Starting Chemo May 2008
Comments
-
Otter, I think I'll have a whiskey 'n seven (whatever the feck THAT is) in your honor. I think about this a lot..the yellow light means 'prepare to stop'. Red means stop. I have never been one to support arguing with the police, but it would make an interesting discussion..prepare to stop, not actually stop. Well hey! You played the Cancer-Card without realising it! so..well done! Kristy, good on you for getting rid of THAT little fashion-statement! I cannot imagine staples..who invented THAT technology?? Myself? I much prefer a nice neat subcuticular suture. (Thanks Otter!) Anyway, make sure you step away from that stove, Kristy, and give someone a little turn! (What's up with my formatting??) I cooked 2 x corned beef and 3kg of teryaki chicken for the boys to take camping with them so BOY! am I in the good books! It's been unspeakably hot here today but the ant-action in the yard makes me think there is a bit of a storm coming. XX
-
Otter~ you could have always said that the light was orange and not quite red yet. Its a running joke in our house on what shade of orange the light was when my husband cruises thru it.
Snowy cold day here in ohio. Supposed to get up to 3 inches of snow, which is nothing in the grand scheme of things. Highs in the lower teens BRR!
Debating on which is more important right now.... pay our mortgage bill or buy groceries. I am due a paycheck from work at the moment but the company does not have the money to pay me. It's happened once or twice and other times I get pay checks before I put in the time. I have a few more days to decide and I'm hoping work comes thru for me with some money. On the brighter side I will be doing taxes tonight, I believe, and doing those electronically. Those usually get deposited within a week after I file them.
Burned up my new computer at work the other day. I've only had the darn thing for about 3 weeks. We had it sitting on the floor under the desk in an area made for the comp case. With me sitting right next to the door, I have a small space heater behind me. Boss turns it on before I get there so I don't get cold and I flip it off when I leave. Saturday nite we went over to network the comps together and play games, and my computer kept shutting off. Turns out boss had turned on the heater and bumped it to where it faced directly at my computer box. With it being a hopped up computer to run high end graphics programs it puts out alot of heat anyway, then you add the heater into the mix. Thankfully it only zapped my power supply. I didn't realize just how much heat it put out until the computer was gone to the shop. It probably dropped 10 degrees in my corner easily.
Tomorrow is herceptin 5 I think it is.. starting to lose count at this point. Just keeping my eyes on september for when it is all done. I need to figure out if I can get bc.org on my cellphone so I can keep up with you ladies during the day at work. Hubby got me the new samsung behold for cmas, its all touch screen like the iphone. Had to get internet service on it for a month to get my rebate. Personally I'd much rather look at the net on the computer, its like using dialup its so slow on the phone.
Ok enough rambling, just felt like I haven't contributed much lately cause I haven't had anything exciting going on. I do check in multiple times a day cause I am addicted to you ladies! lol
hugs and slobbers
Kristy~ did you get your snail mail from me?
-
I simply cannot wait to have hugs and slobbers from Jen in real life!
Kerry, Whisky and 7 is rye whisky and (british style fizzy) lemonade.
I am supposed to be busy, just checkin' in.
Today is my cancerversary. I got diagnosed a year ago.
-
Noelle, so did I. One year ago today, I had the digital mammo + ultrasound + US-guided biopsy that started this whole thing.
Hey, we're still here, right? That's a good thing.
Locally, a whiskey 'n 7 (or, "Seven and seven") is whiskey with 7-up. So it is light and fizzy, just like you said. I liked whiskey sours when I was young, so maybe the fizzy lemonade would work both ways. I normally don't drink the "hard stuff"--haven't for decades; but yesterday it just seemed like a good plan.
Jen/Sable, sorry to hear you fried your 'puter. Sounds like you gals in the north country are needing more than a space heater. That cold is coming our way Friday and Saturday mornings: 14 degrees (F) in the Deep South is pretty extreme. But, it's nothing, compared to that hyphenated stuff that's up north right now. Brrrrrrr!
