Starting Chemo April 2009
Comments
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Happy Birthday Lena!!!!!
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Happy Birthday, Lena. You have no expiration date so I am wishing you many, many more happy birthdays
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Happy Birthday Lena! Well said Helen! Wishing you many happy returns!
Hope everyone has a good weekend, hugs to one and all, Judy x
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Happy Birthday, Lena. I am going to a party tomorrow and have to bring a dessert so I am making a CHEESECAKE in honor of you! I will think of you as I eat my slice!!
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OK got a question for you all here....
I just got back from a walk to the pharmacy to pick up my Lunesta and some contact lens wetting solution, and, as I walked home, I saw this young guy walking his dog. He was wearing shorts but no shirt. But we all know why men can do that but women can't (unless they go to a nudist camp or get a job in Hooter's maybe?) -- because of their BREASTS.
Well now that I don't have any breasts, I wonder if I'd be "allowed" to go out wearing ONLY shorts or ONLY a pair of jeans? Not that I'd actually do it or anything, certainly not now with the still a bit too much Frankenstein chest, but after that all heals.....? Gosh THAT could be a real trip -- IF by that time I learn to get used to my new body, anyway. Nope, I'm still not used to it, still feeling condemned to black and dark colored tops because that HIDES my totally flat chest (which my Pack Rat actually TOLD me he hoped I'd get used to, so maybe I'll show it to him this weekend...er MAYBE). But maybe someday, if I live long enough. I used to love to start up a good shocking ruckus back in the day......
Gardening: Canteloupe and zinnias are way in the lead, but some of everything I planted is growing at least. So the cherry tomatoes will be planted on schedule this weekend.
And yesterday we had one of "those" kinds of downpours -- the heavy downpour on a day when the temperature is at least 80 -- a carwash downpour -- only I had to "waste" it, because of the thunder and lightning (so bad I shut down my entire Network). Oh well. Maybe next time.
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Hi, everyone! Lena, so good to see you back on the boards and glad you are recovering from the BMX and all of the after-surgery "stuff". I had rads in May-June of 2009 after the chemo, and after the horrors I suffered with chemo and all of the side effects for the side effects, rads was a walk in the park! I was vigilant with my skin, keeping it well moisturized with everything they recommended and it held up really well, just got very dark at the end, which faded eventually. I did notice a bit of fatigue, again, towards the end (I had 33 tx, one daily - to the breast, and lymph area where they did the sentinel node biopsy). the fatigue wasn't too bad, I was just a bit more tired in the afternoon (I had mine at around 4 pm each day, so I could work and then get zapped and head home to rest).
Happy summer to everyone - hope you are all doing well. Had my mammo/ultrasound and all is clear, and a follow up with bs gave me an all clear for the next 6 months. Follow up with onc next month and seem to be doing okay with the tamox, but I know she is going to want to put me on an AI soon and I will not do it. either I will stay on tamox or go without, but I tried every AI and for me, they were terrible. The pain and fatigue were just like with the Neulasta (I saw a few comments a few pages back about that) and I felt like I was a cranky 80 year old instead of a cranky 48 year old.
I also get some post-traumatic flashbacks, especially from chemo time, if I smell a certain smell, or eat something I could only eat during chemo. and, I gave away all of the tops I wore post surgery, too traumatic to have them. And of course, i still have minor freak outs about weird pains, symptoms, etc.
Been busy traveling for work - any of you on FB see my frequent conference updates. Just came back from Naples, FL - 5 day conference that actually allowed for half day sessions, so we could lounge by the pool. I brought my husband and we made a little vacay out of it - it was heaven, relaxing by the pool, actually sitting motionless or floating when it got too hot (90+ in Naples this time of year). Before that was Boston, which would have been nice, except I was recovering from that flu/upper respiratory/eye infection/incredible body aches thing going around and it was cold and rainy during my trip. anyone who has rain, please send it down to my area of South Florida - we are in an "exceptional" drought and praying for rain before our beautiful lawn/trees/flowers go away.
Wishing everyone a great weekend - we're not doing much, still kind of in that vacation state of mind.
