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Old 09-13-2013, 02:53 PM   #1
LeahM
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Let me be your voice

Hi All,

I have been offered, and I have accepted, an opportunity to spend two hours on Montel Williams couch with an "oncology expert" and my own beloved Breast Surgeon Dr. H. Chung.

This meeting will take place on Fri Sept 20 and I have a list of things I want to say (as I hear NEDenise in my head saying "we are aware, now lets find a cure"), points I want to make etc

What would you say if you could? I would love to speak for you!

Leah
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39 year old wife, mother of one and nurse.
April 20, 2012: Dx Invasive Ductal Carcinoma
April 25, 2012: ER+(5%), PR-, HER2+++
May 10, 2012: BRCA 1,2 Negative
May 23, 2012: MUGA Scan EF 70%
May 31, 2012: B/L Mastectomy. 2/2 nodes removed and CLEAR!! Power Port placed. 2 Drains. 2 Expanders placed
June 5, 2012: Drains OUT! Ahhhh..
June 12, 2012: Final Pathology Report, .8x.3cm tumor. Micromets to 1 node .35mm under cytokeratin staining. Stage 2A. Onc says "you are lucky to have found this early"
July 10, 2012: Started 6 rounds of TCH with weekly H
Sept 5, 2012: MUGA 65%
Sept 20, 2012: CAT scan of brain clear!
Oct 23, 2012: LAST TC! AMEN! Continue Herceptin every three weeks until July 2013.
Nov 19, 2012: Port out!
Dec 5, 2012: Started radiation
Dec. 10, 2012: MUGA 65%
Dec. 13, 2012: Turned 40. BEST BIRTHDAY EVER!
Jan 23, 2013: Last radiation. Told I am NED. Continue Herceptin every three weeks till July 2013.
Jan 29, 2013: Begin 5 years of Tamoxifen.
Feb 28, 2013: CT Scan with Contrast of lungs. 5mm and 4mm nodules of unknown origin. Rescan in 3 months.
Mar 6, 2013: EF 60%
May 8, 2013: Exanders out, implants implanted...abd. lipo and fat moved up. Girls are looking good!
June 3, 2013: CT Scan with Contrast of lungs. Previous nodules gone. New nodules (2mm and 3mm) found. Rescan in 3 months. So sorry I opened this can of worms...
June 11, 2013: EF 60%
June 25, 2013: Last Herceptin. wow...
Aug 20, 2013: Tumor markers within normal limits. Xray to sore left ribs shows no disease or fractures.
Sept 9, 2013: CT of lungs shows no disease. Closing this can of worms and moving on.
Nov 20, 2013: Tumor markers within normal limits. Severe Vit D deficiency, started on prescription Vit. D. Blaming chemo for this.
Feb 2014: Tumor markers within normal limits.
May 2014: Tumor markers within normal limits. Graduated to twice yearly onc appts.
Oct 2014: Tumor markers within normal limits.
May 2015: Tumor markers WNL. Bone density scan fine. Bone scan and xray of ribs shows "something" 4th right rib. Could be healed fracture but if it is healed why does it hurt?
Nov 2015: Tumor markers WNL. Follow up bone scan clear.
Feb 2016: Syncope! WTF? Dizzy too. Brain scan clear, ECHO EF 60%, Halter Monitor shows heart is fine. Viral? I will never know.
June 2016: Tumor markers WNL.
Oct 2016: Stabbing pain right eye. Long story short, trigeminal neuralgia.
Nov 2016 Brain MRI clear.
Jan 2017: Tumor markers WNL, still getting weird pain right rib area, and sometimes right upper chest. Xray x2, Bone Scan, Breast MRI all clear. Scar tissue? Rads. I may never know.
www.onmywaytosurvivorhood.blogspot.com
www.thechemobag.com
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Old 09-13-2013, 05:08 PM   #2
tricia keegan
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Re: Let me be your voice

Hi Leah,

I'm highly triple positive (with positive nodes) and my Onc believe's its better for me to continue on Arimidex for ten years, I have some side effects but will continue if it keeps me cancer free, I'd like to ask if the Onc expert agree's with hormone therapy for ten years and I know the trials are not finished yet but would like to know their views. Thanks!
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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 09-14-2013, 12:02 AM   #3
StephN
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Re: Let me be your voice

What a great opportunity! Guess you do not know the "air date"?

WE ARE aware, but there are always underserved groups such as might tend to watch a show like Montel. Maybe speak to the younger women "out there" who might think BC could never happen to them. The onc might have some stats to throw into the discussion.

MHO it would be good to chat with the onc about the fact that BC has so many different forms, with differing symptoms. That it is not just ONE disease.
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Live in the moment.

