Illinois ladies facing bc
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Hi amosmaom. This is a wonderful group of women. We don't discriminate by stage only by location. (Well not really since we have folks in AZ and WA these days). Welcome. I'm not being treated at Northwestern but I don't live that far away. (Lincoln Park). Let me know the next time you're in town. If I'm not working I'll meet up.
Joan I hope you infection gets squashed by that antibiotic. I might be able to meet for lunch if I'm not working. Ironically I'm getting inked the next day at my PS (near northwestern).
Robo no hair on your legs yet
Glad you are starting to feel better. Makmak Hows Gabby?
Long day today. I came in at 1pm… left after 8pm. So much for a 1/2 day. I have a feeling tomorrow might end up being a full day too. Still don't know if I'll be working next week. I hear January can be slow.
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Susan:
I trust in the ebb and flow of the universe. I trust that life's bigger than what I can see. I trust that there is a divine order beyond my control. And I trust that no matter what happens, I will be all right.
Oprah Winfreysometimes we don't get to pick and choose --- and you know there would never be a way to find out how strong we really are if there were not things to test us. There is a season and time to everything and everyone and I'll admit, it is much easier to be philosophical in a situation that does not concern me other than I love and care about you....and to that extent about your loved ones. I just know and feel that accepting our powerlessness makes us able to withstand whatever happens. You know that I don't believe in luck, chance, or anything just happening. So all we can do about most things is to pray for acceptance of what will be and the strength to deal with whatever that outcome may be.
Of course in the meantime....I will be praying for a positive outcome, and hope with all my heart and soul that it comes out that way.
Hugs, Jackie
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Amosmom, welcome and this is a good place to hang around. The majority of us are definitely not Stage IV, but we have no problem hanging out with you. We are here to help each other and you are one of us. These women are pretty much always up for having a good time and just about anyone can do that..........so your in.
Saying hi to Spunky, Lisa, Robo, Joan ( how dare that boob ) and mdg, hawk Lago, & Wendy. I'm running late -- didn't get hone until after 8 p.m. tonight so need to get settled down. I'll be looking for all of you in the morning again.
Hugs, Jackie
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Feeling stressed out. I had to call my surgeon and have him call my primary doct to get the pre-op work up set up....I should have to be the one dealing with this.
It doesn't help that we got anew provider and I ve to start this process all over again. The old compan won't transfer any information to the new one.
Surgrey is a wk from tomorrow.0 -
Lisa7290---So sorry that on top of everything you have to deal with insurance. But if you learn anything on this board, learn to be your own advocate, do everything yourself so it gets done in YOUR timeline and make copies of EVERYTHING!!!! It helps to have all those boxes ticked BY YOU so you know everything is all set up and done so you can then concentrate on you. Hugs!
Jackie...you said to Susan what I always say ...."it is what it is"...but you said it so beautifully and so much better than I ever could. You truly have a wonderful gift.
Have a wonderful, happy Thursday! Hope you gals waiting see HAIR!!!!!0 -
Lisak Wendy is so right. Before my BMX there were so many screw ups (ended up firing my gyno but that's a long story, place that I got my mammos/US took 3 tries to get the right US disk, hospital had me scheduled for the wrong kind of biopsy even after I questioned it, given someone elses blood test script!) You really need to watch all of this… but this first surgery was the scariest and most stressful for me.
The doctors usually catch these things though.
BTW I am now on my 3rd insurance starting Jan 1st since this thing started… another long story.
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Happy New Year!
We had a nice week in Michigan with friends. Good times but too much food!
My laptop blew up while we were there and I couldn't check in (I do not like browsing the web on my Blackberry). It is amazing how dependent we are on computers!
Susan - prayers for your dd and her baby! I am the opposite and always think positive so I will send positive thoughts your way!
Joan - hope the infection clears!
Hi to all the new girls! Back to work now...
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Self-care is critical to having a strong inner foundation.
Taking good care of YOU means the people in your life
will receive the best of you rather than what is left of you.
- Lorraine Cohen0 -
Lisa....the quote is for you and for everyone who has to "track" down their own answers for their care. I was fortunate in that I wasn't required to seek out my medical team, nor needed tests, exams or anything -- I lost my insurance and by fortune had the V.A. ( Veteran's Administration ) to use. Just how things worked out....I feel I got better care than I might have had I still had my lost Insurance. -- but I did not pick and choose --- had to take what was offered and it turned out to be fantastic. Like Wendy says.....in my case it is what it is or was what it was......but most of you are in the position that YOU have to take charge.
Thinking most of medical care these days, no matter what you are doing is probably better when you take a very active part.
Sunny day....getting up to 60 today!!!!!! WHAT ???? This just isn't our normal winter weather and as usual, I'll enjoy but underneath worry about that old shoe -- hope you are getting something tolerable there.
Joan, you are coming back to quite tolerable. At least makes having to come back have a decent side to it.
I'll be checking in after work, and will see you all then. Here's to a positive day for everyone.