Hi, rock! Another great, new avatar for you! I just realized, it will be summer where you're going. That will be nice, compared to the NYC weather this week. You and Kerry can gloat for the next few months.
And, Jen/Sable borrowed the hair I had last October/November. That's okay--I was through with it.
Hugs and slobbers from here, too (or, to borrow a phrase from AlaskaDeb, "Bugs and Fishes")...
otter
-
Jen,
Thanks for the snail mail- it totally made my day!
Otter, I had staples after the mastectomy also (way more of them for that surgery than this hysterectomy).
Yesterday pooped me out so I have slept and rested all day today lol- leftovers for dinner tonight.
Kristy
-
yup still here!
yay!
It is
-11 degrees Celsius here which= 12.2 degrees FahrenheitNo big deal if you bundle up.
Otter. Lemonade in Britain is exactly like 7up.
this is from the American guide to speaking British...
Lemonade - Lemonade in England is a clear, sparkling, lemon flavoured drink that is either drunk as it is or added to lager to make shandy. Seven-up and sprite would both qualify as lemonade in England.
http://www.effingpot.com/food.shtml
Gotta run!
N
-
See, that's why I love these boards so much! Now I know that if I'm ever in England and I order "lemonade", I shouldn't expect something made from freshly squeezed lemons.
'Course, there are many other reasons why I love this particular thread, but I'll get all sappy if I start with that. Y'all know what I mean, though.
Luv and hugs,
otter
-
Noelle, I cannot bring myself to say "happy cancerversary". So instead I will say "Cancer. It is. And may it not be anymore."
Kristy -- Staples? OW. Heal as fast as you can. Has anyone made you some mashed potatoes and gravy? Because I think that would help you heal.
I am cold and hungry. Basically, I am a character in a Dickens novel. I have not taken off my hat since I got here -- indoors or out. It's not that it's all THAT cold. It is just ENGLAND. I am looking forward to my 118 hour flight because the plane should be warmer than I am right now. Brrrrrrrrrrr. I feel so bad for women in England who are bald right now.
-
okay, so what's lemonade called in England? Yes, its so cold here in wisconsin, they cancelled school for tomorrow. mainly because of the buses and bus stops. Our low tonight is -15F and our high tomorrow is 1. Yep, no typo, really 1 degree.
I'll do what I can to pitch in but its pretty ugly here too. I work for a large contractor and right now we're looking for work. My dh is in advertising, automotive and real estate...shall I say more. Things will get better. We just need to conserve.
Sitting here with semi permanent color on my head. Gonna wash that damn grey right out of my head.
-
Oh girls, more laughs. What amusing feckers we all are. Rock, you look like a mysterious movie star 'of Middle Eastern appearance' (as police reports say here in Australia). Or a traditional singer from Moldovia, or something like that. Def NOT Dickensian, although it must feel like it in those temperatures! It is picture-perfect warm and lovely here. The boys got away camping all right..even though the 15yo sooked and whinged and stayed in his room while Drew and the 2 x 12 yos packed all the gear. I'm glad they're gone..I need a rest..sigh. Not as much as our Kristy, but. Kristy! Hope you're taking it easy and HAVE WE MOVED OUR BOWELS TODAY, M'AM? Just keeping the hospital theme going there for you, Kristy. Happy C-Day, girls! We live to laughhahha at cancer.XXX Got to go and buy some milk..not for my cat Christina (who is sitting on the arm of the couch and resembling a hovercraft) but for my friend Robyn who is coming for a cuppa and some girl-talk. And don't we all love that!
-
Otter - had to chuckle at your police story. My second day back to work I was pulled over for a moving violation. The woman gave me a ticket without thinking twice. While I was on STD for 5 months, they posted no left turn signs in downtown Minneapolis to help with traffic after the bridge collapse. Never knew they were there - tried to explain - got the ticket anyway. I wanted to say, "do I not look like I have been through enough?" Smile and move on.
