Yesterday I went to Piedmont Rehab and Fitness Center in Fayetteville to have my Lymphedema assessment. I was surprised when I went in and saw what looked like a very well organized gym before me. On almost every piece of equipment was an elderly person obviously using the machines for post operative rehabilitation. I felt awkward and out of place sitting there waiting for my name to be called. I wondered what machine they would place me on and if I would be able to do whatever therapy they decided I needed to do.
After about thirty minutes, a young, blonde woman came up to me and asked if I was Bonnie. I stood up and greeted her. She took me back to a separate examination room and began asking me a lot of medical history questions, nodding her head and entering my answers in the laptop on her little desk. After we'd completed the questions, she had me undress from the waist up and sit on the exam table.
Alison, the Lymphedema specialist, brought an extractable tape measure and a blue marker over to the table. She sat in front of me and began to measure different intervals up my left arm. She started at the wrist and measured then made some blue markings on my arm. Next she went up about 4 inches and did this again but this time, she recorded the numbers from her first measurement on my arm. As she recorded each measured circumference, I tried to see what she was writing on her notepad but couldn't. After she finished the left side, she did the same thing on the right side and then proceeded to measure my chest area and around each armpit. When she had completed all measurements and recordings, I looked down at my arms and laughed. She looked at me in a confused way and I said, "I have markings all over my chest from the radiation mapping and now I have markings up and down each arm too. I sure look funny! It's a good thing I don't have to go anywhere but home after I leave here!"
Next Alison pulled out some anatomy charts and began to explain to me how the lymph system works. She used a lot of medical jargon and asked repeatedly if I understood what she was talking about. I told her that I had wanted to be a nurse when I was growing up so when I went to high school, I focused on anatomy and physiology as well as biology. "That's great," she said, "most people look at me like a deer caught in headlights when I explain this to them." I was thankful I had a good knowledge of medical terminology and was able to understand her explanations without asking her to go in to more detail.
The treatment plan would involve lymphatic massage as well as my having to wear a compression camisole and two lymphedema sleeves. Alison said I'd also have to wear gauntlets to prevent the lymphatic fluid from traveling down my arms into my hands and wrists. Gauntlets? I was suddenly feeling a little medieval. She said she'd have to order all of those things and fax the orders over to my surgeon for her signature. As soon as we got that, she'd contact the insurance company for their approval and then I'd go to an offsite location for fitting. Before I left, Alison showed me how to do lymphatic massage on myself and she explained that my radiation could exacerbate the swelling. I am hoping it doesn't. My Lymphedema isn't as bad as some cases, Alison explained. She said some people come in with legs or arms as big around as tree trunks. I am so thankful I don't have that problem! I can't imagine how uncomfortable those people must feel and how embarrassed they must be to go out in public. People can be so cruel and judgmental.
Prayer request: Please pray that my lymphedema does not get worse as I go through radiation. There is no cure for it but the symptoms can be treated with compression and massage. (Mine seems to worsen late in the day after I've been very active with my arms.) Thank you in advance for praying!
©bonnie annis all rights reserved
Saturday, August 23, 2014
Friday, August 22, 2014
Lymphedema
I had hoped I wouldn't get it but it appears that I have a case of Lymphedema in both arms. This is not uncommon for women who've had lymph nodes removed after breast surgery. The Lymphatic system is impeded and Lymphatic fluid can no longer drain properly so it has to collect somewhere in the body. Mine has decided to collect right around and under my armpits.
When I wake in the morning, the swelling is minimal because I've had my arms propped up all night long on pillows, but by mid morning, the tops of my arms are huge. They're so swollen I can barely get my shirt sleeves over them. I'm thankful a friend had recently given me some larger sized blouses and the width of the sleeves on those accommodate my "fat" arms well.
This morning I will be seeing a physical therapist in Fayetteville named Alison Franklin. She's certified in working with Lymphedema patients. I have no idea what she's going to do to help relieve the situation but I have appointments lined up with her for every other day next week and for several weeks following. I imagine I'll be on the road a lot in between these appointments and my radiation appointments.
It would be nice if breast cancer patients could go in, have surgery and just be done never having to worry about anything else again, but as it goes, most women end up having additional physical problems, treatments, and other issues to deal with for long periods of time. And just when you finish all of the required treatment plans and think you're home free, a new disease creeps in...Canceritis. Canceritis is the fear of recurrence of Cancer. So, you see, breast cancer isn't a once and done type of deal...it's a life changing, mind boggling menace. Not only does Canceritis affect the patient, it also affects the patient's family. Who wants to sit around wondering if every new lump or bump might be the return of a horrible disease?
In the words of Scarlett O'Hara, "I don't want to think about that right now!" I'll cross that bridge when I come to it. Right now my focus is to get this Lymphedema under control so it doesn't travel on down my arms and cause me to be unable to do the things I am able to do right now. If it gets worse, they'll put me in compression sleeves. There is no cure for Lymphedema. That's one reason it's so important for me to remember not to have any needle sticks, blood pressures or any kind of skin injuries to either arm because any of those things can highly exacerbate the situation.