Hugs, Jackie
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Happy New Year to everyone! Went to Atlanta to visit old friends (two other families who also moved out of Michigan a few years ago). Had a good time, but car trips can be stressful at times. They have a very nice aquarium in Atlanta. Tasted some southern BBQ, too.
Kelly--congrats on getting the drains out!
A trip to Traverse City in June was one of the best sister weekends my sisters and I went on....it was unseasonably warm, and beautiful. Love the cherry gift shops and wine tasting. The coastline nearby was so beautiful....
I was focusing less on BC and more on family over the holidays...now it is back for two more chemo treatments before rads.
I'm so glad to see the sun is coming up earlier and staying up longer again!!
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Thanks all for the great vacation ideas. I have a lot to research and dive into thanks to your suggestions.
Susan, your daughter and future grandchild are in my thoughts. Please keep us posted.
MDG, Dr. Fine did grafting for you? Where did he graft from? Does this mean you don't have to get tattoos?
Amosmom...let me know when your next appointment is and I will try to schedule my check in with Dr. Fine on the same day/approx time. I am supposed to see him near the end of Jan, and its just to check on how my fipples are healing...so in and out appointment, and very flexible.
Looking like we might just have a mini get together at NW in Jan with a few others here.
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Thanks everyone! You are all the best. I cannot tell you how grateful I am for your care and concern. I hope that I can give to you in the way you give to me. I will keep you posted.
Lots of chatter here. Corinne, as you get closer to zeroing in on your summer destination, let me know if you are interested in Waupaca. The better places get booked by February and some lakes are better than others. I can tell you more. This is definietly a family place and in no way spa-like.
Where is Laura? I miss her posts!
I am going over to the health club (actually it is a park district facility in Glenview) daily and I want it to become a habit. They say you have to do something for five weeks before it becomes a habit and hard to give up. I have a ways to go as I could easily give it up right now!
Lisa, it sounds like a tangle to me. When I am under the weather, I want people to take care of it all. Wendy and Jackie give the best advice, however, and again I am reminded that we need to be strong even when we feel so vulnerable. Again, easier said than done. Do you have a friend or family member who can go over all your plans with you to help find anypossible loopholes? Or does the doctor have a person on staff who can help you organize? I know my oncologist had an office manager and she was great about coordinating events.
Have a good day, dear ladies, and thank you again for being there for me. I have decided that we have three things in common: we have or had breast cancer, we generally all live in Illinois, and we pretty much are the most caring people on the face of the earth.
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I'm here! Have been a lazy butt!
We're doing a lunch bunch on January 13th...Schaumburg area. If anyone's interested send me a PM.
Welcome to the new girls. Sorry you're here, but glad you found us.
Have a nice day...back later.
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Hi, Corinne ~ We (my DH and I; he is a rock and hasn't missed any appts!) are downtown on the 9th and the 16th in the afternoon, if that works for you. Would love to say Hi! Just let me know.
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Hey, everyone ~ What I meant when I said I scared the crap out of the Stage I/II women in the support group is that my initial Stage II diagnosis was in 1998 ~ after lumpectomy, chemo, rads and 5 years on Tamoxifen, I had been NED since 2004, and had not given a thought to the possibility of mets until I had shortness of breath in December 2009. My reaction to this round is very different from 1998 ~ of course, I am also 13 years older, and my reactions to a lot of things are different!
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zap - Sorry to hear that DD is back on the monitor, but I am glad to hear that she's with an MFM group now. I know the "unknown" can be very scary, but it sounds like they're both in good hands, and much has already been ruled out. Hugs to all of you.
amosmom - Interesting to read about how your reactions to things have changed a lot since your first dx. I haven't had a recurrence, but I do often think about how different I was 6 years ago when this all started. I like to think this unwelcome life "experience" we've all had has definitely made us stronger women, with a bit more insight into ourselves and the world around us.
Pardon my babbling... lol.
LisaK - GREAT advice from Wendy about the necessity of being your own advocate. It's annoying dealing with the red tape between doctor's offices, insurance companies and hospitals, but SO important. Good luck to you with your surgery.
Nancy Jill - Glad you were able to focus on family for the holidays. Back to getting that pesky chemo done and behind you now!
Joan - No fair having a nasty infection ruin a perfectly good trip! Hopefully that Levaquin will do its thing and you can enjoy the rest of your time there.
I've only been home a week post-op and I'm starting to get a little stir-crazy. As much as I always think I want to stay home full-time, I think I really suck at it. LOL. The new boobelas are looking fine, although still sore at the incisions. My symmastia repair area is (as I thought) the most painful and slow to heal area. I'm wearing my (notreally) sexy thongbra most of the day and night, and almost getting used to it. There are still a couple of divots where he put some power-stitches in for the symmastia repair, but I'm told those will lessen in time.
Looks like a ridiculously warm day for January out there. I think I'll open a few windows and get a winter airing out of the house. Unless the windows are stuck that is. My pecs aren't really ready for battling jammed windows right now!
