2012 sisters
Comments
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Maddymac: no my surgery was actually on the 27th.
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It is sweet to hear your voices, sharing so much. i hear knowledge of how hard it is, even when all is going ok.
MyDH asked me if I wanted to go to Santa Barbara for a few days. I felt a sadness wash over me as I remembered that we had gone there at New Years, right before I got my MRI biopsy results. I suddenly started to cry and said I can't go back there...I didn't know then what was about to happen. Life changed. Trying to stay upbeat, but there are moments.
Thanks for listening. -
Thanks for sharing so much. i hear knowledge of how hard it is, even when all is going ok.
MyDH asked me if I wanted to go to Santa Barbara for a few days. I felt a huge sadness wash over me as I remembered that we had gone there at New Years, right before I got my MRI biopsy results. I suddenly started to cry and said I can't go back there...I didn't know then what was about to happen. Life changed. Trying to stay upbeat, but there are moments.
Thanks for listening. -
Jaz, what my post clearly did NOT say upon my re-reading of it, was that yes, the drains suck bigtime (which I guess is what they are supposed to do) and because (I thought) our surgery day was the same, I empathized extra. Which, upon re-thinking, makes no sense anyway. I empathize whether it's the same day or another day or on another planet.
Oh, Lisa2012 my dear, I hear you, and I hear the sorrow shot through with your strength. You're here, and Santa Barbara will be here when you are ready for it. The only thing I am ever sure of when I wake up these days is that life will contain at least one painful and at least one joyful moment that day, and sometimes the joy is damned hard to find.
I wish I had sufficient brain to say evrything I mean to say, and to remember whom to say it to, but I clearly don't right now. Instead I will just say, whether you are resting or rising, I wish all of you peace and ease. -
Sorry I just can't respond to everyone today.
Yesterday was a kick in the gut. Went for my last taxol and the MO informed me the tumor is larger than last time. On the bright side he sent me for an ultrasound when did show it larger but filled with pockets for what they believe to be dead cells so we went ahead with the last tx.
I get to meet the the BS on Monday to get that going. Just want this crap out of me!
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Well, I have been awake now for almost two hours (it's 6am), so thank you all for keeping me company with your posts!!!! I laughed, was informed, smiled, felt companionship, and empathy, but mostly was in awe of all of you ladies!!!!
Although it sucks to be here, what a great group!
What determines whether you have surgery or chemo first? Does everyone have TE's put in if they are going to have reconstruction? Is a BMX always an option? (I don't want to take any chances).
I woke up because my left underarm hurts. I think everyone knows why I can't go back to sleep.I have at least three lumps under my arm and my dh says it probably hurts because I am focusing all my negative energy there.
Thanks for letting me rant randomly, I am so happy to see so many happy dances!!!!! You are all so encouraging! Have a great weekend!</p -
Taking a few quiet minutes for myself before my family wakes up and starts the day so thought I'd say good morning. Feeling a bit brighter today and thankful that surgery day is almost here and I can get this show on the road already.
lisa2012 - consider yourself hugged; you are not alone.
lostinmo - I'm sorry. What crappy news to have to hear after going through all the chemo. But it sounds like maybe it did do something, even if not everything you hoped it would do. Sending you giant hugs today.
Hope you all have a bright, sunshiney (but not too hot) day!
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luvmyfam - I missed your post. I too wonder how the decision is made to do chemo or surgery first. My BS didn't really give me the option. She said surgery, followed by chemo - and I went with it. I think a bmx is always an option - especially if you have positive nodes. Everyone has their own personal feelings about their body - but I'm personally under the opinion of get it out. I don't have much to conserve, so didn't opt to go that route. And I hear you about the underarm pain. I have one known positive node there and I was just telling my hubby how sore my underarm felt when I applied my deoderant this morning. Surgery day for me can't get here fast enough now... Have a good one!
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LuvMyFam, my lumpectomy was determined by a few things like: how operable my tumor was - if it had looked to be invading the pectoral muscle that might have changed the approach and concerns; the fact that I'm in a rural area and though we have a good cancer center we do not have a dedicated breast surgeon - it would have taken longer to go to a larger hospital and consult one and I wanted the cancer out, out out! and then I would not have been at home for part of recovery and that's a big problem for me with a special medical diet; I still think I want a BMX after chemo is done but now at least I don't feel quite so urgent about figuring out where to go and how to do it.