MY STORY SO FAR ~~~~
Found suspicious lump 9/2000
Lumpectomy, then node dissection and port placement
Stage IIB, 8 pos nodes of 18, Grade 3, ER & PR -
Adriamycin 12 weekly, taxotere 4 rounds
36 rads - very little burning
3 mos after rads liver full of tumors, Stage IV Jan 2002, one spot on sternum
Weekly Taxol, Navelbine, Herceptin for 27 rounds to NED!
2003 & 2004 no active disease - 3 weekly Herceptin + Zometa
Jan 2005 two mets to brain - Gamma Knife on Jan 18
All clear until treated cerebellum spot showing activity on Jan 2006 brain MRI & brain PET
Brain surgery on Feb 9, 2006 - no cancer, 100% radiation necrosis - tumor was still dying
Continue as NED while on Herceptin & quarterly Zometa
Fall-2006 - off Zometa - watching one small brain spot (scar?)
2007 - spot/scar in brain stable - finished anticoagulation therapy for clot along my port-a-catheter - 3 angioplasties to unblock vena cava
2008 - Brain and body still NED! Port removed and scans in Dec.
Dec 2008 - stop Herceptin - Vaccine Trial at U of W begun in Oct. of 2011
STILL NED everywhere in Feb 2014 - on wing & prayer
7/14 - Started twice yearly Zometa for my bones
Jan. 2015 checkup still shows NED
2015 Neuropathy in feet - otherwise all OK - still NED.
Same news for 2016 and all of 2017.
Nov of 2017 - had small skin cancer removed from my face. Will have Zometa end of Jan. 2018.
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Old 09-14-2013, 05:17 AM   #4
sarah
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Re: Let me be your voice

Hello,
1.Is anyone working on something for inflammatory bc?
2.Also how to help with radiation side effects or at least warn people of these so they can act upon them quickly - I've had fibrosis in my lung and a totally collapsed/blocked heart artery - I had chest pain and thought it was asthma, turned out to be a heart attack. Not sure how often this occurs but might be helpful to warn women about chest pains and possible heart issues.
3.Agree, we don't need any more awareness we need cures. we need better and cheaper tumor testing to pinpoint what will help.
We will all be waiting to hear what happened.
thanks
sarah
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Old 09-14-2013, 06:08 AM   #5
JillaryJill
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Re: Let me be your voice

PREVENTION TOPIC:
I would like to address the whole dense breast issue. Dense breasts photograph white on a mammogram and a cancerous tumor photographs white. I had mamograms every year since I was 40 and my cancer was not caught until I was Stage IIIc with a large tumor. When looking back all of my mammograms had a disclaimer, due to patient having dense breasts certain lesions may not be detected. Many women that I talk to that are routinely having mamograms, I ask them, what type of breast tissue do you have? Do you have dense breasts? Very few of them know what I am talking about. I think Dr.'s need to tell every patient if they have dense breasts and tailor diagnostic imaging to the breast type. i.e.: mammogram plus ultrasound, or breast mri. Or perhaps is there new technology coming in breast imaging where if you have dense breasts, the healthy tissue photographs purple or something and the cancer cells photograph white. Dramatic example I know but you get my point.
WOMEN WHO ARE DIAGNOSED:
Also, I would like previously diagnosed women to search out and find a clinical trial to help advance the science of this horrible disease. I had no idea how long new drugs are delayed because of the long recruiting phase of these drug trials. I think we need awareness in this area.
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DX November 2010
Brain MRI, CT of lung, liver, bone, all clear
Double Mastectomy w/expanders December 1, 2010
ER- PR- Her2+++, grade 3, 12 positive nodes out of 15
Stage IIIc
Started TCH/Chemo December 31, 2010
6 rounds TCH
Herceptin every 3 weeks for a year
33 rounds of TomoTube radiation, to chest wall, neck, skin and lymph area
September, 2011, MRI to lower spine, hips, DX bulging disk, L4 & L5, pain not from cancer
Expanders removed, implants in Dec 1, 2011
Finished Herceptin, December 21, 2011
August 2012, CT of chest and abdomen, all ok
Enrolled in MC1136 Phase I Peptide Vaccine Trial at Mayo Clinic, Rochester, Minnesota
March 2013, First Vaccine
April 2013, 2nd Vaccine
May 2013, 3rd Vaccine
June 2013, 4th Vaccine
July 2013, 5th Vaccine
August 2013, 6th Vaccine Done!
September 2013, Mayo visit, Echo results 68, vaccine did not effect my heart! Blood work normal.
January 31, 2013, Mayo visit, Echo normal
February 23, 2014, Numb lips on right side, Brain MRI, normal!
June, 2015, Finished the trial at Mayo Clinic. Feels good!
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Old 09-14-2013, 07:42 AM   #6
karen z
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Re: Let me be your voice

LeahM,
Let us know the air date when you know.
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Old 09-14-2013, 11:31 AM   #7
'lizbeth
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Re: Let me be your voice

Leah,

What a wonderful opportunity! I will watch for sure, as soon as you know the air date to watch give us a shout.

