Illinois ladies facing bc
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Morning, everyone!
Joan you are an over achiever with those drains Give yourself, and your fingers a little rest and time to recover. Your presentation sounds wonderful!
Welcome, and hugs to you, Val.
Lago, sorry about the job. The right one is out there for you, and all I can say is it's their loss. Love red licorice and the Pooh bear cartoon. My son used to love that bear!
C-square, good luck today. I did 4 AC, and did not take anything with me to tx. Tx at 9AM, and home about 12:30. I think it was faster because I was first of the day. No nausea, but some heartburn and fatigue. Slept more, and took Mylanta, extra strength, and got through it. I know you will too.
lisak, congrats on finishing up chemo! If you are hormone receptor negative they don't usually give you Tamoxifen or any other meds after chemo.They suppress hormones which are not the cause of triple neg tumors. I'm triple neg, and had 4AC and twelve weekly taxols. Then rads and finished. More than 6 years later, and dong well! Some women feel a little upset about having no more follow up meds, but I just looked at it as no more se's to deal with.
Jackie, I am really enjoying the quotes. Thanks for that.
Zap, I'm still rereading that wonderful paragraph you wrote awhile back. You are a talented writer, and the kids are so lucky that you keep working as a sub. it would be a loss to them if you didn't.
Have to get going, and get some things done. All of you, have a great day!
PS Wendy....do I have to go look for the temp on my own deck? You've got me spoiled!
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invisible2 - I found out yesterday too! I am not BRCA positive either! Praying for b9 for you tomorrow!
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Don't Envy Other Folks
Don't think when you have troubles
That your neighbor goes scot-free
Because he shows a smiling front
And battles cheerfully.No, Man! He, too, has troubles,
But herein the difference lies,
While you go idly moping round,
The other fellow tries.Don't envy other people;
Maybe, if the truth you knew,
You'd find their burdens heavier far
Than is the case with you.Because a fellow, rain or shine,
Can show a smiling face,
Don't think you'd have an easier time
If you could take his place.‘Tis hope and cheery courage
That incite one to retrieve
One's past mistakes, to start afresh,
To dare and to achieve.So smile, and if perchance you light
The spark of hope anew
In some poor sad and burdened heart,
All honor be to you.-Anonymous
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C-squared --- probably late....but I like Doxie's ginger tea. Ginger is a good thing. I am a big fan of Vernor's Gingerale......which I learned to really like when I live in Detroit, Mi for several years.
Valerie....thinking of you today as well. Hope you come through everything just fine with your valium glow.
You know.....sometimes I just marvel at the determination and strength of all of you. Got to thinking of you Jenn and the huge amt. of trepidation going into your first chemo.......and here you are --- able to present a picture that is not so bad. Guess the above poem really describes you. For every one....Jenn is Madismonny.
Lago's games are a good idea too. I didn't have a way to "play" but did do crossword puzzles during chemo...always good for me, even now due to transitory amnesia twice.
It is going to be so beautifully warm today......we will pay for it tomorrow.....heavy rain all day the weather forecast said...sigh !!!!! Hope they are wrong, but the bright side is....according to them, it's only rain.,....not thunderstorms, so no sound effects.....just a lot of water.
Enjoy your day everywhere and to those in procedures.....good positive vibes coming your way.
Pat/Smerf.....you are so wonderful with your encouragements -- they are just like a quote. This thread is chock full of can do and will do people.
Ok, Wendy.....Smerf is right.....and Rita....where are you???
Have a beautiful day.
Hugs, Jackie
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C-Squared -- thinking of you today, AC sista! And you as well, Valerie. I love Edwards's Hospital (even though I drive right past it to get to CDH for my treatments). Hello to everyone else this morning, too. Here's to all of us having great day (after a bit of an icky one for me yesterday)!
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Hi Ladies,
I am newer to the site and saw this group and was wondering if I could join you? I am in Schaumburg, IL. I had a lumpectomy to the right breast on 12/2/11, port put in 12/16 and have completed chemo - 4 A/C and 4 Taxol. I started 30 rounds of radiation this past Monday. I am getting my radiation at NW Community in Arlington Heights.
I work full time, am married and have 2 younger girls.
Hope you all have a terrific day!
Diagnosis: 11/11/2011, IDC, 2.1cm, Stage IIA, Grade 3, 0/5 nodes, ER-/PR-, HER2-
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Welcome Wishn. I really hate when someone so young gets struck down with this ugly disease. Sounds like you have been through alot already. I found rads to nothing more of a daily nuisance, until the last couple weeks when it began to zap my energy. You will do fine. Keep checking in.