Noelle - another significant milestone and a stronger, healthier you!
Kristy - glad to hear that you are feeling better, take care of yourself!
-20 tonight here in MN, high tomorrow of -6. Someone say something warm
Jean
-
Okay, you wild women....I am going to begin taking femara tonight .... for only five years. Anyone got any advice? Good wishes? Goo to check in with you all. Rock, you look great. Can't write right now, but I will take all femara advice...I don't think any of you are on this, right? Are most of you tamoxafining?
-
Congratulations on your anniversaries. I've been lurking on this site since my diagnosis in September so this might be a good time to tell you all how much I admire both your relationships and your success. I still read the sections that relate to my stag in the treatment. I visited may other group sites but this one just has it all. I hope that our group ends up as close as yours. You should unite on Oprah. Just a thought.
Best wishes,
Renee
-
To all of you in the "not fit for human life" temperatures...I send you warm thoughts. Really really warm thoughts.
Kristy - Staples on your mast??? wow! I had them on all 3 of my c-sections but couldn't imagine having had them on my chest.
Noelle - I'm with Rock...kind of hard to be wishing a "happy" anniversary but then....we ARE here thankfully!
Eddie - I've been on Arimidex for several months now. I'm not sure how Femara compares but for me on the Arimidex...early morning stiffness is my biggest complaint. I also take Caltrate (supposed to be 2 X day but I only remember one) and Tums with Calcium. I take the Tums because the Caltrate causes ...ahem...gas.
I had my follow up with my surgeon today. He says I look great and everything is looking healthy. I asked for the name of a plastic surgeon. I'm seriously considering the reconstruction. Hubby is against it only because it isn't important to him and he doesn't want to see me suffer any more. I keep thinking...I'm only 44. Women in my family live a very long time. I can't see living the rest of my life lopsided. My prosthetic is uncomforable and rubs on my incision and is harder than my remaining breast. I just always know its there. So...I don't wear it ever. So, I will pursue this option...reluctantly.
Hello and warm hugs to everyone!
-
Renee~ if Oprah called tomorrow to tell me to hit the airport, I'd be there in a heartbeat! Hopefully she is buying LOL
Colder than snot here right now. Roxi has me beat for tomorrow's high... supposed to get to 8 here. brrrrRRRRrrrrr Only thing keeping me going is an occasional hot flash... har har.
Otter~ funny you say that about me borrowing your hair. I noticed that in different stages we all tend to take the same exact pics and post them. I'll only keep it for a bit then pass it on to the next person.
Rock~ is your trip fabulous so far????
Noelle~ I have a special hug and slobber saved up just for you daulink.
Kristy~ I had staples when I had my c-section. They freaked me out! I only had them for 2 days but the one time I touched them was unreal. Felt like a railroad track on my tummy. And unfortunately for me I am a fast healer....... some of mine had skin growing over them already when they went to take them out. Ouchie!
Eddie~ I wish you no se's on your new drug. It's all got to get better as we go along right?
Me~ I'm a malibu rum and pinneapple/orange gal. Got a big ole bottle in the other room as I type. Bought for me last year when this all started. It's waiting for just the right moment then watch out I'm gonna use a straw!
-
Wow - lots to catch up on. Dh was home last night and monopolized the computer.
It pains me to read about how the economy is hurting everyone. Dh and I both work for the state of California, which is not doing too well by any means. We will either get a 10% pay cut for 18 months or "IOU"s instead of paychecks next month. Great.
Rock - Love the avatar and hope you warmed up!
Noelle and Otter - I, for one, am particularly glad you are both still here. I think all of us are. There is a local commercial for a cancer center that has people saying the phrase "I found out on the [insert day of choice, i.e., first day of school, day I returned from my honeymoon, day of our family reunion]" and it makes me think of us at that time. So, not to be morbid, but I would like to hear what it was like/we were doing when we got "the news". I will post mine soon, but the arm is starting to hurt again. Probably should do something about that...