I am curious as to what Montel will be asking. Would he be kind enough to give you the questions before the show so that you can be prepared? Can we see the question please?

Tell us a little more about your breast surgeon. I tried to google H. Chung Breast Surgeon and couldn't find information.
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Old 09-14-2013, 11:53 AM   #8
Andrea Barnett Budin
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Re: Let me be your voice

I have dense breasts. Mammo prior to being dx w/4th stage invasive lobular bc was NORMAL. I now get a sono at the same time.

I think my dghtrs (40s now) should get both. I think it's an insurance thing. Yes to mammos, reluctant to pony up the extra bucks for sono.

I also wish I had known -- I self-examined monthly. I never had a lump. Would ask friends, what exactly am I feeling for? It's like a marble or a pea.

I would learn that the general hardness in my left breast, that fit into the palm of my hand (as I turned 50/post menopausal) was in fact bc! ANY CHANGE IN YOUR NORMAL BREAST IS A SIGN YOU NEED TO SEE A BREAST SURGEON -- I now know, and now advise!

I also wish I had had a sono at the time of the last mammo prior to dx.

I believe Montel had bc. Don't quote me.

Would love to be on that couch with you. But yes, please BE OUR VOICE, Leah! And thank you for speaking out for women everywhere!

Andi
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'95 post-meno dx Invasive LOBULAR w/9cm tumor! YIKES + 2/21 nodes. Clear mammo 10 mnths earlier. Mastec/tram flap reconst/PORT/8 mnths chemo (4Adria/8CMF). Borderline ER/PR. Tamoxifen 2 yrs. Felt BLESSED. I could walk and talk, feed and bathe myself! I KNEW I would survive...

'98 -- multiple mets to liver. HER2+ 80%. ER/PR- Raging, highly aggressive tumors spreading fast. New PORT. 9 mnths Taxotere Fought fire w/fire! Pronounced in cautious remission 5/99. Taxotere weekly for 6 wks, 2 wks off -- for 9 mnths. TALK ABOUT GRUELING! (I believe they've altered that protocol since those days -- sure hope so!!)
+ good old Vit H wkly for 1st 3 yrs, then triple dosage ev 3 wks for 7 yrs more... The "easy" chemo, right?! Not a walk in the park, but not a freight train coming at 'ya either...

Added Herceptin Nov '98 (6 wks after FDA fast-tracked it for met bc). Stayed w/Vit H till July '08! Now I AM FREE! Humbly and eternally grateful for this life-saving drug! NED since '99 and planning on keeping it that way. To hell w/poor prognosis and nasty stats! STOPPED VIT H JULY '08...! REMAIN STABLE... Eternally grateful...Yes is a world & in this world of yes live (skillfully curled) all worlds ... (e e cummings) EVERY DAY I BEAT MY PREVIOUS RECORD FOR # OF CONSECUTIVE DAYS I'VE STAYED ALIVE. Smile KNOWING you too can be a miracle. Up to me and God now...
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Old 09-14-2013, 11:56 AM   #9
Andrea Barnett Budin
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Re: Let me be your voice

Montel Williams, On Dr. Mehmet Oz Show, Admits Emotional Eating Following Double Mastectomy (VIDEO)

Andi
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'95 post-meno dx Invasive LOBULAR w/9cm tumor! YIKES + 2/21 nodes. Clear mammo 10 mnths earlier. Mastec/tram flap reconst/PORT/8 mnths chemo (4Adria/8CMF). Borderline ER/PR. Tamoxifen 2 yrs. Felt BLESSED. I could walk and talk, feed and bathe myself! I KNEW I would survive...

'98 -- multiple mets to liver. HER2+ 80%. ER/PR- Raging, highly aggressive tumors spreading fast. New PORT. 9 mnths Taxotere Fought fire w/fire! Pronounced in cautious remission 5/99. Taxotere weekly for 6 wks, 2 wks off -- for 9 mnths. TALK ABOUT GRUELING! (I believe they've altered that protocol since those days -- sure hope so!!)
+ good old Vit H wkly for 1st 3 yrs, then triple dosage ev 3 wks for 7 yrs more... The "easy" chemo, right?! Not a walk in the park, but not a freight train coming at 'ya either...

