Saturday, November 29, 2008
Chemotherapy Flight
The airplane had been boarded. Flight attendants had given all the directions. Seatbelts were fastened. All electronic devices had been turned off. The plane was headed down the runway. All of a sudden the plane grinds to a halt. The passengers sit and wait. And wait. And wait. After 4 hours of sitting, the Captain gets on the intercom and announces that the flight will not be taking off. We have gone nowhere. The plane returns to the gate and we all disembark. We will have to rebook our flights for another time.
This is how I felt on Wednesday. It was my first chemo treatment. After questions, bloodwork, hookup and pre-steroid/benadryl infusion they flipped the valve for the Taxotere (the first of 2 drugs to be infused). The plane was headed down the runway and my throat began to close up a bit. They stopped the plane. Pumped me full of MORE Benadryl and steroids and flipped the valve again. Got flushed. Felt like my chest was being compressed. They stopped the plane and brought me back to the gate. I will have to rebook my flight.
I am feeling good physically this weekend.
I'm not 25% done with my chemo at this point.
What a mixed bag.
Thank you SO much again to all my friends and immediate thanks to those who were with me for my first flight!
Sally....Thanks for the cuddly purple blanket (way better than the regular airplane blankets), the laughs, the hugs and the right words at the right time.
Stacy....Thanks for keeping my toes on ice so my nails wouldn't fall out and for the wonderful support!
Karen....Thanks for the expertise and for holding my hand.
Renate.....Thanks for popping in for a 'Mom Hug'
Wednesday, November 26, 2008
These Are a Few of My Favorite Things
Chemo School
Monday was chemo school. Andre met me there and the sweet nurse Brenda talked nonstop for 3 hours about side effects, drugs, support systems, wigs, nausea as well as other bodily functions, and I don't even remember what else. I think Andre took 8 pages of notes. It was quite overwhelming.
Yesterday I went to see the surgeon (thank you Renate) and the news was good. She removed 2 more CENTIMETERS of margin in my last surgery and there was no evidence of any cancer cells in the removed tissue. Way to get a good chunk of it, Dr. Paulishak-Thank YOU! When she removed this tissue, she really just needed to 'connect the dots' as she went into the same incision as before. It hasn't bothered me at all and there is no swelling, although when she told me how much she removed, it dawned on me that 'hmmmm......maybe there is swelling and it will really shrink up', but that's ok because I am reassured that it is OUTTA THERE! Amazing how perspective changes.
My first day of chemo is today. I will head in to the hospital at 1:30 and sit there for 3-4 hours with a needle connected to my port as it goes on to kill any rapidly dividing cells. Even though my 1/2 dose of Ambien (to help me sleep) only lasted until 4am, I am feeling surprisingly calm. I stayed super busy last night and it kept my mind off of what's to come. I am going to a Kundalini yoga class at the Y at noon. I am really excited for this pre-chemo activity as it should be a wonderful meditative focus and hopefully I can go into the next day's activity with a clear calm mind.
Several friends have volunteered to come visit and for that I am very grateful. You ALL give me strength and it is appreciated more than I can express.
Yesterday I went to see the surgeon (thank you Renate) and the news was good. She removed 2 more CENTIMETERS of margin in my last surgery and there was no evidence of any cancer cells in the removed tissue. Way to get a good chunk of it, Dr. Paulishak-Thank YOU! When she removed this tissue, she really just needed to 'connect the dots' as she went into the same incision as before. It hasn't bothered me at all and there is no swelling, although when she told me how much she removed, it dawned on me that 'hmmmm......maybe there is swelling and it will really shrink up', but that's ok because I am reassured that it is OUTTA THERE! Amazing how perspective changes.
My first day of chemo is today. I will head in to the hospital at 1:30 and sit there for 3-4 hours with a needle connected to my port as it goes on to kill any rapidly dividing cells. Even though my 1/2 dose of Ambien (to help me sleep) only lasted until 4am, I am feeling surprisingly calm. I stayed super busy last night and it kept my mind off of what's to come. I am going to a Kundalini yoga class at the Y at noon. I am really excited for this pre-chemo activity as it should be a wonderful meditative focus and hopefully I can go into the next day's activity with a clear calm mind.
