Starting Chemo February 2009?
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Welcome Bev!!! As Webwriter stated, I just had my last chemo on AC!!!!
Carol0371 --Hope you feel better!!! (((hugs)))
Bev!!! Sorry you had to join us, but you will be comforted, loved, and offered friendship and love from your fellow sisters!!! You're gonna beat this!! What grade/stage/type cancer is it?
Jancie---When you get your Neulasta shot has it been refrigerated? Mine gets refrigerated then administered to me!!
Apple--you could be Webbie's secretary!!!!
Webbie-- you're the best, but all of us women rock, right??? LETS HEAR IT FOR US GIRLS!!!
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Bethie 1 - Yes, they do refrigerate my Nuelasta shot but when they start treatment with the anti-nausea and steroids, at that time they take the shot out of the refrigerator so that it warms up to room temperature and then when the nurse gives it to me she pushes it in ever so slowly. I think this might be the reason I have never had a SE with the neulasta shot and I have never taken Claritan or anything else.
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Just a quick check in, I have GOT to go get Monkey...but I solved the mystery about steroid dosages among our Oncos today!
It's a very simple philosophy difference. I'm swelling like an overfilled water balloon and was convinced at the last to TX's that the Decadron was "expired." I just seemed to be adjusting to it or something. The allergic type reactions just get worse and worse. So anyway, that's how it came up. (See it's working! I'm typing and I can't shut up!)
He's going to change me to the pills before and after. (I still get a "healthy" dose in my IV) The reason he didn't do it before is because steroids (duh) cause side effects of their own. He didn't want to ENSURE those side effects in trying to PREVENT one I might not get. Since I didn't get it until #5, I avoided several extra dosages of them. Now we have to start them, but it's okay. Only one more after today! (Not that I think this is the better way. In fact, I think I might've needed it at least two ago, if no the whole time.)
Point being, that we were right, it IS a personal preference by Onco thing. But it's also nice to know the philosophy behind the preference. Some want to throw everything up front, some want to conserve some. If you ever want to argue for either side with your Onco, you'll likely be successful. Just thought you should know.
and Bethie, you're right. We ALL ROCK! Three Fury Cheers for everyone. (And pass the steroids, I need to get some crap done!)
((Hugs!))
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I thought I would share what the SE specialist said to me today regarding all of my SE's.
She totally understood what a circle jerk situation I was in. Can't sleep - no energy to exercise - gain weight - get depressed - no ambition - tons of fatigue and on and on.
Then I was prescribed Mirtazapine which I was to take 1/2 at night. The drug is normally used for psychotic reasons and depression but taking 1/2 of the dosage it acts as a major sleep aid.
Great - I could finally sleep more than 2-3 hours BUT I was feeling drugged up the entire day to where I didn't want to get out of bed. I just felt hungover all of the time.
So here is what we are doing - I am going to take a full dose (15 mg) of the Mirtazapine so I will get the anti-depressant part of it and also it won't knock me out so bad. I know it sounds weird but the lower of the dose the more it acts as a knock out sleep drug.
On top of that I will take 10 mg of Ritalin in the morning and then another 10 mg at lunch time. That will wake me up out of my induced slumbor, hangover, etc. to where I will actually get out of bed and start going back to a normal routine.
I did tell her that I was aware of the SE of Taxol and that would be happening here in 3 more weeks and we talked about L-glutamine and B6 - she said to take the daily recommended dosage. I told her that I got the info here at BCO - we share all of secrets to dealing with SE's and she laughed and said she had heard of BCO and was happy that I had this support group.
She did say to be careful about taking alternative type medication while on Chemo and I told her that I was aware of this and would not take alternative type medicine until AFTER my conventional treatment was done. She said that she does acupuncture and that she can help me with fatigue once I start radiation so I will probably go for that. She laughed when I told her that my horse get acupuncture about every 4 months.
I am so glad that I got an appointment with this lady. My oncologist recommended that I see her as he could tell how frustrated I was getting.
We talked about my eyes burning but we both know there is really nothing we can do about it.
