January 2013 chemo group
Comments
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Re: hair loss... Most of mine came out an Saturday. I shaved the rest as close as I could and then put a little cotton sleeping hat (skull cap) on it and forgot about it. The rest has been slowly coming out without me even noticing. I wore my "dress up" wig out to a party with friends on Saturday night and they really liked it...in fact one of the men must have told me 5 times how much he liked my look! And he meant it....hummmmm I knew I had bad hair, but really? Was it that bad??? Anyway, my wigs are my new best friends hahah...
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I'm feeling like that guy with the (really) bad comb-over. I know I've got to shave it but I just can't bring myself to do it yet.
I admire those of you who have just done it and gotten it over with.
My big girl panties must have gotten lost in the dryer wormhole with all the lost single socks.
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LeeA, you have to post a picture for us to see. Lol
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Hi everyone,
I'm new to this group and new to this whole mess.... I have my third weekly taxol and herciptin treatment tomorrow and was hoping to keep my hair ...... But yesterday it started coming out big time so I just finished ordering wigs and hats etc... It makes me feel pretty stupid but I think I was almost more upset yesterday then I've been since this all started, and I wasn't expecting it to start coming out sooooo dramatically....
I like the big girl panties comment....I just can't imagine shaving my head and actually seeing nothing but a bald skin.... Can you go straight from hair to wig without passing go (or any mirrors) -
jayjayc - I love your avatar and I love your idea ("from hair to wig without passing go - or mirrors"). Wow. You seriously have captured my entire hair crisis with that one sentence.
I feel silly calling it a crisis, I mean - I've given up two breasts (one of them supposedly perfectly fine) for this cause but gee whiz, this hair thing has really thrown me for a loop. I knew it would. Or I figured it would - but I didn't think I would be quite this stubborn about taking the clippers to it.
Tonight I dragged out a wicker basket full of hats I had in the closet. Hats I haven't tried on for years. Each one looked more ridiculous than the one before. I've never worn hats because I look like a damn fool in hats. And I have wig-regret. I'm really glad I don't have to go too many places and even gladder I don't know too many people. And it's not like I had great hair. I didn't. My mom has always been blessed with thick, full hair - even now that she's in her seventies. Mine, on the other hand, has been flyaway and fine.
I probably really was a candidate for the cold caps but too late now. Waaayyyy too late now.
Welcome to the group, jayjayc. I also like the wording on "new to this whole mess." Amen, sister. What a not-so-fine mess it is.
And I see you're on the Herceptin ride as well. Wheeeeee!
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My first TC treatment was 1/10. My hair started falling out by 1/22. On 1/23, I couldn't sleep, as usual even though I take Clonazepam, similar to Xanax. Went into the bathroom and started combing and running my fingers through my hair. About 90% of it fell out. I climbed back in back giggling hysterically fully intending to wake my husband to let him have a good laugh. When he stirred and reached out to comfort me because he thought I was crying, I burst into tears. Then we laughed. The next day, I cut all the long pieces that were left. Then on 1/25, my husband buzzed my head. It seems like I still have the 10% there, which makes me wonder if I'll be completely bald. Hmmmm.
As for my poor little boy. My husband took him to the orthopod today at the direction of the ER staff. One of the bones is set O.K. The other is definitely not. He is scheduled to go to surgery on Wednesday. The orthopedic surgeon will attempt to reset the bone in a closed reduction procedure while Peyton's under general. If he can't reset it properly, he'll have to perform an open reduction and use pins and wires. I'm scheduled for TC #2 the following day. So not looking forward to this. I'm just so glad Dan's home from work this week.
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LeeA you really get it and now I don't feel as silly as I did.....
I don't want to jinx myself but I've been really lucky so far (except of course for that pesky cancer thing) I just had the lumpectomy and sentinel node removed and skipped the really scary chemo by just doing weekly taxol and herciptin..... So I knew keeping my hair was probably asking to much...... But I really really wanted to keep it..... I'm like your mom and my hair has always been the one thing I got complemented on..... I mean even during the early stages of treatment I had nurses compliment my hair Two different times...... And how stupid does that make them..... It was long and auburn.......
i cut it too shoulder length last week and cried on my way home but had really started to like it and then bam.... You know how cats shed, well that's me now......and heaven forbid I run fingers through it ...... I end up with a handful.... I did fine myself almost laughing at work today when I started pulling pieces off my sweater.....
