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Old 01-21-2012, 10:26 AM   #1
Britbee
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Question Just curious

Since coming on these boards I have had three chemo sessions and met a lot of wonderful people. Some have been introduced to me through others, some I have met since I started a blog. I have found the blog to be very therapeutic and enjoy also reading others and their journeys.
Today I would like to ask a question about something that has been bothering me. I find I am a little more sensitive since I was diagnosed with cancer and so maybe this just me.
When I was first diagnosed I was sent to a very sweet oncologist who saw me through the first while until after my mastectomy.
When I went for my first appointment to discuss the first chemo session which I was to have the next day there was a lady oncologist sitting there that I had never met. Not saying she was not versed in my history and had a very nice manner but she was not the original doctor I had seen before. Same office, just different doctor.
She was there for my second chemo and by this time I was happy enough seeing her.
My third chemo it was a different doctor again and he did not even know I had a port! He asked how my veins in my arm were holding up. Obviously had not read my chart properly. Also he gave me a little talk about how there were no guarantees that I would be cured and set me back about a month mentally.
Ok sorry about being so long winded but my question is have the rest of you been tossed around like a beach ball between oncologists or have you seen the same one all the way through. The ladies I have already asked said they stayed with the same one. This is something I would prefer as how can anyone know me if they are different each time? Or am I being super sensitive and getting the care I need and should just get on with it??
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Diagnosed June after Mammogram.
September 26th 2011 - Left breast Mastectomy and axillary Dissection:
Ductal carcinoma in situ nuclear grade 3
Lobular carcinoma in situ focal
Paget's disease of nipple
One of 12 axillary lymph nodes with metastatic carcinoma
Negative for extranodal extension
Metastic tumor deposit measures 1.5 cm in maximal dimension
ER 0/8 PR 0/8
Her2 +
Treatment node positive HER2+ breast cancer treatment
Chemotherapy FEC-DH
Herceptin for remainder of year.
Chemo starts November 25th 2011.
Blog: http://importanceofmammograms.wordpress.com/

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Old 01-21-2012, 10:40 AM   #2
NanaJoni
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Re: Just curious

My oncologist is part of a large group of hematologist/oncologist specialists. In my two years of being under treatment and follow-ups I have seen another dr. in the group only twice when Dr. Shipstone was out of town. Also I saw a nurse practitioner once when I was having gastro problems but she had been with my onc at several of my appts so was well-known with me. If this continues you may want to specify a particular dr or ask whey you're being handed around- it may be typical of the practice so you might want to pursue another office. It really bothers me that you feel "mentally" set back by this. Your mental and emotional state are as important now as the physical.
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Joni -64 yrs old -
3/01/10: found lump in rt.breast
3/12/10: mammogram/ultrasnd/biopsy-invasive bc & DCIS; 2 tumors (2cm er-/pr-/HER2-& 1.8 cm er-/pr-/HER2+); grade 3;poorly differentiated
3/24/10:sent.node biopsy clear
3/31/10:bi-lateral mx.;atypical ductal hyperplasia-lft side
4/21/10:wound revision-infection/scarring 4/28/10:seromas both sides
5/21/10:port installed,TCH chemo (6 x 3 wks); Herc,-1yr; 33 rad tx after chemo
07/2010: port not working-2nd port didnt'work;3rd port opposite side.
07/2010: 2 weeks after 3rd port surgery, threw 3 pulm. emboli-IVC filter installed; warfarin
08/2010: hospitalizations w/3 of chemos; decision to stop after 4th-on to radiation in Oct 2010;Herc cont.
12/03/2010 - finished 33 rads Hooray!! cont. Herc. every 3 wks
4/2011 - pneumonia ??? Nope-radiation pneumonitis. No more Herc.
5/2011 - NED!!! port out.
8/2011 - clean PET & CT scans.Still NED
7/2012 - Still NED/very blessed.
2/2013 - 6 mos checkup-all clear. CA2729 down frm 13 to 11.
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Old 01-21-2012, 11:07 AM   #3
ElaineM
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Wink Re: Just curious

Even if you go to a large medical group you have a right to request the same doctor each time you visit. The only time you should be seen by another doctor is when your doctor is out of town or has to attend a meeting. A person is usually more successful when that person can work with the same doctor most of the time.
Good luck and take good care of yourself.
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Old 01-21-2012, 12:00 PM   #4
BonnieR
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Re: Just curious

