Nurses with Breast Cancer

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  • RitaD
    RitaD Member Posts: 30
    edited March 2011

    Sorry about the typing Patti,didn't notice till now.Back at work,they allowed me to come back part-time first month,then I go full swing ahead. Still get kind of wiped out at times.Just went back to onc. yesterday,so far so good.Looks like spring is around the corner here. Started some seedling of veggies inside and plan to have a nice organic garden when it warms enough to plant.Take care,Rita

  • Bailey5
    Bailey5 Member Posts: 63
    edited March 2011

    Hello all:

    I've been mostly reading now x six months. Kinda shy...

    Anyhow, I just completed phase 2 of reconstruction

    (ie. Fipples, lipo hips and ultrasound-guided lipo(for thumb-

    sized necrosis to B breasts)

    No lift.(per PS--dunno why not)

    Much better than my 8/6/10 B MX w/tram flap; I had 3 months of visiting

    Nurses coming by to dress my wounds!)

    Less nausea after the anesthesia. No BM yet and Surgery was 3/21/11

    But I'm taking Meds for that.

    I have B arm pain generalized; and b chest. Area pain& bilateral belly pain; at about 10 w/o

    Meds and goe to about6-7 after pain Meds! Any tips please advise. Thank you

    Oh yeah I'm a school nurse but I'm not sure I'm going back(strenuous) to school nursing!

    I do have off until 8/10 to decide. Anyone else give up dreamjob after

    Going through this?? My administration was unfair, an unjust throughout the

    Past 9 months!! (mainly insurance issues; but nasty discriminatory derogatory

    Unjust letters added so much stress; not sure I can go back physically or emotionally!

  • NativeMainer
    NativeMainer Member Posts: 10,462
    edited March 2011

    Bailey--glad you found us, glad you posted!    To answer your question, I got my dream job teaching in an ADN nursing program shortly after diagnosis. I was fortunate to have a lot of support from fellow faculty, I would not have gotten that kind of support from the home care agency I left.  Nurses and healthcare employers can be very unsupportive of nurses who develop an illness.  We're expected to take care of everyone BUT ourselves all the time.  The stress of the way you were treated is certainly adding to your pain.  Are you taking your pain meds regularly?  Taking them on a scheduled basis can help keep pain from getting out of control.  What are you taking for pain med?  Can you add some tylenol or advil?  It's surprising how much help those can be when taken with pain meds.  Just be sure there isn't some already in your pain meds.   Make sure you are taking a stool softener AND a laxative to get the bowels going again, Sennokot S works well. Drink lots of water, too, try for 2 liters per day.  Talk to your PCP about getting on an antidepressant for a while, that will help with pain and with the anxiety/stress/anquish you are experiencing.  Take your time about making any decisions right now.  You have a while, take the time.  

    edited to remove a stupid statement about checking the Nurses with bc thread, forget where I was for a moment!  Cancer brain strikes again!

  • NativeMainer
    NativeMainer Member Posts: 10,462
    edited April 2011

    WARNING--RANT AHEAD----WARNING--RANT AHEAD

    There's been a lot of talk over the years about nurses eating our young.   I would like to propose that nursing students have begun eating nursing faculty and instructors.  I know, because it's happening to me.  I am a full time faculty in a 2 year ADN program.  This is my fourth, and will be my final year teaching.  Why am I leaving teaching?  Because I cannot figure out how to teach competent, quality nursing while simultaneously pleasing the new breed of "student consumer."  Earlier this semester, a semester in which I was dropped into a new clinical facility without any orientation or support, with about 2 week's notice, the students complained to the program director that I wasn't providing them with the experiences they need.  They weren't getting OR observations (it took me a while to figure out who to contact and how to reach her to set that up), that I was not allowing them enough independance with med administration, that I wasn't giving them enough different experiences, especially not enough complex wound care, that they didn't like getting doubled up on patient assignments.  So I changed the way I did things.  I pushed them into more independance with med admin.  I don't double up the assignments at all anymore.  I arranged extra OR rotation times.  I have continued to double check that diagnoses and problems aren't assigned to a particular student more than once.  Today I called into a meeting with the director. Why?  The students are complaining that I am not supervisiong them closely enough during med admin.  They're getting patients that are too hard to manage without a second student to help.  Three of the 7 seven stufdents didn't get one of the "best" OR rotation slots.  Only one student gets the complex wound care patient when there is one on the unit.  I"m trying to hurry them up too much and not sweet and pleasant when I'm doing so (this means that I come and get them out of  the break room when there patient rings the call bell).  Somehow I'm supposed to magically fix this and make the last 3 weeks of clinical perfect.  