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Jancie-- great!!! My SE from everything are minimal at best, fatigue and queasy!!!
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Webbie-- here's some virtual steroids--the best I can do for now!!! (((hugs))))) I agree with your opinion about the philosophy drs. use. My onco dr. raises my chemo any needed % based on my bloodwork. If my bloodwork is good, he leaves my chemo alone; if not he raises the chemo. Very conservative, sensible, but he checks which is the RESPONSIBLE thing to do. Good info for all of us to be aware of!!
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Hi Everyone - You ladies are an amazing bunch.
Webwriter - you are too funny!
Kerry - I was really praying that the taxotere was going to give you a break. No such luck. I assume that you have 2 more to go. I spoke to a bc patient that finished her treatments last week. She said that she lost all of her eyebrows but her new ones came in just a couple of days later. Here is hoping we could all be so lucky. I think you are on on the same chemo regime as I am. (3 FEC's and 3 taxotere every 21 days.
Artemsis - I had bilateral mastectomy with immediate reconstruction with saline implants on Dec 23/08. The plastic surgeon told me that it was my only option. Although I have further surgeries; I am happy with the results so far.
I had my mid chemo blood test today. So, I am day 12. My neutrophils were .48. Need to build them up for the final blood test exam on April 2nd. Anyone have any pointers? I am trying to increase my protein intake and am also eating shitake mushrooms.
Take Care Everyone - We are in the middle of a snow storm in Winnipeg.
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Webbie, here I am stressed about taking my major dose of steroids for tomorrow's Taxol, and I read your post. What was I thinking?? This is my chance to get stuff done!!!
Michele, sorry you are still puking. Sending you a Virtual Engraved Golden Bucket with hugs, girlfriend. I wish we could pretend we were on a beach and it would stop, but that doesn't seem to work, does it?
A&D cream (vaseline + lanolin) is wonderful for nether regions, dry skin, and diaper rash.
Apple, love the Bishop & the Boob story.
I too experimented with a DIY set of tatas. Mine were made from the Amoena puffy things they gave me in the hospital and a Walmart Sports bra...but it rode up too much, especially in church it seems. So I went back to Walmart, the fishing aisle (full of men this time of year) and got me some 3/4 oz Lead Sinkers. Poked a couple into each puffy and it helped keep em down somewhat. Felt pretty clever for a few days, till a sinker fell out on the bathroom floor....CLANG.....fortunately only DH was around to hear it.
Artemis, after my first bilat in 2002 I had saline implants which I loved. Comfy, every bra fit, even had a nice lil cleavage. In 2008 found a 2.5 cm lump alongside the implant which is why I'm here now. When they did my 2nd bilat "revision" this January, they discovered a second 5 cm tumor, must have been hidden under the implant. Just something to consider. Personally I'm done with implants; if something grows back I want to see it. I just got fitted for silicon prostheses, and so far I'm happy with them. They seem pretty comfy; the bras are Functional rather than cute but I can live with that. No more cleavage, though... (this requires planning when swimming or bending over).
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Clang ha ha (Sue50)
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Gotta go get my meds and stash myself in the bed. But!
There's a wonderful thread here if you need a laugh. Which I do. Often. It's worth reading the ENTIRE thread, tho it will take about a week. I almost double (triple, since it's also in my blog) posted it here, but thought the better when I realized I had only seen a couple of you on it.
From the great Rock (of RockTheBald fame) I give you: The Road to Hell...Laughter is the Best Medicine. (My Hell Pavement Patch is on page 46--Thanx to Michelle for the correction!)
I swear. You can't make this sh*t up!
(Will post photo proof when I'm through playing with it. I decided to leave it, swap for the right kind and turn it into a game.)
I hope you laugh as hard and Auntie A and I did!
Love,
Web
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Chemo TX #3 tomorrow... a bit of dread tonight. I have to say that I am so glad I am not alone in feeling some of these SEs. I don't want anyone else to feel them, but I felt really alone before I joined this board. I had also had a *lot* of people tell me how much better chemo was and how so and so breezed through it all and hardly missed a day of work and yada yada yada. I was really thinking something must be wrong with me to feel so lousy. And I had five children with nice long labors and no drugs. hmmmm. normally pretty stoic. This stuff is real --yes it is doable, but don't let anyone tell you it is easy!