Is this some peculiarity of Canadian medicine? Otherwise, I would ask to see the doctor of your preference. And you REALLY don't want to see that male doc again! We have to speak up and be our own advocates or we can get lost in the shuffle. Be the squeaky wheel when you have to.
Recently my dental office handed me off to a new guy. I told them I have been coming to that practice longer than most of the staff has been working there and I wanted MY dentist who knows me.
Anyhow, don't ever blame yourself for being "too sensitive". We are entitled to feel vulnerable and it is up to the professionals to put us at ease. That it what we pay them to do. Good luck and keep the faith!
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Post menopause
May 2007 Core biopsy, Rt breast
ER+, Pr-, HER2 +++, Grade 3
Ki-67: 90%
"suspicious area" left breast
Bilateral mastectomy, (NED on left) May 2007
Sentinel Node Neg
Stage 1, DCIS with microinvasion, 3 mm, mostly removed during the biopsy....
Femara (discontinued 7/07) Resumed 10/07
OncoType score 36 (July 07)
Began THC 7/26/07 (d/c taxol and carboplatin 10/07)
Began Herceptin alone 10/07
Finished Herceptin July /08
D/C Femara 4/10 (joint pain/trigger thumb!)
5/10 mistakenly dx with lung cancer. Middle rt lobe removed!
Aromasin started 5/10
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Old 01-21-2012, 02:19 PM   #5
karen z
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Re: Just curious

I am not in Canada (Atlanta, GA, USA) but I have had one and only one oncologist (as well as one breast surgeon/one radiologist, etc.) for the last seven years. I was under treatment (lumpectomy/chemo/radiation/Herceptin) during 05-06 but I still see my same oncologist and breast surgeon when I have check-ups. I would insist on seeing the same person if possible (and one you like and think is good). I would put up a major fuss about that.
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Old 01-21-2012, 08:37 PM   #6
caya
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Re: Just curious

I had my mastectomy at Princess Margaret Hospital in Toronto, had one breast surgeon, and only saw him before and afterwards. He discharged me after 3 years.

My oncologist and chemo treatments were at Mount Sinai Hospital, connected to Princess Margaret. I had the same oncologist from Day 1. Sometimes when I was going for treatments, another oncologist would see me, but I could always ask to see MY oncologist. For all the followups over the years, I have only seen my original onc. He just retired (-:, and he introduced me to my new onc. at my last visit.

all the best
caya
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ER90%+/PR 50%+/HER 2+
1.7 cm and 1.0 cm.
Stage 1, grade 2, Node Negative (16 nodes tested)
MRM Dec.18/06
3 x FEC, 3 x Taxotere
Herceptin - every 3 weeks for a year, finished May 8/08

Tamoxifen - 2 1/2 years
Femara - Jan. 1, 2010 - July 18, 2012
BRCA1/BRCA2 Negative
Dignosed 10/16/06, age 48 , premenopausal
Mild lymphedema diagnosed June 2009 - breast surgeon and lymph. therapist think it's completely reversible - hope so.
Reclast infusion January 2012
Oopherectomy October 2013
15 Years NED!!
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Old 01-22-2012, 09:41 AM   #7
sarah
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Re: Just curious

I'm in France but...
Same chemo oncologist for every treatment over the 6 years and she's still there. Always saw my overall treatment protocol oncologist whenever I wanted and made an appt. to see him. I changed radiologists (my choice) and then only ever saw him, he was always there when I went through radiation and could slip in and see him if I had a question.
Seems very odd that you keep getting different oncologists. It is very important to have the same one because he/she knows your history and you and also because you need to feel comfortable enough with him/her to ask questions and talk about your treatement.
I could understand in a large hospital that during chemo the oncologists on call on the floor might change but not your leading oncologist.
Is this something to do with the hospital? Definitely speak to someone and tell them you are very uncomfortable with this. You should chose the oncologist you want, not just the one on call.
Sorry you're going through this when you're having your treatment.
take care,
health and happiness
Sarah
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Old 01-22-2012, 01:15 PM   #8
tricia keegan
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Re: Just curious

