Breast cancer-CMF or AC?
If you've been through either CMF or AC chemotherapy for breast cancer, I'd REALLY appreciate your feedback. I'm needing to choose between these two options to follow up my lumpectomy surgery in February. I'm specifically interested in how tired you were and for how long during each cycle. I have 2 young children (2 & 4yrs)and I'm trying to choose wisely. I know no one's experience will tell me exactly what mine will be, but I'm just trying to get an idea of what to expect. Thank you bunches!
Also, if you had the AC chemo and are several years from your treatment, have you had any problems with your heart?
Comments
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Hi, 1Supermom,
I have had two rounds of AC and have two more to go. The tiredness has not been overwhelming. If I lay down, I may fall asleep. But there has not been overwhelming tiredness. The antinausea medicine is good and I don't get sick. The steroids I take for the first 5 days of the cycle really give me a boost, so actually I feel pretty good. The second and third week is when your blood counts will go down, and there is another opportunity to feel tired. I just don't overdo it. My blood counts went down pretty low and mouth sores took over, so now I get a shot of white cell stimulator on day 2. You need to get your rest when you can. I find it harder to sleep at night. And the other side effects (constipation, indigestion, mouth sores, dry mouth)are more irritations than anything. Good luck to you.
Mary A.0 -
Supermom, last summer I did dose dense AC treatments. Thats 1 treatment every two weeks, instead of every three. I was told the % of non-recurance was higher and I wanted it over with ASAP. After every treatment, the following day I had to return for a white blood booster. This shot was AWFUL! By the third day my entire body hurt, even my tongue. By the fourth day it was a little better and by the 6th day I was ready to do almost anything. The 2nd week was a breeze. But keep in ming everyone reacts differantly. While I was doing radiation, I went out and rode motorcycles so I could get my endorcement and rode my Harley to my last treatment. I was also worried about my heart and the damage chemo and radiation might cause. My Mother had lung cancer and died of congestive heart failure. I do believe that CMF is suposed to be easier on your heart. I'm only 47 and worry if my heart will be ok later on. Some choice isn't it!! I wasn't offered CMF, just the AC and Taxol, but I refused the taxol. I didn't have lymph node envolvment. Well, good luck and God Bless. Amelia0
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Mary,MaryA said:Hi, 1Supermom,
I have had two rounds of AC and have two more to go. The tiredness has not been overwhelming. If I lay down, I may fall asleep. But there has not been overwhelming tiredness. The antinausea medicine is good and I don't get sick. The steroids I take for the first 5 days of the cycle really give me a boost, so actually I feel pretty good. The second and third week is when your blood counts will go down, and there is another opportunity to feel tired. I just don't overdo it. My blood counts went down pretty low and mouth sores took over, so now I get a shot of white cell stimulator on day 2. You need to get your rest when you can. I find it harder to sleep at night. And the other side effects (constipation, indigestion, mouth sores, dry mouth)are more irritations than anything. Good luck to you.
Mary A.
Thanks so much for sharing your experience. And good for you for being halfway done. I've heard similar reports from other people, so it seems your experience is more common. And I've also heard that the anti-nausea meds are really good. But having to take steroids is a new one for me. I guess I'll find out more on my next trip to the doc. Good luck w/the remainder of your treatments!0 -
Amelia,amelia said:Supermom, last summer I did dose dense AC treatments. Thats 1 treatment every two weeks, instead of every three. I was told the % of non-recurance was higher and I wanted it over with ASAP. After every treatment, the following day I had to return for a white blood booster. This shot was AWFUL! By the third day my entire body hurt, even my tongue. By the fourth day it was a little better and by the 6th day I was ready to do almost anything. The 2nd week was a breeze. But keep in ming everyone reacts differantly. While I was doing radiation, I went out and rode motorcycles so I could get my endorcement and rode my Harley to my last treatment. I was also worried about my heart and the damage chemo and radiation might cause. My Mother had lung cancer and died of congestive heart failure. I do believe that CMF is suposed to be easier on your heart. I'm only 47 and worry if my heart will be ok later on. Some choice isn't it!! I wasn't offered CMF, just the AC and Taxol, but I refused the taxol. I didn't have lymph node envolvment. Well, good luck and God Bless. Amelia
Wow! You're like Rambo! The 3 week cycle is rigorous enough for me. I'm not overly concerned about the heart issue, but I'm sober about it. I'd like to hear from some women who did the AC 20 yrs ago and see what they say. But the Lord has given me a scripture about this, so I'm putting my trust there: Psa 73:26 My flesh and my heart faileth: but God is the strength of my heart, and my portion forever. He'll be the strength of your heart too. Thank you for your input. Best wishes!0 -
