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Old 11-22-2009, 12:18 AM   #1
Catherine
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How did you discover your cancer?

Since many of us found our own lumps, I thought it might be interesting if we all updated our profiles to include how our lumps or how our cancer was discovered. If you want to do this go to your profile, and then to edit profile. I was never good at SBE, but I always believed in knowing your body. Here is my update:
__________________
Catherine


Found my own lump in the shower
April 2006 at the age of 58
Stage IIB, ER- PR- HER2+++ multi focal tumors, largest 2.3cm
Chemo first: AC/Taxol over 16 weeks
Bilateral mastectomy Sep 06
33 rads after the surgery
1 year of Herceptin completed Dec 07
15 years and no recurrence as of April 2021

Last edited by Catherine; 12-18-2009 at 11:35 PM.. Reason: spelling errors
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Old 11-22-2009, 12:20 AM   #2
harrie
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Re: How did you discover your cancer?

mammogram, showed small calcifications
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*** MARYANNE *** aka HARRIECANARIE

1993: right side DCIS, lumpectomy, rads
1999: left side DCIS, lumpectomy, rads, tamoxifen

2006:
BRCA 2 positive
Stage I, invasive DCIS (6mm x 5mm)
Grade: intermediate
sentinal node biopsy: neg
HER2/neu amplified 4.7
ER+/PR+
TOPO II neg
Oncotype dx 20
Bilat mastectomy with DIEP flap reconstruction
oophorectomy

2007:
6 cycles TCH (taxotere, carboplatin, herceptin)
finished 1 yr herceptin 05/07
Arimidex, stopped after almost 1 yr
Femara
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Old 11-22-2009, 12:24 AM   #3
mcgle
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Re: How did you discover your cancer?

Same as Harrie.

Mcgle (UK)
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Old 11-22-2009, 12:50 AM   #4
SoCalGal
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Re: How did you discover your cancer?

Felt my boobies.
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1996 cancer WTF?! 1.3 cm lumpectomy Er/Pr neg. Her2+ (20nodes NEGATIVE) did CMF + rads. NED.
2002 recurrence. Bilateral mastectomy w/TFL autologous recon. Then ACx2. Skin lymphatic rash. Taxotere w/Herceptin x4. Herceptin/Xeloda. Finally stops spreading.
2003 - Back to surgery, remove skin mets, and will have surgery one week later when pathology can confirm margins.
‘03 latisimus dorsi flap to remove skin mets. CLEAN MARGINS. Continue single agent Herceptin thru 4/04. NED.
‘04 '05 & 06 tiny recurrences - scar line. surgery to cut out. NED each time.
1/2006 Rads again, to scar line. NED.

