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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 28, 2007 09:19 pm
Anyone starting Chemo in August 07?Kim-I'm so sorry to hear about possible mets, but a positive story for you. I was talking to someone at the cancer center just today who shared that her friend had bc with bone mets 15 years ago and she is ned still today. she had done additional chemo back then and it took care of the mets. Don't give up hope for a cure! I know its easier said than done, but it can happen! Kidsmom |
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Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Nov 28, 2007 09:10 pm
Starting Rads in December, come join me!!!Hi girls, My simulation and tats were yesterday. I got 5 tattoos and I thought they hurt. I'm not really wimpy, but the ones in my underarm area really really hurt. I was surprised that two tatoos are on my right side (my tumor was in my left). Any body else have tatoos on both sides? I found the whole process more embarrassing than anythng else previously. The doctor (who I've never met) came in and started marking on me with a sharpie, the nurses who were really nice, taped wire all around my breast and shaped a mold for me. It was just a long time to lay there half naked with my arms over my head in a cold room. I'm glad its over. My rads start next Wednesday. Tuesday is my dry run where I guess they double check everything. I'm kind of bummed about the timing. All next week I'll have to take a half day off work for my treatments, then they move to 3:30 pm. I teach junior high so I get out at 2:25. My son is 20 months and having surgery next Friday to have his adnoids out and tubes put in both ears. The poor guy has been having a much tougher time than me lately. My kids put things in perspective and I keep telling myself, better me than them. Thanks joeyann for all the information. I feel better prepared for what to expect during the actual treatment now. Kidsmom |
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Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Nov 26, 2007 07:07 pm
Starting Rads in December, come join me!!!Hello girls, I am going tomorrow at 7:30 am for my simulation and to meet with a nurse about what to expect. Then in the afternoon I get another bone scan. Its going to be a fun day (yeah right). I am concerned about getting the ct and bone scan in the same day though. I told the radiologist about the bone scan and he didn't seem concerned. Anybody have a similar experience ? Thanks, Kidsmom |
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Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Nov 19, 2007 06:54 pm
Starting Rads in December, come join me!!!Hi girls, Count me in for December. I have my consult on November 21st. Not sure about the simulation test. Amber I am 34, I can only sympathize with how you feel at 29 with BC. I have a 3 1/2 year old girl and 20 month old son too. I had 8 mm idc and 2 of 9 nodes positive. The nodes were both larger (almost double) the original tumor size. I am curious how the rads and holidays will go too. Hope you have a great Thanksgiving Kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 13, 2007 08:19 pm
Anyone starting Chemo in August 07?Girls, My PS said 25% of implants fail after radiation. He said he doesn't like those odds and strongly recommends implants with radiation. I'm not sure what to do either. I originally had lumpectomy, but oncologist suggested a mastectomy could improve overall survival. But I have to have rads and don't want the major surgery of a DIEP or tram flap. I am glad to be done with chemo, but as I still feel like crap this week, I'll appreciate being done more when I can move without hurting and can feel me figners and toes again. Hope you all enjoy the Thanksgiving holiday, kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 10, 2007 08:57 am
Anyone starting Chemo in August 07?Kim - I'm so sorry to hear about your friend. What a tragic situation. I am glad your done with chemo though. Everyone keeps telling me congratualations, but I am not sure what to think. My oncologist was out of town. The nurses hadn't even scheduled me to talk to the NP or anyone. I was so bummed. I have all these questions about what to do now and I didn't get to ask them to anyone. I am having the numb fingers and toes still. It hasn't gone away since my 3rd treatment (2 weeks ago) and I have had a very sore spot behind my left shoulder blade for about a month now. I really needed to see my onc. They scheduled me to see him next week so I will have a chance. Doesn't that seem weird not to meet with your doctor on your last treatmetn? Has anyone heard from kaye? Hope she's doing OK. Ladies who had problems with your treatment and had to end early- it is out of your control and so you should just feel relieved your done. It wasn't your choice- but I can understand your concerns. Luckily someone made the decision for you though and they are informed about what is in your best interest longterm. Would the extra treatment be worth it if I made you so sick you were hospitalized? I hope everyone enjoys they're weekend. Kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 8, 2007 04:33 pm
Anyone starting Chemo in August 07?Harley, I'm glad to hear your doing OK after your surgery! Do you still have to have rads? Hope yousleep some tonight Kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 4, 2007 12:01 pm
Anyone starting Chemo in August 07?Angie, I am so worried about not being able to hug/pick up my little ones. I'm glad your husband is helpful. That makes a big difference. Was not having a mastectomy an option for any of you who did? I originally had a lumpectomy but when I asked my onc for numbers in regard to reoccurance he looked things up on Adjavant online and came up with a 1 in 4 chance of reoccurance and a 1 in 5 chance for death in the next ten years even with chemo and rads. That's when we started the discussion about mastecomy again. I originally wanted that, but was talked out by the surgeon. My onc assummed that with a mastectomy I wouldn't need the rads. That meant I couldn have implants which had a quicker recovery time. Now with the rads and that not being an option I keep wondering if I should have the mastectomy? Or just wait and monitor????? These decisions are too hard to make. I can also relate to everybody with the people wanting you to be OK. Everytime I complain the least bit to my dad, he just says, keep your chin up. It makes me want to scream. My mom had bc then passed after a two year battle with lung cancer. He knows what its like and still doesn't have any empathy. thanks for listening again, Kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 3, 2007 09:22 am