When I wake in the morning, the swelling is minimal because I've had my arms propped up all night long on pillows, but by mid morning, the tops of my arms are huge. They're so swollen I can barely get my shirt sleeves over them. I'm thankful a friend had recently given me some larger sized blouses and the width of the sleeves on those accommodate my "fat" arms well.
This morning I will be seeing a physical therapist in Fayetteville named Alison Franklin. She's certified in working with Lymphedema patients. I have no idea what she's going to do to help relieve the situation but I have appointments lined up with her for every other day next week and for several weeks following. I imagine I'll be on the road a lot in between these appointments and my radiation appointments.
It would be nice if breast cancer patients could go in, have surgery and just be done never having to worry about anything else again, but as it goes, most women end up having additional physical problems, treatments, and other issues to deal with for long periods of time. And just when you finish all of the required treatment plans and think you're home free, a new disease creeps in...Canceritis. Canceritis is the fear of recurrence of Cancer. So, you see, breast cancer isn't a once and done type of deal...it's a life changing, mind boggling menace. Not only does Canceritis affect the patient, it also affects the patient's family. Who wants to sit around wondering if every new lump or bump might be the return of a horrible disease?
In the words of Scarlett O'Hara, "I don't want to think about that right now!" I'll cross that bridge when I come to it. Right now my focus is to get this Lymphedema under control so it doesn't travel on down my arms and cause me to be unable to do the things I am able to do right now. If it gets worse, they'll put me in compression sleeves. There is no cure for Lymphedema. That's one reason it's so important for me to remember not to have any needle sticks, blood pressures or any kind of skin injuries to either arm because any of those things can highly exacerbate the situation.
It's always something! Tomorrow I'll give an update on what the therapist did for me today. Thank you for stopping by and reading my blog. I'm sure you're learning more about Cancer than you ever dreamed you might. My prayer for you is that neither you nor someone you love will ever have to deal with Cancer but chances are, someone you know will be diagnosed with it soon. When and if they are, hopefully my blog will have given you some tidbit of valuable information or some small shred of encouragement to pass on to them. It's not an easy trial to get through but it is doable.
One of my favorite quotes is “The strongest of all warriors are these two-Time and
Patience.”- Leo Tolstoy. Time and patience, those are the things a breast cancer patient learns well during their journey. I've always been a impatient person. I've always been a hurry up and get it done type of person...typical type A personality, but since I've had cancer, I've had to learn to slow down and just wait. That's one reason I stopped wearing a watch...to remind me to just take time...to just take one moment at a time and that's all I can do.
© bonnie annis all rights reserved
Thursday, August 21, 2014
Fear is sin
This morning, as I was reading my Bible, I came across a verse that I'm sure I've read many times before in the past, but today, it just grabbed my attention like no other verse had in a very long time. This is the verse I read: "...everything that does not come from faith is sin." Romans 14:23
Wow...EVERYTHING that does not come from faith is sin...EVERYTHING. Now that's pretty clear! As I continued to think about that verse, I realized something I'd never realized before...FEAR is sin. Oh, but wait a minute...you say! Fear is an emotion. Well, yes, it is an emotion but fear is so much more than that. Fear is a lack of faith!
Have you ever thought about fear being a selfish act? It is! When we fear, we are choosing to believe what WE want to believe about something instead of trusting in what God says about it. We are choosing to put the fear above God! And anything put above God is considered an idol. Was I idolizing fear??? I certainly didn't think so but...
I have been very fearful lately. As you might imagine, Cancer can do that to you. Even after surgery and knowing the doctor said she thinks she got it all, I've been fearful there might be some Cancer cells lurking around in my body somewhere. In fact, radiation therapy just confirms that fear...why would they feel it necessary to irradiate my body if they weren't thinking that some rogue Cancer cells might just be swimming up my blood stream or sliding through my lymph system? Fear had attached itself to me during that first phone call telling me the mass was malignant. And that fear had been gleefully taking piggyback rides on my back ever since. That is, until I decided to shake it off today after reading this verse.
God gave me a clarity that I'd never experienced before. In Hebrews 11:6, the Bible says, "without faith it is impossible to please God." Now if fear is a lack of faith, then how did I expect to be able to please God if I was afraid??? Fear certainly doesn't come from faith so I realized that it indeed was a sin.
When you're struggling with a serious illness, it's easy to fall into the trap of only hearing and believing what the test reports show or what the doctors tell you. It's easier to believe the black and white than to have faith in what you can't see or understand. But, as a Christian, I know God expects me to walk by faith and not by sight. 2 Corinthians 5:7 says "for we walk by faith not by sight." So in order for me to walk by faith, I have to choose not to fear!
Why had I not realized beforehand that fear is a sin? I knew unbelief was sin but I never connected that fear is too. After understanding this concept, I had no choice but to let it go. I had to pry those greedy little fingers of fear off my back and cast it away. I feel so much lighter now...
