Happy Thanksgiving one day late! I hope everyone enjoyed the day with family and friends.
I should have posted this back at the end of September but, again, that procrastination problem I'm working on...
I had my scans toward the end of September and with all humility and joy I can tell you that they were clean. My internventional radiologist/SIR-sphere-inserter-doctor, doctor Nosher who has been reading all of my scans since my SIR-sphere procedure 2 years ago said he couldn't find "a single solitary thing." The report stated that no new lesions, or previous existing lesions were detected.
Speechless. I really don't know what to even write. There are no words to describe the gratitude for getting another chance at life. There are no words to adequately thank all those who have been praying their guts out for me, those who know me and haven't even met me.
What can I ever say to Dr. Moriarty, and all my doctors and nurses who have helped save my life?
To my family, friends, my children, my husband? These feelings of gratitude, humility and joy I have not been able to express with words, I hope I can express them, if God's mercy stays with me, in how I live the rest of my life.
Thank you for your continued prayers and love my friends.
All Great Things,
Karen
I want to dedicate my clean, healthy scans in honor of my father-in-law Frank Shanahan who past away this past October 4th. You are deeply loved, and deeply missed. Still waters run deep.
Friday, November 23, 2012
Thursday, August 30, 2012
Summer Update
Hello to all! It has been a long time since I posted, I know. But things have really been that quiet. They have been ordinary, mundane, nothin-doin. And that my friends, is a gift.
I'll go straight to the logistics. My CEA continues to hover around 4.5. It has been that way, for at least 10 months, I think. I haven't had any scans since my last one in March. Dr. Moriarty wanted to wait 6 months (first time in 5 years!) for the next one, as long as my blood work/CEA was normal. I begrudgingly agreed. I knew it was a positive thing, but I also found it very unnerving to wait so long. I almost felt like I was being a bit arrogant. Like "hey look at me I'm so way cool and better so I am totally waiting 6 months man!" But yet I waited and now September is upon us and wheels are in motion for setting up my scan appointment soon.
I have also been seeing Dr. Moriarty once a month still to get my port flushed and blood work done and to just meet and see how my health is faring.
In anniversary news, as of August 10th 2012, it has been 2 years since my last chemotherapy treatment. I have not had any chemotherapy treatment or Erbitux. Hopefully, if all goes well with my scans, October 26th of this year, it will have been 2 years since my SIR-spheres procedure, and my last procedure full stop.
Okay so this whole 5 year deal? The fact that I am alive, and thriving, and to this date, no clinically detectable cancer to speak of? Miracle, my dear friends. And I do not use this word lightly. Just two months ago, this past June, another friend of mine battling the same stage 4 cancer as I, passed away, she had to leave behind her 7 year old boy and her husband. She was 33 years old. Out of respect for her desire for privacy I won't give her name. I also don't speak of her for sympathy on my part. I speak of my lovely friend, because that should also be me, or she should also be me yes? Do you see?
Every morning when I wake up-BOOM-an amazing gift. But wait, it gets better, more amazing gifts to follow! Then I have two healthy happy children that I have the privilege of caring for and raising, and a husband who works so hard, and loves me BOOM! WAIT!! It gets even better!! I am not sick, I feel great, I can walk on my own two feet, take care of my self. BOOM! Make my kids something that resembles breakfast, sit and watch cartoons with them (with my coffee of course)- BOOM, BOOM, KABOOM! Pure, pure, pure gift, upon gift upon gift of life. And that's just my morning my friends.
Every day, every single day, I marvel and I am deeply grateful that I am alive. Because I really shouldn't be. That will never escape me, nor leave me. If it ever does I should be slapped...hard.
Each day that I open my eyes, is a great day. I don't think I am really able to even say "I had a bad day today." What? No way. It may be a stressful day. It may be a sad day. It may be a difficult day. But I am in that day present and accounted for. It is a most precious gift that I don't take for granted. When we are out with the kids, or the kids and I are outside blowing bubbles or something, I am thinking and feeling that I cannot believe I am getting to do this! That emotion pours in, resonates and flows through my whole body and I am deeply, deeply grateful and very humbled. This happens every day with me.