Added Herceptin Nov '98 (6 wks after FDA fast-tracked it for met bc). Stayed w/Vit H till July '08! Now I AM FREE! Humbly and eternally grateful for this life-saving drug! NED since '99 and planning on keeping it that way. To hell w/poor prognosis and nasty stats! STOPPED VIT H JULY '08...! REMAIN STABLE... Eternally grateful...Yes is a world & in this world of yes live (skillfully curled) all worlds ... (e e cummings) EVERY DAY I BEAT MY PREVIOUS RECORD FOR # OF CONSECUTIVE DAYS I'VE STAYED ALIVE. Smile KNOWING you too can be a miracle. Up to me and God now...
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Old 09-14-2013, 12:01 PM   #10
Andrea Barnett Budin
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Re: Let me be your voice

WOW! What a story. (I just listened to the video...)
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Andi BB
'95 post-meno dx Invasive LOBULAR w/9cm tumor! YIKES + 2/21 nodes. Clear mammo 10 mnths earlier. Mastec/tram flap reconst/PORT/8 mnths chemo (4Adria/8CMF). Borderline ER/PR. Tamoxifen 2 yrs. Felt BLESSED. I could walk and talk, feed and bathe myself! I KNEW I would survive...

'98 -- multiple mets to liver. HER2+ 80%. ER/PR- Raging, highly aggressive tumors spreading fast. New PORT. 9 mnths Taxotere Fought fire w/fire! Pronounced in cautious remission 5/99. Taxotere weekly for 6 wks, 2 wks off -- for 9 mnths. TALK ABOUT GRUELING! (I believe they've altered that protocol since those days -- sure hope so!!)
+ good old Vit H wkly for 1st 3 yrs, then triple dosage ev 3 wks for 7 yrs more... The "easy" chemo, right?! Not a walk in the park, but not a freight train coming at 'ya either...

Added Herceptin Nov '98 (6 wks after FDA fast-tracked it for met bc). Stayed w/Vit H till July '08! Now I AM FREE! Humbly and eternally grateful for this life-saving drug! NED since '99 and planning on keeping it that way. To hell w/poor prognosis and nasty stats! STOPPED VIT H JULY '08...! REMAIN STABLE... Eternally grateful...Yes is a world & in this world of yes live (skillfully curled) all worlds ... (e e cummings) EVERY DAY I BEAT MY PREVIOUS RECORD FOR # OF CONSECUTIVE DAYS I'VE STAYED ALIVE. Smile KNOWING you too can be a miracle. Up to me and God now...
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Old 09-14-2013, 02:15 PM   #11
Jackie07
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Re: Let me be your voice

Please remind the audience about the imperfection of mammograms. My recurrence was not found until almost 4 years because the new growth was mistaken for scar tissue! Luckily I finally made an appointment with the original surgeon and had an mammo ordered through her. That's when the Stage IIB recurrence was confirmed.

Pay attention to your body and listen to your heart. When in doubt, check it out!
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http://www.kevinmd.com/blog/2011/06/doctors-letter-patient-newly-diagnosed-cancer.html
http://www.asco.org/ASCOv2/MultiMedi...=114&trackID=2

NICU 4.4 LB
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3 Infertility tmts 99 > 3 u. fibroids > Pills
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3-11 Appendectomy - visually O.K., a lot of puss. Final path result - not cancer.
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 09-14-2013, 03:06 PM   #12
suzan w
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Re: Let me be your voice

Side effects...such as chemo brain, loss of libido, maybe speak to the huge financial ramifications...
Congrats to you for this wonderful opportunity!
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Suzan W.
age 54 at diagnosis
5/05 suspicious mammogram-left breast
5/05 biopsy-invasive lobular carcinoma with LCIS,8mm tumor,stage 1 grade 2, ER+ PR+ Her2+++
6/14/05 bilateral mastectomy, node neg. all scans neg.
Oncotype DX-high risk
8/05-10/05 4 rounds A/C
10/05 -10/06 1 yr. herceptin
arimidex-5 years
2/14/08 started daily self administered injections..FORTEO for severe osteoporosis
7/28/09 BRCA 1 negative BRCA2 POSITIVE
8/17/09 prophylactic salpingo-oophorectomy
10/15/10 last FORTEOinjection
RECLAST infusion(ostoeporosis)
6/14/10 5 year cancerversary!
8/2010-18%increase in bone density!
no further treatments
Oncologist says, "Go do the Happy Dance"
I say,"What a long strange trip its been"
'One day at a time'
6-14-2015. 10 YEAR CANCERVERSARY!
7-16 to 9-16. Extensive (and expensive) dental work done to save teeth. Damage from osteoporosis and chemo and long term bisphosphonate use
6-14-16. 11 YEAR CANCERVERSARY!!
7-20-16 Prolia injection for severe osteoporosis
2 days later, massive hive outbreak. This led to an eventual dx of Chronic Ideopathic Urticaria, an auto-immune disease from HELL.
6-14-17 12 YEAR CANCERVERSARY!!
still suffering from CIU. 4 hospitilizations in the past year

as of today, 10-31-17 in remission from CIU and still, CANCER FREE!!!
6-14-18 13 YEAR CANCERVERSARY!! NED!!
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Old 09-14-2013, 03:12 PM   #13
Mtngrl
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Re: Let me be your voice