Michele
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Amy, you MADE cheesecake? WOW! How did it turn out?
Michele!! If Tamoxifen is still working for you and you're not developing serious problems, stay on it! Even if you and your doctors "got it all" between your surgery, chemo and rads and you're taking whatever kind of hormonal treatment to PREVENT RECURRENCE, I can tell you this. It stands to reason that if Tamoxifen can keep a Stage IV patient with considerable tumor burden STABLE (me, for instance), it's probably reasonable to say it will likely keep a cancer-free patient with NED (you, for instance?) from recurring. I was on Tamoxifen for 5 months after I finished chemo, and it kept me stable. Not only did it keep me stable -- my tumors did not grow and my bone met became slightly less active, but I HAD NO PERCEPTIBLE SIDE EFFECTS from it. Alas, the key word was "perceptible" -- my oncologist found that goddamn deep vein thrombosis on one of my scans (which I had no idea about till he told me: it was totally asymptomatic and STILL is), and Tamoxifen DOES increase the likelihood of blood clots -- so that's why he took me off the Tamoxifen, started having me treated for the blood clot and gave me a prescription for Femara. And there I took that horrible turn onto the Aromatase Inhibitor Boulevard and got lost for a year.
You're right, Michele, you do NOT want to be on AIs with those SEs! I had 'em too, I have tried ALL the AIs -- Femara, Aromasin and Arimidex, in that order, and THEY WERE ALL EQUALLY TERRIBLE. Yes, they kept me stable for a year (the Arimidex failed a few weeks before my spring 2011 scan though, hence the wakeup of my original tumor, a tumor in my other breast, and the little crop of skin mets), but between the chemo and AIs I lost two years of life which was WORTH living. And yes indeed -- feeling like a cranky 80 year old instead of a cranky 48 year old -- I was 48 when I started Femara -- that's EXACTLY HOW I FELT!! -- on ALL the AIs!
Ahhh, OK -- so if I try to have Afternoon Rads I won't be tired in the daytime? (Hmmm, maybe I won't need to take sleeping pills anymore either?) I think maybe I could live with that. Will also keep the skin moisturizer thing in mind. I'm still waiting to be set up with the radiation oncologist, so I still don't know yet when my rads start or how much I'll have to have. I have the feeling now that Dr. R (surgeon) and Dr. C (oncologist) are probably conspiring together, plotting and scheming. I mean, now that the Lab Rat has somehow barely managed to survive being systematically poisoned for two years with toxic chemicals and hormone deprivation and subsequently dissected, let's see what radiation on top of all that will do?
SQUEEEEEEEEEEEEEK! Maybe it's time to bite the mad scientists, before it's time for the necropsy. LOL
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Chelev - good to hear from you! I totally get the post traumatic flashbacks - especially with smells and food. Some days it is worse than others, but still definitely a big part of my life. Sounds like you and your husband had a good break.
Lena - I enjoy your posts, they always give me something to think about. You know, I have no idea if I would walk down the street with no top on, even though I don't have breasts. I am not sure I would have done before - but definitely something to think about.
I am feeling very tired at the moment, a lot of stressful stuff going on with the move, but on the whole I am doing ok.Titan - it has been a while, I hope everything is ok with you.
Hugs to one and all, Judy x
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Hi everyone. Just popping in for a moment. Michele, great to hear from you. Lena, I also love your posts - full of amazing information and thoughts - I once went on a nude beach - in Guadeloupe when I was 28 years old. I was at a Club Med with my then husband. For sure I would not go topless now - I don't even look at myself if I can avoid it. I am learning about the micro fat grafting or lipofilling, where they can give you new breasts by liposuctioning the fat from elsewhere and implanting to create breasts. No major surgery. Has anyone investigated that?
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Wow, Helen, no, I never heard of the micro fat grafting to make new breasts. Too late for me now on that one though -- I lost all my excess weight so there's nothing left to make breasts out of anymore...not even if I eat a slice of cheesecake (with a chocolate rat cookie) each and every day for the rest of this week. Which I'm going to be doing.