Several friends have volunteered to come visit and for that I am very grateful. You ALL give me strength and it is appreciated more than I can express.
A Variety Package of Tears, Kids and Lessons From Leeches
25 September 2008
In my world right now, tears and cancer go hand in hand. Sometimes the tears lasts only a moment....in which it may literally only be 'a' tear. There are shower at the Y tears, meditation tears, reiki induced tears (these are cleansing and brought on by connection and looking deep within, as well as my reiki friend), tears in the middle of the night, wig shopping tears, hat shopping tears, tears from thoughtful cards, tears brought on by the right words at the right time, tears from a thoughtful gift from a friend, tears from a thoughtful card or gift from a student, tears brought on through a shared journey with someone else going through cancer, tears at the dr, tears for fears, tears of frustration, tears of "Why?, tears of joy, tears of thankfulness, tears of love
All of these tears are good for me, whether they are sad or happy. They help me with acceptance and connection to others.
There have been situations when I have been shocked at how strength can wade through the thick mud of tears and I can breathe through them. I told my students about my cancer last Thursday. I was honest, open,showed them my port and was able to get through it with only one mini-moment of catching a tear that began to well (as my teammate quietly slipped his handkerchief into my hand...thank you, Gordon). They asked great questions, honest questions, and were wonderful through it all. They had a few tears, but mostly what I felt was a lot of love. One student came to me later that day and looked me in the eye and said, "Ms. Sommers. So. It's official. You're losing your hair." He asked it twice and my reply was, "Yes I will, but I'll still be the same person inside." I guess it was his way of accepting it and after my answer, he just said, "Ok." and went on to his usual 7th grade antics. I chuckled and shook my head in a situation that might normally bring on a tear or two. He came to me yesterday and said, "Maybe I'll shave my head." Another chuckle and shake of the head.
Another student was very upset that others were focusing so much on 'the hair thing'. His sister has an immune deficiency disease and doesn't have any hair. He told me that despite his sister's hair loss, he is so glad she is still around and he loves her very much. I let him know how he had a wonderful perspective of the whole thing and he would be SUCH a great help to me as well as to the rest of the class for his insights. (He informed me yesterday that he is moving, dangit!)
Incredible thoughtfulness in all forms lands in my lap every day. Teachers I don't know very well, parents who don't know me but volunteer to come clean my bathroom or come make me laugh, coworkers who have battled or are battling this as well, students who approach me with incredible words...they are sometimes uncomfortable, but always encouraged because I don't want secrets or unanswered questions. One of my teammates came to school on Monday with his head shaved. His wife reluctantly said 'ok' (thanks, Kelly) and he was so funny as he lifted his chin, raised his bald head, puffed out his chest and acted like he will be listened to more by his students (who listen to him anyway partially due to 1st quarter lunch detentions). Combine that with his sweet giggle and "Oh, geez" and he makes me smile a LOT! Another person I work with (who needs to remain anonymous) came to a meeting one day with burned copies of the movie Crazy, Sexy, Cancer and the Sex in the City episodes where Samantha has cancer. Thoughtfulness hits me in so many ways! And then there is my student teacher John who has been wonderful about covering classes while I am come in late and leave early for Dr. appointments. I am so appreciative of that! I also can't say enough about the "humanness" of my principal and assistant principals. Their understanding, support, and willingness to help is overwhelming!
When I was an 18 year old river guide at Dear Old Camp Icaghowan, I had 10 girls paddling down the Namekogan River in Wisconsin. Rules were pretty 'lax'. Jumping off bridges and cliffs were activities throughout the day. I would hear rapids coming up and say, "Hey guys, we better put our lifejackets back on." Small trees were downed and HUGE bonfires lit our campsites through the night. Bears were chased. One of the rules I did really stick to was shoes were ALWAYS on your feet (except when one of the kids had REALLY nasty blisters and we made a flip flop for her out of maxi pads and duct tape). I went down to the water one day to wash my feet. It was slow moving and all I wanted to do was take off those wet shoes I was forcing us all to wear. No kids were around, so I did just that. It felt so good to wiggle my toes in the mud. I got out of the water and 'SURPRISE!' My feet were FILLED with leeches. Of course it reminded me of the scene in the movie African Queen but I had to completely supress my first impulse which was to scream at the top of my lungs for my campers to come down to the river and 'GET THESE NASTY SUCKERS OFF ME!' I knew they would freak if I did. From the depths of my gut, I summoned the calmness to gently call up to them, "Hey you guys, could someone bring me the salt shaker?" Of course they came running down to see what was going on, proceeded to freak out (because that is often 12 year old girl group mentality), and handed me the salt shaker. I knew I had to be calm and spoke through their screeches, "It's ok. No big deal. Look...they come right off." And they did.