    Fuck it.  I've already turned in my resignation for the end of the semester.  I told the director today that I'm not sure I can go back to clinical with this group, and I really don't want to.  Right now I am seriously considering going back to the office over the weekend, packing up all my stuff and disappearing.  Send them all an e-,mail that I am resigning immediately so they can get an instructor who better meets their needs.  (little history--we were 5 weeks into the semester before all the clinical instructor positions were filled.  No way they'll find another instructor to finish the semester. Not that they know that.)  

    You know what the topper is?  Whoever it was that complained actually told the director that I must be expecting special treatment because I had cancer.  

    In the mail today is a request to teach a summer session.  7 weeks, once a week for 2.5 hours, getting LPNs up to speed  and ready to jump in at the second year level next fall.  For $825.00,  I'm sending it back with a take this job and shove it note.  

  • 2Hands4me
    2Hands4me Member Posts: 484
    edited April 2011

    So sorry to hear you've had to deal with this experience! Seems the younger work force (in general) has a different work ethic. They want the pay with as little effort as possible. At my husbands work, they come in late, call in sick, don't show up, or don't dress well. At my job, we hired several new people into our rather small department. So many just want the social aspect with the doctors, or don't want to do the on call hours, or want to do things their own way regardless of how it is usually done. It's really too bad that the new students are already functioning with this behavior. (It's all about ME!) How can we change what they haven't been taught by their parents? Yet if we lose the experienced nurses..... what will happen to the next group of nurses - and PATIENTS????

    I certainly understand your frustration! Can you find work in another area of interest where you can make a positive impact on patient care?

  • NativeMainer
    NativeMainer Member Posts: 10,462
    edited April 2011

    2Hands--I have already had a second interview for a home health position with the agency I already do some per diem work for.  I also have 2 other applications out for direct care jobs.  Any one of them will nearly double my income in addition to being direct patient care positions that I will enjoy and be good at.  My choice now is to try to finish out the semester or walk away now and make a statement.  Another long term faculty member is retiring at the end of the semester for pretty much the same reasons (plus age) and another one announced her retirement today, and I know she has had similar experiences recently. 

    I am scared to death about what is going to happen to patient care in the future.  I'm even more scared about what is going to happen to me when I have to be a paitent in the future. Nursing education is becoming a business of recruiting students, getting their tuition and passing them through.  As long as they pass NCLEX everyone who counts is happy with the school. Nurses have no responsibility to the profession or patients anymore.  

  • Jo_Ann_K
    Jo_Ann_K Member Posts: 277
    edited April 2011

    Native,

    Kudos to you for putting your needs first! It is a sad commentary that today's nurses have been sold a bad bill of goods that they will go into nursing and all be managers and won't have to do any of the dirty work like actually "care" for a patient's most basic needs.



    I also came from the generation that worked as long as I was needed, even if the clock passed eight hours. I never left a patient in need without someone taking over. I CARED for my patients in every way.



    Today, I work outside of the healthcare system for the first time in my career. I use my nursing informatics skills for a government contractor. The envt is calm. People respect each other and actually help as needed. The lack of stress is quite an adjustment, but oh so lovely. No more of the crap and desperation for me. Foronce, I will come firsy!