I'm sure you'll know what to say. My consistent message is, "You're not as likely to get breast cancer as you think. But if you do get it, you're much more likely to die from it than you think." A downer, but the truth.
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_____________________________
4/19/11 Diagnosed invasive ductal carcinoma in left breast; 2.3 cm tumor, 1 axillary lymph node, weakly ER+, HER2+++
4/29/11 CT scan shows suspicious lesions on liver and lungs
5/17/11 liver biopsy
5/24/11 liver met confirmed--Stage IV at diagnosis
5/27/11 Begin weekly Taxol & Herceptin for 3 months (standard of care at the time of my DX)
7/18/11 Switch to weekly Abraxane & Herceptin due to Taxol allergy
8/29/11 CT scan shows no new lesions & old lesions shrinking
9/27/11 Finish Abraxane. Start Herceptin every 3 weeks. Begin taking Arimidex
10/17/11--Brain MRI--No Brain mets
12/5/11 PET scan--Almost NED
5/15/12 PET scan shows progression-breast/chest/spine (one vertebra)
5/22/12 Stop taking Arimidex; stay on Herceptin
6/11/12 Started Tykerb and Herceptin on clinical trial (w/no chemo)
9/24/12 CT scan--No new mets. Everything stable.
3/11/13 CT Scan--two small new possible mets and odd looking area in left lung getting larger.
4/2/13--Biopsy of suspicious area in lower left lung. Mets to lung confirmed.
4/30/13 Begin Kadcyla/TDM-1
8/16/13 PET scan "mixed," with some areas of increased uptake, but also some definite improvement, so I'll stay on TDM-1/Kadcyla.
11/11/13 Finally get hormone receptor results from lung biopsy of 4/2/13. My cancer is no longer ER positive.
11/13/13 PET scan mixed results again. We're calling it "stable." Problems breathing on exertion.
2/18/14 PET scan shows a new lesion and newly active lymph node in chest, other progression. Bye bye TDM-1.
2/28/14 Begin Herceptin/Perjeta every 3 weeks.
6/8/14 PET "mixed," with no new lesions, and everything but lower lungs improving. My breathing is better.
8/18/14 PET "mixed" again. Upper lungs & one spine met stable, lower lungs less FDG avid, original tumor more avid, one lymph node in mediastinum more avid.
9/1/14 Begin taking Xeloda one week on, one week off. Will also stay on Herceptin and Perjeta every three weeks.
12/11/14 PET Scan--no new lesions, and everything looks better than it did.
3/20/15 PET Scan--no new lesions, but lower lung lesions larger and a bit more avid.
4/13/15 Increasing Xeloda dose to 10 days on, one week off.
7/1/15 Scan "mixed" again, but suggests continuing progression. Stop Xeloda. Substitute Abraxane every 3 weeks starting 7/13.
10/28/15 PET scan shows dramatic improvement everywhere. All lesions except lower lungs have resolved; lower lungs noticeably improved.
12/18/15 Last Abraxane. Continue on Herceptin and Perjeta alone beginning 1/8/16.
1/27/16 PET scan shows cancer is stable.
5/11/16 PET scan shows uptake in some areas that were resolved on the last two scans.
6/3/16 Begin Kadcyla and Tykerb combination
6/5 - 6/23 Horrible diarrhea from K&T together. Got pneumonia.
7/15/16 Begin Kadcyla only every 3 weeks.
9/6/16 Begin radiation therapy on right lung lesion that caused the pneumonia.
10/3/16 Last of 12 radiation treatments to right lung.
11/4/16 Huffing and puffing, low O2, high heart rate, on tiniest bit of exertion. Diagnosed as radiation pneumonitis. Treated with Prednisone.
11/11/16 PET scan shows significant improvement to radiated part of right lung BUT a bunch of new lung lesions, and the bone met is getting worse.
11/22/16 Begin Eribulin and Herceptin. H every 3 weeks. E two weeks on, one week off.
3/6/17 Scan shows progression in lungs. Bone met a little better.
3/23/17 Lung biopsy. Tumor sampled is ER-, PR+ (5%), HER2+++. Getting Herceptin and Perjeta as a maintenance treatment.
5/31/17 Port placement
6/1/17 Start Navelbine & Tykerb
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Old 09-14-2013, 03:24 PM   #14
IrvineFriend
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Re: Let me be your voice

I actually have a big issue in total with breast cancer in particular. At least in my area, which is Orange County (So CA), all the support groups meet during the day (hospital programs), where the prostate cancer groups and other cancers that include men all meet in the evenings so men can actually get support and work while going through all these appointments. It's so chauvinistic to assume every woman stays at home.

I did not know the enormous amount of time at appointments that would be involved before this. I would let people know what a typical breast cancer patient actually has to go through on a day to day basis just to be treated.