This experience really taught me a lot about leading and group mentality. When I'm at school, my students give me strength. When I tell students from previous years, the last thing I want to do is cry....oh, I may have a tear or two but that's ok. I explain things to them and answer questions. I focus on the cancer being out of my body and the chemo and radiation are precautions so it doesn't return. It is big ugly pothole between now and when my hair grows back. It scares the hell out of me. The strength and the deep breaths that I take in order to explain things to them are really good for me (kind of like the leeches.)
There it is. A plethora of tears, kids and crazy camp stories.
Thanks again for strength, support and love.
In my world right now, tears and cancer go hand in hand. Sometimes the tears lasts only a moment....in which it may literally only be 'a' tear. There are shower at the Y tears, meditation tears, reiki induced tears (these are cleansing and brought on by connection and looking deep within, as well as my reiki friend), tears in the middle of the night, wig shopping tears, hat shopping tears, tears from thoughtful cards, tears brought on by the right words at the right time, tears from a thoughtful gift from a friend, tears from a thoughtful card or gift from a student, tears brought on through a shared journey with someone else going through cancer, tears at the dr, tears for fears, tears of frustration, tears of "Why?, tears of joy, tears of thankfulness, tears of love
All of these tears are good for me, whether they are sad or happy. They help me with acceptance and connection to others.
There have been situations when I have been shocked at how strength can wade through the thick mud of tears and I can breathe through them. I told my students about my cancer last Thursday. I was honest, open,showed them my port and was able to get through it with only one mini-moment of catching a tear that began to well (as my teammate quietly slipped his handkerchief into my hand...thank you, Gordon). They asked great questions, honest questions, and were wonderful through it all. They had a few tears, but mostly what I felt was a lot of love. One student came to me later that day and looked me in the eye and said, "Ms. Sommers. So. It's official. You're losing your hair." He asked it twice and my reply was, "Yes I will, but I'll still be the same person inside." I guess it was his way of accepting it and after my answer, he just said, "Ok." and went on to his usual 7th grade antics. I chuckled and shook my head in a situation that might normally bring on a tear or two. He came to me yesterday and said, "Maybe I'll shave my head." Another chuckle and shake of the head.
Another student was very upset that others were focusing so much on 'the hair thing'. His sister has an immune deficiency disease and doesn't have any hair. He told me that despite his sister's hair loss, he is so glad she is still around and he loves her very much. I let him know how he had a wonderful perspective of the whole thing and he would be SUCH a great help to me as well as to the rest of the class for his insights. (He informed me yesterday that he is moving, dangit!)
Incredible thoughtfulness in all forms lands in my lap every day. Teachers I don't know very well, parents who don't know me but volunteer to come clean my bathroom or come make me laugh, coworkers who have battled or are battling this as well, students who approach me with incredible words...they are sometimes uncomfortable, but always encouraged because I don't want secrets or unanswered questions. One of my teammates came to school on Monday with his head shaved. His wife reluctantly said 'ok' (thanks, Kelly) and he was so funny as he lifted his chin, raised his bald head, puffed out his chest and acted like he will be listened to more by his students (who listen to him anyway partially due to 1st quarter lunch detentions). Combine that with his sweet giggle and "Oh, geez" and he makes me smile a LOT! Another person I work with (who needs to remain anonymous) came to a meeting one day with burned copies of the movie Crazy, Sexy, Cancer and the Sex in the City episodes where Samantha has cancer. Thoughtfulness hits me in so many ways! And then there is my student teacher John who has been wonderful about covering classes while I am come in late and leave early for Dr. appointments. I am so appreciative of that! I also can't say enough about the "humanness" of my principal and assistant principals. Their understanding, support, and willingness to help is overwhelming!