I've been set free from the deceitful grip that fear had on my life. Now it has no power over me because I'm choosing to walk in truth instead of believing a lie straight from the pit of hell.
Fear, worry, doubt...all lies! If you're struggling with those sins today, release them! Replace those lies with truth from God's Word. Walk in faith, even though you can't see a thing...just know that He's got you in His hand and He's never going to let you go! Remember that EVERYTHING that does not come from faith is sin....EVERYTHING.
©bonnie annis all rights reserved
Wow...EVERYTHING that does not come from faith is sin...EVERYTHING. Now that's pretty clear! As I continued to think about that verse, I realized something I'd never realized before...FEAR is sin. Oh, but wait a minute...you say! Fear is an emotion. Well, yes, it is an emotion but fear is so much more than that. Fear is a lack of faith!
Have you ever thought about fear being a selfish act? It is! When we fear, we are choosing to believe what WE want to believe about something instead of trusting in what God says about it. We are choosing to put the fear above God! And anything put above God is considered an idol. Was I idolizing fear??? I certainly didn't think so but...
I have been very fearful lately. As you might imagine, Cancer can do that to you. Even after surgery and knowing the doctor said she thinks she got it all, I've been fearful there might be some Cancer cells lurking around in my body somewhere. In fact, radiation therapy just confirms that fear...why would they feel it necessary to irradiate my body if they weren't thinking that some rogue Cancer cells might just be swimming up my blood stream or sliding through my lymph system? Fear had attached itself to me during that first phone call telling me the mass was malignant. And that fear had been gleefully taking piggyback rides on my back ever since. That is, until I decided to shake it off today after reading this verse.
God gave me a clarity that I'd never experienced before. In Hebrews 11:6, the Bible says, "without faith it is impossible to please God." Now if fear is a lack of faith, then how did I expect to be able to please God if I was afraid??? Fear certainly doesn't come from faith so I realized that it indeed was a sin.
When you're struggling with a serious illness, it's easy to fall into the trap of only hearing and believing what the test reports show or what the doctors tell you. It's easier to believe the black and white than to have faith in what you can't see or understand. But, as a Christian, I know God expects me to walk by faith and not by sight. 2 Corinthians 5:7 says "for we walk by faith not by sight." So in order for me to walk by faith, I have to choose not to fear!
The more and more I studied this morning, God revealed to me that part of the reason I haven't been sleeping is due to fear. Of course, I have physical pain too, but if I can release the fear completely, God will supply His peace to fill the void the fear was occupying in my mind. In 1 John 4:18, the Bible says, "There is no fear in love [dread does not exist], but full-grown (complete, perfect) love turns fear out of doors and expels every trace of terror! For fear brings
with it the thought of punishment, and [so] he who is afraid has not
reached the full maturity of love [is not yet grown into love’s complete
perfection]." God's perfect love contains no fear! And I know as His child, He lives inside of me so, His love is inside of me too and therefore, fear can't possibly reside in me!!!
Why had I not realized beforehand that fear is a sin? I knew unbelief was sin but I never connected that fear is too. After understanding this concept, I had no choice but to let it go. I had to pry those greedy little fingers of fear off my back and cast it away. I feel so much lighter now...
I've been set free from the deceitful grip that fear had on my life. Now it has no power over me because I'm choosing to walk in truth instead of believing a lie straight from the pit of hell.
Fear, worry, doubt...all lies! If you're struggling with those sins today, release them! Replace those lies with truth from God's Word. Walk in faith, even though you can't see a thing...just know that He's got you in His hand and He's never going to let you go! Remember that EVERYTHING that does not come from faith is sin....EVERYTHING.
©bonnie annis all rights reserved
Wednesday, August 20, 2014
Lonely nights
In the late 50's and early 60's, "I love Lucy" was my favorite television show. She always made me laugh hysterically at her funny antics. Once when I was watching her show, I wondered why she and Ricky slept in separate beds. I think I asked my mother about it and she said something along the lines of it being for modesty's sake...it wasn't proper to show them sleeping in the same bed. Sex certainly wasn't openly televised back then!
Last night I made the decision to sleep in one of our other bedrooms. My poor husband had been hanging onto the side of our king sized bed for too long! He'd been gracious enough not to complain as I added more and more pillows to our bed in hopes of finding a comfortable sleeping position, but neither of us were getting a sound night's sleep. It was strange as we kissed each other goodnight and went off toward separate rooms. For twenty one years, we've slept together unless one or the other of us was extremely ill or contagious. I'd grown accustomed to his snoring and he'd grown accustomed to my tossing and turning. It would be odd sleeping apart from one another. Before turning in, Phil helped me arrange the wedge shaped pillow in the middle of "my" bed and he placed the other pillows all around it as necessary to elevate my arms. We stood back and looked at my little "nest" of pillows and then turned to each other and gave each other a halfway smile knowing we weren't going to be beside each other tonight.
