Forum Replies Created
- Replies
-
-
- September 26, 2014 at 3:02 pm
As you said Ginger- "God is Good!" Thank you for sharing this wonderful and promising news. This is so uplifting for those of us in the middle of therapy. I am stage 4 with liver and lung mets and just finished my 4th infusion yesterday. I too have had minimal if any S.E. except being tired.Although my belly is growing it seems to have stablized. My oncologist does not want to rescan for 6 weeks in order to give the Yervoy the best shot at having some effect on my tumors before scanning. God willing I will be able to share similar news in 6 weeks! Please share what some of those new adventures might be ๐
-
- September 26, 2014 at 3:02 pm
As you said Ginger- "God is Good!" Thank you for sharing this wonderful and promising news. This is so uplifting for those of us in the middle of therapy. I am stage 4 with liver and lung mets and just finished my 4th infusion yesterday. I too have had minimal if any S.E. except being tired.Although my belly is growing it seems to have stablized. My oncologist does not want to rescan for 6 weeks in order to give the Yervoy the best shot at having some effect on my tumors before scanning. God willing I will be able to share similar news in 6 weeks! Please share what some of those new adventures might be ๐
-
- September 26, 2014 at 3:02 pm
As you said Ginger- "God is Good!" Thank you for sharing this wonderful and promising news. This is so uplifting for those of us in the middle of therapy. I am stage 4 with liver and lung mets and just finished my 4th infusion yesterday. I too have had minimal if any S.E. except being tired.Although my belly is growing it seems to have stablized. My oncologist does not want to rescan for 6 weeks in order to give the Yervoy the best shot at having some effect on my tumors before scanning. God willing I will be able to share similar news in 6 weeks! Please share what some of those new adventures might be ๐
-
- July 23, 2014 at 11:16 am
Cheri- Our stories sound too familiar though I pray that you do not follow the same progression as me.I have been followed at a major cancer center all along with a Specific Melanoma Program. Perhaps I had been a bit naive surrounding this whole diagnosis over the past 3 years and of course in hindsite wish I had done a bit more research at that time. I will have to go back to my record to share with you my exact staging at that time though it was far along because obviously in that "area" I could not even see or know that it was there! With "neg margins and negative nodes" I thought I was ok.I did not have an initial CT screening at the time of diagnosis. PET/CT scans were never part of or offered as part of my follow-up screening. I was seen by either my dermatologist or my GYN/ONC surgeon every 3 months for visual/physical exams. So when I had unexplained lingering fever-I thought it was some virus-I was thrown off gaurd to discover that my melanoma had returned.
My sister recomended that perhaps you try to petition your insurance company to see if they would cover periodic scans or talk with your physician to see if there are any screening studies/research out there that you could be a part of.
Blessings on you as you continue on this journey.
Theresa
-
- July 23, 2014 at 11:16 am
Cheri- Our stories sound too familiar though I pray that you do not follow the same progression as me.I have been followed at a major cancer center all along with a Specific Melanoma Program. Perhaps I had been a bit naive surrounding this whole diagnosis over the past 3 years and of course in hindsite wish I had done a bit more research at that time. I will have to go back to my record to share with you my exact staging at that time though it was far along because obviously in that "area" I could not even see or know that it was there! With "neg margins and negative nodes" I thought I was ok.I did not have an initial CT screening at the time of diagnosis. PET/CT scans were never part of or offered as part of my follow-up screening. I was seen by either my dermatologist or my GYN/ONC surgeon every 3 months for visual/physical exams. So when I had unexplained lingering fever-I thought it was some virus-I was thrown off gaurd to discover that my melanoma had returned.
My sister recomended that perhaps you try to petition your insurance company to see if they would cover periodic scans or talk with your physician to see if there are any screening studies/research out there that you could be a part of.
Blessings on you as you continue on this journey.
Theresa
-
- July 23, 2014 at 11:16 am
Cheri- Our stories sound too familiar though I pray that you do not follow the same progression as me.I have been followed at a major cancer center all along with a Specific Melanoma Program. Perhaps I had been a bit naive surrounding this whole diagnosis over the past 3 years and of course in hindsite wish I had done a bit more research at that time. I will have to go back to my record to share with you my exact staging at that time though it was far along because obviously in that "area" I could not even see or know that it was there! With "neg margins and negative nodes" I thought I was ok.I did not have an initial CT screening at the time of diagnosis. PET/CT scans were never part of or offered as part of my follow-up screening. I was seen by either my dermatologist or my GYN/ONC surgeon every 3 months for visual/physical exams. So when I had unexplained lingering fever-I thought it was some virus-I was thrown off gaurd to discover that my melanoma had returned.
My sister recomended that perhaps you try to petition your insurance company to see if they would cover periodic scans or talk with your physician to see if there are any screening studies/research out there that you could be a part of.
Blessings on you as you continue on this journey.
Theresa
-
- July 21, 2014 at 8:51 pm
Thank you Mary for this very valuable information. I am being treated at a major Comprehensive Cancer center and do feel that I can address possibilities of other treatment courses with my oncologist. I did get my cKIT report back and I do not have that mutation.
I will be doing further homework surrounding the information you have shared with me prior to my appointment this week.
You are 2 years out from your surgery…Did you recieve immunotherapy? If so what were they using then.
Theresa
-
- July 21, 2014 at 8:51 pm
Thank you Mary for this very valuable information. I am being treated at a major Comprehensive Cancer center and do feel that I can address possibilities of other treatment courses with my oncologist. I did get my cKIT report back and I do not have that mutation.
I will be doing further homework surrounding the information you have shared with me prior to my appointment this week.
You are 2 years out from your surgery…Did you recieve immunotherapy? If so what were they using then.
Theresa
-
- July 21, 2014 at 8:51 pm
Thank you Mary for this very valuable information. I am being treated at a major Comprehensive Cancer center and do feel that I can address possibilities of other treatment courses with my oncologist. I did get my cKIT report back and I do not have that mutation.
I will be doing further homework surrounding the information you have shared with me prior to my appointment this week.
You are 2 years out from your surgery…Did you recieve immunotherapy? If so what were they using then.
Theresa
-
- July 21, 2014 at 3:09 pm
So happy to hear from you Becky. I am still awaiting the final report on the C-Kit mutation for me knowing that this may offer other therapies if the Vernoy is not effective.
Of course my oncologist responded re. the Essiac Tea that they really discourage any other herbal/ non-traditional therapies while undergoing FDA approved therapies. This was the answer that I expected and I am disappointed but always HOPEFULL.
Hoping to hear from Jerry.
Theresa
-
- July 21, 2014 at 3:09 pm
So happy to hear from you Becky. I am still awaiting the final report on the C-Kit mutation for me knowing that this may offer other therapies if the Vernoy is not effective.
Of course my oncologist responded re. the Essiac Tea that they really discourage any other herbal/ non-traditional therapies while undergoing FDA approved therapies. This was the answer that I expected and I am disappointed but always HOPEFULL.
Hoping to hear from Jerry.
Theresa
-
- July 21, 2014 at 3:09 pm
So happy to hear from you Becky. I am still awaiting the final report on the C-Kit mutation for me knowing that this may offer other therapies if the Vernoy is not effective.
Of course my oncologist responded re. the Essiac Tea that they really discourage any other herbal/ non-traditional therapies while undergoing FDA approved therapies. This was the answer that I expected and I am disappointed but always HOPEFULL.
Hoping to hear from Jerry.
Theresa