When I was an 18 year old river guide at Dear Old Camp Icaghowan, I had 10 girls paddling down the Namekogan River in Wisconsin. Rules were pretty 'lax'. Jumping off bridges and cliffs were activities throughout the day. I would hear rapids coming up and say, "Hey guys, we better put our lifejackets back on." Small trees were downed and HUGE bonfires lit our campsites through the night. Bears were chased. One of the rules I did really stick to was shoes were ALWAYS on your feet (except when one of the kids had REALLY nasty blisters and we made a flip flop for her out of maxi pads and duct tape). I went down to the water one day to wash my feet. It was slow moving and all I wanted to do was take off those wet shoes I was forcing us all to wear. No kids were around, so I did just that. It felt so good to wiggle my toes in the mud. I got out of the water and 'SURPRISE!' My feet were FILLED with leeches. Of course it reminded me of the scene in the movie African Queen but I had to completely supress my first impulse which was to scream at the top of my lungs for my campers to come down to the river and 'GET THESE NASTY SUCKERS OFF ME!' I knew they would freak if I did. From the depths of my gut, I summoned the calmness to gently call up to them, "Hey you guys, could someone bring me the salt shaker?" Of course they came running down to see what was going on, proceeded to freak out (because that is often 12 year old girl group mentality), and handed me the salt shaker. I knew I had to be calm and spoke through their screeches, "It's ok. No big deal. Look...they come right off." And they did.
This experience really taught me a lot about leading and group mentality. When I'm at school, my students give me strength. When I tell students from previous years, the last thing I want to do is cry....oh, I may have a tear or two but that's ok. I explain things to them and answer questions. I focus on the cancer being out of my body and the chemo and radiation are precautions so it doesn't return. It is big ugly pothole between now and when my hair grows back. It scares the hell out of me. The strength and the deep breaths that I take in order to explain things to them are really good for me (kind of like the leeches.)
There it is. A plethora of tears, kids and crazy camp stories.
Thanks again for strength, support and love.
Tuesday, November 18, 2008
Truly From the Depths of my Heart
One of the things I've always believed is that friends "DO" for each other. So many of you have done so much for me throughout this whole process. Sometimes my 'thank yous' are in person and sometimes I whisper a silent 'thanks', but ALWAYS I am appreciative of what you are giving me throughout this whole ordeal. My regret is that I can't send each of you a thank you note for everything you have done. These are just a few of the gracious acts that have been so unselfishly given and I thank you for:
somehow 'knowing' that you should call and then meeting me at the Dr on September 18th when the 'C Bomb' was dropped, cussing for me, holding my hand, crying with me and farting at just the right moment so we could have a much needed giggle, dropping a feather off with my newspaper, looking up information for me, bringing me amazing quiche with homegrown garden greens, crying with me, comforting me, doing reiki for me and helping me with visualizations, visiting me at school even though you could have had a sub job that day, emptying the dishwasher, doing the dishes, taking walks, giving me naturopathic advice, calling and being ok if I don't return the phone call for a few days, making me laugh, driving out to visit, offering to come to visit, spending the night, helping me with my blog, helping me with scarf fashion (I may need some more of that), being patient with my tears even though you are busy, fed exing my radiology reports, purple flowers, any flowers, scar massage oil, coconut oil, Messiah's Handbook, letting me comment on your eyebrows, allowing me to come in late and leave early from school for appointments so I don't have to use precious sick days, biking on the flats when you might want to bike on hills, encouraging me to join the Y, beautiful furniture to replace my 'college look' concrete and planks, a beautiful handmade twig table, books on diet, cancer and fun, going to the doctor with me, taking copious notes at the doctor, helping me think of questions to ask the doctor, calling to ask me about my Mountain Chalet schedule and being flexible because I don't know what the effects of the chemo will be, loaning me your favorite crystals, listening with love, wearing purple, bringing me tea that helped you when you were pregnant and feeling crummy, sharing your kids with me, being gentle in encouraging me not to read about chemo side effects at night, calling when I haven't heard from you in years, calling when I haven't heard from you in days, calling when I haven't heard from you in hours, e-mailing, slumber parties with popcorn and sorbet, taking me out for dinner, Peace of Mind relaxing therapy, being there when I wake up from surgery, answering my phone and taking messages, kind loving words, ordering my tv converter box, taking time off from work to be my second set of ears, painting my deck, hugging me when I walk into the office at school, letting other people know what is going on with me, embracing me with love, giving me phone numbers of other cancer survivors, sitting and holding my hand in the dark, flying here from Salt Lake to spend time with me, pomegranate juice, Allison's basketball jersey for 'Dig For the Cure', packages of thank you notes, sending prayer bars, sweet cards with thoughtful words, ordering a Livestrong Notebook, wearing a Livestrong bracelet for me, passing on your Livestrong bracelet when I happened to see you hiking, commenting on my blog, foot rub lotion, talking to me about your cancer, helping me breathe through my tears, the right words at the right time, all the positive thoughts you send.