Ohhhhhhh Did I just say CHEESECAKE?????????
OMG YUMMMMMMMMMMMMMM!!!!!!!!!!!! My Pack Rat came over with the birthday cheesecake last night, which had a surprise trim of chocolate cookie rats surrounding the cheesecake on the platter. They had almonds for ears, twizzie stick pieces for tails and so on: totally edible but so cute I felt bad about eating them, but can't help it, they smelled so good so I ate one, it tasted as good as it smelled and looked, so now I'll have to eat all of 'em. And since I so rarely WANT to eat chocolate, you know THESE are GOOOOOOD!
The cheesecake was totally TO DIE FOR!!!!!!!!! My Pack Rat was shocked while I ate it, he said I sounded like I get when I'm sexually aroused and was seriously wondering if cheesecake was an aphrodisiac! Yeah he actually asked me if cheesecake made me horny! LOL It doesn't, but the last time I had cheesecake THIS GOOD was a number of years ago on one of my very rare "fancy restaurant" dining out occasions...some Italian place, I don't even remember the name of it. But THIS cheesecake was EQUALLY WONDERFUL as the fancy expensive restaurant's. I knew she was a good baker (my Pack Rat's cousin's wife), but I never had her cheesecake; I don't even know if she's ever even MADE cheesecake before, but it wouldn't surprise me if this was her first one. The woman is a freakin' FOOD WHIZ, for both cooking regular meals and baking all kinds of desserts. I've had various of her cookies, plus pie, brownies, carrot cake, "orangies," banana bread and fresh baked bread too. So what happened was my Pack Rat asked her what went into a cheesecake, she told him, he bought it all and she turned it into a cheesecake and came up with the little rat cookie idea herself. So last night we each had a slice of cheesecake (mine was bigger LOL) and a chocolate rat cookie, and I am going to RELISH a slice of that cheesecake and a chocolate rat cookie EVERY SINGLE DAY THIS WEEK!!
Oh, and he also gave me a 750 GB portable HD, too. OMG. Not only will I be able to carry the content of ALL my computers around with me to access on the iBook, I'll be able to use those 250 GB drives I'd bought for the Quicksilver for the Music Project (digitizing my whole music collection of records and tapes to MP3s.).
Pasteurella's is almost ready to be painted (just one more round of caulk and some sanding), too, plus, of course, the decorative stuff.
I think it was the wine but something made me "brave" enough to show the Frankenstein Chest to my Pack Rat after doing my evening round of PT exercises, which I showed him prior to taking my shirt off and showing him the Chest. It shocked the crap out of him -- he said he'd pretty much known what to expect, only mine was much BETTER than he expected to see! :-O OMG. He said the surgeon did such an extra fabulous job I ought to profusely compliment her -- a FEW times, not just once.Then he also complimented ME on having such a sleek and streamlined body. He actually still thinks I'm sexy to LOOK at! :-O And now that my shirt was off, he stripped me the rest of the way naked with his TEETH! (yeah, he did). No time to turn off the light, so this was the first time we did it with the light on in what, almost two years?! He even says I look UNIQUE now and he thinks my body is in better shape now than it was when he met me! So okay, I actually got inspired to do something I was originally thinking that post-BMX I probably wouldn't ever want to do again, even in the dark: jump his bones and ravish him.
Oh....and that business I had for my first two weeks after surgery with that difficulty opening my mouth/painful clicking jaw -- not only is it all gone now, it passed the final test. See, I didn't eat JUST cheesecake and a chocolate rat cookie for dessert last night..... ;-)
(well hey, he made me explode a FEW times, so I say he DESERVED to be eaten alive, raped and pillaged! LOL)
OK, I got some Sims modding stuff to do.....catch you next time....
I'm probably going to need a nap later..........
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Helen, I completely understand you and also find it hard to look at myself. The implants sound interesting, I am going to see if I can find out anything about it.