Anyone starting Chemo in August 07?Angie-I'm glad to hear your recovery is going OK. I am not looking forward to my bilateral mastectomy. Are you able to pick up your kids? Do you have help with that? Kaye-thanks for thinking about me. I am done with chemo with Friday the 9th. I don't write often, so that is so sweet that you remembered. I read almost everyday and feel like I know you all but recently have just felt so overwhelmed by everything I can't even type. How many of you are having rads even after a mastectomy? I posted on the rads thread a similar question. I don't know why, but I was sure I wouldn't need them if I had a bilateral mastectomy. Now I find out I do and that changes the kind of reconstruction I can have. I tell you, I was so upset after my meeting with the rads oncologist. My sister and I were in the room and when he came in he looked at both of us and said, pointing to me, it must be you I'm here to see or your with the traveling gypsies. I'm assuming this comment was in regard to the scarf I was wearing rather than a wig. I was so taken aback, but didn't even say anything to him about being so rude. He was one of those Drs who hasn't been a patient or had family as one lately. He continued to tell me how bad my situation was because of my age and triple negative status. I have stayed pretty positive during this whole experience but after meeting with him I just wanted to cry. My sister worries about me so much that Ididn't want her to see me upset, but then I broke down at school yesterday when the other teacher's were asking me how I've doing. I just feel like I need a mental break from all of this crap. i thought I was nearing the end, now it appears I'm not even close to the halfway mark. sorry for being so depressing. I appreciate just being able to vent to someone who understands the frustration. I hope you all have a good weekend. My kids are excited the leaves are down and we can make a big pile to jump in. Those are the things I'm trying to focus on again. Seeing their smiles and happiness at the little things. kidsmom |
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Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Nov 3, 2007 09:07 am
rads after mastectomy?I had a lumpectomy in July 07 for a 0.8 cm lump 2 of 9 nodes were positive, and a triple negative. I'm almost finished with my chemo 4 A/C, and 4 taxol and after doing more reseach decided with the encouragement of my oncologist to do a bilateral mastectomy. My mom had bc at 57, I'm only 34 but BRACA negative. I met with a rad oncologist to confirm I wouldn't need radiation if I had the mastectomy and was shocked when he said I would need it. He said 5 weeks with 3 beams, the boosters for the 6th week could be skipped because my original tumor was small. He said my age, tumor grade (3), triple negative status, and the fact the tumor was double the size in both nodes as the original in breast, required the radiation even with mastecotmy. I was going to have implants but PS won't do them if I have radiation. I'm fairly thin and he said the chance of them failing with radiated skin is too great. My only options for reconstruction are TRAM or DIEP. I have two little ones 1 and 3 and the recovery for those are so great. I'm tramatized for the first time since this whole BC thing began. I"m going to get a second opinion, but wondered if anyone in their 30's or 40's received radiation after a mastectomy and chemo? Thanks, |
Posted in:
Tests, Treatments & Side Effects + Breast Reconstruction, Created: Oct 18, 2007 07:15 pm
How did you decide?Girls, thank you all so much for sharing your stories and for your advice. I was node positive (2 out of 9). My original tumor was small 8 mm, but my node tumors were twice as big. I understand the risk of mets being the one that may kill me, but the 25% reoccurance rate within ten years was after chemo and rads. I just don't want to have to do chemo again if I can prevent it. I am BRAC negative, but my mom had BC at 57 then passed from lung cancer at 64. Two great aunts also had ovarian cancer we think. All in all, I just want to be there for my kids when they are older and if getting new boobs increases the chances of that, its worth it to me. I am meeting with a surgeon and plastic surgeon from Cleveland Clinic in Ohio on Monday to further discuss options. Has anybody worked with a plastic surgeon from there? I hope you all have a great weekend, thanks again, Kidsmom |
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Tests, Treatments & Side Effects + Breast Reconstruction, Created: Oct 17, 2007 06:56 pm
How did you decide?Hello girls, I already had a lumpectomy and am almost finished with chemo (4 a/c and 2 of 4 taxol done). When I asked my onc for the chance of recurrance I found out it was 25% within the next 10 years. That seems awful high to me, I'm 34 and have a 1 and 3 year old. So I'm meeting next week with the surgeon and plastic surgeon to discuss a bilateral masectomy with reconstruction. I'm suppossed to have 6 weeks of radiation after chemo, but I guess that won't need to happen if I have the masectomy. Thanks for any advice you can give me. Kidsmom How did you guys base your decision for what kind of reconstruction you picked? |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 15, 2007 07:02 pm
Anyone starting Chemo in August 07?msmagoo- I'm a triple negative too, but my onc never said anything about indefinate chemo??? What stage are you? Where are you located? Maybe your oncology could recommend a therapist. In my area, Toledo, Ohio, there are several outreach programs just for breast cancer survivors. Maybe you can go to a group meeting and get some referrals from other survivors. Kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 14, 2007 05:09 pm