Thank you, thank you, thank you. It doesn't seem like enough but know it comes from the depths of my heart. Love to you all.
somehow 'knowing' that you should call and then meeting me at the Dr on September 18th when the 'C Bomb' was dropped, cussing for me, holding my hand, crying with me and farting at just the right moment so we could have a much needed giggle, dropping a feather off with my newspaper, looking up information for me, bringing me amazing quiche with homegrown garden greens, crying with me, comforting me, doing reiki for me and helping me with visualizations, visiting me at school even though you could have had a sub job that day, emptying the dishwasher, doing the dishes, taking walks, giving me naturopathic advice, calling and being ok if I don't return the phone call for a few days, making me laugh, driving out to visit, offering to come to visit, spending the night, helping me with my blog, helping me with scarf fashion (I may need some more of that), being patient with my tears even though you are busy, fed exing my radiology reports, purple flowers, any flowers, scar massage oil, coconut oil, Messiah's Handbook, letting me comment on your eyebrows, allowing me to come in late and leave early from school for appointments so I don't have to use precious sick days, biking on the flats when you might want to bike on hills, encouraging me to join the Y, beautiful furniture to replace my 'college look' concrete and planks, a beautiful handmade twig table, books on diet, cancer and fun, going to the doctor with me, taking copious notes at the doctor, helping me think of questions to ask the doctor, calling to ask me about my Mountain Chalet schedule and being flexible because I don't know what the effects of the chemo will be, loaning me your favorite crystals, listening with love, wearing purple, bringing me tea that helped you when you were pregnant and feeling crummy, sharing your kids with me, being gentle in encouraging me not to read about chemo side effects at night, calling when I haven't heard from you in years, calling when I haven't heard from you in days, calling when I haven't heard from you in hours, e-mailing, slumber parties with popcorn and sorbet, taking me out for dinner, Peace of Mind relaxing therapy, being there when I wake up from surgery, answering my phone and taking messages, kind loving words, ordering my tv converter box, taking time off from work to be my second set of ears, painting my deck, hugging me when I walk into the office at school, letting other people know what is going on with me, embracing me with love, giving me phone numbers of other cancer survivors, sitting and holding my hand in the dark, flying here from Salt Lake to spend time with me, pomegranate juice, Allison's basketball jersey for 'Dig For the Cure', packages of thank you notes, sending prayer bars, sweet cards with thoughtful words, ordering a Livestrong Notebook, wearing a Livestrong bracelet for me, passing on your Livestrong bracelet when I happened to see you hiking, commenting on my blog, foot rub lotion, talking to me about your cancer, helping me breathe through my tears, the right words at the right time, all the positive thoughts you send.
Thank you, thank you, thank you. It doesn't seem like enough but know it comes from the depths of my heart. Love to you all.