Hope everyone is doing ok today. Hugs to all, Judy xxx
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Lena - I'm just speechless
. You often have that effect on me after reading one of your posts...lol. I saw the movie Bridesmaid on Saturday, which was really funny, but also way more explicit than I expected, and guess who I thought of while watching it - - none other than our Lena and her Pack Rat!
Everyone have a good week
Geri
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Lena, I love your posts. Glad that there's lots of good lovin in your life. Read the threads on bco about micro fat grafting. Sounds good
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Hi Everyone! I'm here and I'm fine..glad you guys are too! Actually LMAO at Lena's posts of her and Mr PR...maybe I should have my DH read some of these posts..ha ha..if he only knew!
Been way to busy..but shouldn't have stayed away this long..with weddings going on (we have like 5 in 4 months), wedding plannings, working (when i can fit it in)..plus my son transferring to OSU this fall..we have been busy...
Sorry I haven't posted but I think of you guys all the time...hope everyone is doing well....you all seem to be...good to see.
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Titan, thanks for coming by and it is great that you are so busy with all the good stuff! Long may it last!
Hope everyone is well, hugs to one and all, Judy x
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Good to hear from you Titan, and glad you are so busy with "good stuff"
Lena - I saw a commercial on cable tv tonight for "Pack Rat Storage Bins" - made me smile
Hope everyone is having a good week!
Geri
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Hi all,
I've been dealing with a flare up of lymphedema due to a rose bush poke. I'm back on antibiotics too. My arm, chest and back swelled up. Pulled a muscle in my neck when drying off after a shower. Man sometimes this new normal really sucks. Lena...I believe all the LE is due to rads. Although mine was focused on my nodes, as only two were removed during surgery, the flash path report showed no cancer. Post surgery it came back with cancer and so the rads main goal was to fry my nodes...well they did a good job of it. I did ok with energy going through rads but I got burnt to a crisp...actually my skin turned black and my surgery scar totally fell off. Most drs can't find where the surgery site was, they always say oh there...I say no that's where the cosmetic portion was then I have to point to the scar. Actually, I guess that's a good thing I can say about rads. The worst part of rads was the daily trips to the drs. It was a pretty easy process until the last two weeks for me too. BTW I was the only one on the rads board that had super bad burning. I'm I recalling this correctly Titan?
Today my rose bush poke blistered up so I had to call the doctor, I think it might be an allergic reaction to the topical antibiotics.
I'm feeling tired again. My assistant starts her sabbatical tomorrow (3 mos) so my work load is doubled. If I can make it through mid July (our busy time) I will be fine. Oh well...not much I can do about it. It doesn't help that I have a cold on top of everything.
I hope everyone is doing ok. I'm glad to hear somewhere in this world the weather is good. Spring has yet to start here in Oregon. Did someone say summer is suppose to be starting soon? We are going from winter to summer if it ever happens. I'm sick of rain and wearing coats.
Sorry I'm a little cranky tonight.
Hugs to all.
Betsy
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Oh Betsy I'm sorry the le has flamed up again. It does suck. Sounds like life is stressful for you right now and I agree this new normal isn't fun. I hope you feel better soon
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I went up to see my parents in NYC for the last 2 days. Really good time with them, but I could not WAIT to be home in my nice quiet neighborhood. New York is SO overstimulating. So much noise, crowds, traffic. I cannot imagine dealing with that all the time.
Yes, Lena - I made the cheesecake. it really isn't a hard thing to make if you have the necessary tools (heavy duty mixer, springform pan). I love to bake but we do not need the treats in the house, so I usually bake something fancy when we go somewhere, so I get the fun of doing it, and get to eat ONE piece, and then it all gets eaten by OTHER PEOPLE! It's a good system.
I was REALLY tired when I got home last night.
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Betsy - so sorry to hear that you are having a hard time at the moment, it always seems to come at once doesn't it? I hope you feel better soon and that you get some sunshine in Oregon too! In the meantime, I am sending you (((((Hugs))))). I also hope that work doesn't become too much for you either.
Amy - glad you had a good trip, I love NY - very busy and noisy, but I just love it. Not sure I could live there though. Hope you are resting up from your trip.