Phil has never had any problem getting to sleep. He works so hard and such long hours that as soon as his head hits the pillow, he's out. I, on the other hand, have always had trouble being able to relax and drift off to sleep...so much so, that the doctor had recently given me a sleeping aid to use for the next few weeks so my body could heal properly. I closed the door to my room and climbed into bed. It took several minutes to get positioned so my arms were above my heart, but I did it. Taking my book and my book light, I began reading where I'd left off the night before. I was deeply engrossed in a Stuart Woods' book. After reading a while, my eyes began to get heavy (thanks to the sleeping pill) and I slipped on my eye mask and inserted my foam ear plugs (a habit from sleeping with my snoring mate.) I don't remember falling asleep but I assume I did because the next thing I knew, I heard Phil leaving for work.
It was strange having to make up two beds this morning. It made me very sad that we hadn't been able to sleep together last night. I'm glad Phil was understanding of my desire to give him a peaceful, uninterrupted night's sleep and my need to spread out and take are of my arms. I remembered what he said last night as we parted ways, "even if we sleep in separate rooms, you know I still love you. Nothing is ever going to change that." I responded with a soft, "I know." And that's the way love is...it doesn't matter what comes our way. When you love someone, you always want the best for them. You put their needs above your own. You learn to be selfless and giving.
I am thankful we were both able to get a good night's sleep last night. It looks like we'll be doing this same routine for many more weeks to come. I'll miss his snoring, but I know he's only on the other side of the house and if I get to feeling better, I can always sneak over there and crawl under the covers with him.
I'm praying for a quick recovery but I know I still have quite a ways to go. When radiation begins, right after Labor day, I may be spending much more time in bed than I am now. The doctor has already told me that radiation causes extreme fatigue. I don't sleep well now, but I imagine, from what she's told me, that won't be a problem in weeks to come. Maybe it's best that we're sleeping in separate rooms for a little while...that way, Phil can get good sleep and so can I. It's amazing how much our bodies depend on uninterrupted sleep. The doctor told me that without good sleep, our cells can't rejuvenate and multiply. I definitely need my cells to get all the help they can get right now, so separate beds it is! I am holding on to the fact that this won't last forever and one day soon I'll be back in my own king sized, cool top, memory foam bed. I'll be snuggled up tightly against my husband and I may just leave my ear plugs out that first night so I can hear his beautiful snores all night long and be reminded that he's right there next to me. What do you think...should I do it?
I can just imagine Lucy doing an episode similar to that, can't you? I can just picture her funny face trying to cope with Ricky's loud snoring and in fact, there may have been an episode like that already but I just can't remember. She would probably hit him in the head with something and wake him up. I can just see him rising quickly out of bed yelling, "LUUUUUCCCCCYYYY" in his sexy Cuban accent and then chasing her around the room as she begins with her famous crying "WAAAAAA." (be sure and check out this funny video of one of Lucy's antics...it will really make you smile!)
Watch Lucy sleep
©bonnie annis all rights reserved
Last night I made the decision to sleep in one of our other bedrooms. My poor husband had been hanging onto the side of our king sized bed for too long! He'd been gracious enough not to complain as I added more and more pillows to our bed in hopes of finding a comfortable sleeping position, but neither of us were getting a sound night's sleep. It was strange as we kissed each other goodnight and went off toward separate rooms. For twenty one years, we've slept together unless one or the other of us was extremely ill or contagious. I'd grown accustomed to his snoring and he'd grown accustomed to my tossing and turning. It would be odd sleeping apart from one another. Before turning in, Phil helped me arrange the wedge shaped pillow in the middle of "my" bed and he placed the other pillows all around it as necessary to elevate my arms. We stood back and looked at my little "nest" of pillows and then turned to each other and gave each other a halfway smile knowing we weren't going to be beside each other tonight.
Phil has never had any problem getting to sleep. He works so hard and such long hours that as soon as his head hits the pillow, he's out. I, on the other hand, have always had trouble being able to relax and drift off to sleep...so much so, that the doctor had recently given me a sleeping aid to use for the next few weeks so my body could heal properly. I closed the door to my room and climbed into bed. It took several minutes to get positioned so my arms were above my heart, but I did it. Taking my book and my book light, I began reading where I'd left off the night before. I was deeply engrossed in a Stuart Woods' book. After reading a while, my eyes began to get heavy (thanks to the sleeping pill) and I slipped on my eye mask and inserted my foam ear plugs (a habit from sleeping with my snoring mate.) I don't remember falling asleep but I assume I did because the next thing I knew, I heard Phil leaving for work.
It was strange having to make up two beds this morning. It made me very sad that we hadn't been able to sleep together last night. I'm glad Phil was understanding of my desire to give him a peaceful, uninterrupted night's sleep and my need to spread out and take are of my arms. I remembered what he said last night as we parted ways, "even if we sleep in separate rooms, you know I still love you. Nothing is ever going to change that." I responded with a soft, "I know." And that's the way love is...it doesn't matter what comes our way. When you love someone, you always want the best for them. You put their needs above your own. You learn to be selfless and giving.