3/07 Heartbreaking news - mets! lungs.sternum. Try Tykerb/Xeloda. Tykerb/Carbo/Gemzar. Switch Oncs.
12/07 Herceptin.Tykerb. Markers go stable.
2/8/08 gamma knife 13mm stupid brain met.
3/08 Herceptin/tykerb/avastin/zometa.
3/09 brain NED. Lungs STABLE.
4/09 attack sternum (10 daysPHOTONS.5 days ELECTRONS)
9/09 MARKERS normal!
3/10 PET/CT=manubrium intensely metabolically active but stable. NEDhead.
Wash out 5/10 for tdm1 but 6/10 CT STABLE, PET improving. Markers normal. Brain NED. Resume just Herceptin plus ZOMETA
Dec 2010 Brain NED, lungs/sternum stable. markers normal.
MAR 2011 stop Herceptin/allergy! Go back on Tykerb and switch to Xgeva.
May-Aug 2011 Tykerb Herceptin Xgeva.
Sept 2011 Tykerb, Herceptin, Zometa, Avastin.
April 2012 sketchy drug trial in NYC. 6 weeks later I’m NED!
OCT 2012 PET/CT shows a bunch of freakin’ progression. Back to LA and Herceptin.avastin.zometa.
12/20/12 add in PERJETA!
March 2013 – 5 YEARS POST continue HAPZ
APRIL 2013 - 6 yrs stage 4. "FAILED" PETscan on 4/2/13
May 2013: rePetted - improvement in lungs, left adrenal stable, right 6th rib inactive, (must be PERJETA avastin) sternum and L1 fruckin'worsen. Drop zometa. ADD Xgeva. Doc says get rads consultant for L1 and possible biopsy of L1. I say, no thanks, doc. Lets see what xgeva brings to the table first. It's summer.
June-August 2013HAPX Herceptin Avastin Perjeta xgeva.
Sept - now - on chemo hold for calming tummy we hope. Markers stable for 2 months.
Nov 2013 - Herceptin-Perjeta-Avastin-Xgeva (collageneous colitis, which explains tummy probs, added Entocort)
December '13 BRAIN MRI ned in da head.
Jan 2014: CONTINUING on HAPX…
FEB 2014 PetCT clinical “impression”: 1. newbie nodule - SUV 1.5 right apical nodule, mildly hypermetabolic “suggestive” of worsening neoplastic lesion. 2. moderate worsening of the sternum – SUV 5.6 from 3.8
3. increasing sclerosis & decreasing activity of L1 met “suggests” mild healing. (SUV 9.4 v 12.1 in May ‘13)
4. scattered lung nodules, up to 5mm in size = stable, no increased activity
5. other small scattered sclerotic lesions, one in right iliac and one in thoracic vertebral body similar in appearance to L1 without PET activity and not clearly pathologic
APRIL 2014 - 6 YRS POST GAMMA ZAP, 7 YRS MBC & 18 YEARS FROM ORIGINAL DX!
October 2014: hold avastin, continue HPX
Feb 2015 Cancer you lost. NEDHEAD 7 years post gamma zap miracle, 8 years ST4, +19 yrs original diagnosis.
Continue HPX. Adding back Avastin
Nov 2015 pet/ct is mixed result. L1 SUV is worse. Continue Herceptin/avastin/xgeva. Might revisit Perjeta for L1. Meantime going for rads consult for L1
December 2015 - brain stable. Continue Herceptin, Perjeta, Avastin and xgeva.
Jan 2016: 5 days, 20 grays, Rads to L1 and continue on HAPX. I’m trying to "save" TDM1 for next line. Hope the rads work to quiet L1. Sciatic pain extraordinaire :((
Markers drop post rads.
2/24/16 HAP plus X - markers are down
SCIATIC PAIN DEAL BREAKER.
3/23/16 Laminectomy w/coflex implant L4/5. NO MORE SCIATIC PAIN!!! Healing.
APRIL 2016 - 9 YRS MBC
July 2016 - continue HAP plus Xgeva.
DEC 2016 - PETCT: mets to sternum, lungs, L1 still about the same in size and PET activity. Markers not bad. Not making changes if I don't need to. Herceptin/Perjeta/Avastin/Xgeva
APRIL 2017 10 YEARS MBC
December 2017 - Progression - gonna switch it up
FEB 2018 - Kadcyla 3 cycles ---->progression :(
MAY30th - bronchoscopy, w/foundation1 - her2 enriched
Aug 27, 2018 - start clinical trial ZW25
JAN 2019 - ZW25 seems to be keeping me stable
APRIL 2019 - ONE DOZEN YEARS LIVING METASTATIC
MAY 2019 - progression back on herceptin add xeloda
JUNE 2019 - "6 mos average survival" LMD & CNS new single brain met - one zap during 5 days true beam SBRT to cord met
10/30/19 - stable brain and cord. progression lungs and bones. washing out. applying for ds8201a w nivolumab. hope they take me.
12/27/19 - begin ds8401a w nivolumab. after 2nd cycle nodes melt away. after 3rd cycle chest scan shows Improvement, brain MRI shows improvement, resolved areas & nothing new. switch to plain ENHERTU. after 4th cycle, PETscan shows mostly resolved or improved results. Markers near normal. I'm stunned but grateful.
10/26/20 - June 2021 Tucatinib/xeloda/herceptin - stable ish.
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Old 11-22-2009, 02:32 AM   #5
Brenda_D
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Re: How did you discover your cancer?

By accident, I brushed against a lump. I had a clear mammo 6 months earlier.
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12/12/06- IDC Stage III, 4x A/C, 35 rads, Herceptin 1 year
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Old 11-22-2009, 05:51 AM   #6
lkc Gumby
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Re: How did you discover your cancer?