Bless you all.
My chemo regime:
I hr before CT--oral --2 steroids, 1 benydrll, tylenol, 1 Emend. Just before -some sort of antihistamine by IV.
For 2 Days after chemo 2 steroids twice/ 1 Emend
As needed for breakthrough nausea: Ativan (Lorazipam)/ Compzine (have not taken yet -the side effects sounded horrible to me) I have, however, used the Ativan --especially to get some much needed sleep.
I had a reaction to the Taxotere last time, so they have now prescribed the steroids for the day before, day of, and day after chemo...
My bad SEs for approximately 6 days: constipation (including delicate issues!) and its opposite, chemo farts!, hair loss, joint pain especially knees, 2-4 days of ear-ringing -I *hate* this one -especially since I am a musician, bald and itchy head, depression/fog, chemo brain --this bothers me the most!, fatigue, sore mouth, irritability (husband says!), nothing tasting good, weird cravings, hot flashes, preference for plastic ware over regular silverware, sore nails (but no fallout or blackening), etc...and then the fog lifts, the sun shines, and I return to myself.
My good SEs: heightened appreciation for everyone and everything, life is sweeter. renewed sense of spirituality and purpose, outpouring of love and support from friends (not always the ones I thought would be there!) and family, much more positive overall (although the strong depressive fog/Mack truck after TX#2 really freaked me out...during it, I thought it was forever....when it lifted, I knew immediately it was chemical and short-term -I have asked my husband to remind me if it happens again ...)
Some positive changes I have made:
I send a lot more cards and letters/ little gifts --they have lifted my spirit so much that I must pass it on --and I find doing that lifts my spirit as well.
I am much less mousy about my needs.
I no longer let people dump work on me in the workplace -I make sure it is mine before I take it on. I also freely state my opinion (nicely worded of course). I ask for time off and stay home when I am sick. I take off to attend school events for grandparents.
I quit smoking again -this time for good!
I sought out and started going to a pyschotherapist -figured this was a good time to look at the lack of balance in my life -good stuff!
If I want it or someone I love wants it and I can afford it, I do it. (go to a beautiful place, sign up for a seminar, buy a book, etc...)
I started posting instead of lurking...(it's a metaphor, too.)
Anyone else have some good SEs to share?
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Hey guys - thanks for your kind thoughts over the last couple of days. Man, that Taxatore really knocked me for six. I spent two days in bed, which I have never had to do before - not even after my Surgery! But, yesterday the pain was not nearly as bad and I mostly just slept, and this morning I feel remarkably better, so "knock-on-wood" the worst is over!
I think my biggest problem was not keeping on top of the pain, and it got really bad. Once I started taking the Tylenol #3's I was able to get a handle on it - of course, now I am constipated....so I'm taking pills to take care of the SE's from the pills I am taking to take care of the SE's from the Chemo. Great.
Bev - great to "meet" you again! I'm glad you have joined us. My Onc said about 50% of people get joint pain - fingers crossed it won't hit you as hard. I did use Ice Mitts by the way, and so far so good. If it is any consolation, the chemofog doesn't seem as bad on the Taxatore....My WBC for Tx #3 was 1.65 - I was so worried that it would be too low. For #4 it was 10! The wonder of Steroids.....! I don't know what you can do to raise them, noone seems to think anything helps. I've been eating more meat and fat as I feel better with that anyway.
Sue - love the Sinker Story - now try going through Security at an airport!! I am not going for recon either - I may change my mind in the future, but at the moment I am happy being "half boy" It doesn't look that bad actually. Also still thinking of getting the other one removed.....no-one who has done it seems to regret it. I wish I had thought more about it before my initial Surgery, it wasn't really presented as an option to me and I wish it had been.
datadrudge - Oh, yeah, I have heard all the stories of how so and so "breezed through" Bahh. I can't imagine this is a breeze for anyone. I do think it is a bit like having a baby and labour though - it will not seem as bad when we are looking back. But, as I said to my poor long suffering Husband the other day - It is the least fun I think I have ever had, Ever.