Supermom, I was going to write scripture that I found through prayer and the bible, but for some reason, I didn't. When I was first told I had an aggresive breast cancer, I was frozen in shock and immediatly turned to God for help. I went to the bible, my mother in law suggested I do this, and just opened it and tried to read for some comfort. I couldn't because I was crying to hard. I closed the book and came back later to try again. When I opened it the 2nd time, it was the same page. The phone rang so again, I closed the book. Later on the 3rd try, wouldn't you know it, it was the same page. This is what I found: Joshua 1:9 "Be strong and be of good courage. Be not afraid, neither be thou dismayed: For the Lord God is with thee wither thou goest." Every time I remember those words and that day, I get a renewed sense of well being. I know in my heart, that no matter what happens, I am not alone. God bless
Supermom, You are in my prayers, Amelia0 -
Hi #1, I was diagnosed stage II, grade III in January 2003. I chose mastectomy followed by 4 cycles of AC. I cleaned my house, took care of my pets, got myself to all doctors appointments and even cut the grass well into my 3rd treatment. I did have to get the neulasta shots after each one to boost white cell production as well as procrit after the 4th to boost red blood cells. I spent a weekend in the hospital on IV antibiotics following my last cycle but was back to feeling pretty good by Sunday. I took anzamet (insurance covered the $100 per pill cost) for nausea the first 3 days following each treatment and never threw up. It's great stuff. My heart is strong and I have no fear of the treatment down the road. You might find someone who was treated with CMF 20 years ago since we've had it since the mid to late 70s but AC just became available in the 90s. If I had it to do all over again, I'd choose AC again over CMF. There are fewer reported side effects with AC (other than hair loss) and I can't imagine doing 6 months of anything when I could get it over in just 2. You're lucky to have a choice. My oncologist felt strongly that I needed the intensity of AC and I agreed. My friend, Leslie, had 6 cycles of AC and worked part time through it all (she's 44). Good luck with your decision.0
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I was 47 when I was diagnosed with BC. I had a lumpectomy, AC and radiation 4 years ago. My feeling at the time was to "get it overwith", which is why I went with AC and not CMF (my oncologist said that the stats were about the same with either of them). I didn't have small children, mine were in college -- trying to keep up with young ones is a consideration -- do you have anyone that can help you out, so you can rest? In my case, the tiredness was culmulative ... as I had more treatements behind me, it took longer to bounce back. After my first treatment I had terrible nausea, but the doctor prescribed a better anti-nausea med and after that I didn't have any problems. The baldness didn't bother me as much as losing my eyebrows and eyelashes, by the last treatment, I got the mouth sores. I worked throughout my treatments and was able to take an afternoon or day off when I just couldn't stay at work. I was also able to walk 3+ miles daily with my walking partner (we didn't walk the day after my treatments). The radiation was a "piece of cake" compared to chemo. There are times during treatment that you wonder if you're going to make it to the next treatment, but you do. Knowing what I know now, I would do it the same. Be patient and kind to yourself...and enjoy those little ones of yours.0
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Hi:
If you haven't done so already, it's a good idea to thoroughly research these different regimens while comparing the details of your path report, to try to get a better idea of which may offer the best result for your particular situation. Ex: Some studies demonstrate that A/C offers advantages over CMF, particularly for tumors that are Her2/neu positive, while a slower growing, hormone positive, less aggressive cancer may be more suitable for CMF therapy. If you go to www.nci.nih.gov you will find a lot of info which may be helpful.
I had 4 rounds of A/C followed by rads, post lumpectomy. The day of infusion wasn't a problem but the next 3 days were, for me, days of being tired and feeling edgy from the large doses of Decadron. I had some intermittent periods of feeling queasy but no vomiting, etc.. I took Anzamet on the day of treatment and for 3 days following, which helped a lot, I believe. Drinking plenty of fluids also helped. I never had mouth sores or experienced very low counts, etc.. I rinsed 3 times/day with baking soda (a great oral moisturizer which also helps balance the ph in the mouth). I also brushed my teeth with baking soda, using an ultra soft tooth brush. Toothpaste was just too harsh, burned and tasted most unpleasant. My dentist also prescribed an ointment, prior to my beginning treatment, which I could apply if I should get a nick or irritation inside the mouth (from foods, brushing, etc.). I never needed it though.