Renee - Lurk all you want. And I like the Oprah idea!
-
Eddie, I've been on Femara for I think 3 months. My onc ( a German seriously up on his chemicals) insists that letrazol is the premium cancer-killer for E+ post meno women, so Femara it is. I have been shocked by the hand and feet pain, especially the feet and especially first thing in the morning. No more springing out of bed for me, and no gambolling down the stairs, or running down (late for work). Now here's the thing: I was going to quit. I am made of cast iron, but I could not bear the hot flushes or the broken feet. But then I remembered that I am a May O'8 girl and we LAUGHHAHA at cancer, so I decided to experiment. I altered the time I took the tablet. No difference. Then I started to take a half tablet at 7am and a the other half at 7pm. The hot flushes are amazingly far fewer (and remember it's summer here..so..hot nights). I also doubled my dose of glucosamine from 1500mg to 3000 (one tablet morning and night). No more phantom carpel-tunnel syndrome, and the feet are much better. I discussed the half-tablet biz with my onc today. He was able to find out that it was fine as far as the actual tablet absorption goes. He is finding out if the more even dose, rather than one big whammy per day, is going to change the effectiveness of the drug. I'll keep you posted because this is a very important piece of information for anyone who likes to walk on their feet
The Oprah thang! S-w-e-e-e-e-t! What could be cooler than a May reunion??? Hell, I can be a media-ho if I have to be! Would it be best to get flown to South Africa? That would be cool too! When did I find out I had cancer...hmmm...that would be after I woke up from an induced coma (for ARDS) ROFL! Did I dream this last year up? Anyone feel like that? XXX Karin, I'm getting the pic organised TONIGHT! XXX
-
I'm in for the TV reunion, but prefer Dr. Phil to Oprah.....you are right, Renee, we are very lucky here to have each other.
I found a lump, went to my gyno, got scheduled for a mammo. At my mammo center they read it right then. They told me they wanted another mammo of the left breast. They told me they wanted to do an ultrasound. In the ultrasound room was a female technician and a female trainee, and we were joking around while the gel was placed on my breast. When she placed the wand on my breast, they both immediately got profoundly quiet. Although I wasn't officially given the news for five more days, that is when I knew. I was at work when I got the official news. I told my husband on the phone. I went downstairs and found a woman, any woman, and told her and cried. On a very deep level I still have trouble believing it.
Off to Georgia for a few days, and I'll be offline. Love you guys and I will miss you. Back on Sunday (that's Monday for you, Kerry)
Sue
-
me and the BF talked about this last night. He had a false memmory about when i told hime. I will post about it later. Gotta go bundle up for the trek outside.
-
Noelle thanks so much for the package that just arrived...it was like christmas all over again. I won't mention whats in it for those who haven't recieved theirs yet,,,,but one of those things I will be using right away as my arm has been achy lately and it looks like this is just what i need. Thanks sweetie!
Hmmmm...let me think back, found the lump in the shower at the end of January, obsessed over it for a couple weeks thinking that tomorrow it wouldn't be there...finally went to doc in beginning of Feb. , mammo & ultrasound on Feb. 14 ( I could clearly see a mass on the ultrasound so had an inkling of how this might play out)...Feb 28 had needle biopsy......March 4 while driving my daughter to an appt. got the call on the cell phone told them i would call back.(can't talk and drive and it's a good thing cause that info would of sent me into the curb or another car!) Got dd into appt. returned the surgeons call and got the info that would change my life forever and i was to see him in 2 days to discuss our options.....It was a beautiful day and i was down by the water so just went for a walk and pondered what was ahead. I remember that phone call like it was yesterday.
On a tastier note...beverage of choice...an ice cold beer on the beach or with popcorn watching a thunderstorm. Also i must admit i love my ceasars...vodka, clam juice , tobasco , worsteschire and lemon...and in my more refined moments a glass of white wine.