I love your list of "Good" SE's too - I think I will get less upset by other people. It has certainly opened my eyes to what is important in life. I certainly will care a lot less about a lot of things, and a lot more about a few.
Anyhow, I aim to stay awake ALL day today! Hope you all have a good one too.
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hey Web... it is page 46. LOL!
Sue~ I have a removable silicone uniboob. It is pretty comfy. I'm still getting used to putting my boob on in the morning...
Datadrudge~ Love your list... I'm not feeling very positive today (still sick) so I won't be adding to it but I enjoyed reading yours.
Apple~ So how are you doing??
Kerry~ How's the knee pain? Better yet?
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Still feeling good after first Taxol tx. Now if getting my blood thinner levels would just cooperate, I'd be all set. I now have to go in for 2 more blood draws a week to check my coumadin levels, my poor veins can't take it!
I did turn pretty red yesterday in the face/neck. I was glowing. Actually, it was the healthiest I've looked in a while, lol. It went away pretty quickly. Other than that, I've had a slight 'tummy ache' feeling, not nauseous, nothing like on AC.
Judy
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Datadrudge - i really liked the way you summarized your side effects.
as to the sore mouth.. i notice that i sleep with my mouth open. Long term cancer patients often have issues with tooth decay and decline.
so .. i try to avoid sugar, carry toothpicks in my car, floss, brush with baking soda upon occasion, use prevident (a remineralizing toothgel i got from the dentist years ago).. there is a new one out that helps your teeth stay healthy.
nothing really relieves the mouth pain for me, but it sure helps with any sort of craving i might have.
my onc. gave me some hydrocodone.. omgosh.. they help so much. at 52 with arthritis pains, i sail thru my days without pain. those little pills help alot. i am taking 1/3 the daily maximum and still reaping benefit.
it's off to chemo today after i power clean the basement, getting ready for the tax auditor and bookkeeper to come over.
(thank goodness i fired myself from boookkkeeepingg five years ago. i absolutely hate that sort of thing.
have a great day all.
pureed apricots anyone?
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oh yeah..
Wet and Wild a super cheap makeup line has come out with an excellent eyebrow kit - it works SSSOOOOOO well.
2 colors, some 'wax' and an excellent little brush.. it took me a couple times to learn how to apply it sparingly.
i bought two different color schemes, brown and smoky brown.. they were out of the lighter selection.
3.99!
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Well, thats good to know - I am going to be needing it soon!! I've never used any type of eyebrow makeup, but i think I am going to have to learn at this rate!! They are certainly getting sparse....and i have always had such bushy eyebrows. Perhaps as a reward for going through this they will grow back in a nicely shaped arch....!!
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Kerry - like you I have never used eyebrow make up nor do I pluck my eyebrows. I got a kit from the Look Good Feel Good class but I still have my eyebrows and eyelashes.
Ok, what is weird - my hair started falling out 2 days after TX #2 on A/C. I could pull clumps of hair out so I had my head shaved. There was probably about 1/8" of hair left and that hair has NOT come out. Most of my hair in the "southern region" has come out but not all of it. I really figured by now my head would be bald and smooth but instead I have hair left mostly on the top but on the sides it is very sparse. So if that hasn't come out yet does that mean my eyebrows and eyelashes are going to stay in? I go for my last A/C next Wednesday. Now I wish I hadn't buzzed it so close.