I am thankful we were both able to get a good night's sleep last night. It looks like we'll be doing this same routine for many more weeks to come. I'll miss his snoring, but I know he's only on the other side of the house and if I get to feeling better, I can always sneak over there and crawl under the covers with him.
I'm praying for a quick recovery but I know I still have quite a ways to go. When radiation begins, right after Labor day, I may be spending much more time in bed than I am now. The doctor has already told me that radiation causes extreme fatigue. I don't sleep well now, but I imagine, from what she's told me, that won't be a problem in weeks to come. Maybe it's best that we're sleeping in separate rooms for a little while...that way, Phil can get good sleep and so can I. It's amazing how much our bodies depend on uninterrupted sleep. The doctor told me that without good sleep, our cells can't rejuvenate and multiply. I definitely need my cells to get all the help they can get right now, so separate beds it is! I am holding on to the fact that this won't last forever and one day soon I'll be back in my own king sized, cool top, memory foam bed. I'll be snuggled up tightly against my husband and I may just leave my ear plugs out that first night so I can hear his beautiful snores all night long and be reminded that he's right there next to me. What do you think...should I do it?
I can just imagine Lucy doing an episode similar to that, can't you? I can just picture her funny face trying to cope with Ricky's loud snoring and in fact, there may have been an episode like that already but I just can't remember. She would probably hit him in the head with something and wake him up. I can just see him rising quickly out of bed yelling, "LUUUUUCCCCCYYYY" in his sexy Cuban accent and then chasing her around the room as she begins with her famous crying "WAAAAAA." (be sure and check out this funny video of one of Lucy's antics...it will really make you smile!)
Watch Lucy sleep
©bonnie annis all rights reserved
Tuesday, August 19, 2014
X marks the spot
This morning, I left for the Radiation/Oncology center at 10:15 a.m. under a light, misting rain. All the way to the center, a little Honda was following me so closely, I thought she was going to rear end me. Of course, I had to give her a little brake check to get her off my tail because I didn't want to have a wreck before making it to the center for my appointment.
I entered the Radiation/Oncology office and swiped my ID scan badge that I'd been given on my last visit. Each time I enter for tests or treatment, I will need to swipe my badge so they can record my visit. A nurse I hadn't met yet came out to get me. She had trouble pronouncing my last name so I told her to make it easy on herself and just call me Bonnie. She laughed and took me back to the dressing room. After donning a lovely seafoam green gown, I waited for Pam, the nurse, to return.
We walked down a long hallway and Pam led me into a room with a huge CT machine in the center of the room. It looked like a huge, cavernous, mouth waiting to devour me! She had me stand beside the CT table while she mixed up some sort of solution and poured it into a very large black bag that looked a lot like a Hefty garbage bag. She squished the solution around inside of the bag for a few minutes and then flattened it out on the table. She told me that she was going to position me and needed me to hold that position while she helped me lie back onto the black bag. "Before you lie back, just know it's going to be quite warm," she said. She took my arm and helped me begin to lean back. It was painful to lie flat. I hadn't been in that position since my surgery. I'd been sleeping at night propped up on a wedge shaped pillow with pillows under each arm for support.
As Pam continued to lean me backward, all of my chest muscles were pulling and tugging. They were so tight and I was surprised at how much it hurt. She saw me wince a few times and told me she would try to hurry in the process. As my back touched the bag, I could feel instant warmth surrounding my body. The extreme heat felt wonderful to me but Pam said, "most people find this very uncomfortable." I told her that I was always cold and it felt great to me.Within a few minutes, the liquid foam she'd poured into the bag began to harden around me. She explained that the foam mold they were making would be used each time I came for treatment, and would help ensure that I was positioned exactly the same way each time.
Dr. Santiago entered the room and said hello. She was talking to me but I couldn't see her because the foam mold held my body so that I couldn't turn my head. Finally she realized I was unable to move and she came around the table to the other side. She explained that she was about to do my mapping and the marks she would make on my torso would provide guidelines for the radiology tech during treatment. I couldn't see what she was doing. At times, I could feel her making marks on my body but in the areas around my incisions, I didn't feel a thing because my skin is still numb there. I had no idea how many marks the doctor made, but she continued to draw on me for several minutes. Pam placed clear dot sized bandages over the top of many of the markings. She explained to me that those dots were very important and I should not get them wet or allow them to be removed. When she was finished placing the clear bandages, Pam ran me back through the CT machine again. The machine whirred loudly and sounded like a small jet engine. The only thing painful about the procedure was the way I was having to lie on the table with my arms outstretched over my head.
Finally we were done and Pam helped me sit up. I felt a little dizzy at first. She had me sit there a few minutes until I felt well enough to stand. I was led back into the dressing room and told to place my used gown in a biohazard bin. When I removed the gown to put my shirt back on, I glanced in the mirror. I had markings all over my chest and abdomen. I also had a mark in the center of the side of my neck. I had asked Dr. Santiago about the wide range of marks while she was placing them on me and she told me that the field she'd chosen was to ensure all of the Cancer would be eradicated. She said they were being very aggressive with the treatment plan and the reason they were going as high on my neck as she'd marked was because the Cancer liked to travel that route. The mirror revealed several lines, dots, and even a huge X just under the location of where my right breast used to be. I took a picture of my torso while looking in the mirror. I won't put it on this blog post, but I did want to keep it for my own personal documentation of this journey.