Four days post infusions, I'd feel fine again. I continued to garden, bike ride, walk and jog, daily Yoga, going out to dinner...pretty much maintaining a normal routine. I took care not to be around large groups of people (and always avoided anyone who had a cold/flu and groups of young children) for the first week following treatment. After that I felt great during the infusion interims.
Unfortunately, I did get a tummy virus, between treatments 2 and 3 but that too passed with no other problems or difficulties.
I have not experienced any cardiac side effects from chemo or rads but sometimes and I'm 3 years out. Much literature states that people do have cardiac problems with the Adriamycin, although it's more common with Herceptin. Typically, these are people who had some pre-existing cardiac problems according to the research. Others, in studies, have developed late cardiac effects, attributed to Adriamycin, who had no previous known conditions. In people with known cardiac problems, there are cardio protective drugs which can be used to lessen the chance of any damage. Ejection fractions can be minimally reduced, immediately following treatment in a small percentage of patients but typically returns to normal with time. You will find more detailed info about this at the site I suggested. Hope that helps some.
Most every hair on my body was gone, by the time I had the 4th cycle. We're all different but for whatever reason, losing my hair was not a huge deal for me. I had expected it may be but was pleased when it wasn't. My brows and lashes were the last to go but not every one fell out, and since they were the first to grow back in and did so very quickly, it wasn't much of a deal either.
Attitude is very important, I think, and you may also want to look into some supplements which may be helpful with some of the side effects of treatment, as this can greatly effect your particular chemo experience and how you feel overall. Do your homework and discuss it with your dr. though as some supplements can interfere with the benefits of chemo.
Good luck and keep in mind that chemo is not the nightmare it was just 10 years ago and many women do very well, even continuing to work. The main thing is to listen to your body and respond accordingly to its needs. When you need additional rest, take it, when you need some time alone, take that too. Treat yourself to little pleasures which are relaxing and/or stimulating,
whichever you need at the time, and remember that so many of us have come through chemo quite well and the chances that you will too, are excellent!
Love, light and laughter,
Ink0 -
Hi, Supermom. In 2002 I was diagnosed with Stage I invasive cancer, 1.8 cm., no nodes, ER/PR negative, Grade 3, HER2/neu negative. I had the same decision you have - whether to do CMF or AC chemo. My oncologist recommended CMF because (1) it wasn't in my nodes, (2) I was HER2/neu negative and (3) because of my age (54) and being post-menopausal for years. He said if any of those points had been different, he would have recommended that I do AC instead. He said AC is more toxic and while there is about a 1% better recurrence rate with AC, for me he didn't think it was a worthwhile trade-off. I had a second opinion and decided to do CMF. I was worried about the potential for heart damage (I already have heart mitral valve prolapse and didn't want any further heart issues). I'm totally happy with my decision, but this is a very personal choice. I'm sure there are others out there with my stats exactly who chose AC. I didn't lose my hair, but was plenty sick on CMF despite all the great meds to deal with nausea (Zofran, Kytril, Decadron, Ativan, etc.). Go figure. Everyone reacts so differently, it's hard to predict. I wasn't hideously tired though and worked full-time throughout my 6 months of CMF. Did end up needing shots for the low white blood count and spent one Sunday in the ER with an infection. But no matter which way you decide to go, chemo is definitely do-able - we're here to prove that true! Good luck to you.0
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I had high doses of Adriamycin as a child for synovial sarcoma. That is why it was difficult for my doctors to decide on a chemo plan now that I have infiltrating ductal carcinoma Stage IIIb. I had a baseline MUGA scan, 2 doses of AC, a repeat MUGA scan (no change in heart muscle function) and then 2 more doses of AC. There was a great response with regard to the tumor size. Then they changed my chemo to Taxotere. No significant response! I had surgery 1 week ago. Modified radical mastectomy, and removal of about 18 lymph nodes. I am doing fine now. I feel that the AC was well tolerated and had a significant effect with regard to tumor shrinkage. I also have 4 children and worked F/T. The kids are 11,10, 6, and 6 mos. I had to stop working during treatment. (I worked with children and that would have been too risky while my immune system was comprimised)I think you should go for it. You have to think of the big picture. You might have a little tougher time now, but a better chance of surviving this horrible disease! Good luck and God bless!0