Congrats Leah and thank you for being the voice!

Andi, I have the same experience except I was stage III. There is a law that I believe has passed at least in CA and many other states requiring doctors to inform their patients of their density status if they have dense breasts. Mine are so dense my plastic surgeon thought I had implants already when she first took at look and felt them.
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Live in Orange County, CA

Diagnosed with DCIS Oct. 2012

Bilateral Dec. 19, 2012
IDC, ER/PR-, Her2+++, Grade 3
Stage IIIa
15.6 cm
4/14 nodes + macrometastases
First thing each morning, I try on my bathing suit. Then, nothing worse can happen the rest of the day.
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Old 09-14-2013, 05:48 PM   #15
Andrea Barnett Budin
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Re: Let me be your voice

The mammo tech would typically take you to the other waiting area... The radiologist would check the pics and if more were needed, back in you'd go.

I ALWAYS HAD TO RETURN TO THE SCENE OF THE CRIME. I was told, by way of explanation -- you have very, very dense breasts. And that was the end of it. Dense breasts meant you needed more angles taken.

Never ever was a sono recommended. Except when I presented with a 9 cm solid mass at mastec! Then, they did a sono, to confirm the unbelievable! Previous mammo was normal.
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Andi BB
'95 post-meno dx Invasive LOBULAR w/9cm tumor! YIKES + 2/21 nodes. Clear mammo 10 mnths earlier. Mastec/tram flap reconst/PORT/8 mnths chemo (4Adria/8CMF). Borderline ER/PR. Tamoxifen 2 yrs. Felt BLESSED. I could walk and talk, feed and bathe myself! I KNEW I would survive...

'98 -- multiple mets to liver. HER2+ 80%. ER/PR- Raging, highly aggressive tumors spreading fast. New PORT. 9 mnths Taxotere Fought fire w/fire! Pronounced in cautious remission 5/99. Taxotere weekly for 6 wks, 2 wks off -- for 9 mnths. TALK ABOUT GRUELING! (I believe they've altered that protocol since those days -- sure hope so!!)
+ good old Vit H wkly for 1st 3 yrs, then triple dosage ev 3 wks for 7 yrs more... The "easy" chemo, right?! Not a walk in the park, but not a freight train coming at 'ya either...

Added Herceptin Nov '98 (6 wks after FDA fast-tracked it for met bc). Stayed w/Vit H till July '08! Now I AM FREE! Humbly and eternally grateful for this life-saving drug! NED since '99 and planning on keeping it that way. To hell w/poor prognosis and nasty stats! STOPPED VIT H JULY '08...! REMAIN STABLE... Eternally grateful...Yes is a world & in this world of yes live (skillfully curled) all worlds ... (e e cummings) EVERY DAY I BEAT MY PREVIOUS RECORD FOR # OF CONSECUTIVE DAYS I'VE STAYED ALIVE. Smile KNOWING you too can be a miracle. Up to me and God now...
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Old 09-15-2013, 07:13 AM   #16
LeahM
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Re: Let me be your voice

Thanks for your input Ladies! I have jotted everything down and will bring it with me on Friday. I received a lengthy email last night from a producer that took me the better part of 3 hours to respond to. I did indicate that I would like to know what we would talk about, what I would be asked, in advance and I do believe that long email full of questions was my answer.

I also, at the end of my return email, asked if I would be given a chance to ask the experts some questions. I hope so.

From what I understand it will be a two hour in studio conversation, no audience. It will then be edited to appear on his Health and Wellness TV show and a series of "webinars". As soon as I have air dates I will let you know. At this point all I know is it will be in the fall. I was told to wear "fall colors", long sleeves, no white, no jeans. So...I went shopping!! And I made a hair apt for Wed., but this hair is a hot mess these days!

Funny story...when I was first contacted I was told taping was in April..so I figured ok, this gives me time to get it together, to grow my hair...so imagine my surprise when last Thurs I find out taping is this Fri, Sept. 20. I almost backed out at that point.