As I looked at the markings on my torso, I couldn't help but think it looked like a pirate's treasure map. I thought it was funny that I had a huge X in the center of my belly. "X marks the spot," I said, hoping none of the staff heard me. (Somewhere I remembered I'd read that phrase was put into use by the British army long ago. They would mark a piece of paper with a black x and would place it over the heart of someone sentenced to death.The acting officer would say "X marks the spot" and the firing squad would shoot the x. Pirates later took up the phrase using the X to indicate the position of a buried treasure.)
I placed my gown in the biohazard bin and as I left the center for the day, Pam said, "see you next week. We'll go over the results of the CT scan with Dr. Santiago and she'll review the treatment plan with you again. More than likely, your radiation won't start until the day after Labor day." I was glad to hear that...a few more weeks of "normalcy."
On the way home, I stopped by the grocery store to pick up a few things. I had to remind myself not to lift anything heavy with my right arm. Both arms are still very swollen from the lymphedema but I was told to be very cautious with the right arm. When I got home, I was extremely tired. I can't wait to show my husband the "treasure map" on my chest when He comes home from work. I just know he's going to laugh when he sees it. I love hearing him laugh. Laughter has been in short supply around here lately and I could sure use a laugh today.
©bonnie annis all rights reserved
I entered the Radiation/Oncology office and swiped my ID scan badge that I'd been given on my last visit. Each time I enter for tests or treatment, I will need to swipe my badge so they can record my visit. A nurse I hadn't met yet came out to get me. She had trouble pronouncing my last name so I told her to make it easy on herself and just call me Bonnie. She laughed and took me back to the dressing room. After donning a lovely seafoam green gown, I waited for Pam, the nurse, to return.
We walked down a long hallway and Pam led me into a room with a huge CT machine in the center of the room. It looked like a huge, cavernous, mouth waiting to devour me! She had me stand beside the CT table while she mixed up some sort of solution and poured it into a very large black bag that looked a lot like a Hefty garbage bag. She squished the solution around inside of the bag for a few minutes and then flattened it out on the table. She told me that she was going to position me and needed me to hold that position while she helped me lie back onto the black bag. "Before you lie back, just know it's going to be quite warm," she said. She took my arm and helped me begin to lean back. It was painful to lie flat. I hadn't been in that position since my surgery. I'd been sleeping at night propped up on a wedge shaped pillow with pillows under each arm for support.
As Pam continued to lean me backward, all of my chest muscles were pulling and tugging. They were so tight and I was surprised at how much it hurt. She saw me wince a few times and told me she would try to hurry in the process. As my back touched the bag, I could feel instant warmth surrounding my body. The extreme heat felt wonderful to me but Pam said, "most people find this very uncomfortable." I told her that I was always cold and it felt great to me.Within a few minutes, the liquid foam she'd poured into the bag began to harden around me. She explained that the foam mold they were making would be used each time I came for treatment, and would help ensure that I was positioned exactly the same way each time.
Dr. Santiago entered the room and said hello. She was talking to me but I couldn't see her because the foam mold held my body so that I couldn't turn my head. Finally she realized I was unable to move and she came around the table to the other side. She explained that she was about to do my mapping and the marks she would make on my torso would provide guidelines for the radiology tech during treatment. I couldn't see what she was doing. At times, I could feel her making marks on my body but in the areas around my incisions, I didn't feel a thing because my skin is still numb there. I had no idea how many marks the doctor made, but she continued to draw on me for several minutes. Pam placed clear dot sized bandages over the top of many of the markings. She explained to me that those dots were very important and I should not get them wet or allow them to be removed. When she was finished placing the clear bandages, Pam ran me back through the CT machine again. The machine whirred loudly and sounded like a small jet engine. The only thing painful about the procedure was the way I was having to lie on the table with my arms outstretched over my head.
Finally we were done and Pam helped me sit up. I felt a little dizzy at first. She had me sit there a few minutes until I felt well enough to stand. I was led back into the dressing room and told to place my used gown in a biohazard bin. When I removed the gown to put my shirt back on, I glanced in the mirror. I had markings all over my chest and abdomen. I also had a mark in the center of the side of my neck. I had asked Dr. Santiago about the wide range of marks while she was placing them on me and she told me that the field she'd chosen was to ensure all of the Cancer would be eradicated. She said they were being very aggressive with the treatment plan and the reason they were going as high on my neck as she'd marked was because the Cancer liked to travel that route. The mirror revealed several lines, dots, and even a huge X just under the location of where my right breast used to be. I took a picture of my torso while looking in the mirror. I won't put it on this blog post, but I did want to keep it for my own personal documentation of this journey.