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Great scripture! Thanks for sharing. Another one the Lord's impressed on my heart is the one in Mark 16...and if they drink any deadly thing, it won't hurt THEM. I'm definitely not looking forward to this, but I'm confident it will come out well. I'm going w/the AC. Thank you!amelia said:Supermom, I was going to write scripture that I found through prayer and the bible, but for some reason, I didn't. When I was first told I had an aggresive breast cancer, I was frozen in shock and immediatly turned to God for help. I went to the bible, my mother in law suggested I do this, and just opened it and tried to read for some comfort. I couldn't because I was crying to hard. I closed the book and came back later to try again. When I opened it the 2nd time, it was the same page. The phone rang so again, I closed the book. Later on the 3rd try, wouldn't you know it, it was the same page. This is what I found: Joshua 1:9 "Be strong and be of good courage. Be not afraid, neither be thou dismayed: For the Lord God is with thee wither thou goest." Every time I remember those words and that day, I get a renewed sense of well being. I know in my heart, that no matter what happens, I am not alone. God bless
Supermom, You are in my prayers, Amelia0 -
Timac,tlmac said:Hi #1, I was diagnosed stage II, grade III in January 2003. I chose mastectomy followed by 4 cycles of AC. I cleaned my house, took care of my pets, got myself to all doctors appointments and even cut the grass well into my 3rd treatment. I did have to get the neulasta shots after each one to boost white cell production as well as procrit after the 4th to boost red blood cells. I spent a weekend in the hospital on IV antibiotics following my last cycle but was back to feeling pretty good by Sunday. I took anzamet (insurance covered the $100 per pill cost) for nausea the first 3 days following each treatment and never threw up. It's great stuff. My heart is strong and I have no fear of the treatment down the road. You might find someone who was treated with CMF 20 years ago since we've had it since the mid to late 70s but AC just became available in the 90s. If I had it to do all over again, I'd choose AC again over CMF. There are fewer reported side effects with AC (other than hair loss) and I can't imagine doing 6 months of anything when I could get it over in just 2. You're lucky to have a choice. My oncologist felt strongly that I needed the intensity of AC and I agreed. My friend, Leslie, had 6 cycles of AC and worked part time through it all (she's 44). Good luck with your decision.
Thank you. I didn't realize AC was so recent on the market. But I think I'm gonna go that route. Thanks for sharing all the other pieces too. It really helps to know what to expect in general and also some of the possible scenarios. It gives me a great place to start in prayer. Thanks for sharing.0 -
Ink,inkblot said:Hi:
If you haven't done so already, it's a good idea to thoroughly research these different regimens while comparing the details of your path report, to try to get a better idea of which may offer the best result for your particular situation. Ex: Some studies demonstrate that A/C offers advantages over CMF, particularly for tumors that are Her2/neu positive, while a slower growing, hormone positive, less aggressive cancer may be more suitable for CMF therapy. If you go to www.nci.nih.gov you will find a lot of info which may be helpful.
I had 4 rounds of A/C followed by rads, post lumpectomy. The day of infusion wasn't a problem but the next 3 days were, for me, days of being tired and feeling edgy from the large doses of Decadron. I had some intermittent periods of feeling queasy but no vomiting, etc.. I took Anzamet on the day of treatment and for 3 days following, which helped a lot, I believe. Drinking plenty of fluids also helped. I never had mouth sores or experienced very low counts, etc.. I rinsed 3 times/day with baking soda (a great oral moisturizer which also helps balance the ph in the mouth). I also brushed my teeth with baking soda, using an ultra soft tooth brush. Toothpaste was just too harsh, burned and tasted most unpleasant. My dentist also prescribed an ointment, prior to my beginning treatment, which I could apply if I should get a nick or irritation inside the mouth (from foods, brushing, etc.). I never needed it though.
Four days post infusions, I'd feel fine again. I continued to garden, bike ride, walk and jog, daily Yoga, going out to dinner...pretty much maintaining a normal routine. I took care not to be around large groups of people (and always avoided anyone who had a cold/flu and groups of young children) for the first week following treatment. After that I felt great during the infusion interims.
Unfortunately, I did get a tummy virus, between treatments 2 and 3 but that too passed with no other problems or difficulties.
I have not experienced any cardiac side effects from chemo or rads but sometimes and I'm 3 years out. Much literature states that people do have cardiac problems with the Adriamycin, although it's more common with Herceptin. Typically, these are people who had some pre-existing cardiac problems according to the research. Others, in studies, have developed late cardiac effects, attributed to Adriamycin, who had no previous known conditions. In people with known cardiac problems, there are cardio protective drugs which can be used to lessen the chance of any damage. Ejection fractions can be minimally reduced, immediately following treatment in a small percentage of patients but typically returns to normal with time. You will find more detailed info about this at the site I suggested. Hope that helps some.