SBE in shower, 9 mos after " clear Mammo"
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Linda

Dxed Stage IIIC May 05, 12 pos nodes
er/pr -neg,Her -pos
LVI
Right partial mast & partial axillary dissection-June14,2005
Right modified mast-no clear margins- June 30, 2005
DD AC x4
Taxotere X4 with Herceptin
Rads x 35( 5 fields )
Left prophylactive mast( atypia & hyperplasia found ),
put on Tamoxifen x 1 yr; D/ced due to endometrial thickening
bilateral recon (saline implants)May 06
Nipple recon July 06
metformin 2010
removal of implants due to severe encapsulation, insertion of gummies 2013
Reclast Q yr
NED!!!
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Old 11-22-2009, 06:23 AM   #7
Laurel
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Re: How did you discover your cancer?

Routine Mammo at age 48, small invasive tumor less than one cm which could not be felt on exam.
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Smile On!
Laurel


Dx'd w/multifocal DCIS/IDS 3/08
7mm invasive component
Partial mast. 5/08
Stage 1b, ER 80%, PR 90%, HER-2 6.9 on FISH
0/5 nodes
4 AC, 4 TH finished 9/08
Herceptin every 3 weeks. Finished 7/09
Tamoxifen 10/08. Switched to Femara 8/09
Bilat SPM w/reconstruction 10/08
Clinical Trial w/Clondronate 12/08
Stopped Clondronate--too hard on my gizzard!
Switched back to Tamoxifen due to tendon pain from Femara

15 Years NED
I think I just might hang around awhile....

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Old 11-22-2009, 06:27 AM   #8
Sheila
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Re: How did you discover your cancer?

Calcifications on mammo, clear mammo 6 mos before, biopsy of area revealed IDC, then left mastectomy...at age 49.
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"Be kinder than necessary, for everyone you meet
is fighting some kind of battle."



Hugs & Blessings
Sheila
Diagnosed at age 49.99999 2/21/2002 via Mammography (Calcifications)
Core Biopsy 2/22/02
L. Mastectomy 2/25/2002
Stage 1, 0.7cm IDC, Node Neg from 19 nodes Her2+++ ER PR Neg
6/2003 Reconstruction W/ Tissue Expander, Silicone Implant
9/2003 Stage IV with Mets to Supraclavicular nodes
9/2003 Began Herceptin every 3 weeks
3/2006 Xeloda 2500mg/Herceptin for recurrence to neck nodes
3/2007 Added back the Xeloda with Herceptin for continued mets to nodes
5/2007 Taken Off Xeloda, no longer working
6/14/07 Taxol/Herceptin/Avastin
3/26 - 5/28/08 Taxol Holiday Whopeeeeeeeee
5/29 2008 Back on Taxol w Herceptin q 2 weeks
4/2009 Progression on Taxol & Paralyzed L Vocal Cord from Nodes Pressing on Nerve
5/2009 Begin Rx with Navelbine/Herceptin
11/09 Progression on Navelbine
Fought for and started Tykerb/Herceptin...nodes are melting!!!!!
2/2010 Back to Avastin/Herceptin
5/2010 Switched to Metronomic Chemo with Herceptin...Cytoxan and Methotrexate
Pericardial Window Surgery to Drain Pericardial Effusion
7/2010 Back to walking a mile a day...YEAH!!!!
9/2010 Nodes are back with a vengence in neck
Qualified for TDM-1 EAP
10/6/10 Begin my miracle drug, TDM-1
Mixed response, shrinking internal nodes, progression skin mets after 3 treatments
12/6/10 Started Halaven (Eribulen) /Herceptin excellent results in 2 treatments
2/2011 I CELEBRATE my 9 YEAR MARK!!!!!!!!!!!!!
7/5/11 begin Gemzar /Herceptin for node progression
2/8/2012 Gemzar stopped, Continue Herceptin
2/20/2012 Begin Tomo Radiation to Neck Nodes
2/21/2012 I CELEBRATE 10 YEARS
5/12/2012 BeganTaxotere/ Herceptin is my next miracle for new node progression
6/28/12 Stopped Taxotere due to pregression, Started Perjeta/Herceptin
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Old 11-22-2009, 07:04 AM   #9
alicem
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Re: How did you discover your cancer?