  • RitaD
    RitaD Member Posts: 30
    edited April 2011

    Native Maine,Nursing has changed so much. Agreed,work ethics have changed with the younger generation of nurses.Not sure what you did in the end,keep us posted.At my job we are struggling with new nurses. We had a big retirement incentive and with that ,nurses left with tons of knowledge and experience. Standard of care is declined and definately not dedicated as before.

  • NativeMainer
    NativeMainer Member Posts: 10,462
    edited April 2011

    In the end, given that I couldn't say anything negative to a student without it being reported as retaliation, I gave my notice on the grounds that I could not ensure patient safety in the clinical setting.  Got to drop that bombshell on the students last Wednesday.  I start a weekend job with a local home care agency on the 25th.  I already work there per diem, so it won't take long to get up to speed with the computer charting, admission processes, and hospice care.  I've done it all before, enjoy it and am good at it, and most home care patients are appreciative or at least courteous.  I'll be making $5K more per year working 32 hours (before weekend and call differentials) than working full time teaching.  The employer evals the university was getting back (granted very few employers do that but a very few still do) are indicating that new grads are not team players, not dependable, not good at working collaboratively.  More and more patients are refusing student nurses due to bad experiences with new grads.  The program I just left re-worked it's vision, mission and values.  There is no mention of the patient, clinical competency or collaborative care.  It's all about "holistic care" that includes "self care" by the nurse.  Crazy. 

  • jacgrehanjul
    jacgrehanjul Member Posts: 17
    edited April 2011

    Happy Oncology Nursing Month.  ONS Video Contest:

    http://www.youtube.com/playlist?p=C686AEDE9943C68F

    Some will make you LYAO!

  • cajmi
    cajmi Member Posts: 80
    edited December 2011

    Hi All,

    Yet another addition to the group.  I've spent the last 3 weeks since my abnormal mamm reading and was very pleased to find this group.  So, now it's official, I've been diagnosed with DCIS intermediate grade with focal necrosis and calcs, ER+/PR+.  I will get more info tomorrow when I meet with the surgeon.  I have spent my 8 year nursing career at a major pediatric hospital working the night shift.  I would love to ask some questions if anyone has time to spare. I'm really curious about some of the reconstruction techniques and results.  I'm very anxious about the prospect of rads and tamoxifen and wonder if mastectomy wouldn't be a better decision as I have a sister who was diagnosed with stage 4 IDC last year.  So, if anyone wants to chat, drop me a line:>  Thanks and God bless you all!!! Carolyn

  • NativeMainer
    NativeMainer Member Posts: 10,462
    edited December 2011

    Hi, Carolyn, welcome to the club no one should ever have to join.  The first peice of advice I would give you is to take your time, do your research, don't let anyone rush your decision making.  The second piece is to not let anyone know you are a nurse.  Once the docs/office staff etc find out you are a nurse they stop giving info, assuming you know everything you need to know becuase you are a nurse.  They won't stop and think that pediatric nurses never take care of breast cancer patients.  I had a bad time with rads (someone's got to be in the less than 5% who gets the bad side effects, after all) so I won't speak to that at all.  As to mastectomy/recon, that's a personal choice, and no one approach is right for everyone.  I finally had the other breast removed and both reconstructed becuase I couldn't deal with the annual mammogram appointment for the remaining breast, with the inevitable extra views every year.  While reseraching reconstruction be sure you talk to a PS who does DIEP recons, PS's who do not do them often give the wrong info about them and surprsingly few actually are accrediteded to do DIEP.  No PS in Maine is, despite a couple saying they do the procedure.  There are implant procedures, skin sparing mastectomies,  and lots of options, besure to take your time looking at all of them before you decide what you want.  How old are you and how old was your sister when she was diagnosed?  If either of you were younger than 50 then BRCA1 and 2 mutation testing is in order.  These mutations inc the ris of breast and ovarian cancer and strengthen the argument for mastectomy (and sometimes oopherectomy). 