I woke up after 7.5 hours of sleep again so if that's my post chemo sleep pattern I'll take it. My stomach has definitely not been hurting as much but I absolutely had to get some calories in me this AM. I have a lot of frozen smoothie cubes in my freezer so I grabbed a couple of those and that seemed to be just the ticket. Being frozen they kind of numbed my mouth so I'm not tasting the chemo meds, just nice cool soothing sensation.
I'll keep the meals small today and for a few days, not that my body gives me much choice if it's like the last time through. Neulasta later today and then in my bed for a few days of fever probably... I have lots of DVDs checked out from the library and lots of documentaries and oooooold movies downloaded from the youtube. I like being prepped.
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lisa2012-I feel for you and BIG ((((((((((((HUGS)))))))))))))))
luvmyfam-Chemo before or after is determined by your med team with info to the type of cancer, stage, and size of the tumor. Some aggressive cancer that are bigger in size will get chemo to shrink them before operating on, and not all reconstruction is TEs. Some opt for no reconstruction at all at the point of surgery and reconstruct at a later date or or at all. Others use methods of removing your own tissues and muscles from other areas like tummy and back to reconstruct breasts and others like myself who were candidate for 1-step to implants.
lostinmo-Sorry to hear about your chemo and the size of your tumor, now that part is done you could concentrate on getting your cancer out.
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Good morning ladies! Hope everyone is feeling better today.
Lisa, we are here to listen if nothing else! Maybe Santa Barbara will be a nice place to go for you again, maybe you will just find another beautiful place to go instead. I hope you are feeling better. This is a roller coaster ride...from hell.
Lostinmo, I see you have hit a low point on the roller coaster too, I feel your pain. Sorry to hear that the tumor didn't shrink. Don't lose hope though, the fact they think that there are lots of pockets of dead cells is good. According to my pathologist husband, he says that he puts no stock in size of tumors during or after chemo. Sometime all the dead cells cause a inflammatory reaction that causes things to swell. And scar like tissue gets left behind. Those cells don't just disappear, they die and something has to happen to them and something is left behind. They will know when they take out the f'ing cancer and look at it under a microscope. Now chemo is behind you, time to look forward as hard as it is, and get the damn cancer out of us.
Luvmyfam, I did chemo first because I am trying to preserve the breast and do a lumpectomy. I have a large aggressive tumor and teeny tiny titties. Doing chemo before or after has no affect in my case (or any case I think) on survivor rates or recurrence rate.
Allurbaddays, hope the side effects and your stomach calm today. Sounds like you have a plan!
My surgery isn't for a couple of weeks. I will probably think way too much about it between now and then. My husband keeps shoving aside the topic and saying that this part is easy. Maybe he is right but it isn't him getting pieces of him whacked off soon. He has never (thank goodness) had surgery. I am finding the sympathy lacking a bit. Though I think that he means well and generally we arent ones to dwell on things we can't control and mull and worry. He and I are of the general attitude to take care of business and move on. And maybe that is what I need, talking about it might just get me more worked up. But I don't think he has any idea how this is affecting me. This is deforming surgery. I know it isn't a vital organ but still I am kind of used to what I have being where it is.
Anyway despite that rant I am feeling pretty good. I am going for a walk before it gets any more ridiculously hot out there. Best wishes sisters! -
ramols - Not silly!! I couldn't have children so didn't have that apect of attachment but still got very sentimental before surgery and really still miss them. BUT have done well and wasn't as emotional after the surgery as I thought I would be. A fill of the TEs at surgery helped some I believe.
Soyandpepper - absolutely not. Funny, I found while writing that that I liked writing, just didn't love the topic! I hope that you are doing well. Where are you in your journey?
Happy Saturday and thinking of you all daily.
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Thanks, ladies. Today we are having a small party for son (turning 24 today) and me (57 yesterday.)
First social event at our house in 3 months. Just family and some friends, maybe 15 people. It's a beautiful day, will probably be about 75. I'm a bit nervous but once it starts I'll be fine -
Lisa, you will be fine, have fun and Happy Birthday to you both.