Microcalcifications on a mammogram at the age of 52.
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9/15/08 (age 52) - Mammo: calcifications
9/22/08 - Biopsy: DCIS, grade 3. ER,PR status: Pos. in 75-90% of tumor cells.
10/01/08 - Ob/Gyn appt.: found complex, mostly cystic mass on right ovary - 11cmx12cmx 8cm
10/15/08 - Hysterectomy & Oophorectomy, Lumpectomy: Cyst on uterus, not ovary - all was benign. Breast - 5 of 6 bad margins. 2 Sentinel Lymph nodes removed, both negative. Stage 0, Tis, N0
12/11/08 - Mastectomy & DIEP reconstruction: Surprise! 2 cm Invasive DC, grade 2 found. One benign internal mammary lymph node. Stage 1, T1c, N0, all clean margins. ER+ (Proportion Score = 2/5, Intensity Score = 2/3) and PR+(Proportion Score = 3/5, Intensity Score = 2/3)
HER2 score = 3+
1/09/09 - Oncotype DX: Recurrence S/core of 60 !?!?! ER status is NEG!! PR staus is NEG! HER2 score = 12.2 (still positive, greater than 11.5 is positive).
1/20/09 - Started chemo: TCH
5/26/09 - FINISHED CHEMO!
1/05/10 - FINISHED HERCEPTIN!
1/22/10 - Port-a-catheter removed!
3/07/18 - Still NED
9/10/23 - Still NED
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Old 11-22-2009, 08:05 AM   #10
whatz
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Re: How did you discover your cancer?

I was mildly sore on my left breast which led me to investigating (comparing left to right). Found lump on left. Mamo 6 months earlier was clear.
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4/09 suspicious lump in left breast
5/09 biopsi lead to diagnosis ER/PR -
Her2+.Grade 3,full masectomy left breast,sentinel nodes clear,Stage 1
6/09 Adriamycin + Cytoxan 4 treatments (every 3 weeks) followed by Taxol + Herceptin, 1 treatment weekly for 12 weeks, followed by Herceptin for 40 weeks
MRI Brain 4/10 clear
CT Body 4/10 clear
PET Body 2/11 clear
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Old 11-22-2009, 08:17 AM   #11
Montana
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Re: How did you discover your cancer?

Microcalcs on yearly mammogram
__________________
Diag. Oct. 2004 age 54 left breast
Stage 1 grade 3; 6mm IDC; unknown amount of DCIS
with comedo necrosis; node neg.
Nottingham Grade 7/9
ER 91% PR 62%; Her2 3.6 by ICH; KI-67 35%

Nov 2004 Lumpectomy; SNB failed so had
full axillary clearance;
Dec 2004 2nd lumpy for clean DCIS margins.

Jan/Feb 2005 4 A/C dose dense;
33 rads finished 6/2005;
Began 5 years Arimidex in 6/2005
No Herceptin
9/2007 Quit Arimidex due to severe side effects.
NED
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Old 11-22-2009, 08:32 AM   #12
Margerie
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Re: How did you discover your cancer?

SBE age 38 (no family history)
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Are we there yet?


Dx 10/05 IDC, multi-focal, triple +, 5 nodes+
MRM, 4 DD A/C, 12 weekly taxol + herceptin
rads concurrent with taxol/herceptin
finished herceptin 01/08
ooph, Arimidex, bilateral DIEP reconstruction
NED
Univ. of WA, Seattle vaccine trial '07
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Old 11-22-2009, 09:24 AM   #13
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Re: How did you discover your cancer?

Both times: MRI

Marilyn
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Old 11-22-2009, 09:41 AM   #14
Lien
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Re: How did you discover your cancer?

I found a new lump at age 44. Had cysts and b9 lumps since I was 25.

I wondered, Marilyn, why you had the MRI? Did you feel something? Wat it seen on a screening mammo?

Jacqueline
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Diagnosed age 44, January 2004, 0.7 cm IDC & DCIS. Stage 1, grade 3, ER/PR pos. HER2 pos. clear margins, no nodes. SNB. 35 rads. On Zoladex and Armidex since Dec. 2004. Stopped Zoladex/Arimidex sept 2009 Still taking mistletoe shots (CAM therapy) Doing fine.
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Old 11-22-2009, 09:54 AM   #15
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Re: How did you discover your cancer?