But bald.... I just know I'll have a funny looking head with moles and zits and who knows what else....
Thanks for making me feel less alone -
Hi Ladies,
I am leaving the fog. Day 5 post chemo and yay, I could leave the house today! Went to the supermarket, had a walk and ate 3 meals. Woop woop! Not going to call feeling healthy too early (learnt my lesson after gloating on day one on a steroid high) but I am feeling so much better. I have a meeting with my onc pre next treatment to nail this bowel spasm stuff. Also seem to have picked up my son’s cold which is a bit worrying but it’s not been bad for him so hopefully it won’t knock me about. Thanks to everyone for their kind words.
I have a wig at the ready and I really like it. We’ll see how much I like it when I have to wear it. LOL. Jayjayc, the ‘go to woah’ could be a plan. My son starts 4 year old kinder next week and I am thinking about wearing it from the get go so that all of the mums have no idea I am sick. I cut all my hair off very short in readiness for the baldness but the wig is darker and longer than I have it now so it would look super obvious in a couple of weeks. My husband really likes it which cracks me up! I bought a few turban/beanie things online on the weekend and although in principle I am cool with wearing them, they really do scream CANCER PATIENT. I guess I’ll adlib and see what I feel like on what day. I wonder if there may even be some days when I’m game to ‘nude nut’ it!
Watta, my aunt had BC and chemo and still wears her wig every day. She finished chemo 18 months ago. She says BC was the best ever for her hair as she now has no bad hair days! Seriously, she loves her wig and rocks it. She is always being asked where she has her hair done. It looks so natural. There are some minging ones out there so I guess it’s trial and error. When I bought mine, the guy helping me had the WORST hair piece on ever and I nearly left the shop. Fortunately I stuck it out and bought one that you can part any way which makes it seem more like real hair and you can see scalp through the part line. I have spent the last 2 weeks getting nits out of my son’s hair and we all had treatment so a plus will be that I won’t be susceptible to those manky little critters for a while!
cancernoway, hope you feel better soon. I have done exactly as you have suggested and am eating what feels good and what I can get down in the first few days post treatment. The kale, smoothies, salads and broccoli shoots will be back on deck soon
Ciao for now,
Jubby xox
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Carpet and drapes FINALLY MATCH!!!! LOLOLOLOLOL oh dear I knew this would be the bunch of women I'd love. So, no hair, no leg hair, pit hair, down there hair, etc... I feel like a siamese cat. I guess now they (the guys) cant bitch when there is hair in the drain. HA!
Bryona- I too find it rude that this cold made itself comfy in my body. It can leave now.
Colleen- Hope you are feeling ok from happy hour. My nurse told me to alternate the anti nausea meds to see which ones worked the best. And I definitely take the ativan before sleep. Stay hydrated!!! Eat what you can handle. keep your strength up... (my face felt flush with the steroids the first day or so... no numbness)
Jubby- Welcome back from the fog. Sorry you caught your sons cold. Same over here on that end. Kids... they are magnets for germs.
jayjayc- I had bra strap long hair. I cut it short a few days after xmas and then a pixie cut a week or so after my first TX. I was afraid to be bald. I was so scared that I would have some weird lumps on my head. I has my DH buzz it and I had about a 1/8 inch long haircut.. oddly, I liked it like that. Now I am almost completely bald. just some stubble left. Just another hurdle in our journey.
Good morning to all of you! I am so blessed to have found all of you. Who suggested that we needed a little village where we all could live close by during our treatments? Fantastic idea! Think of the roar of laughter coning from the village walls!!!
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My 8 year old niece called last night to tell me that she and her 2 sisters (10 and 4) bought "cancer scarves" to wear to school in honor of Aunt Amanda. She was going on about the cancer scarves with the "cancer signs"..hers is pink, her sister's is black with pink cancer signs. I said, you mean the cancer ribbons? She said, yeah, the cancer signs..we support your cancer. Haha!! I love that kid. The best was that she bought me a scarf that says survivor.
It feels really good to be the favorite aunt, and I'm an INLAW! I've spent a lot of my medical leave sewing doll clothes for their American Girl dolls and these kids brag about what I've made. It's really good therapy. -
Amrdbit, my hair took the same course as yours. Pretty well all gone on the north and south poles, but still have face peach-fuzz, arm hair, and that 2-oclock shadow on my legs. I call it a 2-oclock becuase it isn't even enough to worry about shaving. It hasn't grown out, but hasn't fallen out yet either.