Monday, November 17, 2008
Today's Surgery
I was at the hospital at 6am and surgery began at 7:30 (time does NOT fly when you are being poked and prodded). The surgery went fine. Dr. Paulishak went into the same excision from 6 weeks ago, "dug out" more margins (I did request that she get plenty) and they put in a port on my right side. (The port is basically a 'portal' to my superior vena cava...the main vein that goes to my heart and then the rest of my body. This is my 'poking site'. They will administer the chemo through this, take blood through this and it makes access to my insides much easier. It does stick out which grosses me out but apparently the pain will be less.) The surgery went well and I have a pretty cool x-ray of the port and the tube that goes into my vein (these look GREAT on an overhead projector).
Andre brought me in this am, Renate spent the day with me and Sally and I are having a slumber party tonight. I didn't dare have more than 3 bites of my yummy lentil soup because it is a bit spicy and I don't want to throw up. I'm saving room for popcorn and mango or peach sorbet later. This surgery was much easier. We sat on the deck in the sun after we got home, I took a nap for a couple hours and I'll go to bed early tonight.
This part is behind me. Each one of these hurdles is that much closer to being DONE!
Andre brought me in this am, Renate spent the day with me and Sally and I are having a slumber party tonight. I didn't dare have more than 3 bites of my yummy lentil soup because it is a bit spicy and I don't want to throw up. I'm saving room for popcorn and mango or peach sorbet later. This surgery was much easier. We sat on the deck in the sun after we got home, I took a nap for a couple hours and I'll go to bed early tonight.
This part is behind me. Each one of these hurdles is that much closer to being DONE!
All Call for Ideas
17 November
"Chemo School" is this Monday. At this point, they will be dripping poison into my body the day before Thanksgiving. Not all types of chemo cause hair loss. The two I am receiving do. I'm realizing that I'm attached to my hair and that's just the way it is. I cry over the thought of losing my hair. I know it will grow back, but not until after I have lost it all. I thought of an idea, but could really use your help. I dug out a few hats and tried them on. I will be knitting my first hat. My friend Sue (http://suesun40@blogspot.com) helped me with a little bit of scarf tying. She also had a very sexy wig; lots of body, beautiful flouncing curls at the bottom, looks like one of those conditioner commercials. If it were my real hair, it would take electric curlers, lots of mousse and about an hour....and it would last a maximum of 2 minutes before falling!
Here is my idea. I would like to get my hair cut before it falls out and attach it somehow to some type of hairband. I could wear the hairband and put a hat over it. That way I could keep my hair as a "souvenir" and at least feel comfortable in situations where I want a bit of hair. I'm calling on you, my incredible creative community, to help me with this.
My "All Call" to you is to help me come up with a way to attach it to a headband.
1. What type of headband should I use?
2. In order to attach the hair to the band, do I use superglue? Duct tape? Windex?
When I talked with Sue (my trailblazer, in that she has gone through 3 chemo treatments so far and is sharing info, laughs and tears), she stressed that if I want to do this, my hair needs to go before I get too far into chemo. Apparently hair gets all strawlike fairly early on with treatments.
Thank you SO much in advance for your creative wigging! Perhaps we can start a trend among chemo patients!
"Chemo School" is this Monday. At this point, they will be dripping poison into my body the day before Thanksgiving. Not all types of chemo cause hair loss. The two I am receiving do. I'm realizing that I'm attached to my hair and that's just the way it is. I cry over the thought of losing my hair. I know it will grow back, but not until after I have lost it all. I thought of an idea, but could really use your help. I dug out a few hats and tried them on. I will be knitting my first hat. My friend Sue (http://suesun40@blogspot.com) helped me with a little bit of scarf tying. She also had a very sexy wig; lots of body, beautiful flouncing curls at the bottom, looks like one of those conditioner commercials. If it were my real hair, it would take electric curlers, lots of mousse and about an hour....and it would last a maximum of 2 minutes before falling!
Here is my idea. I would like to get my hair cut before it falls out and attach it somehow to some type of hairband. I could wear the hairband and put a hat over it. That way I could keep my hair as a "souvenir" and at least feel comfortable in situations where I want a bit of hair. I'm calling on you, my incredible creative community, to help me with this.
My "All Call" to you is to help me come up with a way to attach it to a headband.