    I personally had DIEP reconstruction.  I was emotionally upset at the thought of putting a foreign body (implant) into my breasts after having them removed.  I opted not to have skin sparing procedures becuase that felt like only doing half the job to be.  I know that 's not statistically true, but the emotional response is as important as any other response you have, and worth paying attention to.  I was not a candidate for tissue exapnder/implant on the irradiated side anyway, since the tissue was so damaged by the radiation. 

    Some things to consider regarding mastectomy/recon:  where the scars will be and what they will look like--tissue taken from another site leaves a scar at that site.  Recovery time, with lifting limitations and the like vary from procedure to procedure.  There are areas of numbness left by any of these surgeries, often permanent, and it's important to know where those areas will be.  The total length of time of the entire recon varies by procedure.  Almost all procedure except the skin and nipply sparing ones are multiple step, requiring multiple procedures/surgeries.  If you opt for non-skin sparing mastectomy, then you will need to think about nipple recon and arueole tattooing to "finish" the job.  I put finish in quotes because I chose not to have nipples made or tattooed, so I am considered "unfinished" in the recon world.  Not that I care.  

    Another thing to keep in mind is that recon can be done anytime.  I had a lumpectomy, rads, mastectomy due to rads damage, then spent a year researching recon and wound up going out of state for bilateral DIEP.  Which is another factor, what procedures are available locally and which require travel with associated extra costs and time.  

    So have you got twice as many questions now as before I started?Wink

  • rc778
    rc778 Member Posts: 56
    edited December 2011

    Hi Carolyn,

    I was diagnosed with DCIS last Nov and tomorrow will be a year since my BMX.  I chose to go that route because of a family hx, very dense breast tissue, and my nature of being a worrier.  I got immediate reconstruction with expanders, which I think were the worst part of the whole experience.  Once the fills started though, they did not bother me as much.  The surgery was not as horrible as I expected.  Pain wasn't an issue...pca pump for 1 and half day, po narcotics for 2 days then motrin when needed.  The lack of energy was my main complaint, but I got it back within 1-2 months.  I had my permanent implants put in in May.  They look good but are nothing like having your own breasts.  I still am not used to the lack of feeling/sensation, but I would do it again if I had to.  Hopefully you'll get some feedback on rads and tamoxifen as I did not use these.  Feel free to PM me if you have any questions.  Good luck.

  • cajmi
    cajmi Member Posts: 80
    edited December 2011

    Hi All,

    Had my appointment with the surgeon yesterday who suggested just what I had guessed, lumpectomy with rads and tamoxifen.  I asked about an MRI and he was intially not on board until I reminded him of my family history and explained that I had reservations about rads and tamoxifen. I told him I understood that this could show addidtional areas that would require biopsy, but even though they would most likely be benign, it might push me more toward MX. I am 48 years old and my sister was diagnosed at 52, so he also decided to do the genetic testing.  After talking to his nurse, I found out that a large percentage of recons fail after rads, and may docs won't even attemp it.  Anyone have any input on that?

    At this point I am scheduled to meet with plastics on Jan 5 and Genetics on Jan11.  I assume that if I proceed with BMX that I won't need to take the Tamoxifen does anyone know if this is true? 

    I know that BMX seems a bit extreme and I don't want to overeact, but I feel as if I'm making a decision based on facts and not emotion.  I do however, want to make sure I have all my facts correct.

    I have an HMO, so I am resticted to the system.  If I choose to do the BMX with recon, they do not perform the DIEP procedure.  My general surgeon said he was comfortable with a skin sparing and possibly part of the areola, but not the nipple.  I assume this may provide a better cosmetic appearence. Obviously, the plastic surgeon will be able to provide me with better info regarding this.

    Does anyone have a ballpark estimate of how much DIEP would cost without insurance?  There are several docs in the area who actually do perform the procedure.

    Has anyone had the BMX and really regretted the choice? All opinions welcome, as I want to consider all angles before making this huge decision.

    Nativemainer, thank you for all the information!!!  Now I have all kinds of good info to ask the PS.

    RC778, Thank you too for your response!!!  What made you choose implants over a DIEP or TRAM procedure?