We are very busy here with the sorting and packing which takes both a physical and emotional toll on me and last night I had a particularly bad night, very restless, it was like every time I thought about something I needed to do, I woke up! Hope tonight will be better.
Hope everyone is having a good week, take care, Judy x
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That sucks about the lymphedema, and being exhausted, Betsy. Ummmmmmm thanks for the warning about rads too, I think..... :-P I'm hoping that the "what to expect/most likely side effects" parts of the talks I had with the nurse and radiation oncologist I saw today are more in line with how I'll react to rads, than how YOU did (lymphedema was not even mentioned). I guess that's because my nodes were NOT EVEN TOUCHED while I was having my BMX, and, I'm not getting the rads in the armpits. I'm getting them on my chest (where my breasts used to be), that right ribcage area where I had the skin mets taken off, and the very lowest part of my neck.
Yeah I'm a little surprised on how much of my body is getting them -- I thought originally it was just going to be where the skin mets were, but...oh well, and I am doing this WHY?!
I'm recovering at a normal rate with regards to my current range of motion in terms of 4 weeks post-BMX (tomorrow), but now I have to RUSH it! As in MORE exercises to do at home, PT TWICE a week for the next couple weeks instead of once a week! I have two doctors (my oncologist and surgeon) who, if matters could have only proceeded 100% to THEIR plans -- would have both dragged me kicking and screaming into the radiation chamber THIS week! And why didn't they? Because I'm still not able to lie down and even GET my arms over my head, much less be able to hold them up that way for however long it takes to do the simulations or getting the rads. Hence the rush! They want me physically ready to have simulation on July 1st so I can get rads ASAP. Dose: 33 total (28 regular, 5 booster).
Oh this is going to be fun.... ---NOT--- ....and I'm doing this WHY?!
Nope Amy, I don't have the necessary baking equipment to make cheesecake. Probably just as well -- that is NOT something I need to have in the house at any other time than around my birthday. I'm glad you survived NYC. The crowds and noise and traffic are precisely why I refused to go there in the last 12 years (ever since my divorce which meant no more being dragged there by the husband) -- even though I lived "only" 20 mins away by train. And I'll just BET you were exhausted when you got back from that place.
Judy -- last summer I was where you are now -- organizing and packing up for a big move. Not as big as yours, but big. And yes it WAS exhausting and overwhelming.
Geri, yeah I've heard of the Pack Rat Storage Bins. There's even a moving company called Pack Rat. LOL
Titan it's actually good you have a life and don't have to come here much! LOL
Hope you're doing OK, Helen.
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Lena - good to hear that you are recovering at a normal rate. I found the PT really helpful after my BMX.
Hope everyone has a good weekend and is doing ok. Sending you all hugs, Judy x
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Judy - please post some details about your move. When do you leave and where are you settling when you go back home? Same place you lived before? Do you have a house there waiting for you? Is it your husband's job that is responsible for the move?
And for your children - are they bilingual and can do school in either language? Are they excited about going back or sad to go? It must've been quite an experience for them to have a few years here.Sorry for so many questions and I hope none are too personal. But it is such a long time that we know each other, I would love to get some background on your big adventure.
And...my sympathies re the packing. We had some painting done this week and had to empty a large # of closets. The house LOOKS like we are moving even though we aren't! It is total disarray and I can't wait to have everything back in order. So even though it is a MUCH smaller scale, I appreciate a little bit what you are facing.
Amy
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Speaking of "the house is chaos"....Amy and Judy -- I'm not moving now, and the only painting soon to happen here is on the porch, so there won't be much disarray from that at all, BUT --
Remember when I mentioned that during the week preceding my BMX I moved a lot of my stuff (core canned and dry foods; pots and pans) out of cabinets and on to the kitchen table so I'd be able to get at it before my ROM recovered? Well herein lies a tale...