Regrettably, I wasn't doing SBE's. My husband found my lump...geez, what a mood killer!!!

Hayley
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Hayley
Oklahoma

3/35/2009 - Diagnosed, age 39
5/7/09 - Mastectomy and reconstruction started. Two tumors found. Tumors were side by side. DCIS tumor was 2.8 cm, ER-, PR-, grade 2. Invasive tumor was 1.1 cm, poorly differentiated, grade 3, ER+90%, PR+95%, HER2+3. Thankfully, no node involvement.
5/29/09 - Second surgery resulting from difficulty healing from mastectomy.
6/2/09 - Began Herceptin treatments
6/23/09 - Began Taxotere and Carboplatin treatments along with Herception every 3 weeks.
10/06/09 - Completed Taxotere and Carboplatin - Yeah!!!
10/27/2009 - Herceptin maintenance and began Femara
12/10/2009 - 2nd stage reconstruction surgery
2/2010 - Body rejected saline implant
3/18/2010 - Second stage reconstruction using silicone implant
5/4/10 - Completed Herceptin - YEE-HAA!
May '10 - Body rejects silicone implant...taking a break.
11/29/10 - Hysterectomy
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Old 11-22-2009, 11:04 AM   #16
Debbie L.
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Re: How did you discover your cancer?

It would be interesting to ask this question of those who have died. Let me rephrase that. It would be interesting to know the answer to this question for those who have died of their breast cancer.

I suspect the answers would be very similar.

FINDING a breast cancer does not necessarily equate (alas) with SAVING A LIFE. Most of us on this list, btw, are too new to the game to say our life has been saved.

TREATING a breast cancer - yes, that does save some lives. But again, and alas -- not all lives, not yet.

As for finding your own lump - no one is saying that women do not find their own lumps, nor that they should NOT find their own lumps. I saw a stat that of the breast cancers that are not found by mammography, 80% are found by the women themselves, and not when doing formal BSE. No one is saying to ignore our breasts, nor to ignore suspicious findings in our breasts. The science is saying that
doing a formal monthly exam in a specific manner does not improve outcome for women whose breast cancer is detected in this way.

I don't know how to say it more clearly. Take two groups of 100 women. Teach one group to do excellent breast exams and have them do them every month. Tell the other group of women to let us know if they notice anything different with their breasts. The rate of death from breast cancer will be exactly the same in both groups. We could get into the harms caused by the hyper-vigilance of BSE but we don't even need to. Even if there were no harms, why would we advise doing something that makes no difference to outcome?

Why would we want to spend millions of dollars telling women to do something that does not help them?

I don't understand why some of this anger is not directed at the fact that we've been deceived by the screening and awareness propaganda all these years.

Debbie Laxague
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3/01 ~ Age 49. Occult primary announced by large (6cm) axillary node, found by my husband.
4/01 ~ Bilateral mastectomies (LMRM, R elective simple) - 1.2cm IDC was found at pathology. 5 of 11 axillary nodes positive, largest = 6cm. Stage IIIA
ERPR 5%/1% (re-done later at Baylor, both negative at zero).
HER2neu positive by IHC and FISH (8.89).
Lymphovascular invasion, grade 3, 8/9 modified SBR.
TX: Control of arm of NSABP's B-31 adjuvant Herceptin trial (no Herceptin, inducing a severe case of Herceptin-envy): A/C x 4 and Taxol x 4 q3weeks, then rads. Raging infection of entire chest after small revision of mastectomy scar after completing tx (significance unknown). Arimidex for two years, stopped after second pathology opinion.
2017: Mild and manageable lymphedema and some cognitive issues.
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Old 11-22-2009, 12:39 PM   #17
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Re: How did you discover your cancer?

Hey DL, I would like to take a stab at an alternate take on your conclusion....
Quote:
Even if there were no harms, why would we advise doing something that makes no difference to outcome?
Nothing makes a difference in our ultimate outcome. We all die one day. From something. If not from a disease or an accident or an act of malice, then from old age. There is no such thing as "saving a life" - it should actually be called "extending a life" - even if it is a firefighter pulling a person out of a burning building.