Colleen ask your onc about the face numbness. I would worry that the pain meds might not interact nicely with the chemo. Did you go through the list of all drugs, rx or not, with them prior to chemo? I'm so overly cautious now about what I take that I worry about when or if to take Advil or Tylenol anymore.
jayjayc, Ciao Bella! We are all right there with you sista. The hair thing was the biggest worry for me. I've always beens somewhat vain, with long or "big" hair. But honestly once it started coming out I couldn't wait to get it off. It turned my stomach to see the strands in my hands and flying around the bathroom. I still refuse to go completely bald, just don't have the balls or desire, or the liking of how it looks. I'm not as confident and strong as our Skigirl, but I've been sporting hands and scarves and now don't even think about it. I thought I would want a wig because it would make me feel more complete, and it actually made me feel more fake and like this cancer thing was real. Okay, so the head wraps make it real too, but at least I didn't feel so self conscious like I was "fake" faking it that way. They do have awesome wigs out there. I've seen ladies that look amazing in them. One lady I met had short hair all her life, and how sports a long wig. When I first met her I didn't even know it was a wig. So you will definitely find your way and make it work and will find you are comfortable in your own shoes still.
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MandyNJ- Kids are so good at making it all seem so simple. I cherish the moments like that with my son. I bought him mousse soap for the shower and he wrote 'I love you mom' on the wall in the shower. He didn't tell me. I went in to pick up after him and saw it on the wall and it make me all warm and fuzzy inside. Wear your scarf proudly and stand tall that you ARE the favorite aunt!
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Round 2 done! Still not sure if I will have 4 or 6. I do remember( at least I think I do ) MO telling me that if I do good through the treatments then I will definately do 6 or if I get sick I will need just 4. Does that make sense? I have not been "sick" thanks to all of the anti nausea meds. I do have terrible aches & pains though. An awful rash has also developed along my would be hairline & my upper back. It's extremely itchy & looks horrible.
My hair is pretty much gone, I have a wig but have yet to wear it. I need to take it in to be trimmed up & thinned out . Maybe then I will wear it. It feels so fake as it is. I have some beanie style hats but need scarves or lighter hats that I can wear indoors & not be so hot. I''m sure there is probably a thread as to where to buy hats & scarves online & such but I missed it. Suggestions welcome please.
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LeeA~Does your bad comb over look anything like Donald Trump? That would make me buzz my hair pronto!
I had my long hair cut in a pixie the night before 1st chemo. On day 17 I noticed every time I ran my hands through my hair there were quite a few hairs on my hands. On day 21 I woke up with hairs all over my pillow, so had my son buzz it that day. Now this is day 12 after AC #3, I still have my buzz cut. Haven't lost any of the stubble as far as I can tell. I still have my lashes & brows too.
I'm not sad that I buzzed it. I could tell chemo had made it dry and lifeless. Like a dead animal on my head. This way I get a fresh start. My hair was auburn, but I always wanted to do it bright red with blond streaks. Not highlights. STREAKS. So when it comes back in, this 62 year old broad is going to ROCK IT!!!
Hang in here Girls. It will get better. The hair grows back. Too bad the boobs don't.
Blessings
Paula -
I forgot to say, that even though I haven't lost my buzz, it isn't growing at this point either.
Paula -
Kimmeam- try these...
http:/www.modestworld.com/Ways-to-wear-a-head-scarf-rectangular.asp
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Good morning, ladies (and men - if there are any insane enough to lurk) -
Paula, Donald Trump? I wish! I had Donald Trump mornings when I had shoulder-length hair.
I went a little crazy with the clippers last night after my husband fell asleep. I tried to shave off what was left but now I look like I'm ready for those FEMA camps that Jesse Ventura blathers on about - but in my case it's FELINE EMERGENCY MANGE ACT.
My husband calls these things he's offered up to do the job "clippers" but I think it's really a beard trimmer (or an eyebrow shaper). Maybe I'll just take my damn Ped-Egg to it when I've woken up enough (no, no, I won't - I'm not that stupid/sadistic).
At 12:05 a.m. I went out for the first time since the Neulasta shot last Thursday.