I have always seen myself as a very strong person able to deal with whatever hits me in the face. However, when one of my noisy neighbors decided to tell my husband's exwife and his daughter that I had BC I totally lost it. I called her up when I found out at 9:30 pm and chewed her out. This lady used to babysit for the kids when they moved to Utah after being taken away from their mother due to her being a crack w*ore. She KNEW this but didn't think twice of telling them about my personal medical condition, yet NOT ONCE did she call me to ask me how I was doing and believe me I mentioned that several times. My stepdaughter is a juvenile delinquent who has been to juvy court 5 times already in the past 2 years since she decided to run away and go live with mom who sets no rules, no boundaries, no structure and NO consequences. The girl was enticed to live there so she could do as she pleased when she pleased, etc. After spending almost $100K in court to get custody we were going to be dammed if we spent another dime because everytime we said no, she would run to dear mom. BTW, they are quite the pair, they smoke pot together and drink together and have been doing so since the girl turned 14. And I wanted them to know I had BC? Not only that they are both violent and I don't have the energy to defend myself so I am totally expecting them to harrass the crap out of me when my hubby is not around. The girl just went to court this week facing charges of assaulting my husband. She knew about this court date for a month and yet proceeded to get arrested one week before her court hearing for (1) out past curfew - 1:00 am (2) drinking alcohol and; (3) lying about her age to the police officer. Mom of course hid this information from us but we got the call from the probation supervisor. So because we still retain legal physical custody my husband is still responsible for her actions even though she is living with an insane bi-polar mom.
I so don't need that personal stress on top of my BC and neither does my hubby who has been so supportive of me but also is stressed out because he sees his own daughter ending up in adult prison when she is 18.
So trying to find something positive in my life is really hard right now. I wanted to go to the barn and just forget about everything but we have a snow storm today. I am now happy that the specialist yesterday got me on some anti-depressents. Never been depressed in the past even though believe me I have had a life that would cause most people to commit suicide starting from the age of 5 years old. I so don't deserve this crap.
I did manage to take a walk around the block last night in the rain and I am going to go walk over to a friend's house this morning - up that darn hill going there and up another hill coming back. I took my Ritalin so hopefully I will get some energy really soon.
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Jancie - just what you needed - sorry you have to deal with this crap - one positive is you only have one more AC - yeah! This will END! I also still have a fuzzy head (actually prickly) but not enough that the hair would have looked decent - and I still have my brows and lashes - I'm hoping they stay! I also still have to shave my legs - go figure - not as often but they are definitely growing and I actually am kind of happy about it in a weird way! I hope your "new" drug combo works for you too!
Datadrudge - thanks for the good SE list - I have taken off of work during chemo and although it's the crappiest (and only) extended time off from work I have ever had - I am happy to be home for my kids for once in my life - so that's a positive!
Sue - LOL to the sinkers! Sorry you have had to endure this more than once in your lifetime - did you chemo with the first DX?
Webbie - thanks for the steroid/onc info - my onc is definitely conservative - I'm only scheduled for Benadryl with my first Taxol - no steroid - I definitely try the less is more approach - I think the SEs from all of these drugs are worse than the actual SE they trying to mask.
Bethie - yeah no more AC!!!!!!!!!!!!!!!!!!!!!!! I start Taxol on the 31st - I'll keep you posted!
Judy - you rock - I'm so glad you're doing well on the Taxol - hope you can get the rest straightened out too and soon!
Hope everyone has a good day - it's rainy and cold in PA today - it's making me sleepy - well I'm always sleepy but I have an excuse today
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Hi Fabulous Furies- I feel like Kerry Mac--- in pain, tired and find it impossible to function. Stayed in bed and yelled at my family for talking on the phone. Not a good situation. Everyone is very frustrated. i am day 7 of first taxotere and i feel a bit better. Made it to work-sometimes focusing on work and maintaining a semblance of the status quo seems to make it easier
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I'm writing you all from my chemochair Husband is seated beside me. I'm in for a rough week, we've all been there.
I am IMing with my mom from Michigan. The webcam is on so we can talk and see each other. She couldn't be here in person, this is the next best thing.