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Ok, don't be in a huge hurry to get your drains taken out. Mine came out at 8 days after surgery and were both draining under 15cc a day. Now I have a seroma on my lymph nodes that is not going away at almost 7 weeks out. I don't want to get it drained becuase I've already had an infection there but guess will see what my surgeon says next week.
Allyourbaddays, report back on how the fasting went. Just wondering if it actually helps.
And yes, I do get sick of talking about BC! Sometimes I just resolve to have a BC free day and pretend it didn't happen. I think it helps.
Happy birthday, Lisa! After my surgery I was super hungry and wanted carbs. Thought I would lose some weight from major surgery, but no!
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Lisa: Sending you a big hug and a Happy Birthday! You'll be able to go back to Santa Barbara again, but I know how you feel. I used to love going to Monterey (always have even before we moved to Northern CA) but now when I think of Monterey, it's the place where I'm being treated for BC and just doesn't hold the same memories for me anymore.
Allurbaddayswillend: (love that) That's a fantastic idea about the frozen smoothie cubes. I'm going to have to try that.
So I have decided that I will have my DH shave off my hair this coming Friday (my 1st chemo date is 7/11). Our little guys had their heads shaved yesterday and they asked if I was going to have mine done with them, too (they're excited to cut my hair as best they can beforehand). I just couldn't do it last night, but.... I am 95% sure about this Friday. I decided that chemo is not going to decide when my hair is gone, but I will. I hope I stay strong about my decision.
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CMartin-I'm 9 weeks out from my NSBMX with 1-step to implants! Now in the process of deciding whether or not I'm going to do chemo. No radiation since I do not have node involvments, but the chemo part is very diffcult since I'm not sure the benefit outweight the risks in my case, still waiting on my hormone receptors and had a consultation with one MO who was an ass cause he assumed I was doing chemo and I was there to just talk about my benefits and risks. He went on and on about the different cocktails he would use if my Er was + or - and her2 + or -. He also downplayed the side effects a lot, my main concern is putting toxic chemical in my body. There's no stat. for someone my age (35) and even my oncoplastic surgeon whom I trust a great deal told me that chemo is optional for me.
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Happy Birthday Lisa!
teeball, i think its a great idea to shave it beofre the chemo makes it fall out. I buzzed mine as soon as I got more than a few strands when i ran my fingers through my hair. For me it was 3 weeks after the first treatment. But no matter when you do it you are the one in control that way.
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MaddyMac: Thanks
lisa: Hoping you and your son have a great birthday celebration with your family, wishing much joy and laughter!
Lostimo: I'm sorry to hear about your tumor not shrinking but I'm sure these feelings will be eased when you go in for surgery to get this stuff out! There is a sense of relief when you get it out and hear clean margins! Hang in there
Luvmy fam: I think my surgery before chemo was determined based on my tumor size and positive nodes? Not exactly sure, but I remember the doctor saying something like that.
Ramols: Glad you're feeling better, hoping that you enjoy a peaceful and happy weekend heading into surgery on Tuesday!
allurbaddayswillend: good idea about the smoothie cubes, I'll save that for when I start chemo, enjoy your movies, hope you feel ok.
Jpmomof3: Sending you hugs, I think that our families think that being strong and positive means not talking about our feelings and fears, I think that it is good to rant and talk things through, it helps me to move forward; anyway, to be able to do that from time to time and get it out of my system. Hope you enjoyed your walk..
DianaNM, I have come to agree with you regarding rushing to get the drains out after hearing so many stories about taking them out to soon, I have an infection in one of my drains but worry about getting them out to soon and dealing with different side effects so I'll just deal with the one I have now. I'm sure all this will pass soon.
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jazlaumir and DianaNM - re: drains - I had surgery on the 29th and have been a little impatient in regards to my drains and when they can be removed; I tried to make an appointment Thursday afternoon for early next week but they wouldn't let me and I was frustrated about this. Thanks for the reminders that they are serving a purpose and that thankfully, so far my recovery has gone smoothly without complications so I need to be patient with this area.