I know tomorrow is not promised. I knew about it before, but now I have lived it and I am still living it. Cancer is always lurking back there. I try not to pay it much mind, but yes with scan time, comes the "scanxiety" but to think about that now would be wasting time, not living in the present, not focusing on being able to write to all you amazing people who have prayed, supported, loved and cheered my family on these last 5 years. I selfishly ask please don't stop praying!
I have had the privilege of speaking with a lot of different people out there who most specifically have stage 4 colon cancer. I know I don't have a lot going on, but I will continue with the blog because people need to know that there is hope. There is a place in all of the dark world of cancer where people can get to wellness. I don't just mean myself. There are many others out there. If there is anyone new to this blog there is a great calendar out there called the Colondar. It has 12 different stage 4 colon cancer survivors featured on it. They are all young people diagnosed with colon cancer at a very young age such as myself. On the cover is a woman who is an 11year stage 4 cc survivor! Go to www.colonclub.com and the calendar is featured there. It is an amazing source of hope. If you know of someone who may find this helpful please pass it along.
Once my scans are done and all is known I will post the info. Please pray all is clear. Thank you ahead of time.
Thank you all again for your unfailing love and support to our family. We thank you for it and are very grateful to be so blessed. Let's continue to pray for one another, and live fully in the present.
Much love,
Karen
I'll go straight to the logistics. My CEA continues to hover around 4.5. It has been that way, for at least 10 months, I think. I haven't had any scans since my last one in March. Dr. Moriarty wanted to wait 6 months (first time in 5 years!) for the next one, as long as my blood work/CEA was normal. I begrudgingly agreed. I knew it was a positive thing, but I also found it very unnerving to wait so long. I almost felt like I was being a bit arrogant. Like "hey look at me I'm so way cool and better so I am totally waiting 6 months man!" But yet I waited and now September is upon us and wheels are in motion for setting up my scan appointment soon.
I have also been seeing Dr. Moriarty once a month still to get my port flushed and blood work done and to just meet and see how my health is faring.
In anniversary news, as of August 10th 2012, it has been 2 years since my last chemotherapy treatment. I have not had any chemotherapy treatment or Erbitux. Hopefully, if all goes well with my scans, October 26th of this year, it will have been 2 years since my SIR-spheres procedure, and my last procedure full stop.
Okay so this whole 5 year deal? The fact that I am alive, and thriving, and to this date, no clinically detectable cancer to speak of? Miracle, my dear friends. And I do not use this word lightly. Just two months ago, this past June, another friend of mine battling the same stage 4 cancer as I, passed away, she had to leave behind her 7 year old boy and her husband. She was 33 years old. Out of respect for her desire for privacy I won't give her name. I also don't speak of her for sympathy on my part. I speak of my lovely friend, because that should also be me, or she should also be me yes? Do you see?
Every morning when I wake up-BOOM-an amazing gift. But wait, it gets better, more amazing gifts to follow! Then I have two healthy happy children that I have the privilege of caring for and raising, and a husband who works so hard, and loves me BOOM! WAIT!! It gets even better!! I am not sick, I feel great, I can walk on my own two feet, take care of my self. BOOM! Make my kids something that resembles breakfast, sit and watch cartoons with them (with my coffee of course)- BOOM, BOOM, KABOOM! Pure, pure, pure gift, upon gift upon gift of life. And that's just my morning my friends.
Every day, every single day, I marvel and I am deeply grateful that I am alive. Because I really shouldn't be. That will never escape me, nor leave me. If it ever does I should be slapped...hard.
Each day that I open my eyes, is a great day. I don't think I am really able to even say "I had a bad day today." What? No way. It may be a stressful day. It may be a sad day. It may be a difficult day. But I am in that day present and accounted for. It is a most precious gift that I don't take for granted. When we are out with the kids, or the kids and I are outside blowing bubbles or something, I am thinking and feeling that I cannot believe I am getting to do this! That emotion pours in, resonates and flows through my whole body and I am deeply, deeply grateful and very humbled. This happens every day with me.
I know tomorrow is not promised. I knew about it before, but now I have lived it and I am still living it. Cancer is always lurking back there. I try not to pay it much mind, but yes with scan time, comes the "scanxiety" but to think about that now would be wasting time, not living in the present, not focusing on being able to write to all you amazing people who have prayed, supported, loved and cheered my family on these last 5 years. I selfishly ask please don't stop praying!