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Hi ladies! Im currently going through chemo at RUSH but have an upcoming BMX in february, where did you ladies go??? Im located in Barrington
anyone near by????0 -
Welcome KatieP. I am in Geneva and have my docs at NW. Many of us have had BMX so ask any questions you like.
Corrine Dr Fine used my stomach skin and c section scar for my grafts. PM me if you have more questions or want to chat. I did put one photo on the photo board a few weeks ago. I have to update it though.0 -
I did meet with dr fine! He was very nice! Who was your breast surgeon at NW?.. Im also getting dr.s who tell me i dont have to do both but because im 23 they understand why i would want to... How did you ladies decide MX vs. BMX? Whatd they say at northwestern? Im currently at Rush, i liked their team approach over NW but that was my second choice. I saw dr. Khan
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Welcome Katie
I see Dr. Bethke and Dr. Fine at NWMH. Are you with Dr. Witt? He has a great reputation too.
I made the choice to have a BMX, although I had ILC in the left breast only. I chose a BMX, and the decision was mine. I was told that a lumpectomy was not an option for me (small breast to begin with, would have to have a MX) so I chose a BMX to reduce the chance of it returning and for symmetry reasons. No regrets.
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I chose bmx due to dense breasts and concern they could miss another cancer. Also for symmetry. Much easier than trying to match the natural to the reconstructed. No regrets either.
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However be aware that you will lose sensation which is really hard to deal with. I didn't think it would because I was not that sensitive before but it is.
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HI Katiep, Welcome. I am nearby in Crystal Lake. Went to NW for my BS who is Dr Nora Hansen, director or the Lynn Sage Comprehensive Breast Center there. She is wonderful. She layed out my options and made me DECIDE. Easy for me.. with two very dense breasts. Just wanted them both OFF. At your age, it is very understandable that you would be interested in reconstruction.
Levaquin seems to be doing the trick for my infection. Thank God. Will be interesting to see how my next consult with PS goes on Jan 16th at NW.
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Corinne- thats how i feel totally, theyre telling me that the chance is low but i just dont trust that, also ive never been symmetrical and would like to be.. Do you ever wish you still had sensation? And yes im with dr. Witt and i love him more then words. What incisions did they do at NW? I want skin sparring but dr witt creates an ellipse around the nipple so a little bit of skin goes, but ive seen where they just take the areola?
Hopefulhealing- mine are dense too and fibrocystic so very lumpy which is what worries me i also dont want mammos and mris for the rest of my life and to always be afraid theyd find something... Sensation is something i worry about, but i didnt like my boobs before so id cover them up anyway during those kind of moments... Haha i thought about doing nipple sparing on the non cancer side.. But i duno if thats crazy.
Joan- you are close! Im actually in bhills right by fox river grove. I saw that you got rads, is the infection from rads? Did you get rads while you still had the TEs? Whatd that timeline look like? Does it put off the exchange for a long time? Any issues during rads? Theyree saying i need rads bcuz of my age even tho my nodes were neg.... So rads is my biggest worry on top of deciding whether to do bmx or umx im def leaning toward bmx i think the odds are just against me and i have to be extra careful0 -
Katie - I'm in Hawthorn woods...not far from you. I had my treatment (chemo and rads) and surgeries at Good Shepherd. Very with all. I'll PM you my Dr's names.
We are meeting for lunch in Schaumburg on Friday, January 13th...feel free to join us! EVERYONE here is invited!
Best wishes to you.
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Katiep just to let you know a friend of mine was diagnosed a 2 years before me. She just had a lumpectomy and rads. She didn't do hormone treatment (issues with tamoxifen). She was diagnosed 2 years later just after my 4th of 4 chemo tx in her other breast. She again did lumpectomy rads and this time luprin shots and AIs. She's 49.
It's true what the say about sensation. Remember you will be watched very closely now. Rush is know for their imaging. I wish I had been going there for my mammos. I bet they would have found my a lot sooner.
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LauraGTO - i too was at good shephard i live 5 min from there and had dr. Witkowski who i LOVED. He did my lumpectomy... However the radiology dept missed additional tumors in my imaging that the university of chicago saw from the same immages.... So i went through that surgery for nothing and now need more. Im very pissed at GSH but im glad none of this has happened to you...
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OUCH! Wow...sorry to hear that! My experiences with them were great...yes, I am fortunate. A different hospital missed my 4cm TUMOR for 5 years...I am very pissed at them. So...I know the feeling! Arghhhhhhhhhhhhhhhhhhhhhhh!
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Welcome Katie....glad you found our wonderful group but it infuriates me that this disease is making a 23 year old women need to remove her breasts. Damn cancer!!!!
I'm in Geneva with Mdg....I was diagnosed at age 35 and had my BMX in June. I just finished my chemo at RUSH on dec. 13th. Love the team!!!!
I didn't get any emails regarding the lunch bunch on jan. 13th???? I changed my address about a month ago.... I better send my new one to you Laura!!!0 -
MadMom I don't think she sent one. I didn't get one either.
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