
Hello from Texas
What a unique greeting, right?
Seems that Kate’s Grand Adventure has taken a turn down a new road. Yes, I’m still dealing with the gastric bypass, and all that means, but I have a new challenge to tackle and subdue, or overcome. Friday I had an appointment with my doctor and I got some “not so good” news. Seems I have something called Invasive Ductile Cancer, or IDC. What that translates to in plain everyday English is Breast Cancer. Mine is “stage 2” which means that my cancer is not only in my right breast, but also in the lymph glands under my right arm.
My breast surgeon (and I never thought I would write that particular phrase) is in a hurry to start treatments since I am at stage 2. She said I’m not stage 1 which is the earliest diagnosis, and means the cancer is only in the milk ducts of the breast and has not spread. Stage 2 means that the cancer has decided to spread out and has invaded at least one lymph node under my right arm. There are two more stages after this, but fortunately for me I got a guilty conscience when my heart doctor lectured me and went for the dreaded mammogram.
I go tomorrow (Monday) to have a port installed in my chest wall just below my collar bone on the left side. This will allow my oncologist (another phrase I didn’t think I’d ever say) to inject the chemo therapy directly above my heart, and that will allow my heart to disperse the chemo more quickly and efficiently. Evidently I am being scheduled for chemotherapy treatments weekly for the next 4 to 6 months. Up side to that is I get to start a new fashion trend at my work. Since I’ll be loosing my hair (at least that’s what the paperwork my doctor gave me said) and I have a whole wardrobe of hats and big earrings, my new look will be hats and gaudy ear rings. Can hardly wait!
After the chemo I will have 6 to 8 weeks of radiation therapy on a daily basis. The paperwork says that this won’t make my hair fall out. Not too sure why she put that since my hair will be gone if not from the chemo then from the bypass! The radiation is, evidently, very finely focused and will only be aimed at 4 to 6 sites within the breast, and several sites in the lymph node.
After these two treatment “Modalities” I will go through several tests including MRI, bone scans, and CT of my chest, abdomen and pelvis. These will be to see if the tumors have been reduced, and to be sure the cancer has not spread to any other sites. These tests may be combined with a newer test called a PET scan, but I’m not too sure about this test. I’ll learn more as time goes by. Other things my doctor is going to be watching is my bone density, I don’t want to develop osteoporosis, and my heart, as evidently chemo and radiation can be heard on the old ticker.
After all these treatments (it looks like at least 6 months to a year of various treatments) I will be evaluated for surgery. If the treatments have successfully reduced the tumors, I may only need what is called a Lumpectomy. That’s where they go in and only remove part of the breast tissue. If not they will do a complete mastectomy. One of the concerns I have is if they only do a lumpectomy, will there still be cancer cells floating around in there that could settle again in my breast? If there is a chance of that happening I’d rather they just take the whole breast.
I’m also thinking about reconstruction. According to my Mother, (who faced most of these questions 2 years ago when she was diagnosed with Cancer), reconstruction is a lot of pain for something you don’t really need (the breast). But then again she is 80, and was 78 when facing those questions. She is also a “mini”, which means that although she is 5’6” she only weighs less than 120 and has never had more than a 36B. I, on the other hand, am 2 inches shorter but have always been buxomy. I asked my surgeon if it was possible to take tissue from my remaining breast (or tummy) and build another breast. I really don’t want silicone. She said that was a possibility. I must admit, I like the idea of being a B cup instead of a DD cup, so IF I decide on reconstruction, that is something I’m going to think about real hard.
According to everything I’ve read so far my attitude can have a very profound impact on my treatments, both in the success and the amount of nausea and pain I encounter. I’ve always been a very positive person so I’m thinking that I’ll not have as much pain, etc as some of the horror stories I’ve heard. Besides my positive attitude, I have a strong support group, and a very strong faith in God. The way I look at it, I’m almost 60 and in those years God has always taken superb care of me. There’s no reason he won’t do so now either.
Before you point out that I have cancer, and some people don’t consider that superb care, I must remind you that everyone has free will. Free Will has as much to do with how we care for our bodies as how we act in other arenas. I looked down a list of things that can contribute to a woman’s chances of getting breast cancer. There were 14 or 15 items on that list, including smoking, overweight, sedentary lifestyle, among other things. On that list I can claim all but one and that was drug usage. So my attitude is, IF I did the crime (not taking care of myself) then I have to pay the time…(or walk the line of cancer therapy).
Lastly for today, I figure that IF the cancer takes my life I’ll be in heaven with my Savior, and that’s a Win situation for me….WHEN I beat the cancer, I get to stay here and have more fun with friends and family…That is also a WIN situation for me. So whatever happens, I’m getting a win/win situation …who can argue with that?
Stay tuned for the next blog. Don’t know for sure when that will be, but I think I may be writing you a bit more often than I did before. Pray for me…I need it and you probably need the practice!