I have had the privilege of speaking with a lot of different people out there who most specifically have stage 4 colon cancer. I know I don't have a lot going on, but I will continue with the blog because people need to know that there is hope. There is a place in all of the dark world of cancer where people can get to wellness. I don't just mean myself. There are many others out there. If there is anyone new to this blog there is a great calendar out there called the Colondar. It has 12 different stage 4 colon cancer survivors featured on it. They are all young people diagnosed with colon cancer at a very young age such as myself. On the cover is a woman who is an 11year stage 4 cc survivor! Go to www.colonclub.com and the calendar is featured there. It is an amazing source of hope. If you know of someone who may find this helpful please pass it along.
Once my scans are done and all is known I will post the info. Please pray all is clear. Thank you ahead of time.
Thank you all again for your unfailing love and support to our family. We thank you for it and are very grateful to be so blessed. Let's continue to pray for one another, and live fully in the present.
Much love,
Karen
Saturday, May 5, 2012
All Good Things
Hello my dear friends and family! I know, it's been over 4 months-whatsa matta wit me? Well ironically, the answer is nothing!!
Like I have mentioned in the past if things are going well then I usually don't have much to report. So here I sit writing to you all feeling very lucky indeed.
I'll start by saying that I met with Dr. Moriarty at the end of February for my monthly check-up and bloodwork. I was sitting in my kitchen waiting to hear from Kathy with my CEA numbers and instead I heard from Dr. Moriarty. Now as you all know I love Dr. Moriarty, but when your oncologist calls you at home-it usually ain't so good. So as my stomach was churning I asked Dr. M "hi...why are you calling me?" (insert nervous laugh here)
Dr. M. said that my CEA was slightly elevated and though he wasn't overly worried or "freaked out" (he tries to use my language) he didn't like the trend. Now mind you it had only gone up a point in a half or so. But when my tumors "act-up" the CEA is usually consistent with that. The last time my CEA started to rise is when my cancer resurfaced after the liver resection.
I was due for scans in about 3 weeks. Waiting that long for scans and results in cancer-time is about...hmm...lets say a year! Add on possibility of new cancer whatever...that's 2 years!! For the first 5 seconds I was like "okay no biggie, it didn't go up that much." That lasted for all of 5 seconds, then I fell to pieces.
For the next 3 weeks I was a mess. I stopped working out, watched a lot of t.v. and sat and stared a lot. I don't like to admit it but I was pretty depressed.
It's not that I am scared of, or worried about treatment. For me, with stage 4 cancer, I just skip over all that and think, "okay is this where I die now?" I hate to be morbid, but this is a cancer blog, and it's how my mind works. That's what rots about cancer. I think especially stage 3 or 4. There isn't anything that anyone can give you or treat you with that can garauntee you get better (and I say this with all the love in my heart, but please don't suggest alternative medicine or diets to me...please). You can do this and that and just cross your fingers and pray it works, and if it doesn't work and your tumors aren't under control you die. So when I say I just skip to the end, that's what I mean. And that what makes your head spin, and takes you into dark places in your mind that your are REALLY tired of going to.
Then I'm thinking, well maybe I just need more chemo or whatever, and guess what? Then I get to watch my children and husband suffer while I walk around like a warmed over corpse. Yippeee!! (heavy on the sarcasm here) Like I said-wasn't feeling so "positive."
So I had my scans on Monday the 20th of March and saw Dr. Moriarty that Wednesday. The report had not come in yet. That means no report-no info-no knowledge this equals Karen having a mental breakdown. I thought my whole body was going to crack in half. As if I was a statue and someone took a chisel at the top of my head, slammed it down and I split right down the middle.
Fortunatley I had the CD with the scan on it so Dr. Moriarty was able to review it with Fran and I. He sat with us for at least 20-30 minutes going over it with us. He felt that barring anything the interventional radiologist Dr. Nosher saw, he didn't see anything outstanding.
In addition, my CEA numbers also went back down. Okay, starting to breathe. The top of my shoulders which had been fused with stress to the bottom of my jawbone for the last 3 weeks started to loosen up a bit. For me though, I NEEDED THAT REPORT!!! I know that anyone with cancer reading this knows where I am coming from. That Friday, the lovely Kathy called me. I was in the food store.