As I looked at the markings on my torso, I couldn't help but think it looked like a pirate's treasure map. I thought it was funny that I had a huge X in the center of my belly. "X marks the spot," I said, hoping none of the staff heard me. (Somewhere I remembered I'd read that phrase was put into use by the British army long ago. They would mark a piece of paper with a black x and would place it over the heart of someone sentenced to death.The acting officer would say "X marks the spot" and the firing squad would shoot the x. Pirates later took up the phrase using the X to indicate the position of a buried treasure.)
I placed my gown in the biohazard bin and as I left the center for the day, Pam said, "see you next week. We'll go over the results of the CT scan with Dr. Santiago and she'll review the treatment plan with you again. More than likely, your radiation won't start until the day after Labor day." I was glad to hear that...a few more weeks of "normalcy."
On the way home, I stopped by the grocery store to pick up a few things. I had to remind myself not to lift anything heavy with my right arm. Both arms are still very swollen from the lymphedema but I was told to be very cautious with the right arm. When I got home, I was extremely tired. I can't wait to show my husband the "treasure map" on my chest when He comes home from work. I just know he's going to laugh when he sees it. I love hearing him laugh. Laughter has been in short supply around here lately and I could sure use a laugh today.
©bonnie annis all rights reserved
Monday, August 18, 2014
Little Miss Know it All
I'm a planner. I like order. I find security in knowing what's going to happen next, so when I found out I had Cancer, I just knew I was going to have to go through Chemotherapy. I made the decision to be proactive. I should have known better but I forged ahead. I was extremely emotional that day.
As My husband and I were driving back from a doctor's appointment, I begged him to stop at the nearest salon. I wanted to get my hair cut short. I don't know why I felt like I had to do it at that very moment, but I did. Maybe I felt like things in my life were totally out of control and that was the one thing I could control at that very point in time, I'm really not sure, but I wanted it done immediately. We stopped at one shop after the other and none of them had any openings for walk ins. On we drove and my tears began to flow. Finally, we came to a Super Cuts. I knew I'd be able to get my hair cut there because they don't take appointments. We went in, waited about ten minutes, and I was in the chair having my precious locks sheared off. I've always loved my hair and wanted it to be long and luscious, but most of my life it's been chin length or shorter. This time it was extremely short because I'd asked the stylist for a pixie cut.
Fast forward...it's been a little over 2 months now since my Cancer diagnosis. I've been waiting for the doctor to say, "you'll begin chemo treatments next week." Imagine my surprise when last week, He told me chemo was unnecessary in my case! I was elated but humbled at the same time. I realized that I had run ahead of God. In my desire to be proactive and cut my hair anticipating chemo, God had other plans. I couldn't help but pray asking Him for forgiveness. I should have waited...should have trusted...should have been patient, but just like most things in my life, I'm always running ahead trying to do things in my own way and in my own timing. God continually reminds me that I'm out of step with Him when I do that. I need to work on that.
My closet is filled with various scarves, hats, and wigs now, both borrowed and new. These are things I won't need now. Yet again, I ran ahead of God. So today, Little Miss Know it All (ME), has decided to stop running ahead of God. I'm going to sync up my steps with Him. Instead of running far ahead of Him, I'm going to temper my gait to match His exactly...and while I often won't know where we're going, I know if I stay close by His side, He'll only take me where I need to go. I won't make the mistake of running ahead of Him and doing things unnecessarily. I won't put myself through unneeded stress. I'll be able to relax and take one step at a time knowing that He knows the way and little Miss Know it All doesn't.
If I hadn't jumped the gun, my hair would be past my shoulders by now. As it is, I'm working on growing out this pixie cut. It's frustrating to grow out super short hair because it takes soooo long to get past that horrid "stuck in your collar" stage. I won't complain though because I know it's my own fault. I'm the one who was in such a hurry to cut it off. God is using this to remind me to be patient.
Why do you think it's important to God that patience grows inside us? It's because God's timing is not our timing. He is always doing more than we see or know. It is important that we never run ahead. He sets the pace and only He knows where the path leads. Our job is just to be willing to walk WITH Him.
As My husband and I were driving back from a doctor's appointment, I begged him to stop at the nearest salon. I wanted to get my hair cut short. I don't know why I felt like I had to do it at that very moment, but I did. Maybe I felt like things in my life were totally out of control and that was the one thing I could control at that very point in time, I'm really not sure, but I wanted it done immediately. We stopped at one shop after the other and none of them had any openings for walk ins. On we drove and my tears began to flow. Finally, we came to a Super Cuts. I knew I'd be able to get my hair cut there because they don't take appointments. We went in, waited about ten minutes, and I was in the chair having my precious locks sheared off. I've always loved my hair and wanted it to be long and luscious, but most of my life it's been chin length or shorter. This time it was extremely short because I'd asked the stylist for a pixie cut.