      Support is a wonderful thing!  Without sharing too much sappy info, I've meet some fantastic women through support groups.  I had a child with Angelman Syndrome who taught me so many wonderful things, one of which was how to deal with difficult situations...  So, this is just another bump in the road.  I am thankful for all of you wonderful women who are willing to share your knowledge and experiencesSmile.

    Thanks again,

    Carolyn

  • Jennt28
    Jennt28 Member Posts: 2,021
    edited December 2011

    Hi all, I'm Jenn and although I'm not technically a nurse I'm hoping that you won't mind me joining you because I'm a cancer clinical trials coordinator running two renal cell trials here in Australia, and like you this means I've got a little bit more initial knowledge about the whole disease/treatment process which I'm finding helpful but also a bit scary because I think I know too much...



    I was diagnosed on 1st December 2011, had a wide local excision with 1 sentinal node removed on the 9th of December and am now due to meet the oncologist his coming Thursday to get "the plan" with all the dates for chemo. I already have an appt set-up with the radiologist on the 17th of January as well.



    My sentinal node was 5mm with extra-capsullar (0.6mm) extension however I declined ALND this week after doing some reading of the latest research. Since I'm ER+ PR+ Her2+ I'm up for the full gammut of chemo and radiation and herceptin and hormone therapy anyway. Feel very good about this decision since a CT scan (brain, chest, abdo, pelvis) this week showed no signs of residual disease in my axilla or anywhere else :-)



    regards Jenn



  • 3girls
    3girls Member Posts: 94
    edited December 2011

    Hi,  I am RN dx in Sept this year.  I am scheduled for AC x4 every 2 weeks and taxol with herceptin every week for 12 weeks. 6 weeks of radiation and herceptin every 3 weeks to complete a year.  This is so overwhelming, initially thought i would be having lumpectomy and radiation- but dx changed after surgery.  I work 3 12 hour nights in an ICU.  My main concern is being able to continue to work through all this as I don;t have much sick time accrued.  I did really well after my 1st AC and am scheduled for my 2nd on Mon.  It's kind of hard having some knowledge- I just took care of apt with heart failure secondary to the AC he received for treatment of leukemia:(  Trying to have a positive attitude and taking one day at a time!  Jen and Carolyn good luck with your appts!  We CAN conquer this!

  • starbeauty
    starbeauty Member Posts: 327
    edited December 2011

    Hi 3girls... I took off right after surgery 4weeks... But other nurses on this board went back after 3 weeks. I wasnt really healed well by then. Started chemo after i went back to work and had the port put in the final week before going back. Then worked through a similar tx plan full time... Went back to school this fall plus worked full time. Trying to finish my MS. It can be done... Exhausting but possible... Hang in there...and try to do what someone told me... Only deal with a week at a time... Don't get too far ahead in your head... Just do what you need to do this week...

  • Janeybw
    Janeybw Member Posts: 199
    edited December 2011

    I didn't know this thread existed!  I just had my exchange surgery yesterday.  It went very well--not too much pain and they already look so much better than the TEs.  Feel much better, too.  My invasive component was too small for chemo, but I am on tamoxifen.  It's been about 6 months now and it hasn't been too bad.  Hot flashes, some joint and muscle pain, and a little foggy brain.  I work with mostly menopausal women, so I joke that I fit in better now!

    I was an L&D nurse and now have been a full time faculty in a community college (ADN) program for 2 1/2 years.  I LOVE my teaching job.  I teach fundamentals and OB (we do 2 quarters a semester).  I have excellent clinical sites and great support from my peers.  Native Mainer--I'm sorry you had such a bad experience.  That is not the culture of our program.  I can't imagine my director calling me in for something like you have described.  We are a public school, so the tuition issue isn't there.  I have heard some horror stories about the private, for profit, schools popping up around here.  