1. What type of headband should I use?
2. In order to attach the hair to the band, do I use superglue? Duct tape? Windex?
When I talked with Sue (my trailblazer, in that she has gone through 3 chemo treatments so far and is sharing info, laughs and tears), she stressed that if I want to do this, my hair needs to go before I get too far into chemo. Apparently hair gets all strawlike fairly early on with treatments.
Thank you SO much in advance for your creative wigging! Perhaps we can start a trend among chemo patients!
Friday, November 14, 2008
Life Is
14 November 2008
Life Is. That's where you go for healing, comfort, energy, perspective.
This was my message tonight when I headed to 'Messiah's Handbook'.
Now all I need to do is make sense of it all.
Second opinions. I was mostly interested in what the oncologist had to say (this is the Chemo Master.....or Devil.....depending on how you look at it). He told me that I was in a grey zone as far as treatment options go. In his very flat tone, he said, "It would probably be ok if you didn't get chemo and it would probably be ok if you did."
He and the radiation oncologist suggested study after study that I could participate in, but once again, it puts me into the hands of "The Randomizers".
So, what am I going to do? After lots of tears (thank goodness for friend's shoulders), I have decided to go ahead and do the chemo. This has been agonizing, although when I learned that my chances for recurrence would be lower if I did it, I think I knew in my heart what my decision would be.
There are times when I can talk about this without crying, times that I have 30 second to 1 minute streams of tears, and times when it lasts longer. I'm sleeping unassisted (no Ambien, yet), and have been doing a lot of working out. I want to be strong when I get my surgery on Monday to put in the chemo port and get more margins "dug out" (my surgeon hates when I use that term). I will then be going to "Chemo School" a week from Monday and am scheduled for my first treatment the Wednesday before Thanksgiving.
I don't know if I can make sense of it all at this point. My hope is that when I move into the 'amateur' role, that I will be able to get perspective. I guess for this moment I just have to keep telling myself "Life Is" and grasp the threads of healing, comfort and energy that are offered to me by so many of you. Thank you for all your help, all your love and your shoulders.
Saturday, November 8, 2008
Illusions and Magic
In the book Illusions by Richard Bach, there is a man named Donald Shimoda who carries a small book around called "Messiah's Handbook: Reminders for the Advanced Soul". The idea behind this book is to hold a question in your mind, close your eyes, open the handbook at random, pick the left or right side, open your eyes and read the answer.
Right after the "C Bomb" was dropped on me, a dear friend gave me that book as an early birthday present. In one of my "breathe through your tears and try to deal with this" moments, I opened the book and read,
"You learn most when you play against an opponent who can beat you"
WOW! It took my breath away. It gave me strength and stopped my tears pretty quickly.
Another evening, I opened the book and the magic stated,
You're master of what you've lived,
Artisan at what you're living,
Amateur at what's next to live.
I was completely WOWED once again!
Last year on November 11 I returned home from another trip of a lifetime. I had spent the last 10 days in Italy with my mom running around medieval cities, eating gelato, and floating within the magical cloud that wraps itself through Italy.
I wouldn't have imagined in my wildest dreams (and my dreams can get pretty wild), that this year on November 11, I would be getting a second opinion about treatment options for cancer. That is my plan for this Tuesday. Andre and I are driving to Denver to meet with a team of surgeons, radiation oncologist, chemo oncologist and perhaps others to see if there is agreement with my doctors here.
I can't say I'm an artisan at this point, but I'm getting through with the help of so many of YOU. I breathe my way through tears, enjoy my family and friends, continue my biking and hiking, try to impart knowledge to 13 year olds and do some laughing along the way.
Amateur. It's what's next. May it be filled with learning and lessons.
Saturday, November 1, 2008
Pineapples in Colorado
Pineapples always remind me of Thailand. The ladies on Khao San Road carve them with speed and dexterity and hand them over for 50 cents. Young gals sell pineapple while sitting in the shade of some abstract limestone karst as tourists make their way to the beach.
It is an absolutely glorious day in Colorado today. I'm glad to be here cutting up my own pineapple on the back deck this morning (although it didn't quite taste the same)!
Subscribe to:
Posts (Atom)