Kathy said the they had the report and on the report it was stated "no evidence of disease." You see, that was in the actual report. Kathy told me she had to read it over a few times to make sure that's what it said before she called me. I was shaking like a leaf and my knees felt like jelly.
Now I have been lucky for months now. My scans for the past year have been very good. The reports have stated, "continuous improvement," "no new growth." That in itself is incredible news.
But for it to say no evidence of disease??? It's winning a billion dollars (tax free) in the lottery except exponentially far better.
Now after reading the last post in December one might say "yes well you were already NED right?" But the last report stated in general terms things look good. But there wasn't any mention that there was no evidence of disease. That has never been in a report of mine-not ever.
To put it in even greater perspective, I have not had chemo since August of 2010. I have not had a procedure done or treatment of any kind since October of 2010. For nothing to grow in that time...to me, its astounding. I am lucky, blessed, and cannot even begin to articulate the depths of my gratitude.
Every day I am grateful. I am grateful each morning when I get up. I am grateful when the laundry room is overflowing with laundry, I am grateful when one of the kids is giving a passionate speech about how homework is mean for kids to do and they will never ever get it done. I am grateful for cleaning the bathroom toilets. I am grateful for every mundane, ordinary thing in life, because guess what, I am alive to live it.
You see I am here. Everyday that I get to wake up and be present in my life is a gift. I am not planning to travel the world, climb Mount Everest, or jump out of a plane. I just want a beautiful, sweet, ordinary life growing up and growing old with my family. I am very blessed to be given that chance right now. I don't know how long the cancer will stay away, a few months, a few years, who knows? But right now I have been given a rare gift in the stage 4 cancer world of being quasi well.
I do have survivor guilt and getting-well guilt for sure. And at times it gives me pause, and I debate wether to publish the next blog post. But that's really just me thinking about what other people would think of me and has nothing to do with helping and informing people, which is supposed to be the point of this blog. So I digress...
Deeply, deeply I thank you for all the prayers, years and years have past, and people still come up to me with the greatest compassion in their eyes and tell me that they are still praying for me. Woah. Blows me away and I humbly thank you . I do continue to pray for all those suffering and all those who I know and don't know who pray for me, so hopefully, the power of many...
Again thank you everyone. Thank you. Lets continue to pray for each other. We all need Jesus in our lives. I don't think it means we always feel like we want to. But for myself when I try to do it on my own, I end up in a muddled mess.
Thank you for all the support for reading this blog. Take care of your health. Get your mammograms, get your colonosopies, if its scary-so what. That just means its something that's scary. It's just an emotion and won't hurt you. But not doing these tests can also kill you. Live in the present, prevent illness where you can, and pray.
Much love to you all,
Karen
Like I have mentioned in the past if things are going well then I usually don't have much to report. So here I sit writing to you all feeling very lucky indeed.
I'll start by saying that I met with Dr. Moriarty at the end of February for my monthly check-up and bloodwork. I was sitting in my kitchen waiting to hear from Kathy with my CEA numbers and instead I heard from Dr. Moriarty. Now as you all know I love Dr. Moriarty, but when your oncologist calls you at home-it usually ain't so good. So as my stomach was churning I asked Dr. M "hi...why are you calling me?" (insert nervous laugh here)
Dr. M. said that my CEA was slightly elevated and though he wasn't overly worried or "freaked out" (he tries to use my language) he didn't like the trend. Now mind you it had only gone up a point in a half or so. But when my tumors "act-up" the CEA is usually consistent with that. The last time my CEA started to rise is when my cancer resurfaced after the liver resection.
I was due for scans in about 3 weeks. Waiting that long for scans and results in cancer-time is about...hmm...lets say a year! Add on possibility of new cancer whatever...that's 2 years!! For the first 5 seconds I was like "okay no biggie, it didn't go up that much." That lasted for all of 5 seconds, then I fell to pieces.
For the next 3 weeks I was a mess. I stopped working out, watched a lot of t.v. and sat and stared a lot. I don't like to admit it but I was pretty depressed.