I donned one of the borrowed Buffs and went to pick up the refill for the anti-nausea med thinking it would be the best time to avoid germs/people. I was semi-right but as I was waiting in one of the militaristic lines (you know, the HIPPAA, you wait here, they wait there, keep your head down, don't listen, don't step over the line) this man approaches me from the side and says "I don't think you want to wait behind her" - I'm all like WTF - don't come near me, I'm out at this hour for a reason (in my mind, that is) but in reality, I politely turned, in my buff, and said "I beg your pardon?" and at that point the woman at the counter, who must have been his wife, significant other, whatever, turns (from that somewhat safe HIPPAA distance) and she's wearing a hospital mask (!!!). He proceeds to say "we called in our prescription - you might want to wait in the other line."
Mine had been called in as well. Probably long before hers was or perhaps before she even needed that hospital mask because my husband is an anal, first-born mensa who does everything on time or before time.
I tried to give him the politest look I could muster without screaming "WHY THE H DOUBLE HOCKEY STICKS IS YOUR WIFE WEARING A HOSPITAL MASK" and assured him that I was, indeed, in the right line - i.e. I've been to this rodeo/CVS before, Mr. Line Organizer, in fact, often enough to get $25 rewards coupons every few months because of all the money we plunk down while we're there getting our various and sundry prescriptions.
So, in summary, I stealthily go out past midnight on a double-pronged mission (first time out with the used buff + shorter line/fewer germs at that hour) and for the first time ever a man approaches me in line (I was the line) AND the woman I'm due to replace at the counter is decked out in a hospital mask.
There isn't enough hand sanitizer for this sh*t, ladies.
Unfortunately, my boy in the bubble suit got delayed in shipping along with my Jetsonmobile somewhere back in the seventies. Oh, and that Race for the Cure™? Missed that as well.
Soon, I must get up and look what I've done to my hair, ma, (the older ones might get that reference to the old Melanie Safka song - recently redone by Miley Cyrus) in the cold, hard light of day.
Have you ever had one of those urges to just get in your car and keep on driving until you drive off the planet? I've had those crazy urges from time to time since childhood and late last night, driving back from the drugstore, was one of those times. Of course, we can't drive away from cancer. We're tethered to it like bald old (I'm speaking for myself here) balls at the end of raggedy cotton ropes (or IV lines).
This is my rant. It won't happen again. Hopefully.
I shall sit in my corner with my lint/hair roller and drool bib and be good for the rest of the day! YaY Cancer!
p.s. I wish you all a peaceful day with little to no side effects - and free of hair-pulling (it's ill-advised
) angst.
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LeeA~You have given me my laugh for the day! Thank you my friend!
Some of those masked strangers may have been protecting themselves. My sister, Jan, who takes me to my chemo said, she wished Id wear a mask to church to protect myself.
She might be right. I just try to avoid hugging and shaking hands for a couple weeks after treatment.
I've survived chemo hell once again. I have one more AC to go. Now that my tastebuds are back, I'm craving Chinese. Combination Lo Mein. Yes, that's the stuff.
Have a Blessed Day
Paula -
Paula, you're right. I might have been standing within feet of my OCD germ soul sister and not even known it. Ships that pass in the night!
I just wish she would have kept her dinghy (husband) on a shorter leash/rope as he was definitely too in my non-masked face for comfort, i.e. the least she could have done was masked him as well!
Also, Skigirl, I love "down there hair" (I mean, I don't love it - but I love your term for it because it's edgy and almost Dr. Seuss-ish). And from what I've observed, that hair is wired differently (no pun intended). Perhaps its genetic purpose is more important than that of the hair on our head, i.e. to serve and protect (heh) our sacred area of fertility. What was it Voltaire said? God is a comedian playing to an audience too afraid to laugh.
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LeeA- i swear you're writing what i'm feeling...even very mellow husband asked me today what was wrong...oh...just that i f****** hate this s***. For me it was MRI day (scary, stupid machine) on top of bonescan day yesterday- i need the stupid tests for lurking insurgents to be over and start the stupid, life-saving f****** chemo. Aaaaauuuuggghhhh!!! 1st appt with the MO tomorrow...hopefully the bonescan results are in and i just have to wait on the MRI- i want EVEYONE to think negative for me, pls?
Carpet vs. drapes- this one has been a bone of contention for me for YEARS. I'm a natural blonde and i work in a VERY male dominated workforce. Joke has always been "Hey Shannon does the carpet match the drapes?" To which my response has always been, "No. Hardwood doesn't have to match the drapes". Shuts 'em up every time. But damnit! Now the capet and drapes are both gonna be hardwood...and husband is bald so we'll MATCH on top of everything else...we work in the same place. Put my painted-on helter-skelter stenciled eyebrows in on top of that...I'm gonna look like Halloween gone bad. Carly Simon's "You're So Vain" is playing in my head...