I'm in Ireland and have the same onc all the time and usually see her at my appts but not always, however during chemo I often saw the Junior Dr's under her which did'nt bother me as knew she was busy doing her clinic and usually they only needed to give me a new script for something and check my BP!!
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Dx July '05 IDC 1.9cm Triple positive 3/9 nodes positive
A/C X 4 ..Taxol/Herceptin x 12 wks then herceptin 1 yr
Rads x 36 ..oophorectomy August '06
Currently taking Arimidex..
June 2011 osteopenia/ zometa x1 yearly- stopped Zometa 2015 as Dexa show normal bone density.
Stopped Arimidex July 2014- Restarted Arimidex 2015 for a further two years on the advice of my Onc.
2014 Normal Dexa scan
2018 Mammo all clear, still NED!
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Old 01-22-2012, 06:08 PM   #9
Bunty
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Re: Just curious

In Australia, under the public health system, I've only ever seen the same onc now for the past 11 years. Like Tricia from Ireland, sometimes through chemo I might see a Registrar, but my onc will always poke his head in to see how I'm doing.

I agree with other comments that you should make it clear what is your preference.

Cheers Marie
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dx Dec 2000 dcis 2.5cm clear sentinel node, ER/PR- Her-2+
lumpectomy, 6 cycles AC, 6 weeks rads
October 2007 three x 2.5cm lung mets. 8 months Taxol, started Herceptin and continue. Significant reduction in lung mets.
June 2011 3cm x 4cm liver tumour. Started Abraxane and continue with Herceptin.
November 2011. Finished with Abraxane, continue with just Herceptin. Liver tumour now reduced to 15mm x 12mm. Lung tumour now 10mm x 0.5mm
February 2012. Scans show everything stable, and brain scan clear.
July 2012. PET/CT scans show I'm in remission - no active cancer!
]Dec CT brain cllear, lungs stable, liver tumour has increased to 20mm. PET scans showed active liver met and active lung thinglet, and possible bone met.
Jan 2013 recommence Abraxane, continue with Herceptin.
June 2013 finish Cycle 6 Abraxane, continue with Herceptin. 30% reduction in liver tumour, everything stable.
December 2013. CA15-3 on rise.
February 2014. PET and CT scans show single liver tumour has increased to 35mm. No other activity.
March 2014. Planned for SBRT for liver met, but couldn't have treatment as tumour too close to bowel. Continue Herceptin.
April 2014. Surgeon advises that I am a good candidate for liver resection, so will have operation early May (after camping holiday). Tumour now 44mm x 29mm.
May 7, 2014. Two liver tumours surgically removed. Third of liver removed, and gall bladder. Am I NED?May 2014. Pathology of tumour shows it's now ER+ (95% staining).
June 2014. CA15-3 has decreased to 18 from a pre-surgery reading of 59!
June 2014. Started Femara, continue with Herceptin.
July 2014. Stop Femara due to severe Osteoporosis. Commence Tamoxifen, continue Herceptin. Waiting to hear if I can have Aclasta infusion.
August 2014. CA15-3 has decreased further to 12 - YAY!
October 2014. Aclasta infusion for Osteoporosis. November 2014, CA15-3 decreased to 11. Scans of liver all clear, something new showing up on lung, but just watching at the moment.
November 2015. Started SBRT on solitary lung met.
November 2015. Bone density scan showed very good improvement so back on Femara - yay!
December 2016. 6 treatments of SBRT radiation on lung. Seems to have had some effect.
June 2016. CA15-3 still stable and low at 9.
June 2016. Started subcutaneous Herceptin replacing infusion.
Jan 2017. LVEF dropped to 46%. Stopped Herceptin.
Feb 2017. Started ACE Inhibitor and BETA Blocker. Still off Herceptin.
Aug 2017. Two new mets - Portacaval lymph node and mediastinal lymph node.
Aug 2017. Blood tests show extremely elevated liver enzyme levels. Many tests to investigate.
Sept 2017. Portacaval lymph node blocking liver bile duct causing liver enzyme and Bilirubin problems.
Oct 2017. 8cm stent inserted into liver bile duct. Procedure caused pancreatitis, and hospitalised for 3 days. Liver enzymes improving rapidly.
Nov 2017. Commenced 4 weeks of radiation on Portacaval lymph node. 5 week break before chemo.
Jan 2018. CT scan. 11 new small liver mets, and new superclavical lymph node med.
Jan 2018. Start Kadcyla. CA15-3 426.
Apr 2018. First scans since starting Kadcyla. All tumours reducing. CA15-3 dropped to 30 from 426.
Dec 2019. Still on Kadcyla, but two small brain mets have been treated in the past month with SRS. CA15-3 stable for 12 months at 11.
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Old 01-22-2012, 06:24 PM   #10
sassy
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Re: Just curious

The first onc I saw was very kind and caring and told me if there was anything I wanted to do, get it done in the next ten years. When I asked if there was something about my cancer I didn't know, he replied "Oh, no--no". At that point my dx was stage two ER/PR positive-nothing on HER2 because I had not been tested.