Kate
What a unique greeting, right?
Seems that Kate’s Grand Adventure has taken a turn down a new road. Yes, I’m still dealing with the gastric bypass, and all that means, but I have a new challenge to tackle and subdue, or overcome. Friday I had an appointment with my doctor and I got some “not so good” news. Seems I have something called Invasive Ductile Cancer, or IDC. What that translates to in plain everyday English is Breast Cancer. Mine is “stage 2” which means that my cancer is not only in my right breast, but also in the lymph glands under my right arm.
My breast surgeon (and I never thought I would write that particular phrase) is in a hurry to start treatments since I am at stage 2. She said I’m not stage 1 which is the earliest diagnosis, and means the cancer is only in the milk ducts of the breast and has not spread. Stage 2 means that the cancer has decided to spread out and has invaded at least one lymph node under my right arm. There are two more stages after this, but fortunately for me I got a guilty conscience when my heart doctor lectured me and went for the dreaded mammogram.
I go tomorrow (Monday) to have a port installed in my chest wall just below my collar bone on the left side. This will allow my oncologist (another phrase I didn’t think I’d ever say) to inject the chemo therapy directly above my heart, and that will allow my heart to disperse the chemo more quickly and efficiently. Evidently I am being scheduled for chemotherapy treatments weekly for the next 4 to 6 months. Up side to that is I get to start a new fashion trend at my work. Since I’ll be loosing my hair (at least that’s what the paperwork my doctor gave me said) and I have a whole wardrobe of hats and big earrings, my new look will be hats and gaudy ear rings. Can hardly wait!
After the chemo I will have 6 to 8 weeks of radiation therapy on a daily basis. The paperwork says that this won’t make my hair fall out. Not too sure why she put that since my hair will be gone if not from the chemo then from the bypass! The radiation is, evidently, very finely focused and will only be aimed at 4 to 6 sites within the breast, and several sites in the lymph node.
After these two treatment “Modalities” I will go through several tests including MRI, bone scans, and CT of my chest, abdomen and pelvis. These will be to see if the tumors have been reduced, and to be sure the cancer has not spread to any other sites. These tests may be combined with a newer test called a PET scan, but I’m not too sure about this test. I’ll learn more as time goes by. Other things my doctor is going to be watching is my bone density, I don’t want to develop osteoporosis, and my heart, as evidently chemo and radiation can be heard on the old ticker.
After all these treatments (it looks like at least 6 months to a year of various treatments) I will be evaluated for surgery. If the treatments have successfully reduced the tumors, I may only need what is called a Lumpectomy. That’s where they go in and only remove part of the breast tissue. If not they will do a complete mastectomy. One of the concerns I have is if they only do a lumpectomy, will there still be cancer cells floating around in there that could settle again in my breast? If there is a chance of that happening I’d rather they just take the whole breast.
I’m also thinking about reconstruction. According to my Mother, (who faced most of these questions 2 years ago when she was diagnosed with Cancer), reconstruction is a lot of pain for something you don’t really need (the breast). But then again she is 80, and was 78 when facing those questions. She is also a “mini”, which means that although she is 5’6” she only weighs less than 120 and has never had more than a 36B. I, on the other hand, am 2 inches shorter but have always been buxomy. I asked my surgeon if it was possible to take tissue from my remaining breast (or tummy) and build another breast. I really don’t want silicone. She said that was a possibility. I must admit, I like the idea of being a B cup instead of a DD cup, so IF I decide on reconstruction, that is something I’m going to think about real hard.
According to everything I’ve read so far my attitude can have a very profound impact on my treatments, both in the success and the amount of nausea and pain I encounter. I’ve always been a very positive person so I’m thinking that I’ll not have as much pain, etc as some of the horror stories I’ve heard. Besides my positive attitude, I have a strong support group, and a very strong faith in God. The way I look at it, I’m almost 60 and in those years God has always taken superb care of me. There’s no reason he won’t do so now either.
Before you point out that I have cancer, and some people don’t consider that superb care, I must remind you that everyone has free will. Free Will has as much to do with how we care for our bodies as how we act in other arenas. I looked down a list of things that can contribute to a woman’s chances of getting breast cancer. There were 14 or 15 items on that list, including smoking, overweight, sedentary lifestyle, among other things. On that list I can claim all but one and that was drug usage. So my attitude is, IF I did the crime (not taking care of myself) then I have to pay the time…(or walk the line of cancer therapy).
Lastly for today, I figure that IF the cancer takes my life I’ll be in heaven with my Savior, and that’s a Win situation for me….WHEN I beat the cancer, I get to stay here and have more fun with friends and family…That is also a WIN situation for me. So whatever happens, I’m getting a win/win situation …who can argue with that?
Stay tuned for the next blog. Don’t know for sure when that will be, but I think I may be writing you a bit more often than I did before. Pray for me…I need it and you probably need the practice!
Kate