Fast forward...it's been a little over 2 months now since my Cancer diagnosis. I've been waiting for the doctor to say, "you'll begin chemo treatments next week." Imagine my surprise when last week, He told me chemo was unnecessary in my case! I was elated but humbled at the same time. I realized that I had run ahead of God. In my desire to be proactive and cut my hair anticipating chemo, God had other plans. I couldn't help but pray asking Him for forgiveness. I should have waited...should have trusted...should have been patient, but just like most things in my life, I'm always running ahead trying to do things in my own way and in my own timing. God continually reminds me that I'm out of step with Him when I do that. I need to work on that.
My closet is filled with various scarves, hats, and wigs now, both borrowed and new. These are things I won't need now. Yet again, I ran ahead of God. So today, Little Miss Know it All (ME), has decided to stop running ahead of God. I'm going to sync up my steps with Him. Instead of running far ahead of Him, I'm going to temper my gait to match His exactly...and while I often won't know where we're going, I know if I stay close by His side, He'll only take me where I need to go. I won't make the mistake of running ahead of Him and doing things unnecessarily. I won't put myself through unneeded stress. I'll be able to relax and take one step at a time knowing that He knows the way and little Miss Know it All doesn't.
If I hadn't jumped the gun, my hair would be past my shoulders by now. As it is, I'm working on growing out this pixie cut. It's frustrating to grow out super short hair because it takes soooo long to get past that horrid "stuck in your collar" stage. I won't complain though because I know it's my own fault. I'm the one who was in such a hurry to cut it off. God is using this to remind me to be patient.
Why do you think it's important to God that patience grows inside us? It's because God's timing is not our timing. He is always doing more than we see or know. It is important that we never run ahead. He sets the pace and only He knows where the path leads. Our job is just to be willing to walk WITH Him.
©bonnie annis all rights reserved
Burned bacon, radiation
This morning I was in the mood for a nice breakfast so I pulled out the eggs and the bacon. Usually, I just eat a bowl of cereal or some Greek yogurt, but today I was actually hungry. I cracked the eggs and scrambled them in a bowl. I didn't really want to cook the bacon on the stove top so I decided to microwave it. I looked on the back of the package of Butterball Turkey bacon for instructions on cooking times but there were none. I figured that I would have to wing it. (no pun intended!)
I put the bacon on a couple of napkins atop a microwave safe place and slid it into the oven. I guessed that it would take about 2 minutes for 3 pieces of bacon. I set the timer and went about cooking the eggs so everything would be perfectly timed and ready to eat. Before the microwave timer went off, I began to smell a rank odor. When I opened the microwave door, I saw the bacon was perfectly cooked on the outer edges but the center had a huge, black, burned area. For some reason, seeing that burned area made me think of radiation.
On Tuesday, I meet with the radiation oncologist for mapping and tattooing. I'll also go through a CT scan and a radiation simulation session. I'm trying to be brave but I'm really nervous about it. The doctor has already warned me that after about the second treatment my energy level will hit an all time low. She said to just "go with it" and rest whenever my body said it needed to rest. I'm not good at resting, but I guess I'll have choice.
The internet has both good and bad information on radiation therapy. Some sites, like breastcancer.org, give good detailed, accurate information while other sites have photos and horror stories on them. I know I shouldn't have done it, but curiosity got the better of me and when I first found out I needed radiation therapy, I Googled it. Some of the photos of burned Cancer patients were pretty severe. As I remembered those photos, my mind went back to the bacon.
I don't know why my bacon burned in the middle...a perfect black circle of crispness, but it made me stop and pray. I asked God to keep me protected from the dangerous radiation waves that might cause burning and scarring. The radiation techs are highly skilled, I'm sure, but it unnerves me to think of myself in a situation similar to bacon in a microwave!
© bonnie annis all rights reserved
I put the bacon on a couple of napkins atop a microwave safe place and slid it into the oven. I guessed that it would take about 2 minutes for 3 pieces of bacon. I set the timer and went about cooking the eggs so everything would be perfectly timed and ready to eat. Before the microwave timer went off, I began to smell a rank odor. When I opened the microwave door, I saw the bacon was perfectly cooked on the outer edges but the center had a huge, black, burned area. For some reason, seeing that burned area made me think of radiation.
On Tuesday, I meet with the radiation oncologist for mapping and tattooing. I'll also go through a CT scan and a radiation simulation session. I'm trying to be brave but I'm really nervous about it. The doctor has already warned me that after about the second treatment my energy level will hit an all time low. She said to just "go with it" and rest whenever my body said it needed to rest. I'm not good at resting, but I guess I'll have choice.
The internet has both good and bad information on radiation therapy. Some sites, like breastcancer.org, give good detailed, accurate information while other sites have photos and horror stories on them. I know I shouldn't have done it, but curiosity got the better of me and when I first found out I needed radiation therapy, I Googled it. Some of the photos of burned Cancer patients were pretty severe. As I remembered those photos, my mind went back to the bacon.
I don't know why my bacon burned in the middle...a perfect black circle of crispness, but it made me stop and pray. I asked God to keep me protected from the dangerous radiation waves that might cause burning and scarring. The radiation techs are highly skilled, I'm sure, but it unnerves me to think of myself in a situation similar to bacon in a microwave!
© bonnie annis all rights reserved
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