Needless to say the ten year time line sent up all kinds of alerts and prior to staring treatment I decided to switch to a facility at a major research center. Good choice because when I heard about the release of herceptin on the national news and thought my cancer sounded very much like it, I asked my new onc (who did not realize I had not been tested) about it, I was immediately tested and stepped into that treatment protocol with Herceptin/Taxol as I had just finished A/C.

I had only one onc through initial treatment, then changed to a different one who had been trained by my onc and was at a facility closer to my home. Good decision there too, he was cutting edge and gave me treatment 7 years ago that are just now becoming the standard of care. As a researcher he was up to date on new developments.

I would want my onc to know me and see me. Your treatment should be a collaboration between you and your doctor, not a hit or miss by whomever happens to be there at the time.
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Rhonda (Sassy)
dx age 45
DX 2/15/05 Stage IIb (at surgery)restaged IIIa
Left mast .9cm tumor 5 of 14 nodes
Triple Positive
4 DD A/C
12 Taxol/Herceptin
33Rads
Strange infect mast site one year aft surg, hosp 1 wk
Herceptin for total of 18 months
Lupron Monthly 4 yrs
Neurontin for aches, pains and hot flashes(It works!)
Ovaries removed 11/09 stop Lupron and Neurontin
Arimidex 6 yrs (tried Femara, no SE improvement)
Tried Exemestane-hips got so bad could hardly walk
Back to Arimidex for year seven
Zometa 2X Annual for 7years, Lasix
Stop Arimidex 5/13
Stop Zometa 7/13-Bi-lateral Stress Fractures in Femurs from Zometa
5/14 Start Tamoxifen
3/15 Stem cell transplant to stimulate femur bone growth/healing
5/15 Complete fracture of right femur/Titanium rods both femurs
9/16 Start Evista stopTamoxifen
3/17 Stop Evista--unwelcome side effects!
NED and no meds.......
14YEARS NED!

Last edited by sassy; 01-23-2012 at 07:11 PM..
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Old 01-22-2012, 11:08 PM   #11
Paty
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Re: Just curious

Hello! I am in Mexico, i have always had same doctors during all my process. I would only change if I decide to do so.
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Dx. June 30th, 2006 at age 43
Lumpectomy rt breast
2.2 cm tumor, 13 nodes all negative
ER-PR+,her2+++
6 FAC
32 Rads
Dx. Lung fibrosis due to radiation
Ended 1 year herceptin in March, 2008
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Old 01-23-2012, 09:32 AM   #12
MJo
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Re: Just curious

I've had same oncologist for six years. I see him once a year now. Only time I saw different onc was when I was hospitalized during chemo for respiratory infection and my onc was out of town at a medical convention. I saw one of his partners then. I definitely think you should ask some questions.
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IDC, Stage I, Grade 2
Oncotype DX Score 32
Her2++ E+P+, Node Neg.
Lumpectomy 11/04/05 Clear Margins
3 Dose dense AC (Couldn't tolerate 4)
4 Dose dense Taxol & Herc. (Tolerated well)
36 weeks Herceptin (Could not complete one year due to decrease in MUGA score)
2 years of Arimidex, then three years of Femara
Finished Femara May 2011
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Old 01-23-2012, 02:05 PM   #13
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Re: Just curious

I've seen the same one since the beginning, August 09. He's in a group of others and if I have an emergency when he's not there I might see another, but he is my doctor and he is the one I see each month. He came to see me when I was in the hospital too, which was for c-diff and not cancer, which I thought was nice.

I wouldn't want to switch from doctor to doctor in an oncology situation. When I was pregnant with my 2nd child, the OB practice I went to did this. But, they told me up front and they gave me an appointment with a different doctor each time so I'd meet them all and they all would meet me. That way, by the time the baby came, I would have had a chance to get to know all the doctors. For a delivery, it made sense to me and I accepted that as part of their practice - but for oncology, where your history can get very complicated I wouldn't want to do that. My file is about 9 inches thick right now, no new doctor can read through all that.