Renee good luck with your journey...the info and the friendships that have been made here is invaluable...there are good things that can come out of the bad!
While i sit with my balmy 2 deg. celsius outside (around 35 F) i feel for all of you getting hit with the cold weather.. bundle up and stay warm!
On to the laundry, dishes and all that other stuff i say i will do later...cheers!
-
I gotta start making lists...
Angels, it looks from your avatar like you've borrowed the #1 hair from ... who had it last? I gave away the #1 hair last November/December, when I claimed the curly (#2) stuff.
Eddie, I've been on Arimidex (anastrozole) since the last week in June '08. That makes it 6-1/2 months. Some oncos think Femara (letrozole) may be a bit stronger than Arimidex; my onco thinks they're pretty much the same based on current evidence. There is a clinical trial called "FACE" (Femara versus Anastrozone Clinical Evaluation) that is supposed to answer some of the questions about relative effectiveness and SE's of those two AI's. Here's a link to a 2007 article about the two drugs: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2001225
My SE's on Arimidex have been minimal. I have the "usual" v*ginal dryness etc. that I would have anyway (to some extent), being 6 years into menopause. I think my hair re-growth may be a bit sluggish, and my hair may be a bit thinner, because of Arimidex, but I can't prove it. Like Adrienne, my biggest complaint is occasional mild stiffness and joint pain, mostly in the morning or when I've been embarrassingly inactive. I just noticed today that I don't hurt at all. Whether that's because I've been more active this week or I'm finally adjusting to the effects of this drug, I don't know. We'll have to wait and see what happens with my bone density. At this point, it's very, very early (hardly detectable) osteopenia.
I'm going to try to send some warmth up northward, and even over the pond to rock, but please remember that I'm using a heat pump to do it. I don't understand all the physics involved with heat pumps. What I do know is, they can only extract the heat that is there. When the air temperature gets too cold, heat pumps don't work anymore. So, tonight and tomorrow night when it gets into the low- to mid-teens here in central Alabama, you'll have to put on your warm jammies and woolly caps and turn on those electric blankets. I'll be in bed, totally covered up with just my nose sticking out. (My dh refers to that as my "snorkel look.")
I'm going to ask for a rain check on the reminiscence about the day I received my biopsy results. It was January 16, 2008--one year ago tomorrow, and two days after the biopsy that forever changed "life as I know it." Kerry, I need your help--what is it we're saying?: "Cancer is an interruption... nothing more" ???
otter
-
Much like Angels, I found mine in the shower in early February. I was hoping it would go away after my menstrual cycle but no such luck. I fretted over it for several weeks after my period. I didn't say anything to anybody. February is a bad month for my family. My late husband died in February as did my grandmother, so I just couldn't handle even bringing it up in that month. I couldn't do that to my kids who have already lost enough. DH knew something was wrong so I finally told him. March 14, I saw our GP. March 31, lumpectomy. April 3rd, I got the dreaded call telling me that I had breast cancer. I was at home and for some reason my DH happened to be home that day, thank God. I don't remember much about the call beyond that. I balled for hours. My family balled with me. Even though my son didn't understand, he knew the family was in distress. Doctor had told me they couldn't get any clear margins, so the next day made the decision, after consult with the doc, to do the mastectomy. That happened on April 10. And here we all are today.
-
Here's my walk down memory lane - and what weird timing, since it was exactly a year ago today that I got the call. My first reaction to Cris's post was that, oh yes, I remembered it vividly. But now that I'm trying to write it down, I realize that there's a lot of vagueness around the edges. I never felt a lump; something showed up on my regular screening mammogram. I got the call about that on my first day back to work after the Christmas-New Year's holiday, and went in for a follow-up mammo and ultrasound the next day. I was really not overly concerned. I remember thinking it was overkill when the nurse coordinator at the breast clinic sat down to educate and reassure me (complete with a little pamphlet on "Understanding Breast Changes"). Yeah, yeah, yeah - you're telling me it's probably nothing, and I believe you, so why the fuss?