And to those of you who can go "commando head"- i saute your bravery. My head is soooooo oddly shaped. I have ridges on the sides and a big, honkin' divot on the top...no hair, i'm gonna look like a car-accident cancer victim. (Shut up Carly.) I HATE the headscarves...as soon as she found out about my diagnoses, my mom went out and bought me a ton of scarves...all polyester, all hideous. Old church ladies would laugh and point if i wore them. They make me feel like a cancer patient...which i know i am...shut up...i just don't like them. I got 3 cool hats from Headcoverings (Newsboy, bucket and girlie-type sunhat for summer and wearing with skirts) and i like those. All UV protective and pretty good looking...although like LeeA, i always thought i looked like a total tool in hats...guess THAT attitude gets to change. And i'm getting a wig- short, synthetic and as close as i can get it to my own hair. I'm thinking i may have the balls to wear JUST a hat to work...definitely my wig...but commando? No way. (Carly is now screaming in my head). I just can't fathom it...everyone will know i am bald (word is spreading around work like WILDFIRE now) but knowing i'm bald and seeing my wacky egg-head are two very different things. And don't get me ranting on the eyebrows again...
Hopefully the MO can tell me tomorrwo when my chemo starts and what kinds so i can stop being a chemo wannabe and join the club for real...we'll be a jan-feb chemo group.
Death to cellular insurgents and here's to being NEGATIVE (did i mention i f******hate tests???) Shannon
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LeeA,
You cracked me up. Yes I have wanted to drive and never come back unfortunatly, wherever I go, there I will be. Obviously I would be taking me with me. For some reason that reminded me of Jimmy Buffet song "Take the weather with you." Great song.
Love people who wear masks and don't know what they are doing. There is a special mask made by 3M called a N-95 that patients or family will pick up in hospitals sometimes, because they are stupid and don't ask for what they need or want. Anyway that mask is used for pts with TB or suspected of TB. The mask doesn't let the person wearing it to release their germs into the air, instead they suck in all the germs out in the environment. It is to protect us/others not the pt. with TB. So the moral of the story is if you are gonna wear a mask be sure and get the right kind. I had a pt come in who is super prejudiced about everything and everyone. He will say they are sick they shouldn't be here, EXCUSE me we are here for sick people. Anyway he came in with a TB mask on one day and I asked him if there was any reason he was keeping his germs from being released into the environment and sucking all the other dirty germs into his lungs. If I thought I would have been able to get back up I would have layed on the floor and laughed my ass off. He is a prick towards other patients and deserved it.
Enough: Sorry for your issue Lee but I would have asked Mr. I am in charge of telling the world what to do, why wifey didn't stay home if sick and he pick up her RX.
Sheryl
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Paula,
I so hate it when I lose my buzz! Oh sorry wrong thread forgot where I was for a minute.
Weird brain cells today they are misfiring I think.
Sheryl
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kimmeam,
http://www.goodwishesscarves.org/
This site will send you a free head cover, it will take about 4-6 weeks but hey it's free and you will still need it for awhile.
Sheryl
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Crack Pugs...which one?
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the one with the zebra... lol or the pink unicorn.
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Shannon,
I went for a MRI for my low back the other day and they ran me into the machine after asking all the appropriate questions. I have the head phones on and fan blowing in my always hot face and just kicked back when all of a Fu...king Sudden!!!! I start screaming Hey,,Hey,, Help, legs up in air kicking beating on machine etc. I don't think anyone was watching me (for crying out loud, put an old woman in a tube and turn your back). Anyway she says, Mrs Burns is something wrong, Yuh Think!!!! I forgot to tell you I had a chemo port!!! I had visions of my chest exploding when the magnet kicked in, (as a nurse for >30 years I have heard and known of some horror stories). She say's oh that is fine no problem. Needless to say I didn't calm down very well for the next 20 minutes and sweat like a hog, Can you say adrenalin rush. Whew!!
Sheryl
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Woke up today feeling "normal". Yay! So glad that is over with.