I really bristle at the theory of "harms caused by hyper-vigilance" because I think women are emotionally strong enough to weather false positives in favor of the power of knowledge.

If the end purpose for all research is to save lives, then we might as well stop now, as nothing in the end will ultimately "save our life." Perhaps the end purpose for all research should be more simply stated as designed to cure disease and remove it as a speed bump in the middle of life along the way to the ultimate outcome all humans face.

As to the quote above, it does make a difference to outcome to the degree that we have some control over our immediate short term outcome. Finding it as opposed to not finding it allows us to take measures to extend our lives, i.e. treating it. I don't know for sure whether or not I would still be alive 6 years later from my diagnosis if I hadn't treated it or hadn't know about it for another few years, but I suspect that given the course of mine, I would not. I would rather have known early and had reasonably "small measure" choices that I tolerate well and incorporate into my life, than find out at stage IV and have less choices, less time and absolutely less hope. Whether that treatment cures it or buys more time, it is valid. And the diagnostics that brought me here (BSE, mammo, ultra sound and biopsy) are all valid, too.
__________________
Brenda

NOV 2012 - 9 yr anniversary
JULY 2012 - 7 yr anniversary stage IV (of 50...)

Nov'03~ dX stage 2B
Dec'03~
Rt side mastectomy, Her2+, ER/PR+, 10 nodes out, one node positive
Jan'04~
Taxotere/Adria/Cytoxan x 6, NED, no Rads, Tamox. 1 year, Arimadex 3 mo., NED 14 mo.
Sept'05~
micro mets lungs/chest nodes/underarm node, Switched to Aromasin, T/C/H x 7, NED 6 months - Herceptin only
Aug'06~
micro mets chest nodes, & bone spot @ C3 neck, Added Taxol to Herceptin
Feb'07~ Genetic testing, BRCA 1&2 neg

Apr'07~
MRI - two 9mm brain mets & 5 punctates, new left chest met, & small increase of bone spot C3 neck, Stopped Aromasin
May'07~
Started Tykerb/Xeloda, no WBR for now
June'07~
MRI - stable brain mets, no new mets, 9mm spots less enhanced, CA15.3 down 45.5 to 9.3 in 10 wks, Ty/Xel working magic!
Aug'07~
MRI - brain mets shrunk half, NO NEW BRAIN METS!!, TMs stable @ 9.2
Oct'07~
PET/CT & MRI show NED
Apr'08~
scans still show NED in the head, small bone spot on right iliac crest (rear pelvic bone)
Sept'08~
MRI shows activity in brain mets, completed 5 fractions/5 consecutive days of IMRT to zap the pesky buggers
Oct'08~
dropped Xeloda, switched to tri-weekly Herceptin in combo with Tykerb, extend to tri-monthly Zometa infusion
Dec'08~
Brain MRI- 4 spots reduced to punctate size, large spot shrunk by 3mm, CT of torso clear/pelvis spot stable
June'09~
new 3-4mm left cerrebellar spot zapped with IMRT targeted rads
Sept'09~
new 6mm & 1 cm spots in pituitary/optic chiasm area. Rx= 25 days of 3D conformal fractionated targeted IMRT to the tumors.
Oct'09~
25 days of low dose 3D conformal fractionated targeted IMRT to the bone mets spot on rt. iliac crest that have been watching for 2 years. Added daily Aromasin back into treatment regimen.
Apr'10~ Brain MRI clear! But, see new small spot on adrenal gland. Change from Aromasin back to Tamoxifen.
June'10~ Tumor markers (CA15.3) dropped from 37 to 23 after one month on Tamoxifen. Continue to monitor adrenal gland spot. Remain on Tykerb/Herceptin/Tamoxifen.
Nov'10~ Radiate positive mediastinal node that was pressing on recurrent laryngeal nerve, causing paralyzed larynx and a funny voice.
Jan'11~ MRI shows possible activity or perhaps just scar tissue/necrotic increase on 3 previously treated brain spots and a pituitary spot. 5 days of IMRT on 4 spots.
Feb'11~ Enrolled in T-DM1 EAP in Denver, first treatment March 25, 2011.
Mar'11~ Finally started T-DM1 EAP in Denver at Rocky Mountain Cancer Center/Rose on Mar. 25... hallelujah.