What bugs me for you is that they didn't explain that they'd do this and let you choose. You should talk to them and ask if you can have just one doctor. If not, I'd probably find some other practice.
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08/17/09 Dx'd.
Multifocal/multicentric IDC, largest 3.4 cm, associated ADH, LCIS, DCIS
HER2+ ER+/PR- Grade 3, Node Negative

10/20/2009: Right mastectomy, reconstruction with TE
12/02/2009: Six rounds TCH, switched to Taxol halfway through due to neuropathy
03/31/2010: Finished chemo
05/01/2010: Began tamoxifen, the worst drug ever
11/18/2010: Reconstruction completed
12/02/2010: Finished herceptin
05/21/2011: Liver Mets. Quit Tamoxifen
06/22/2011: Navelbine/Zometa/Herceptin
10/03/2011: Liver Resection, left lobe. Microwave ablation, right lobe - going for cure!
11/26/2011: C-Diff Superbug Infection, "worst case doctor had seen in 20 years"
03/28/2012: Progression in ablated section of the liver - no more cure. Started Abraxane, continue herceptin/zometa
10/10/2012: Progression continues, started Halaven, along with herceptin and zometa.
01/15/2013: Progression continues, started Gemzar and Perjeta, an unusual combo, continuing with herceptin and zometa
03/13/2013: Quit Gemzar, body just won't handle it. Staying on herceptin, zometa and perjeta.
04/03/2013: CT shows 50% regression in tumor, so am starting back on Gemzar with dose reduction, staying with perjeta/herceptin/zometa. Can't argue with success!
05/09/2013: Discussing SBRT with Radiology due to inability of bone marrow to recover from chemo.
06/07/2013: Fiducial placement for SBRT
07/03/2013: Chemo discontinued, on Perjeta, Herceptin and Zometa alone
07/25/2013: SBRT (gamma knife) begins
08/01/2013: SBRT completed
08/15/2013: STABLE! continuing with Perjeta, Herceptin, Zometa
06/18/2014: ***** NED!!!!***** continuing with Perjeta, Herceptin, Zometa
01/29/2014: Still NED. continuing with Perjeta, Herceptin. Zometa lowered to every 3 months instead of monthly.
11/08/2015: Progression throughout abdomen and lungs. Started TDM-1, aka Kadcyla. Other meds discontinued. Remission was nice while it lasted.

5/27/18: Stable. Kadcyla put me right back in the barn. I have two teeny spots on my lungs that are metabolically inactive, and liver is clean.

I’m beating this MFer. I was 51 when this started and had two kids, 22 and 12. Now I’m 60. My oldest got married and trying to start s family. My youngesg graduates from Caltech this June. My stepdaughter gave me grandkids. Life is fantastic.
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Old 01-23-2012, 04:38 PM   #14
Jackie07
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Re: Just curious

I've had the same oncologist since 2003.

I think your first 'oncologist' was probably your breast cancer surgeon who's regarded as a 'surgical oncologist'. The oncologist you saw after the surgery would be your 'medical oncologist' who overseas your chemo treatment and other follow-ups.

It's possible that you were seeing different doctors because of the holiday season. It won't hurt to get a clarification next time: "Are you my medical oncologist?" You might get an answer like: "No, I'm the [oncology] nurse practioner," or "No, I'm a 3rd year medical student."

Most hospital have oncology team meetings at least once a week to discuss about patient care. Nurse practioners have been assuming more and more responsibilities these days. I hope you will get things clarified soon and get more comfortable with your team.

Sending you good vibes.
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Start Vitamin D3 and Calcium supplement (600mg x2)
10-10 Stopped Exemestane due to r. hip/l.thigh pain OKed by Onco 11-08-2016
7-23-2018 9 mm groundglass nodule within the right lower lobe with indolent behavior. Due to possible adenocarcinoma, Recommend annual surveilence.
7-10-2019 CT to check lung nodule.
1-10-2020 8mm stable nodule on R Lung, two 6mm new ones on L Lung, a possible lymph node involvement in inter fissule.
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Old 01-27-2012, 05:55 AM   #15
Britbee
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Re: Just curious