Most every hair on my body was gone, by the time I had the 4th cycle. We're all different but for whatever reason, losing my hair was not a huge deal for me. I had expected it may be but was pleased when it wasn't. My brows and lashes were the last to go but not every one fell out, and since they were the first to grow back in and did so very quickly, it wasn't much of a deal either.
Attitude is very important, I think, and you may also want to look into some supplements which may be helpful with some of the side effects of treatment, as this can greatly effect your particular chemo experience and how you feel overall. Do your homework and discuss it with your dr. though as some supplements can interfere with the benefits of chemo.
Good luck and keep in mind that chemo is not the nightmare it was just 10 years ago and many women do very well, even continuing to work. The main thing is to listen to your body and respond accordingly to its needs. When you need additional rest, take it, when you need some time alone, take that too. Treat yourself to little pleasures which are relaxing and/or stimulating,
whichever you need at the time, and remember that so many of us have come through chemo quite well and the chances that you will too, are excellent!
Love, light and laughter,
Ink
Thank you, thank you! I think I'm going w/the AC, much because it's overwith quicker. The recurrence numbers for my case were very similar w/both regimens. But thanks for all the practical info especially. I'm sure that will come in VERY handy. But I have one question for you...you said you never had a problem w/low blood counts. Was there anything that you'd attribute that to? Diet? Supplements? From where I'm sitting, other than the hair loss and nausea, low blood counts make up for all the other side effects: anemia, fatigue, more easy bruising and bleeding, and higher risk of infection. I'm 36 yrs old and in very good health. I'm confident I'll come through this just fine, but I'd like to make it as easy as possible on myself. Thank you so much for your input.0 -
Wow. Surgery one week ago and you're online giving support to others. Thank you! And good luck and God bless you too. Enjoy all your babies!twicebitten said:I had high doses of Adriamycin as a child for synovial sarcoma. That is why it was difficult for my doctors to decide on a chemo plan now that I have infiltrating ductal carcinoma Stage IIIb. I had a baseline MUGA scan, 2 doses of AC, a repeat MUGA scan (no change in heart muscle function) and then 2 more doses of AC. There was a great response with regard to the tumor size. Then they changed my chemo to Taxotere. No significant response! I had surgery 1 week ago. Modified radical mastectomy, and removal of about 18 lymph nodes. I am doing fine now. I feel that the AC was well tolerated and had a significant effect with regard to tumor shrinkage. I also have 4 children and worked F/T. The kids are 11,10, 6, and 6 mos. I had to stop working during treatment. (I worked with children and that would have been too risky while my immune system was comprimised)I think you should go for it. You have to think of the big picture. You might have a little tougher time now, but a better chance of surviving this horrible disease! Good luck and God bless!
0 -
epgnyc,epgnyc said:Hi, Supermom. In 2002 I was diagnosed with Stage I invasive cancer, 1.8 cm., no nodes, ER/PR negative, Grade 3, HER2/neu negative. I had the same decision you have - whether to do CMF or AC chemo. My oncologist recommended CMF because (1) it wasn't in my nodes, (2) I was HER2/neu negative and (3) because of my age (54) and being post-menopausal for years. He said if any of those points had been different, he would have recommended that I do AC instead. He said AC is more toxic and while there is about a 1% better recurrence rate with AC, for me he didn't think it was a worthwhile trade-off. I had a second opinion and decided to do CMF. I was worried about the potential for heart damage (I already have heart mitral valve prolapse and didn't want any further heart issues). I'm totally happy with my decision, but this is a very personal choice. I'm sure there are others out there with my stats exactly who chose AC. I didn't lose my hair, but was plenty sick on CMF despite all the great meds to deal with nausea (Zofran, Kytril, Decadron, Ativan, etc.). Go figure. Everyone reacts so differently, it's hard to predict. I wasn't hideously tired though and worked full-time throughout my 6 months of CMF. Did end up needing shots for the low white blood count and spent one Sunday in the ER with an infection. But no matter which way you decide to go, chemo is definitely do-able - we're here to prove that true! Good luck to you.