"I would rather be anecdotally alive than statistically dead."

Last edited by hutchibk; 11-22-2009 at 01:22 PM..
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Old 11-22-2009, 01:13 PM   #18
Becky
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Re: How did you discover your cancer?

But... at least if you are doing BSE and find the lump you do feel as if you were giving yourself your best shot.

I did find mine and at least felt that at that moment (and every moment of every BSE prior to then and after then) that I was doing myself a good turn - something good for myself and my health. I figure it was better to find it at 1.9 cm (and one positive node) than perhaps several months later at 2.6 cm and 3 positive nodes. It is true that either way, I would probably still be here 5+ yrs later (or not perhaps). However, we are all told over and over again that our prognosis is better the earlier we are diagnosed.

So, I will continue to check my boobies once a month. I've learned the lay of my landscape and my new landscape to know if a new tree is there that was not there before and it gives my mind alittle comfort to make sure its okay. I dread doing it, I have to admit (because maybe something IS there this time) but I do it because I feel it is something I do for my health overall. After all, I've come this far and don't want a brand new bc to take me down just because I didn't even know it was there when I could have.

Everyone's different though.
__________________
Kind regards

Becky

Found lump via BSE
Diagnosed 8/04 at age 45
1.9cm tumor, ER+PR-, Her2 3+(rt side)
2 micromets to sentinel node
Stage 2A
left 3mm DCIS - low grade ER+PR+Her2 neg
lumpectomies 9/7/04
4DD AC followed by 4 DD taxol
Used Leukine instead of Neulasta
35 rads on right side only
4/05 started Tamoxifen
Started Herceptin 4 months after last Taxol due to
trial results and 2005 ASCO meeting & recommendations
Oophorectomy 8/05
Started Arimidex 9/05
Finished Herceptin (16 months) 9/06
Arimidex Only
Prolia every 6 months for osteopenia

NED 18 years!

Said Christopher Robin to Pooh: "You must remember this: You're braver than you believe and stronger than you seem and smarter than you think"
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Old 11-22-2009, 01:34 PM   #19
Debbie L.
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Posts: 463
Re: How did you discover your cancer?

(warning, it took me so long to write this that I was timed out and had to sign in again, even though it still knew who I was. sorry for the length but Brenda and I do tend to get going)

Hi Brenda,

You and I have enjoyed this debate before (smile). Correct me if I'm wrong, but my understanding is that your style values finding small things. My thinking is that the biology and response-to-treatment is more important than size. Brain mets excepted.

I think when we've discussed this before, it's been about mets vigilance. I think that we've agreed to disagree - noting that it's partly a matter of style and personality although I do have other concerns (like the cost) about ultra-vigilance when we have no evidence of benefit. Again, brain mets excepted. And I do allow that there is the possibility that one day, we may learn that finding, for example, a small liver met and zapping it, as we do with a small brain met - will be an improvement that extends life. But we don't know that. There's a heck of a lot that we don't know.

But now we're talking about primary detection which in some ways is different (we do have bushels of evidence that seems to say that larger is worse and vascular/lymphatic invasion is worse). The argument to that, which makes sense to me, is that those things (larger, more spread) may not be, in themselves, worse things, or even things that happened because of time - but are simply markers that go along with the more-aggressive (faster growing, more invasive) cancers, and thus the worse prognosis relates to the biology that caused the larger size or farther spread.

You are right, we are all dying. But we are also talking here about saving lives in a breast-cancer-specific way and so I think "saving" lives is an okay way to phrase it. If the cancer doesn't return and some other fire gets us at 90 - well then we can say that we were saved from dying of breast cancer. Can't we? (except now there is the argument that some tumors may never threaten life and/or may regress on their own but my guess would be that those are not HER2+ ones).

What else. Oh yeah. Harms. I didn't even go there because I'm not sure it strengthens the argument. But the harms are not just to peace of mind. The extra radiation is a harm (especially perhaps to the BRCA+ cancers) and the biopsies carry the risk of any surgery plus there are some questions about what role the growth factors involved in wound healing might play r/t cancer occurrence and/or growth. And now with MRSA and other resistant bugs, any invasive procedure becomes more worrisome.