Went to see the Doc Thursday 26/1/12. When another new face walked in I immediately told them I had issues I needed to address. It was a very nice lady called Cindy and she said she just wanted to go over some stuff about the DH chemo I was getting the next day first then I was free to tell her all my issues.
So all these fresh faces I have been seeing are not actual oncologists. There is apparently a shortage of oncologists in Calgary. There is way more cancer patients then oncologists, a fact which I find very sad, each oncologist has "helpers".
Most are Doctors in their own right but are like family Doctors or such. The lady I saw yesterday was a nurse with years of knowledge of breast cancer patients and she also had a Masters Degree in (I forget) something related. The actual oncologist meets with these people everyday and has knowledge of all his patients and gives orders for each which are carried out by his helpers.
Having found this out I still said my feelings about being passed around were still present and even if I saw just one of the helpers each time I would be more comfortable. She told me she would do everything in her limited power to make sure I saw the same person each time and made a note in my file. Another thing she mentioned was that my file was in disarray and she would take the time to put it in order. I mentioned again that different people had seen me each time so no wonder they did not know what was going on if the file was not in order.
Having said all that this lady was the most thorough I had seen since the actual oncologist and I felt better when I left after dealing with her. I was in there over an hour and was one of the last patients that day but she listened to all my concerns and addressed each one. I now have medicine to help me with that awful throat problem I had last time and she showed me my flow chart and told me I was in very good shape going into the next chemo.
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Diagnosed June after Mammogram.
September 26th 2011 - Left breast Mastectomy and axillary Dissection:
Ductal carcinoma in situ nuclear grade 3
Lobular carcinoma in situ focal
Paget's disease of nipple
One of 12 axillary lymph nodes with metastatic carcinoma
Negative for extranodal extension
Metastic tumor deposit measures 1.5 cm in maximal dimension
ER 0/8 PR 0/8
Her2 +
Treatment node positive HER2+ breast cancer treatment
Chemotherapy FEC-DH
Herceptin for remainder of year.
Chemo starts November 25th 2011.
Blog: http://importanceofmammograms.wordpress.com/

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Old 02-16-2012, 01:32 PM   #16
Britbee
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Re: Just curious

Just to wind up this thread. After complaining last time, I actually saw my real oncologist today!! They do listen after all
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Diagnosed June after Mammogram.
September 26th 2011 - Left breast Mastectomy and axillary Dissection:
Ductal carcinoma in situ nuclear grade 3
Lobular carcinoma in situ focal
Paget's disease of nipple
One of 12 axillary lymph nodes with metastatic carcinoma
Negative for extranodal extension
Metastic tumor deposit measures 1.5 cm in maximal dimension
ER 0/8 PR 0/8
Her2 +
Treatment node positive HER2+ breast cancer treatment
Chemotherapy FEC-DH
Herceptin for remainder of year.
Chemo starts November 25th 2011.
Blog: http://importanceofmammograms.wordpress.com/

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Old 02-16-2012, 04:50 PM   #17
Mary Anne in TX
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Join Date: Jun 2006
Location: San Antonio, TX
Posts: 2,357
Re: Just curious

Yea!
Keep standing up for yourself, girl!
ma
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MA in TX.
Grateful for each and every day....

Diag. 12/05 at age 60
Stage II, Grade 3, 4.5 cm primary tumor
ER/PR- Her2 +3 strongly positive
Her2 by FISH 7.7 amplified
vascular invasion
Ki67 20% borderline
Jan - March '06 Taxotere/Adriamycin X 3 to try to shrink tumor - it grew
April '06 Rt Modified Radical Mas, 7 of 9 nodes positive
April - Aug. '06 Herceptin/Taxol/Carboplatin X 8 (dose dense)
Sept - Dec. '06 Navelbine/Herceptin x 8 (dose dense)
Radiation & Herceptin Jan. 22 - March 1, 2007
Finished Herceptin Dec. 10 '08! One extra year.
Port removed August, 2012.
8 1/2 years since diagnosis! 5 1/2 Years NED!
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Old 02-19-2012, 02:24 AM   #18
KsGal
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Join Date: Dec 2011
Posts: 585
Re: Just curious

Im glad you got the result you wanted, and I hope it continues! On the flip side of things, I have seen the same doctor every time, and he is overloaded with patients that he looked at me on my fourth visit and said "Do you still have your primary tumor?". I've had a double mastectomy....ugh.
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Diagnosed in October 2011 Stage IV with metastasis to liver.
January 2012 after double mastectomy, started taxotere, carboplatin and herceptin.
Clear.
December 2012 was diagnosed with five brain mets, and had whole brain radiation.
Around July 2014 two mets in brain, one a residual spot and one new one growing in size. Received Cyberknife on both areas
Clear/NED
April 2015 remain NED
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