Thanks everyone for your words of caution! I am feeling pretty strong and well prepared for my presentation, well except for finishing the PowerPoint. I have entitled my presentation "When Being Strong is the Only Choice You Have". I know that you all know what I mean there. My biggest worry now is getting a hot flash or two and wanting to tear off my clothes in the middle of it! Wouldn't that just top it all off?
This is a 2-night weekend conference, but with my latest turn of events, I will only be attending for a few hours on Saturday to have lunch and deliver my message. My DH insists on driving me back and forth and I will not fight him on that. I still haven't driven since surgery and frankly that is making me mad. I love my new PriusV and my DH is driving it every chance he gets. Wait a minute! Just so he doesn't change my radio presets and start storing his stuff in my cubbies.
Good luck to everyone going through surgeries and treatments today. My DH and I are about to head down to NW for my first post-op with PS. Sure hoping to come home with 3 less drains!
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Welcome wishn4one!!! Lots of gals here in your neck of the woods.0
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Welcome wishn4one! Joan - praying for a few less drains on the way home!
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Welcome wishn.....you have come to a fantastic place with lots of open arms.
Joan.....how many times I have said.....it is just amazing what you can do when you have no choice. You gals all make miracles happen.
Stay well,
Hugs, Jackie
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Hi Wishn...I so sorry you have to be here but know you will be happy you found this gem of a thread.
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Positive thoughts being sent to all those undergoing surgery/treatment.
Wishn4one-Welcome, wish it was under better circumstances though. Stop in often to ask questions, share thoughts and get lots of support.
Glad Lago and invisible got to meet. Sorry I missed the party-I was at Rush last week. (picked up some cute half-price Easter things in the gift shop-apparently there is nowhere I won't shop)
Had my last appt with my PS at Loyola today-I'm really going to miss him, but new insurance doesn't cover Loyola. Feel free to make suggestions-I have no idea where to start to look for a new one.
Hope everyone is well!
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Spunky I was at Rush Tuesday last week. Don't tell me we where there the same day
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hello Illinois ladies, i live down near peoria, Illinois - just started chemo on Friday the 13th. I am 43 years old. Can anyone make some good suggestions about what to do with this acne that the chemo has given me and also the dry/chapped lips. I have used Aveeda, CO Bigelow, Chapstick etc. Maybe i want instant relief :-) Thanks,
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Cindy It's best to ask your onc about something for the acne. I know some folks get it. Sometimes it goes away on it's onw. For dry chapped lips I always found good old petroleum jelly worked best. I also used the Aveeda product as well. If you're going all natural then maybe others can chime in.
Welcome to the IL Ladies Thread. BTW if you are limited on your daily posts (they do that to newbies to make sure you aren't a spammer). You do have unlimited PMs. Be sure to post your full quota a day so you can get of limited post duty.
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How come everyone's always at Rush when I'm NOT???

Spunky.... the one giftshop there has some great stuff, particularly in their sidewalk sales.... I used to shop after my bloodwork and before my chemo! LOL
Welcome Wishn.... glad you found our thread!
Jackie... that's so true about me, look how far I've come in regards to chemo?!?! I was so darn scared, remember my buying EVERY single item post on BCO in regards to possible s/e..... i barely used any of them. I just needed to be prepared for the worst..... And now i'm just impatiently waiting for my hair to grow out more than a "bedhead" looking buzzcut.....
Robo.....how's the hair growth on your end? When are we burning our wigs?
Joan....i remember how annoyed I was with not being able to drive after my BMX.... i didn't drive for over 3 weeks.....
Hopefully you get to reclaim your car SOON!!!! Where's mdg been hiding?? And Mak?
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Lago-I was there on Tuesday-9:30a. It was a follow up with the gynie-onc for my oomph so it was a quickie. It took me longer to park than the entirety of my appt-mind you I'm not complaining, just making an observation.
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Hi ladies, I am out here in the western suburbs. I am back at La Grange where I had radiation for Hodgkin's Lymphoma 20 years ago. I am not thrilled to be back there, but love my doctors. I have my BMX behind me (almost 4 weeks now) and am just working on getting these annoying expanders filled. I was not eligible for more radiation (hence the double mastectomy) and I don't need chemo. I will start Tamoxifen in about a week. Nice to meet you all.
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spunky My appointment was at 9:30 too. Yes the parking was crazy that day. I never saw anything quite like that. I also got my port flushed so it took more than a few minutes. Also, since I haven't been seen by my onc/np in a year (saw my BS 6 months prior) there were lots of questions.