'lizbeth here is a link to my breast surgeon, there is a short video to watch if you wish. On the day of my surgery I remember her holding my hand and rubbing my arm as they put me under:
http://www.lvhn.org/find_a_doctor/profile-1604
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39 year old wife, mother of one and nurse.
April 20, 2012: Dx Invasive Ductal Carcinoma
April 25, 2012: ER+(5%), PR-, HER2+++
May 10, 2012: BRCA 1,2 Negative
May 23, 2012: MUGA Scan EF 70%
May 31, 2012: B/L Mastectomy. 2/2 nodes removed and CLEAR!! Power Port placed. 2 Drains. 2 Expanders placed
June 5, 2012: Drains OUT! Ahhhh..
June 12, 2012: Final Pathology Report, .8x.3cm tumor. Micromets to 1 node .35mm under cytokeratin staining. Stage 2A. Onc says "you are lucky to have found this early"
July 10, 2012: Started 6 rounds of TCH with weekly H
Sept 5, 2012: MUGA 65%
Sept 20, 2012: CAT scan of brain clear!
Oct 23, 2012: LAST TC! AMEN! Continue Herceptin every three weeks until July 2013.
Nov 19, 2012: Port out!
Dec 5, 2012: Started radiation
Dec. 10, 2012: MUGA 65%
Dec. 13, 2012: Turned 40. BEST BIRTHDAY EVER!
Jan 23, 2013: Last radiation. Told I am NED. Continue Herceptin every three weeks till July 2013.
Jan 29, 2013: Begin 5 years of Tamoxifen.
Feb 28, 2013: CT Scan with Contrast of lungs. 5mm and 4mm nodules of unknown origin. Rescan in 3 months.
Mar 6, 2013: EF 60%
May 8, 2013: Exanders out, implants implanted...abd. lipo and fat moved up. Girls are looking good!
June 3, 2013: CT Scan with Contrast of lungs. Previous nodules gone. New nodules (2mm and 3mm) found. Rescan in 3 months. So sorry I opened this can of worms...
June 11, 2013: EF 60%
June 25, 2013: Last Herceptin. wow...
Aug 20, 2013: Tumor markers within normal limits. Xray to sore left ribs shows no disease or fractures.
Sept 9, 2013: CT of lungs shows no disease. Closing this can of worms and moving on.
Nov 20, 2013: Tumor markers within normal limits. Severe Vit D deficiency, started on prescription Vit. D. Blaming chemo for this.
Feb 2014: Tumor markers within normal limits.
May 2014: Tumor markers within normal limits. Graduated to twice yearly onc appts.
Oct 2014: Tumor markers within normal limits.
May 2015: Tumor markers WNL. Bone density scan fine. Bone scan and xray of ribs shows "something" 4th right rib. Could be healed fracture but if it is healed why does it hurt?
Nov 2015: Tumor markers WNL. Follow up bone scan clear.
Feb 2016: Syncope! WTF? Dizzy too. Brain scan clear, ECHO EF 60%, Halter Monitor shows heart is fine. Viral? I will never know.
June 2016: Tumor markers WNL.
Oct 2016: Stabbing pain right eye. Long story short, trigeminal neuralgia.
Nov 2016 Brain MRI clear.
Jan 2017: Tumor markers WNL, still getting weird pain right rib area, and sometimes right upper chest. Xray x2, Bone Scan, Breast MRI all clear. Scar tissue? Rads. I may never know.
www.onmywaytosurvivorhood.blogspot.com
www.thechemobag.com
www.facebook.com/thechemobag
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Old 09-15-2013, 09:52 AM   #17
Becky
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Re: Let me be your voice

A few good things were brought up in this thread.

1. Dense breasts - I think its a crime that we are not informed of this. I actually changed my primary health care provider just after being diagnosed because every year I had my physical and got my mammo through her. As everyone knows, we get a very stunted letter from the mammo facility saying "no changes from last year" and we go on our merry way. However, the doctor gets the bigger, more informational report. When I had my lump, I had to go to the mammo center and pick up all my past studies. They were in a sealed envelope that had a huge sticker on it saying it could only be opened by the doctor (in this case, the breast surgeon that I would be seeing in a couple of hours). Heck with that sticker and I opened the envelope. That's how I found out my lump was cancer (even though I already knew by the way people were treating and talking to me (so gently)). I also read those other 10 reports from over the years. "This woman's breasts are so dense, we cannot see anything. We recommend alternate screening with MRI or ultrasound." EVERY YEAR this was said and I did NOT know and was not told. So I am diagnosed with node positive breast cancer. There should be a law about informing patients about dense breasts and the need for alternate testing with MRI. Get mammo, six months later get MRI. Get mammo, six months later get MRI and so on. I changed doctor's because I was counting on her to tell me.

2. Pinktober - I know we bc gals are sick of it. Me especially since I was diagnosed at the end of August and began everything (surgery early Sept and then chemo in October). With Pink all around me, I felt I could never get away from it even for a moment - shopping at the mall, chain restaurants - pink was everywhere. However, it reminds those who are not affected in anyway (themselves or any family and friends) that maybe they should get a mammogram or a professional breast exam or they think something's up and to stop putting it off. It raises awareness and more importantly, you can't help pink without the green ($). It raises $$$$ for research for the cure. Without the green, the Pink doesn't go away forever. So, it this time of year the Pink really is a downer for me because it was "my time of year" but if Pink produces the Green for a cure or preventative vaccine whatever - I really can't complain. I buy my Cheerios with the pink and yogurt etc so those companies donate the green to eliminate Pink! But I hear ya otherwise.