And that was pretty much my attitude when the ultrasound showed a complex cyst, and through the needle aspiration two days later. The cyst disappeared (poof!), they sent the liquid off to the lab (they gave me the impression this was just a formality), and I forgot about it.
So, I was blindsided when I got a message at work from my Dr's office saying that I should set up an appointment to come in to get my results. That was a little unsettling, but I figured it was some eager-beaver staffer who didn't understand that an appointment was utterly unnecessary.
Then I got "the call" from my Dr. himself. He started off by saying he was very sorry, so of course I knew what he was going to tell me, even if I didn't quite believe it. I remember hearing the words "surgeon," "lumpectomy or mastectomy" and "radiation." At some point, I asked him to hold on for a second so I could get up and close the door. That calmed me down, and I started to hear him better. I remember how awkward and uncomfortable he sounded. At one point, he got to the point in his script (I pictured him with a set of talking points on a notepad) where he was supposed to be reassuring. "It's important to know," he said, "that breast cancer isn't a, isn't a . . . " and then he trailed off, and I could imagine the internal dialog:
"Oh, shit! I can't say "death sentence!" what do I say to her instead? how do I get out of this?"
I felt sorry for him, and interjected, "It's very treatable."
"Yes!" He sounded so relieved that I was relieved, too.
After I got off the phone, I sat there for a little. I wasn't freaking out - didn't cry at all. Mainly, I was thinking about all the different people I'd have to tell (boyfriend, daughter, parents, boss, department, friends), and how and when I should tell them.
And here, as Adrienne said, we all are today.
Linda
-
Renee, we have formed such deep friendships here, welcome and I hope your group connects like we did. It really eased my pain throughout the entire cancer "interruption".
I never found a lump. Had a suspicious cyst in 2007 and we watched it until my mammo in 2008. I reminded my doctor about the cyst and she wrote an open order for a mammo, ultrasound and biopsy if needed. Never expected anything. Had the ultrasound before and was even joined with the radiologist both times. This time seemed different though. The cyst was nothing, instead they saw microcalcifications which sent me for the biopsy. Mammo was February 15th, biopsy was March 18, got the call at work on Friday, the 21st. It was DCIS at that point. My trip to the cancer center March 27th got me the MRI that found the tumor. April 2, lumpectomy. After staging of lump and clear margins, opted for mastectomy April 23.
-
I forgot to mention in my summary that I did have a mammo between my GP visit and the surgeon consult....DUH. I was immediately taken into the ultrasound room after my mammo was done and a somewhat somber man, who made me nervous just by his demeanor, did the ultrasound. Before I left, I had my consult appt with my surgeon. wham bam thank you ma'am.
-
Otter, thanks for FACE link. Kerry and Adrienne, keep me posted. I have take a total of ONE Femara so far. Will keep you all posted as well.
I fell 800 feet down a mountain last February. It was wild then I got up and skiied away. March 15 I was feeling around because I still had minor injuries and was checking to see what bruises were gone and what were not. I found the lump. I figured I had checked it out because I always had a lump of some sort. I asked my friend, an onc, if I should go in...she said, yah, but don't sweat it. I went in at the end of March. I moved all of my stuff from Federal Way, WA to Seattle (because they said it would take 10 days for a biopsy appt and Seattle could give me one a couple of days later). I woke up at 4:44 AM on 4/4 and knew it was cancer as 4 means death in China. I called my brother to tell him and he said that we were not Chinese, but more Native American where 4 is a lucky number. The call came in that morning at work from a nurse who knew NOT how to tell me. She, too, had a script and she was doing the best she could. Even though I already knew I had cancer in my heart of hearts (even the doc doing the biopsy was giving me a phone number for a surgeon) it was still a shocker. My cancer bully friend, Dottie, was nearby and I just remember walking into an office (not Dottie's) and shutting the door and crying. It was awful. That whole first night I kept weeping and saying I wanted to live and I wanted to see my grandkids someday. Each day got a little easier but the first days were darkest as well as the first days of chemo. Now I am convinced we are all going to live a long, long, long time.