One of the reasons for my impatience is that I want to see the surgeon and know what my surgical pathology report reveals so I know what I am facing in the months ahead. They won't give me that appointment until the drains are also ready to come out. I have a suspicion from feeling and looking at my chest that they had to do more of a radical mastectomy than modified as I do not feel muscle under the skin, only bone and my husband has confirmed this with me also. I think from how things feel and where one of the drains is that they also took supra-clavicular lymph nodes. This would mean that the cancer may have been growing into the underlying muscle and that they may have suspected or confirmed other lymph node involvement than just axillary. I know this is a lot to assume and I could be proven wrong, I am a nurse though and I would just like to 'know'.
luvmyfam: my cancer was smaller (1.5 cm) but aggressive and already had established a good blood supply for itself and satellites for a 4.5 cm total area so they wanted it out right away.
lostinmo - thinking of you, the ultrasound of your tumor sounds promising though
ramols - hoping that the nanny interviewing goes well this weekend and that you are in a good place for surgery next week; I will be thinking of you. I was pretty sentimental prior to going into surgery last week -my breast nursed four boys, still looked pretty good and perky for a 54 year old and was well loved; saying goodbye was not easy but maybe having done that preop it has been easier to accept now that I am postop.
lisa2012 - I know you will be enjoying yourself and your friends/family this evening - be kind to yourself tomorrow.
teeball - understand the wanting to control what you can control; enjoy your hair for the remainder of this week and then let it go
, I'll be joining you soon
tazzy - hope you are having a wonderful camping weekend
allyourbaddayswillend - I am very much paying attention to your chemo experience, I also like the smoothie idea and hope that you are having an OK weekend.
Hope I haven't missed too many; I enjoy reading all the posts.
Take care everyone
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allurbadday - I hope you are feeling well and your stomach is cooperating!
jpmom - My husband is the same way. Don't get me wrong, he's a super support and his rock-like way of handling all this is helpful at times, but I wonder if/where/what the real emotions are for him. He has trouble allowing me down/sad times, as he's afraid that is me giving up the fight. To him, this can all be boiled down to removing and killing contained cancer and getting new boobs to boot. I know he gets that there is an emotional component to this for me - and I know he is scared too, but every so often his rah rah attitude kind of pisses me off. But in the end, I know he means well and is there for me 100%. Men just deal with their emotions differently. They are very practical.
cmartin - you are obviously a very strong woman. I'm going to hold onto your comments and try to be as stong post-surgery!
lisa2012 - I hope all went well today with the party!
dianamn - sorry to hear about drain struggles. I hope things clear up soon for you!
teeballmom - good for you about your hair! I don't start chemo for several weeks, but got myself a pre-surgery haircut where I cut off MANY inches. It sure felt liberating. Go get 'em!
soyaandpepper - I'm curious to hear more about your concerns on chemo, and if they have to do with your age. I'm 37 - not much older than you, and was told that because I'm so young, they are going to be very aggressive with my chemo. Wondering if I should be doing more research about the SEs in relation to age?
As for me - had a lovely (although obviously early) date night with my husband and am set to relax tomorrow and spend some quiet time with family on Monday before the big day on Tuesday. Hope you're all feeling well and have a restful evening!
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websister - I missed your post. Good to see you here again. Glad to hear your post-surgery experience hasn't been too bad - all things considered. Keeping my fingers crossed for you on those drains and your post-op pathology report. And thanks for your note about your emotional attachment to your breasts. I think there is something very primal about that nursing connection - and to lose the vehicle of it is sad. But onwards and forward - right! Our children love us for the mom that we are, not for the way we fed them when they first came into this world! And thanks for checking in on the nanny interviews. We met a few possible candidates today and I have a really good feeling about our interview set for tomorrow morning. Rest up and feel good!
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Ramols. - I never thought of myself as strong and was certain I couldn't do this. You sound equally sound and will find the strength In the time that its needed. Thinking of you.
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websister - i just took a peek at your blog and tried to post a response to the "mommy-sat" one, but don't think I accomplished my goal...
Just wanted to tell you I loved your admission in there of getting lost looking at your sons when they talk to you. What a lovely visual. Glad you have so many good men to take care of you right now!
cmartin - thank you. we never really know how strong we are until we need to be. I think Tazzy has a quote like that in her sig line that resonates with me every time i see it
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Thinking of you. Update us when you can.