    I almost always tell them that I am  a nurse and then follow that with the fact that this isn't my specialty so they need to explain everything very well.  They can just explain it at a higher level which is nice for both of us.  The second night in the hospital for the BMX, I had the cutest young new grad who must have been told I was an instructor.  She gave me the most complete head to toe I have ever had.  I smiled the whole time--she even checked my pedal pulses and strength!  For the most part I have had good care.  Yesterday was an outpatient procedure and they were great.  I get pretty goofy when I'm nervous and then with the drugs.  We all laughed a lot.  My poor husband... 

  • 3girls
    3girls Member Posts: 94
    edited December 2011

    Starbeauty,  That's great to know that it can be done!  I have realized that taking it one week at a time is the best way and am thrilled that despite a horrible cold this past 2 weeks I felt good and was able to work.  Happy Holidays!

  • Jennt28
    Jennt28 Member Posts: 2,021
    edited December 2011

    Hi 3girls, You and I almost look like diagnosis twins! I see you had 1/1 nodes as well which is unusual to see...



    regards Jenn

  • rc778
    rc778 Member Posts: 56
    edited December 2011

    Carolyn,

    I didn't consider any other procedures because I needed to get back to work/family asap.  I had heard the DIEP and TRAM recovery times were longer and much more painful, so I honestly did not research them too much.  Also, I had never had any surgeries before so I wanted the shortest one possible.  I'm a little bit of a chicken :)  I did not take Tamoxifen after my BMX.  Let us know how your appointments go...good luck.

  • nurseronda10
    nurseronda10 Member Posts: 209
    edited December 2011

    Can't believe I have never seen this thread, but glad I found it.  I graduated in 1986 with an associates degree in nursing.  I have been working night shift all these years, but know I would feel better mentally and physically if I were on dayshift. I was unable to work during chemo due to being neutropenic starting with 2nd round of Taxotere and Carboplatin and low H/H with 4th, 5th, and 6th rounds.  I had a lot of nausea also.  Just finished Herceptin in October.  Will begin the reconstruction process soon. :o)

  • donnajrn
    donnajrn Member Posts: 154
    edited December 2011

    Hi ladies, what an awesome group.  I have been a nurse since....forever...and still working full time.  I was diagnosed with DCIS 3 1/2 years ago had lumpectomy and radiation.  I have been on tamoxifen for 3 years and was ready to try a trial off of it because of side effects....then I had my routine mammogram!  This (after mammo, biopsy and MRI) showed LCIS..which is, not cancer..but then I say, why does it have cancer in the name!  This just means I am at a higher risk for developing invasive cancer in the future.  I said to someone, a lot of good the tamoxifen did me...but she said: maybe it did work...makes me think.  I also did research when I had my first surgery and read about curcumin....and been taking that for about 3 years also.  So..I am scheduled for surgery next month (excisional biopsy--not lumpectomy cause this is not cancer-but same type of surgery) and depending upon that result.............will either have close follow-ups or go the BMX route.......Here I go again!

    Donna

  • 3girls
    3girls Member Posts: 94
    edited December 2011

    Jenn28,  yes we do look the same!  I see u declined the ALND I did as well, but I keep getting second thoughts after finding out that I was her2+ as well.  My onc says there is a 20-50% chance that there are additional + lymphnodes so it feels weird leaving them in.  He says the chemo and radiation would take care of it- but I feel like I am leaving cancer in my body.  I am sure I will feel better after I talk to a radiation oncologist.

  • Jennt28
    Jennt28 Member Posts: 2,021
    edited December 2011

    No second thought here 3girls. There are quite a few academic papers, including radiology ones that are showing no survival benefit to having had ALND. I choose to look at it as no disadvantage to me.



    My appt with the rad onc isn't until 17th January so will just have to wait until then to discuss with her.



    regards Jenn

  • cajmi
    cajmi Member Posts: 80
    edited December 2011

    Hi All,

     So, I'm a little over a week out from my stereo biopsy and I think I'm developing a seroma.  Anyone have any experience with this?  I just noticed it yesterday.  Lump measures about 2.5cm.  It's a little tender, but not reddened or weepy. 