Yep, I think I'd have chosen CMF in your case too. But I'll tell you, just making the decision at all feels like a load of bricks off my chest. I'm going w/the AC, mostly because it's overwith quicker since the recurrence rates were really similar w/both regimens. I think that'll suit my situation best. But I've really been warmed by all the support I've had from people like you who don't even know me. Thank you and God bless.0 -
Patty,billandpatty said:I was 47 when I was diagnosed with BC. I had a lumpectomy, AC and radiation 4 years ago. My feeling at the time was to "get it overwith", which is why I went with AC and not CMF (my oncologist said that the stats were about the same with either of them). I didn't have small children, mine were in college -- trying to keep up with young ones is a consideration -- do you have anyone that can help you out, so you can rest? In my case, the tiredness was culmulative ... as I had more treatements behind me, it took longer to bounce back. After my first treatment I had terrible nausea, but the doctor prescribed a better anti-nausea med and after that I didn't have any problems. The baldness didn't bother me as much as losing my eyebrows and eyelashes, by the last treatment, I got the mouth sores. I worked throughout my treatments and was able to take an afternoon or day off when I just couldn't stay at work. I was also able to walk 3+ miles daily with my walking partner (we didn't walk the day after my treatments). The radiation was a "piece of cake" compared to chemo. There are times during treatment that you wonder if you're going to make it to the next treatment, but you do. Knowing what I know now, I would do it the same. Be patient and kind to yourself...and enjoy those little ones of yours.
Boy, I didn't think "getting it overwith" would be a deciding factor at first. But it turns out that's the primary reason I'm going w/the AC. I think I'll be a much more patient mommy if I'm in the trenches for 3 mos instead of 6. And I even get better stats that way. Thank you for sharing your experience. And God bless you!0 -
Hi, Supermom
I was diagnosed with Stage II breast cancer with cells in one of the sentinel nodes; had a lumpectomy and nodes removed in November, started chemo (AC) a few weeks later. I have had very few problems. Yes, the first treatment I was very nauseous and tired on days 3-5 and had no appetite. The Lofram I took did nothing. In looking back, I think much of it was stress-induced. The next treatment I used Emend---it worked wonderfully. Yes, I had very little appetite for a few days (this is a problem???!)Yes, I lost some of my hair (about 1/3 to 1/2) starting with the first treatment. It came out in clumps and I cried every day in the shower for a week. I had 4 treatments with AC at 3 week intervals and now I'm going to be having my 3rd treatment with taxotere (also 4 treatments at 3 week intervals). My hair is starting to grow back. I did not take steroids with AC, I am with the T. I'm more tired with the T than with the AC, but it's not horrendous. I'm retired (I'm 56) so I have the luxury of babying myself more. If you can, stop trying to be everything to everyone for a while. Let family members and friends help you. Take shortcuts; don't feel guilty about getting things done. The dust only comes back no matter how much you clean! Appreciate the little things. Keep as positive an attitude as possible, allow yourself a good cry occasionally, and try not to let stress get to you (yeah, right, with 2 little ones to care for!; this is a bump in the road called life and you'll get over it.0 -
Ramapou,ramapou said:Hi, Supermom
I was diagnosed with Stage II breast cancer with cells in one of the sentinel nodes; had a lumpectomy and nodes removed in November, started chemo (AC) a few weeks later. I have had very few problems. Yes, the first treatment I was very nauseous and tired on days 3-5 and had no appetite. The Lofram I took did nothing. In looking back, I think much of it was stress-induced. The next treatment I used Emend---it worked wonderfully. Yes, I had very little appetite for a few days (this is a problem???!)Yes, I lost some of my hair (about 1/3 to 1/2) starting with the first treatment. It came out in clumps and I cried every day in the shower for a week. I had 4 treatments with AC at 3 week intervals and now I'm going to be having my 3rd treatment with taxotere (also 4 treatments at 3 week intervals). My hair is starting to grow back. I did not take steroids with AC, I am with the T. I'm more tired with the T than with the AC, but it's not horrendous. I'm retired (I'm 56) so I have the luxury of babying myself more. If you can, stop trying to be everything to everyone for a while. Let family members and friends help you. Take shortcuts; don't feel guilty about getting things done. The dust only comes back no matter how much you clean! Appreciate the little things. Keep as positive an attitude as possible, allow yourself a good cry occasionally, and try not to let stress get to you (yeah, right, with 2 little ones to care for!; this is a bump in the road called life and you'll get over it.
I love your outlook! Thanks for sharing your experience. It seems w/each response, I gain so many different insights--medical, emotional, etc. I'm sure chemo is no picnic, but I think you're probably very right about the stress factor. I've been honing in w/the Lord and I'm determined to go from strength to strength throughout, over, and beyond this thing. Your regimen is more strenuous than mine. I wish you success and pray for your total recovery.0
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