Hi DeborahC. {{{waves}}}
Did we just get 4 new IL ladies today?! WTF! What is going on?
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Lago....I read an article in a magazine on my way home from Mexico saying the occurrences of BC will rise by 26% by the year 2020...
Stupid cancer!!!!
Welcome Deborah! I'm in the western burbs too! Did you have your BMX in the burbs too?
Edit to fix my bad English....scatter brain sometimes.....lol0 -
Thanks for the welcome. I'm happy to find a friendly group. Yes, I had my surgery at La Grange Hospital. I thought about going to U of C, but I found a great group of local doctors and decided to stay close to home. I had my cancer surgeries at Michael Reese 20 years ago - but that's no longer an option!
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I chose to have my BMX close to home too.... I live in geneva and had it in st. Charles. I ended up needing chemo so I went downtown to Rush for that.
This group is wonderful.....we even get together in person a couple times a year!!! The greatest support system!
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Welcome DeborahC-I'm a west suburbanite too. I chose Loyola for my BMX/recon, but am moving to Rush for insurance reasons.
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So glad you new ladies found us. I'm just home from work and got my chores done here -- almost 9 p.m. so I have mentally shut down as I seem to do lately most nights ( I work from 1 p.m. to 8 p.m. You have come to a great place and we are all glad....but it will take me a while to sort you all out. It is a caring place where hand-holding is a big priority......
Lago didn't say....but she is your linky girl and will have you covered. I put in quotes 365 days a yr.....and try to do it in the morning. There are some nurses here as well as Lago's links so you can get lots of info here if and when needed......in the mean-time we keep you company because it can be a long road and the people who understand best are all wearing the same shoes.
Scary about the "rise" of cancer. Ten yrs. ago I didn't know anyone who had it --- now I'm thrilled when I find people who haven't. It's a backward world isn't it????
Hope you all have an great eveing....what's left of it. See you tomorrow.....
Hugs, Jackie
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Hi to the new ladies. Yes, wish we did not have to meet under these circumstances. You will find lots of companionship here.
Well, my PS was very happy with the way things are looking. In his words, "they are looking beautiful". Gosh, only your PS would say something like that when looking at these reconstructed foobs, right? He had his nurse pull two of the drains. So, I still have one in front and one in the back. AnyWay, it's a lot lighter load and more comfortable. I go back next Thursday and hopefully lose the other two.
Both my PS's nurse and his scheduler commented on how busy my PS has been with breast cancer reconstruction cases. Nurse also mentioned what a rise they are seeing in very young women, in their 20's even. Something is definitely going on. We need a cure, or better yet, a vaccine.0 -
Couldn't decide which moved me more so two for the price of one today:
Obstacles are like wild animals.
They are cowards but they will bluff you if they can.
If they see you are afraid of them...
they are liable to spring upon you;
but if you look them squarely in the eye,
they will slink out of sight.
- Orison Swett MardenFormulate and stamp indelibly on your mind
a mental picture of yourself as succeeding.
Hold this picture tenaciously. Never permit it to fade.
Your mind will seek to develop the picture...
Do not build up obstacles in your imagination.
- Norman Vincent Peale0 -
I'm sitting here waiting for the rain that is coming. I'd like to *not* see this obstacle to the day's enjoyment for me, but it isn't going to work. If I want any impact, I'll have to decide I like rain ( actually don't mind when we really need it ) and develop a great love for liquid ground nourishment.
Joan....you couldn't be more right.....we do need something. People having had or just now getting diagnosed with C should not be in the majority.
Despite what happens today, I am sure loving the Spring green. I can barely make out the house on the next street ( probably about 12-14 acres from me........now that the Spring foliage is all but totally filled in. I'm able to hide back here in the woods now.......just the way I love it.
Hope you all have a great Friday and lots of success whatever you do today.
Hugs, Jackie
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Facebook seems to suggest friends for you "people you may know." Usually they are friends of friend. For some reason Facebook seems to keep recommending my Onc. Not sure how the bots know the connection. I'm a little creeped out about it.
No I didn't friend her.

TGIF and TGITW
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Lago, you must have some particular activity, website, intersest in common with your ONC. Wonder what that would be? My PS has a business page on FB that I have "friended". He doesn't post very often on it, but always is interesting stuff.
Brrrrrr! What happended with this weather? Have a great weekend everyone.
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It must be the ACS. I defriended Komen

Weather… this is actually typical for April. Remember? Maybe our May will be nice. In the past we have had May in April and April in May.
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