It's not that I am scared of, or worried about treatment. For me, with stage 4 cancer, I just skip over all that and think, "okay is this where I die now?" I hate to be morbid, but this is a cancer blog, and it's how my mind works. That's what rots about cancer. I think especially stage 3 or 4. There isn't anything that anyone can give you or treat you with that can garauntee you get better (and I say this with all the love in my heart, but please don't suggest alternative medicine or diets to me...please). You can do this and that and just cross your fingers and pray it works, and if it doesn't work and your tumors aren't under control you die. So when I say I just skip to the end, that's what I mean. And that what makes your head spin, and takes you into dark places in your mind that your are REALLY tired of going to.
Then I'm thinking, well maybe I just need more chemo or whatever, and guess what? Then I get to watch my children and husband suffer while I walk around like a warmed over corpse. Yippeee!! (heavy on the sarcasm here) Like I said-wasn't feeling so "positive."
So I had my scans on Monday the 20th of March and saw Dr. Moriarty that Wednesday. The report had not come in yet. That means no report-no info-no knowledge this equals Karen having a mental breakdown. I thought my whole body was going to crack in half. As if I was a statue and someone took a chisel at the top of my head, slammed it down and I split right down the middle.
Fortunatley I had the CD with the scan on it so Dr. Moriarty was able to review it with Fran and I. He sat with us for at least 20-30 minutes going over it with us. He felt that barring anything the interventional radiologist Dr. Nosher saw, he didn't see anything outstanding.
In addition, my CEA numbers also went back down. Okay, starting to breathe. The top of my shoulders which had been fused with stress to the bottom of my jawbone for the last 3 weeks started to loosen up a bit. For me though, I NEEDED THAT REPORT!!! I know that anyone with cancer reading this knows where I am coming from. That Friday, the lovely Kathy called me. I was in the food store.
Kathy said the they had the report and on the report it was stated "no evidence of disease." You see, that was in the actual report. Kathy told me she had to read it over a few times to make sure that's what it said before she called me. I was shaking like a leaf and my knees felt like jelly.
Now I have been lucky for months now. My scans for the past year have been very good. The reports have stated, "continuous improvement," "no new growth." That in itself is incredible news.
But for it to say no evidence of disease??? It's winning a billion dollars (tax free) in the lottery except exponentially far better.
Now after reading the last post in December one might say "yes well you were already NED right?" But the last report stated in general terms things look good. But there wasn't any mention that there was no evidence of disease. That has never been in a report of mine-not ever.
To put it in even greater perspective, I have not had chemo since August of 2010. I have not had a procedure done or treatment of any kind since October of 2010. For nothing to grow in that time...to me, its astounding. I am lucky, blessed, and cannot even begin to articulate the depths of my gratitude.
Every day I am grateful. I am grateful each morning when I get up. I am grateful when the laundry room is overflowing with laundry, I am grateful when one of the kids is giving a passionate speech about how homework is mean for kids to do and they will never ever get it done. I am grateful for cleaning the bathroom toilets. I am grateful for every mundane, ordinary thing in life, because guess what, I am alive to live it.
You see I am here. Everyday that I get to wake up and be present in my life is a gift. I am not planning to travel the world, climb Mount Everest, or jump out of a plane. I just want a beautiful, sweet, ordinary life growing up and growing old with my family. I am very blessed to be given that chance right now. I don't know how long the cancer will stay away, a few months, a few years, who knows? But right now I have been given a rare gift in the stage 4 cancer world of being quasi well.
I do have survivor guilt and getting-well guilt for sure. And at times it gives me pause, and I debate wether to publish the next blog post. But that's really just me thinking about what other people would think of me and has nothing to do with helping and informing people, which is supposed to be the point of this blog. So I digress...
Deeply, deeply I thank you for all the prayers, years and years have past, and people still come up to me with the greatest compassion in their eyes and tell me that they are still praying for me. Woah. Blows me away and I humbly thank you . I do continue to pray for all those suffering and all those who I know and don't know who pray for me, so hopefully, the power of many...
Again thank you everyone. Thank you. Lets continue to pray for each other. We all need Jesus in our lives. I don't think it means we always feel like we want to. But for myself when I try to do it on my own, I end up in a muddled mess.
Thank you for all the support for reading this blog. Take care of your health. Get your mammograms, get your colonosopies, if its scary-so what. That just means its something that's scary. It's just an emotion and won't hurt you. But not doing these tests can also kill you. Live in the present, prevent illness where you can, and pray.
Much love to you all,
Karen
Subscribe to:
Posts (Atom)