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Holy cow have I missed A TON! I guess that's what happens when you go all anti-social and get buried in doctor's appointments and 20lbs of literature from the cancer 'goodie' bag.
Casseroles - LOL I made chicken/broccoli/potato/cheese, chicken enchilada casserole, baked penne pasta with sausage & 3 kinds of cheese and good old fashioned mac n cheese.
Since my last check in...I've had a contrast MRI, contrast CT and contrast bone scan - talk about a bunch of very cool pictures. Luckily, cancer is localized in the one twin. LOL I met my Radiation Oncologist, love her! I'm still struggling to get along with my very nice breast surgeon...I get that he's the first contact for the newly diagnosed but I'm not fragile and I certainly don't need to 'go back to medical school'. That's his phrase right before he explains what he's going to do and where in a manner much similar to a kindergarten teacher. I also scheduled my first meeting with the medical oncologist and have already run into a snag. The receptionist stated that the MO won't likely do an oncotype test with me. I'm like WHAT?!?!?! The woman hasn't even seen my file! I haven't even had surgery yet! So I called the surgeon and even he is saying that unless at least 1 sentinel node comes back with cancer, that an oncotypeDX doesn't need to be done and my entire treatment will consist of lumpectomy, 6 weeks RADS and 5 years of tamoxifen.
Does this sound reasonable? Suddenly I'm worrying about the choices I made in chosing my team... is my 'invasive' cancer not so invasive?
And while I'm asking all these questions... LOL Does the dye needle in the nipple hurt? Please tell me they numb me first like they did with the core biopsies. And what about the 'wires' that will be inserted that will flank the tumor, does that hurt? I'm a total bundle of nerves; sleep rarely comes, the nightmares have started and all I want to do is eat sweets! LOL
Okies...stepping down on the rant/soap box
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Good morning
Ramols - glad to hear re: nanny, hope today's interview is all it promises to be. Thanks for your comment about my blog post - I'm sure as Mom's all of us look at our children that way, I do love looking at them and it reminds me of something Maya Angelou once said on Oprah -
'Every child deserves to see their parents eyes light up when they enter the room'. Wishing you well for your surgery.
Firestorm - I know what you mean re: whirlwind of scans, I was thinking I would glow in the dark. Invasive means that the cancer broke through the walls of the duct, not that it has metastasized. What they are proposing sounds reasonable if your sentinel node is clean. Re: concerns about needle in nipple - they have you use Emla cream (a topical anesthetic) prior to the procedure but I can't speak to how it feels as I haven't had one. The wire localizations are easier than the core biopsies, they use local freezing before inserting and then tape them down, a bit of a nuisance to deal with prior to surgery but not bad, I had two prior to my lumpectomies in 2009. Hope you can rest and find some time to enjoy the beautiful summer days before your surgery, glad to hear your scan results were clear. -
jpmomof3-thank you for sharing your DH thoughts with me. What he said makes sense. I know that the tumor shrank a lot with the A/C and was really hard. Now it's bigger again but it's smoother and somewhat squishy if that makes any sense. And strangely it sometimes itches, but can't be scratched.
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Party was fun! dH cooked wonderful food, weather was perfect, I made it through fine, just skipped the family walk after guests had left cuz I had run out of steam. I even had a fresh strawberry daiquiri and a piece if cake- two foods that I have not had in three months.
I was reading these posts and got stuck in teeballmom 's one. Could i have had the oopharectomy and mastectomy at the same surgery in November if my doc had done the MRI sooner? Why look back, I know.
Re oncotype: strange how they do or don't do it. I did have it, with clean nodes. It came back a 38 but confused matters about estrogen positivity. I think if there are other indicators that make it seem like chemo is important, like grade and K167 and shape and such, the onco isn't that helpful. I don't know. And the risks if chemo weren't really discussed with me, more the side effects during. Too late now! Done! -
Firestorm, the dye needles don't hurt. The nurse gave me Emla cream and a Saran like patch to put over the nipple area about 2 hours before the dye is injected. I hardly felt the injections at all, and I'm sensitive. The radiologist numbed the area where the rods would be inserted, and while I wouldn't say I didn't feel it, there was not much pain.
Susannah
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