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Hey Ladies,
I feel a little bit more among the living today. I spent almost the entire day on the couch yesterday feeling miserable! Saw an ENT yesterday for my sinus issues and had a ct scan this morning. He says he doesn't want to treat me for an infection if I don't have one so we'll wait to see what the scan says. Also found out I have a pretty bad deviated septum so my nasal passages and my eyes are all swollen from the congestion, he couldn't even get a scope up my nose! This morning at my weekly Onc. I sat in the waiting room waiting for my doctor to come in and give me bad news on my tumor markers... turns out it takes 2 days for the results to come back, which I didn't know. Anyway... he didn't seem "too" concerned that the # spiked 2 weeks ago, he says he doesn't know why but he see's tumor marker #'s go up during treatment. So if he's not too concerned with it now, I won't be either. Won't know this week's # until my next appointment in 2 weeks. So Monday I go for my radiation simulation... ah to begin the next step. Also Onc. says he wants me to keep the port in until radiation is done and I get restaged. I was kinda looking forward to getting this thing out... I feel like it's bad karma to keep it in even though I did my last chemo.
Kerry and Jess-I hope your next Taxotere treats you a little better. Maybe the first one for u will be the hardest as your system adjusts.
Feel good everyone!
Sue
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Hey Sue - I have been wondering how it went for you today. Glad your Onc isn't too concerned. I always feel better after seeing mine, as she is always so upbeat. And really, I think you will find it was just the chemo messing with it. Let us know how the Rad Simulation goes - when are you set to begin? I should be starting mine in June....
Cheryl - how cool you have your Webcam on while getting Chemo! I get so grumpy sitting there, I'm not sure I am fit for anyone to view me.
Jess - yep, I'm day 7 out too, and still only feeling half normal. But hey, at least today I am out of bed! I didn't think it would do this to me.... I've also lost my appetite and I'm finding it an effort to eat, my mouth is sore too. I moan, I complain, blah, blah, blah!!!!
So, who else is counting the "sleeps" until this is done...?
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Sue - I was just looking through your Blog. Great to read your story. My daughters Birthday is Dec 13th too - and I had my surgery two days before. LOL!
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"I can totally relate to wanting to feel Normal AND with squishy boobies too! ... I have been fighting the depression lately since the last AC treatment has made me a couch pillow - literally I cannot do anything but stare at the TV and eat salty carbs - so I feel tired, fat and ugly!" terri, thanks for saying that. I'm not happy that you're blue and blobby-feeling like me, and I know everyone in here is feeling some form of it, but sometimes I just need to hear it ... or read it, ya know?
webbie, thanks for your kind words too. you are such a luv.
Hello and welcome to bev - sorry you have to be here, but glad you found us.
Sue, I've read up on the Oncotype dx test and I can totally sympathize with your fears. i'm glad your onc isn't worried. i hope you start to feel better soon sooner soonest ... Keep your chin up, honey.
Judy, I'm so sorry to hear you've been so sick, on top of everything else, but yay for being done with AC! Sending you all the good vibes in the world, my dear.
Bethie, congrats for making it thru the AC too!
Michele, sometimes my pee is warm, and things are definitely ... different ... in my nether regions. More sensitive, maybe.but that's about it. I'm sorry you're suffering from yet another horrific SE.
Kerry, maybe you passed out from the pain meds? Vicodan/ hydrocodone does that to me (along with making me nauseous, yay.) I bet my onc will tell me to take Tylenol if I have pain with the taxotere. I think if I came in with a bleeding artery, he'd tell me to take Tylenol. *severe rolling of eyes*
BCPrego2008, I can't imagine having to take care of a newborn while on chemo. You get the superhero cape, fershure. At least you have your little antidepressant helping you make it thru. You must get your strength from just looking at her adorable little face. i finally got to meet my new little niece last weekend, and it definately lifted my saggy spirits.
Datadrudge, good SE's ... what a great concept! And megacongrats on quitting smoking!
Jancie, you so don't need that dramarama. Here's hoping your stupid inconsiderate neighbor will soon find out that karma's a bitch.
Artemis, I had to make my decision in a matter of a week. I still can't believe I didn't have a nervous breakdown. (sometimes I think my breakdown is on the horizon. Like, when I'm done with treatment and I have the energy to have a breakdown. *weak laugh*) I opted for a bilateral mastectomy with immediate reconstruction (tissue expanders) - please feel free to PM me and we can "chat" about it in depth, if you'd like. i can't say I'm happy living with the expanders, I CANNOT WAIT TO HAVE MY EXCHANGE SURGERY, but I would definitely make the same decision.