    Carolyn 

  • NativeMainer
    NativeMainer Member Posts: 10,462
    edited December 2011

    cajmi--call the surgeon and get seen today. Seromas can become very large and very painful VERY quickly, and the sooner it's known about the quicker you can get in for drainage if it needs it.  I found out--the hard way--that you can have a lumpectomy & rads and develop a seroma a year later and it is still considered a surgical problem related to the lumpectomy!  Like, who cares, but a year later????? Happened to me, though.

  • AnneW
    AnneW Member Posts: 4,050
    edited December 2011

    Nice to see this thread resurrected!

    NativeMainer, I read through your last posts with dismay. I would have had no clue what to do in your situation, but probably would have left before I got sick from the stress of it. Is this what we'll be turning out for nurses? What's going to happen when they have to work a double shift, or take an extra load when there's no one else to work??

    I have not been in education, other than my current job at a college health center. How does one manage to keep a thick skin, and be tough but fair in assignments and opportunities and expectations?

    Is this unique to younger nursing students, I wonder, who are definitely a spoiled lot (helicopter parents have ruined this genration!)?? A friend of mine went back to school at age 52, to an ADN program. She was probably the hardest worker and most conscientious in her class, and is one of the really good nurses out there, a throw-back to the old days.

    I haven't done hospital nursing since I became an NP 20 years ago. Not sure I could return to that setting if I had to. It's the toughest job in our profession. Good on ya for trying to impact a new generation of nurses. And good on ya for being true to yourself and leaving.

  • fredntan
    fredntan Member Posts: 1,821
    edited December 2011

    Waving hello to everyone,

    I've been off work since my Rt mast in sept. I realized this was/is my 20th year of nursing. I work in Interventional Radiology. I'm prn-I usually worked 3days a week. they technically can't fire me and havn't. they have actually been kind of slow so they havn't really needed me. (our area opened up 2 new hospitals right before the economy failed)

    my story: always had my mammo's yearly. in 09 they sent me back for repeat /c US. guy said it was fine. I switched to one of those new hosp  in '10 mammo normal-but later I'm looking at it and it says same fibroglandular pattern unchanged-it was the cancer. I felt lump in july....you know how rest goes. And now since I felt like someone should have bx'ed this thing-my family and I are now distrusful of local docs. they hauled my ass up to sloan kettering. Had oneof best sx probably in world. nursing care sucked though. I think I have PTSD from that horrible experience.

    woke up in OR when it was over. I said "I need 1 mg ativan, I just lost my breast" didn't get it. got out to recovery, I said where's my PCA? "oh those are reserved for the bilaterals" so they were giving me .2 and .4 of dilaudid-I knew I was screwed at that point. Had the throw ups after I got to my room-they gave me ?pepcid before they gave me the antinausea. I was basically on my own all night. I had to ask my nurse to put my SCD's on. I think I got out of sx at 4pm. it was midnight before they were put on. so many things were done wrong. I complained after I got home to the higher ups/sent in nasty  press gainey. at the end of night my nurse made comment-you know they say nurses make the worst patients. She'd only been nurse 2 years-right bitch-you just wait.

    But I didn't go there for the nursing care. my sx got great margins. Its funny though , both the breast sx and PS both talked to DH after. PS said to DH oh she'll get a PCA and she'll probably need to be in for 2 nights due to pain control. I don't believe he told the ordering pain care docs that he put in 300 mls in that TE. I got my ass out of there that next day.

    It pisses me off cause I'm that kind of nurse that allways goes the extra mile for my patients. They call me the patient whisperer. I love taking someone that is all worked up over there IR procedure. calming them/little bit of drugs and job well done.  

  • cajmi
    cajmi Member Posts: 80
    edited December 2011

    NativeMainer,

    Thanks for the imput!!  I called this am and was told it is probably a hematoma which is very common, but they would see me Tuesday if I wanted.  When I got up this evening, it seems like it might actually be a little smaller, so I guess I'll see how it is in the AM.  I'm scheduled for my MRI tomorrow evening and they got me in to genetics for Dec 29, so things are moving along.  Thanks again for the responseSmile  Carolyn

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