But I think the bottom line is that we're back to our ongoing agree-to-disagree place. You are sure that finding a cancer with BSE a month before you might have noted it by chance in the shower will offer you a longer lifetime - whether from a cure or from control of mets. I am not sure of that. I don't see any evidence that says that might be true. And it bothers me that we are/were spending so much money and effort to tell women to do something that we don't know will help them. I'd much prefer that we spent that money finding out more about breast cancer. Especially important right now is finding out which cancers really are a threat. For us on this board, who are HER2+, that may not seem very important, because all HER2+ cancer may be a threat. But with the majority of breast cancers, it's not so clear.

Debbie Laxague
PS: how do you make that quote box? I can do copy/paste and change colors/fonts but when I click on "quote" below, nothing happens. I'm on another list where the quote thing works, so I don't think it's my computer.
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Old 11-22-2009, 02:32 PM   #20
alicem
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Location: Colorado Springs, CO
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Re: How did you discover your cancer?

I missed the statistics that support the recent mammogram recommendations. What percentage of cancers are found because of mammograms given to women in their 40's? 20%? 10%? What person out there wants that person whose life might be saved - but won't be because of the new treatment recommendations - to be someone they love dearly?

The mammogram that saved my life was done when I was 52. However, it had been too many years since my previous one. Perhaps the calcifications might have shown up on a mammogram 3 years earlier when I was 49 and it still might have been just DCIS, stage 0 and the Her2+++ invasive cancer that had to be treated by chemo would never have happened. I blame myself for this, but I had become complacent. My primary care physician had told me in my early 40's that I would NEVER get breast cancer. HAH!!!

Lets fast forward to the next treatment that might fall under the gun for the next round of "cost savings/harm prevention" - - biopsies. When my calcifications were found, I was told not to be worried because in my particular situation, 90% of the time it would turn up nothing. Because 10% of the time it does turn up cancer, it was the recommendation to have a biopsy. I fell in the 10%. It worries me that the same argument could be made for biopsies in my situation. Statistically, calcifications like mine are nothing. Statistically, 90% of the women are put under the "stress" of a biopsy for no reason. Is the cost of these "unnecessary" biopsies for those 90% TOO GREAT??? In my opinion, NO!! If it weren't for this particular standard of care, I would be facing a different outcome entirely. My mammogram found calcifications. My calcifications led to a biopsy. The biopsy led to a lumpectomy. The lumpectomy led to a mastectomy. The mastectomy FOUND MY INVASIVE CANCER before my lymph nodes became involved!! If it weren't for the biopsy, I believe the cancer would have progressed to the point where my odds of survival were greatly reduced. It scares me that in the future, a women with my scenario might face a totally different result - because it was more important to cut costs.
__________________
9/15/08 (age 52) - Mammo: calcifications
9/22/08 - Biopsy: DCIS, grade 3. ER,PR status: Pos. in 75-90% of tumor cells.
10/01/08 - Ob/Gyn appt.: found complex, mostly cystic mass on right ovary - 11cmx12cmx 8cm
10/15/08 - Hysterectomy & Oophorectomy, Lumpectomy: Cyst on uterus, not ovary - all was benign. Breast - 5 of 6 bad margins. 2 Sentinel Lymph nodes removed, both negative. Stage 0, Tis, N0
12/11/08 - Mastectomy & DIEP reconstruction: Surprise! 2 cm Invasive DC, grade 2 found. One benign internal mammary lymph node. Stage 1, T1c, N0, all clean margins. ER+ (Proportion Score = 2/5, Intensity Score = 2/3) and PR+(Proportion Score = 3/5, Intensity Score = 2/3)
HER2 score = 3+
1/09/09 - Oncotype DX: Recurrence S/core of 60 !?!?! ER status is NEG!! PR staus is NEG! HER2 score = 12.2 (still positive, greater than 11.5 is positive).
1/20/09 - Started chemo: TCH
5/26/09 - FINISHED CHEMO!
1/05/10 - FINISHED HERCEPTIN!
1/22/10 - Port-a-catheter removed!
3/07/18 - Still NED
9/10/23 - Still NED
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