Yesterday I lost my mind looking for an orange (purchased on Tuesday, at one of the med center's little food places) I still can't find. Do NOT ask why or how it ever ended up upstairs, but it did, and I kept meaning to bring it down and put in the fruit bowl on the kitchen table, but have totally NO recollection of having done so. I DISTINCTLY recall picking it up "on my way downstairs" but never making it downstairs, putting it down again on my bedroom dresser, the bathroom windowsill -- and forgetting about it when I actually did go downstairs. On my way home from the radiation oncologist yesterday I stopped at the little store to buy some more fresh fruit (including oranges) and salad veggies, and when I got home -- after 2-something PM since I also had to go to the library to make copies of my thrombophilia panel from last year; onc and I discussed it Weds and I said I'd send it: 3 copies -- one for her, one for the hematologist I'm supposed to see in August, and one for my PCP -- I was totally famished, and decided to make a fresh fruit salad. Immediately I though of "that" orange which I "knew" was "upstairs somewhere." So I go upstairs to get it; I want to eat "that" orange first, and I always include an orange in my fruit salad.
Not only did I NOT find the orange in ANY of the places I remember having had it, but I couldn't find it anywhere else in the whole friggin' HOUSE!!!!!!!!! GRRRRR!!!! After half an hour or so searching and repeatedly searching not only just the places I remembered having it, I also looked in "stupid" places cause I must have obviously done something stupid with it! Now yes, this place is bigger than my old place was, but it's not REALLY big either! I could NOT find it no matter where and how many friggin' times I looked, and right now I'm getting almost as mad telling this story as I did yesterday afternoon while it was happening. Well, once I got pissed to the point where I was hurling all kinds of profane self-abusive verbiage at myself -- I mean for crying out loud it's 2 goddamn YEARS PFC and I'm off the AIs for almost 2 months, what's my frickin excuse NOW except REALLY being a total fucking idiot!! What is this crap is this already?! -- and physically throwing things I gave up and used one of the new oranges to make the fruit salad.
Not only is this orange STILL missing (GRRRRRRRRRR! >:-{ ), later on -- dinner time, I had another problem -- I couldn't find the vinegar to put on my green salad! No, I didn't take this upstairs -- hahaha, and I did find it -- after 10 minutes, of looking on that goddamn overloaded impossible to organize chaos on the kitchen table I haven't been able to eat on in what is now almost a month. And I realize how much that's been driving me crazy the past week or so -- that, and I can't REALLY clean the kitchen unless I get all that stuff on the table put away, and the kitchen now REALLY HAS TO be cleaned totally not JUST for aesthetics/basic sanitary reasons/not letting it degenerate to the point I won't be physically able to do it, but also so I can set the ant traps I bought 2 weeks ago!
AAAAAAAAARGH!!!!!!!!!!!!
Well that's it, I don't frickin care anymore -- the chaos has to STOP NOW. I gotta eat lunch first, but today I'm going to put all that stuff on the table back in the cabinets and if I can't reach some of it, I'll get more exercise by dragging a chair over to stand on.
I hope that orange turns up before there's a trail of fruit flies to help me find it......
:-{
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Lena...could you have possibly eaten the orange and not remembered doing so! Sounds like something I would do.
Remember how many times I said I re-organized when I moved back into my existing kitchen. It takes time...pace yourself. Good luck on your new project.
I know you will fare much better than I did in rads, they really aren't bad but you will get tired. The rads themselves is way easier than the simulation. So don't panic.
Well my arm just started healing a bit this weekend. Pretty much daily the blisters pop then immediately fill up with fluid again. My arm has definitely swelled more than normal. I'm back to MLD (manual lymph drainage) daily and wearing my waffle iron pad at night. My dh talked me into using a sling yesterday to keep it elevated so the lymph fluid couldn't get to my wound. It made sense and even thought I was skeptical I'm happy to report it WORKED! Today is the first morning my skin isn't stretched so tight I thought it would pop. So I'm going to continue it today. I just need to go back to the pt exercises as I don't want my shoulder to seize up again for lack of motion.
Well we got one day of spring on Friday. It was beautiful but yesterday it rained all day again. My furnace is still kicking on every morning. Friday's weather lightened my spirits.
Wishing you all a good week.
