› Forums › General Melanoma Community › Abraxane treatment finally started
- This topic has 15 replies, 5 voices, and was last updated 13 years, 7 months ago by
jag.
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- October 21, 2011 at 12:25 am
although we were worried my wife's blood count would be too low, it tested normal and she started the chemo Abraxane today. Kind of funny, even though she has short hair from the craniotomy and bald patches from the cyberknife, the first thing she said when the doc said, "good news, we can do the chemo", was, "oh, this means I lose my hair". I guess in this case it is good news to be able to put poison in your body…and yes, in 14-21 days she loses all her hair. Treatment is weekly assuming her blood counts stay up.
although we were worried my wife's blood count would be too low, it tested normal and she started the chemo Abraxane today. Kind of funny, even though she has short hair from the craniotomy and bald patches from the cyberknife, the first thing she said when the doc said, "good news, we can do the chemo", was, "oh, this means I lose my hair". I guess in this case it is good news to be able to put poison in your body…and yes, in 14-21 days she loses all her hair. Treatment is weekly assuming her blood counts stay up.
We've also been battling an invisible tumor – the unexplained arm pain persists – although it is being managed well with a heavier daily dose of steroids and a medication called gabapentin, which is an anti-seizure med that has nerve pain reduction qualities. She saw a neurologist yesterday and he is pretty sure there is a small tumor – maybe the size of a grain of sand – and invisible to an MRI hitting a nerve in her C6 cervical spine or in her brachial plexus. She has an EMG, nerve conduction study on Monday. If they can narrow the location down they could in theory radiate it.
Nick
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- October 21, 2011 at 12:32 pm
Nick, Good luck with the chemo, I hope it can hold back those cancer cells for awhile. I am sure your family would love stability thru the holiday season coming up. I follow your blog, and admire how you and your wife are handling this situation, with love, dignity, and honesty. I am still feeling shell shocked after my husband’s craniotomy three weeks ago, and current WBR treatments. Phil is doing well, but I have to remind myself almost every minute to enjoy the moment and not dread the future. My very best to you and your wife, it’s not an easy journey! Here’s to a wonderful weekend with no treatments and doctor appointments. Valerie (Phil’s wife) -
- October 21, 2011 at 12:32 pm
Nick, Good luck with the chemo, I hope it can hold back those cancer cells for awhile. I am sure your family would love stability thru the holiday season coming up. I follow your blog, and admire how you and your wife are handling this situation, with love, dignity, and honesty. I am still feeling shell shocked after my husband’s craniotomy three weeks ago, and current WBR treatments. Phil is doing well, but I have to remind myself almost every minute to enjoy the moment and not dread the future. My very best to you and your wife, it’s not an easy journey! Here’s to a wonderful weekend with no treatments and doctor appointments. Valerie (Phil’s wife) -
- October 21, 2011 at 12:32 pm
Nick, Good luck with the chemo, I hope it can hold back those cancer cells for awhile. I am sure your family would love stability thru the holiday season coming up. I follow your blog, and admire how you and your wife are handling this situation, with love, dignity, and honesty. I am still feeling shell shocked after my husband’s craniotomy three weeks ago, and current WBR treatments. Phil is doing well, but I have to remind myself almost every minute to enjoy the moment and not dread the future. My very best to you and your wife, it’s not an easy journey! Here’s to a wonderful weekend with no treatments and doctor appointments. Valerie (Phil’s wife) -
- October 21, 2011 at 4:35 pm
Many warm hugs to you and Meagan. May the Abraxane do its job with minimal side effects. I so much appreciate her connection to art and color. It's part of what makes life so beautiful (and, of course, a loving partner)!
Blessings to you both~
Cristy, Stage IV
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- October 21, 2011 at 4:35 pm
Many warm hugs to you and Meagan. May the Abraxane do its job with minimal side effects. I so much appreciate her connection to art and color. It's part of what makes life so beautiful (and, of course, a loving partner)!
Blessings to you both~
Cristy, Stage IV
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- October 21, 2011 at 4:35 pm
Many warm hugs to you and Meagan. May the Abraxane do its job with minimal side effects. I so much appreciate her connection to art and color. It's part of what makes life so beautiful (and, of course, a loving partner)!
Blessings to you both~
Cristy, Stage IV
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- October 22, 2011 at 4:04 am
Nick, it is possible that Abraxane could work better than expected. Wishing your wife good luck with the EMG. Hope that they are successful in finding and treating the source of the pain.
Take care
Frank from Australia
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- October 22, 2011 at 4:04 am
Nick, it is possible that Abraxane could work better than expected. Wishing your wife good luck with the EMG. Hope that they are successful in finding and treating the source of the pain.
Take care
Frank from Australia
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- October 22, 2011 at 4:04 am
Nick, it is possible that Abraxane could work better than expected. Wishing your wife good luck with the EMG. Hope that they are successful in finding and treating the source of the pain.
Take care
Frank from Australia
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