Anyone starting Chemo in August 07?Kaye, thank you for the warning about not getting the neulasta. You made me definately think that I should just get the neulasta shot. What kind of claritin are you guys taking. I tried claritin -D the previous shot and didn't notice a difference. Is it just the regular claritin? Hope you all had a good weekend, Kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 13, 2007 08:44 pm
Anyone starting Chemo in August 07?Boy, I feel like I'm making up tonight for not posting much before- I wanted to mention about the taxol study. My onc and I talked about whether to keep me on taxol or switch to taxotere. His take on the study was that if your her2 negative, and estrogen +, taxol would NOT be effective. I'm a triple negative so he wanted me to stay on the taxol. Has anyone else had a discussion about the new taxol study with their onc? thanks kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 13, 2007 08:39 pm
Anyone starting Chemo in August 07?I also wanted to mention that I am going to have a bilateral masectomy now. I originally had a lumpectomy with clean margins, and 2 nodes positive. My onc and I looked at some statistics for reoccurance again, and he agreed with my gut feeling that its better for my to get rid of the "girls". I'm only 34 and with chances of reoccurance greater for us with age and greater once you have bc, I'm kind of screwed. My gut originally told me to get rid of them, but both surgeons I met with said a lumpectomy had the same reocurance rate, and the recovery was so much shorter and with a 18 mths old and 3 1/2 year old and no family in town, and the confusion and fear when originally diagnosed I let them talk me out of what I wanted to do. I really feel that for me, my future will be less anxiety ridden if I trade in these for a new pair sorry for posting so much, I think its the steriods again. welcome to the new people on the thread and hello again to the girls (kaye, june, nash, harley, etc,) whose posts I read religiously. You are all so much support to me even though I don't post often, your always in my thoughts and prayers. Kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 13, 2007 08:33 pm
Anyone starting Chemo in August 07?Jackie-I'm sorry your having such a rough time with the taxol. I felt somewhat similar after my first treatment at day 5, but I think it was more the neulasta than the taxol. Who knows though. Has anyone switched from neulasta to neupogen during chemo treatments? After explaining to my onc about the migraine I had after treatment 1, he said let's skip the neulasta this time. I was sooo happy he said that. Then on Friday when I got treatment 2 I told the nurse I wasn't going to get the shot. She was sooo worried for me and said if she was me she would get the shot. And went on about how if my wbc gets low I won't get my treatment in two weeks. I asked about neupogen because some of you said it was easier on you. She said that's the same as neulasta only its short acting so I would need 5 to 8 shots of it and it still may not bring my count up. I'm so confused with what to do now??? Any ideas. I really like my onc and want to go with what he said (because I hate that nasty neulasta) but am scared to get behind. November 9th has been on my calendar as my last treatment since I started and I really want this chemo to just be over. Any ideas? My taxol #2 is going well again. Yesterday I slept from 6 pm till2 then was awake the rest of the night. I felt like I was hyperactive today. My 3 year old and I were out running errands, then I did a bunch at home. Slept from 5 till 8 pm and I'm awake again. I definately have slept less with taxol, but I don't feel like I'm going to throw up so its a better trade off. Hope everyone is well Kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 4, 2007 08:44 pm
Anyone starting Chemo in August 07?June, I hope your taxol goes well too. Even with my migraine, I still think the taxol is better than the AC. I feel like I'm 80 instead of 34 with all the aches and pains, but those are more easy to deal with than the naseua was. I saw the nurse practitioner today and she said the same thing about my migraine maybe being from the pre-meds from the taxol in combination with the neulasta???? She didn't have a clue about my blood shot eye. She said maybe I just scratched it. Which in hindsight may be true. I was pretty loopy from the benedryl after by treatment last Friday and maybe Idid scratch my eye when I took my contact out??? Hope everyone has a great Friday and weekend! Kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 4, 2007 10:30 am
Anyone starting Chemo in August 07?Hello all, I am home from work for the first time since I started chemo. I have 4 AC done and 1 taxol. I thought the taxol seemed so much easier because I had it Friday and felt pretty much normal Saturday and even walked in the Race for the Cure on Sunday. Monday was my neulasta and then whammy it hit me. Tuesday was sore and achey. Wednesday I felt like my head exploded. Don't know why but I went to work (I teach junior high science) and tried to beg the kids to be quiet because I felt so bad. Most complied but it was terrible. I couldn't even get my kids from daycare. Today its better but still sore and have a headache. Also, my eye was bloodshot the day after taxol and hasn't improved. Has anyone else had the headache from neulasta or bloodshot eyes?? Kaye-I'm so happy for you to be done!! Kidsmom |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 2, 2007 04:38 pm
Craving crunchy salty chips after chemotrigeek, I have gained weight (about 5 lbs) during my 5 chemos and I'm sure its from all the bad food I've been eating. For some reason, I feel justified eating junk because I did chemo and it sounds good. Also, my mouth always has that metal taste so I think I'm looking for salty stuff to try and scape that taste away. Kidsmom |
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