So Pink says early detection and you can't have early detection if you have dense breasts and don't know it. That's my imput.
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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"

Last edited by Becky; 09-15-2013 at 09:55 AM..
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Old 09-15-2013, 10:49 AM   #18
Andrea Barnett Budin
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Re: Let me be your voice

YES, Becky!

Telling me I have dense breasts, and NOT telling me what they write down behind the scenes, should be criminal!

Certainly NOT IN THE BEST INTERESTS OF THE PATIENT!

I have learned through these many yrs (since my '98 recurrence, which "I" FOUND studying and comparing my blood results and hearing the onc say 3x over 6 mnths WHEN PRODDED for more info -- Well, your liver enzymes are "slightly" -- but very very slight -- I asked for a liver sono, which meant an abdominal sonogram).

I NOW GET A COPY OF EVERY REPORT WRITTEN RE TESTS AND PATHOLOGY REPORTS AND SURGICAL PROCEDURES.

But I never realized there was a hidden report re mammos!! We get the short perfunctory letter -- that's it!

Of course, the insurance companies will balk at the added $$$$ expense of MRIs, which are perhaps only necessary for those with "dense" breasts. Lots of politics will enter the equation. But Becky, you are so right on. There ought to be a law!

Patient's rights are listed all over the place at doc offices and facilities but those reports, which you should have every right to, can help you discuss matters with your doc (who should be discussing matters with you anyway!). Those reports can help you determine a plan of action. Alert you.

Thanks for that, Becky!

(One onc used to dictate his report after an exam seated at the counter, talking into the phone, his back to you as you dressed.

I heard him say, The patient presents as being lobular and HER2+ which is highly unlikely! He gave a brief synopsis of my history and said, IT IS REMARKABLE THAT THE PATIENT HAS SURVIVED THESE MANY YEARS...)

I WAS IN THE ROOM! I don't go to that onc anymore...

I did attend an early morning lecture of his with my husband. Granted he is brilliant and is into bc research. He was talking about one patient who... He was talking about me, in a kinder, gentler, inspirational manner...

Andi
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Andi BB
'95 post-meno dx Invasive LOBULAR w/9cm tumor! YIKES + 2/21 nodes. Clear mammo 10 mnths earlier. Mastec/tram flap reconst/PORT/8 mnths chemo (4Adria/8CMF). Borderline ER/PR. Tamoxifen 2 yrs. Felt BLESSED. I could walk and talk, feed and bathe myself! I KNEW I would survive...

'98 -- multiple mets to liver. HER2+ 80%. ER/PR- Raging, highly aggressive tumors spreading fast. New PORT. 9 mnths Taxotere Fought fire w/fire! Pronounced in cautious remission 5/99. Taxotere weekly for 6 wks, 2 wks off -- for 9 mnths. TALK ABOUT GRUELING! (I believe they've altered that protocol since those days -- sure hope so!!)
+ good old Vit H wkly for 1st 3 yrs, then triple dosage ev 3 wks for 7 yrs more... The "easy" chemo, right?! Not a walk in the park, but not a freight train coming at 'ya either...

Added Herceptin Nov '98 (6 wks after FDA fast-tracked it for met bc). Stayed w/Vit H till July '08! Now I AM FREE! Humbly and eternally grateful for this life-saving drug! NED since '99 and planning on keeping it that way. To hell w/poor prognosis and nasty stats! STOPPED VIT H JULY '08...! REMAIN STABLE... Eternally grateful...Yes is a world & in this world of yes live (skillfully curled) all worlds ... (e e cummings) EVERY DAY I BEAT MY PREVIOUS RECORD FOR # OF CONSECUTIVE DAYS I'VE STAYED ALIVE. Smile KNOWING you too can be a miracle. Up to me and God now...
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Old 09-15-2013, 12:23 PM   #19
roz123
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Re: Let me be your voice

in regards to the dense breast issue we are all so passionate about (I also had very dense breasts) I always tell women to ask for and get a copy of each years mammo reports. My doctors dismissed me when I asked her if I had dense breasts - she dismissed me and told me I was fine (whatever that was supposed to mean) the radiologist report clearly gave the same disclaimer as everyone else seemed to have. Knowing my hypochondriac self I would have asked for an ultrasound had I read my report

YOUNG WOMEN - there is still a pubic misperception that this is a disease of older women. I was 42 (so not really considered all that young) but I did recently meet a 25 yr old and know several mid 30 year olds who also had BC - doctors are so ready to dismiss us younger patients because even they are unaware

great opportunity and good luck
keep us posted
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right breast IDC 2.2 cm LVI
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surgery -pCR 0/2 nodes
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Old 09-15-2013, 12:27 PM   #20
NEDenise
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Re: Let me be your voice

Leah!
You go girl!
I have every confidence in your ability to do us all proud!
Denise
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