Betsy
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Hey Lena, losing the orange sounds like something i would do. It is so frustrating. I don't know whether it's old age, chemotherapy brain or just stupidity but this happens to me frequently
Judy, it's such a big move you are making. I have the same questions as Amy. I do hope the move won't be too stressful for you and the family -
Well, the orange STILL hasn't turned up. I DID consider the idea that maybe I'd eaten it and forgotten that I'd eaten it -- while actually looking for it when I first noticed it missing. However, I dismissed it because that particular morning I'd had eggs and garlic roasted potatoes for breakfast with my Pack Rat, and when I eat the garlic potatoes, I don't eat an orange or any other fruit like I do with the lighter breakfasts I normally eat; egg and garlic potatoes (which I make special for my Pack Rat sometimes) is a heavy enough "stick with you" kind of breakfast so I don't "need" a piece of fruit too.
OMG Betsy! That lymphedema business sounds even worse than I figured it was. YUUUUCK, blisters? And how do you FUNCTION?
Hey Helen, don't you have some kind of party coming up soon? Your retirement party, right?
And in other news....I went for a walk yesterday afternoon. All was well until I got to the area by the water about three quarters of a mile from the house. Some people were there fishing (not unusual) -- but suddenly I notice I'm being stared at, by ALL of them, in this "OMG" kind of way. First thing I'm wondering is oh wow do I have a booger hanging out of my nose or something? And then I realize it's gotta be my COMPLETELY FLAT CHEST -- no I didn't have any boogers, I was wearing pants and a T-shirt, and even if I don't LIKE my hair this way, it's definitely "normal" (albeit for someone ELSE LOL). I mention that because other than The Chest, there was nothing odd or unusual about my appearance, and I'd recently had a shower, so I didn't smell bad or anything. If I said I was getting better on the body image issue, I think I spoke too soon, because I was so embarrassed I wanted to die.
:::::sigh:::::
I think most of my ROM is back, though some things still hurt to do (i.e., the newer exercises the therapist gave me last time). Today I seemed to have both enough ROM and enough energy to (FINALLY) clean the whole house top to bottom -- one of the good thorough "once a month" cleanings, which it was time for, especially since I skipped all the weekly smaller cleanings this time because of the surgery...but yeah it wiped me out. It's a beautiful day for a walk but I'm too tired to go in addition to still feeling embarrassed when I think of yesterday. At least I have a clean house to sit around in feeling sorry for myself now.
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You guys are busy...Judy..I know that you are going back to Israel..I just wish we could have met you in person..I know we can talk here just as well but dang..
Ha ha Lena..that I have a life...I guess I am busy with the daughter's wedding, working , having my son home for the summer...etc, etc...there just don't seem to be enough hours in a day to get things done and still have time for ME...and that is when I can come on here..the ME time.
Oh Betsy..the wedding is Oct 1...and the invitation is still open to anyone that feels like coming to Ohio....we have a block of hotel rooms reserved....you can party with the kids late at night if you want to..ha ha.
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Lena, I know several women who go flat and feel very comfortable - in fact they like it. I admit, I can't do it and still have serious body image problems. Everyone is different. Anyone who would be staring at you is an idiot! Retirement party is this Wednesday. I have no idea if anyone is even coming. The flyer goes out to everyone and people can choose to attend or not. I expect there'll be up to 50 people although I know the organizers are hoping for more. But the good news is that donations are almost $1,700 so far
Titan, seems that you are very busy. But at least it's with good stuff
Just, when is your moving date? -
Hi everyone, I am sorry that I have not been by, I am really busy packing up and we have the shippers coming tomorrow and then we move out on Friday. Thank you for all of your interest, we are all finding it very stressful and the kids have mixed feelings. My youngest son (9), is very sad because he only really remembers being here. I think it is going to be hard for all of us.
We are looking for a new place to live at the moment, which is not so easy from this distance, but we have friends looking too.
So, I hope to be able to come by from time to time over the next few weeks.
Sending you all hugs and thanks for your support! At least I don't have to say "goodbye" to you all, because I can come and talk to you anytime
!
Have a great day, Judy x
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- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team