,
You are really strong girl.. My one friend is suffering from cancer.. He is completed his 2rd round of biochemo treatment, But still he didn't loss his hair… So you don't woory about it… it's happened in rare cases…
Ref: payroll management software
______________________
-
- July 13, 2013 at 4:38 pm
Brian,
i am currently NED and I am being treated at the Huntsman Cancer Institute in salt lake city utah. It is a pretty aggressive treatment plan but I personally couldnt live with a 60% chance of survival in 5 years and not do anything about it, I have been told by my doctors (Dr Antebaka and Dr Khong) that this is being looked at as a cure for me ๐ Good luck to you and let me know if you need any more information.
Melissa
-
- July 13, 2013 at 4:38 pm
Brian,
i am currently NED and I am being treated at the Huntsman Cancer Institute in salt lake city utah. It is a pretty aggressive treatment plan but I personally couldnt live with a 60% chance of survival in 5 years and not do anything about it, I have been told by my doctors (Dr Antebaka and Dr Khong) that this is being looked at as a cure for me ๐ Good luck to you and let me know if you need any more information.
Melissa
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