-
I had known I had a lump long before I found out I had cancer. The lump was there for the previous 2 years of GYN visits, but my GYN told me not to worry about it. He said it felt like fibrocystic tissue. And, since my mammograms came back “normal”, he didn’t see any reason to pursue it. It was nothing, he said.
When I asked my PCP for advice, he referred me to a university hospital breast center for further work-up. I admit that I was worried, but I figured this was just covering all the bases and my GYN would be right—it would be nothing.
The radiologist didn’t see anything on the digital mammo, but easily found the lump with US. He did a core biopsy, and said the path results would be back in about 3 days. The radiology tech patched me up, and told me to go home and not worry about it.
Two days later, I was in the kitchen, getting ready to make sandwiches for lunch, when the phone rang. It was the radiologist. He identified himself as the doctor who had done my biopsy, and he said the path report was back. I felt a dark shadow pass through my mind and stop right behind my eyes. I sat down. My husband was standing right behind me.
“I’m afraid it’s cancer,” the radiologist said. But I was sure he wasn’t talking about me. He couldn’t be. My lump was “nothing”. This was someone else we were discussing.
The radiologist tried to be optimistic. He told me the prognosis looked “very good,” because the cancer had been “caught early”—the tumor was “only” 1.6 cm. Just to keep up my end of the conversation, I asked him what type of tumor it was, and he said it was “invasive ductal,” grade 2. He said at that point the cancer was still “Stage 1,” because my lymph nodes appeared not to be involved. He told me I needed to see a surgeon as soon as possible. I said I already had a follow-up appointment with a breast surgeon for the very next day. He said that was “very good,” and he wished me his best.
After hearing the words, “I’m afraid it’s cancer,” I started scribbling some notes, because I knew my mind had switched into some other level of consciousness and I might not remember what else he said. I keep running across that little piece of paper with the scribbled notes, every time I sort through my BC documents. Seeing it still makes me shiver.
otter
-
Good evening brave women of May. I still don't post much, but look in on you all every day. I feel like I know everyone and amost felt like I could have been with Noelle and Rock last week. You all write such sincere, heartfelt thoughts - just like a regular conversation. I admire the feats of bravery that occurred during this last year and can't believe it's time to relive that year as the monumental dates arrive. This week I made my annual gyn appointment which happens to fall on the same date as last year which lead to the mammogram that lead to the U/S which led to ...
Kind of like the story "There was an old lady who swallowed a fly". I didn't feel my lump. I went for a gyn appt because I was just few years behind on the check ups and my 93 yo grandmother found out she had bc. No one else felt my lump, either. It showed on the mammogram. I found out the day before my grandma died that I needed to have a biopsy. Her birthday was January 31 so there are reminders of her and of my ordeal just about month.
But, as you've all said, we are here to start this new year. My hair is on its way back with a lot of gray and curls and could pass as an intended style. I say it is the most expensive perm I've ever had (around $60,000 for chemo) and I have ONE tan boob that cost about the same. I'm still trying to keep a sense of humor and enjoy the funny quips I've read here.
Weather in central Illinois today - high of 0 with wind chill of -15 to -30 and kids were home - just when I had gotten used to them being back on schedule.
I'll try to participate more in the group this year!
Thanks for listening,
Julie
-
Hi, Julie--welcome back!
otter
-
Thanks, Otter!
I finished rads in early October and then made it through my first mammogram and follow up appointments. I still seem to have issues that my family doesn't get and I still just feel comfortable here. This is just a great place to belong!
Julie
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 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