LeeA - You have cracked me up today. Fortunately, only people in this same situation can say that and get away with it because we know how you feel. I haven't had the same feeling about my hair though. I just don't care about it. I'm too concerned about getting all this crap out of my body to worry about my hair and what other people think. My motto through all of this has been, I can't change it so it's time to fix it and to hell with what other people think. As for the old lady and gentleman in the pharmacy, I'm wondering if he was warning you not to get too close because she had something that was contagious and didn't want you getting it. Not that he was afraid you were going to pass something on to her. I'm extremely claustrophobic and the thought of those masks sends me into a tail spin. If the woman did have something contagious, she should have kept her junky butt in the car and let her hubby get her prescription for her instead of lerking around the line pissing people off. Agreed on that one 100%.
Smethot - I looked up some of the hats that you choose and they are adorable and I love them. I have a few scarves and buffs and a couple hats myself, but I love those newsboy hats and will have to get one of those. Keep your chin up and remember you are sooooooo not alone in this. You too, have succeeded in making me smile today. Thank you.
I'm venturing out shortly to go to the bank and to get pet food. I know you are all so jealous but since I haven't been out since Saturday, this is a big deal. If all goes well, I'm going to work tomorrow. Fingers are crossed!
BTW, My Sister in law brought me a piece of peanut butter pie from Frisches and OMG it was the best thing I had ate in days. I know not on the healthy list, but it was so good! Nikki, I know you are from the area so give it a shot.
And finally, after rereading my last post, I have realized I shouldn't post on my tablet. Looks like I was having a mental lapse in my typing. Good grief. Sorry about that.
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Agree - Zebra
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...its pugs...google them...they ALLLLLL look like crack pugs...i have 2 myself...they ARE crack pugs...maybe i'll start rotating avatars...a crack-pug-a-day-calendar?
The Headcovers hats are really nice. The only thing that chapped my ass was that they charged me extra +++ shipping & handling. Not because i live in Canada- I'm used paying extra S & H because Americans think i live in an igloo and travel by dogsled- but because I live in SOUTHERN ONTARIO which Headcovered deemed to be "remote". Now let me tell you, i live in the most populous place in Canada. Southern Ontario is home to over 92 per cent, or 12.1 million, of Ontario's total population of 13.1 million people. One of the most population-dense places in Canada. I do not live in Nunavut. Or Northern Ontario. Its absolutely insane...FEX ED (who delivers for Headcovers) has 2 depots in my city...but its remote and i have to pay extra. But other than that...nice hats.
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Sheryl, wow, I'm glad you got their attention! What a way to spend your time in the tube - all stressed out (and hot) following an adrenaline burst!
cancernoway, this isn't so much about what other people think about me because I really don't know anyone out here. It's more about my OCD weirdnesses, acne scars, desire to hide (believe me, I've even thought about burqas since all of this), etc. Yes, I am weird. I always think about the line from the Doors movie "where's your will to be weird, man?" Well, mine is a srong will. I was a hair twister as a child. I haven't thought about that much since all of this but during times of stress it can creep back in. I'm just one of those odd ducks who sailed (well, sort of) through a double mastectomy but is gnashing my teeth and wailing online about the hair thing. This, too, shall pass. I shall not let cancer steal ALL my joy. Thank goodness I haven't been truly hormonal for years as these outbursts used to be monthly.
smethot, I was looking at ads for French Bulldogs over the past few days (I like to torture myself with the idea of getting another dog during the post-chemo days, this after my husband and I made a pact last summer when we lost our beloved Beagle-mix after 16 years together: "no more pets") .
I grew up with Boston Terriers and had two Boxers during my younger adulthood. That said, I love those pushed in faces. Your avatar choice is splendid although the puppy with the kibble certainly expresses itself well!
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Re: the man with the masked wife - I just don't know what that was all about. Perhaps it was the Universe's way of telling me to calm the f*&^ down and go with the moment instead of being a nervous ninny about everything. I do know that he was sitting down, several yards away (I always survey the territory!), and made it a point to get up and tell me I should go to the other line. Perhaps he was new to the process. Perhaps I looked like I had just dropped off the turnip truck versus out of a Prius.
What I've noticed since living in California (about 14 years) is that people generally tend to steer very clear of one another (physically) unless panhandling is involved so it definitely caught me off guard.
I can only recall one other time when anyone approached me in that drugstore and it was when a woman warned me away from some cellulite cream. She lifted up her shirt and pulled down her waistband and said "look, it didn't work." I thanked her and bought it anyway. Hey, I like the stuff!
Also, I think there's a strange vibe later at night. Back in Indiana, the best Walmart brawls always seemed to happen after midnight.
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- 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