All this T-pain - yikes! Seems like this is a standard SE...?*fret*
Lisa's hair report: Scalp: still a lot of strands, no more falling out. Eyebrows: intact Eyelashes: intact. Underarms: still have to shave every 7-10 days, but only for a few hairs. Legs: stubble every week, could do without shaving, but sometimes I just like to find excuses for a shower lasting more than 3 minutes, hee! Nether regions: a little sparser.
I met the radiologist onc yesterday, but I wasn't impressed. He recommends 6 weeks of treatment, 5 days a week. He said tomotherapy is new, but it's more precise and has less SE. again ... he's one of the top area docs, he must know what he's doing. But ... eh. I don't feel up to getting a second opinion or researching. the center is at my medical practice, close to home and work, I can go in early and be at work by 10 am or so ... but I'm leery that he is just pigeon-holing me into the regular old breast cancer adjunctive therapy compartment. I went along with it for the chemo, even tho I'm cancer-free. But this time, I may balk. Depends on what ALL of my doctors say. Especially my breast surgeon, who I see on 4/20.
Maybe I have a ‘tude about it cuz he said I would need to wait SIX MONTHS after radiation for my exchange surgery! The very thought of waiting that long makes me want to crawl into a hole and die. There's NO WAY I'm waiting that long, dammit.
*in thru the nose, out thru the mouth, in thru the nose, out thru the mouth...*
(((everyone)))
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Kerry-December 13th, what a nice day:-) Yeah, having a birthday party 2 days after you have your boobs removed was an experience, but thank goodness for family support! So I was coming home from the hospital when you were going in!
I should start my rads somewhere around mid-April or so. I'll keep u posted.
Lisa-I have to wait about 6 months for my exchange too! But I'm ok with it, cause I want to do it the right way. I had my last fill on Friday, I'm a little uncomfortable cause these foobs are hard as turtle shells! But like everything else I'll get used to it. All my docs say it's better to wait until after rads for the exchange. I'd rather be on the safe side and heal well first!
Sue
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I see things are back to normal around here! (See Bev! Oh, and when did you start? I'll get you on the list. Anyone Missing! Drop me a line with corrections, updates or chemobrain farts!) I can't keep up again!
Thanx for the correction Michelle! I have an empty (picnic style) ketchup bottle in the bathroom. I fill it with warmish water as needed for nether region cleaning and pain. And yeah, flushable wipes by the dozen.
Housekeeping didn't make it in today. Gotta go see if I'm feeling well enough to run the vac. I'm astonishingly un-sick today. Whatever it is, (more steroids?) I hope it doesn't give anytime soon!
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Terri ~ I don't know if I'll be having radiation or not. If I do, I can still get expanders with my bi lat, but will have to put off having them filled...is that right? Or not?
And I'm no longer feeling all that great with Taxol. I'm so tired now, my joints are aching, and I have little muscle spasms. I just keep telling myself, "Three more to go, three more to go..."
Jamieh ~ I'm not really counting down, but I do have a big calendar on which I mark off the days since starting chemo. It's great to see all the red X's to show how far I've come!
Jancie ~ lumpectomy isn't an option for me. I actually have 3 tumors that need to come out even though 2 are benign; there will be hardly any breast left after that. There are three "questionable cysts" in the other breast, so we're doing bi lat so that I (hopefully) won't have to go through this again.
Beverly, sue50, Lisa810 ~ thanks for your input on implants. I'm really thinking that's the way I'm going to end up going.
Sue50 ~ am I understanding that you had a bi lat and then had another?! Yikes!
Jancie ~ I'm so very, very sorry about your neighbor, step-daughter and the ex-wife. What a mess, and just what you DON'T need right now! *hugs*Hugs to all,
Artemis -
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tres cool! Webbie
i hope my kids don't see that pic.
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