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Old 06-02-2008, 05:59 PM   #1
Alyce
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how do you know you are cancer free?

I usually forget to ask all my questions when I see my Onc. and here is one for all of you who have continued on for more than one year of herceptin. Is there a time when you can be tested to know that you are cancer free? I wonder if you just go for your mamograms and assume that you are cancer free if nothing shows up?
How does your Onc. determine the length of time for you to continue on with herceptin when it goes beyond the year?
Also- I met a woman at my radiation appt. who is being treated again after 22 years, and while she was on chemo this time they found another cancer in her breast. Very confusing to me. So does that mean that a brand new cancer came into existence, overcoming the current chemo?
It would be nice if there was a test to actually tell you that you are cancer free. I am kind of nervous thinking that even while we are taking Femora and herceptin we might still have active cancer cells.
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Old 06-02-2008, 07:17 PM   #2
Mary Jo
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Hi Alyce,

I guess the worst part of a cancer diagnosis are the points you bring up. The uncertainty of it all. The never really knowing what is going on inside our bodies. Of course there are always tests like CT's, PETS, MRI's, blood work etc. but these are not always accurate either.

So, yes, you are right.........it would be nice if there "was a test to tell us if we are cancer free" but that isn't anything we have. So, all we can do is follow up with our oncs., stay on top of symptoms that don't go away and live our lives to the fullest each day AND to always remember that to be a survivor we need to live with confidence and the assurance that none of us know what tomorrow will bring. None of us. Whether having had cancer or not.

Thank God for this day called "today."

Hugs to you...

Mary Jo
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"Be still and know that I am God." Psalm 46:10

Dx. 6/24/05 age 45 Right Breast IDC
ER/PR. Neg., - Her2+++
RB Mast. - 7/28/05 - 4 cm. tumor
Margins clear - 1 microscopic cell 1 sent. node
No Vasucular Invasion
4 DD A/C - 4 DD Taxol & Herceptin
1 full year of Herceptin received every 3 weeks
28 rads
prophylactic Mast. 3/2/06

17 Years NED

<>< Romans 8:28
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Old 06-03-2008, 08:52 AM   #3
atdec05
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Thanks, Mary Jo, for those inspiring words. Something I try to follow but it isn't always easy.

As to a concrete monitoring test, there is promising research to be able to detect small amounts of circulating blood tumors. Of course, nothing currently available.

- Anna
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- Anna

Stage I - DX 9/2005
ER/PR-, HER2+, grade 3, DCIS, IDC multi-focal (1.05cm)
DD 4 A/C finished Jan 31, 2006
Herceptin weekly finished Jan 31, 2007
recurrence to chest wall on last month of Herceptin
Stage 3B - 3/15/07 - 2 carcinomas in dermal lymphatic
Rads finished 6/5/07
12x TH finished 9/10/07
12/07 - Clear scan!
3/08 - 4 month Melatonin trial
1/09 - osteoperosis -
start Alendronate
2/09 - 4-month Simivastin trial
3/13 - take drug holiday after 5 years of Alendronate
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Old 06-03-2008, 02:43 PM   #4
TSund
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There was that encouraging bit on PH differentiation (via baking soda!) but that's a ways out yet
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Terri, spouse of Ruth, Dallas/Ft. Worth area
Ruth dx 05/01/07 (age 50) Filipino
multifocal, several tumors .5 -2.5 cm, large area
Breast MRI showed 2 enlarged nodes, not palpable
100%ER+, 95%PR+, HER2+++
6x pre-surgery TCH chemo finished 9/15/7 Dramatic tumor shrinkage
1 year Herceptin till 6/08
MRM 10/11/07, SNB: 0/4 nodes + Path: tumors reduced to only a few "scattered cells"
now 50% ER+, PR- ???
Rads finished 1/16/08
Added Tamoxifen,
Finished Herceptin 05/08
NOW is the time to appreciate life to the fullest.
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Old 06-03-2008, 04:27 PM   #5
DanaRT
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Mary Jo,

you write, "live our lives to the fullest each day AND to always remember that to be a survivor we need to live with confidence and the assurance that none of us know what tomorrow will bring. None of us. Whether having had cancer or not."

I needed to "hear" this.

Dana
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-Dana-

]
Diagnosed - Nov. 2, 2007 at 45
Lumpectomy - Nov. 13, 2007
Tumor 1.2 cm
Stage 1 Grade 3
ER/PR - Her2 +++ (3.8)
Taxotere/Carboplatin/Herceptin- 6 rounds
Neulasta
Radiation 33 treatments - will be done 6/6/08
Herceptin through 12/08
12/07 MUGA 61%, 4/08 MUGA 60%, 7/08 MUGA 64%
three wonderful daughters, a terrific husband,
Life is Good
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Old 06-03-2008, 04:50 PM   #6
hutchibk
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I needed to read that too!

And I suppose that no-one really knows if they are cancer free - even those who don't yet know that they have it...
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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."
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Old 06-03-2008, 08:09 PM   #7
CindyE
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Yes this is a great thread to read. No one knows for sure. We can only get the treatments and trust God to handle the rest...
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Cindy

L/IDC, 1.2 cm, Stage 1, Her2+, ER+/PR+ at age 48
4/15/2008 Lumpectomy + sentinel node biopsy
Margins neg and Nodes neg (2 tested)
MUGA score 55 on 5/6/2008

Treatment starting 05/08/2008:
Chemo 4 cycles, 3 weeks apart with Taxotere & Cytoxan - Chemo - Done 7/24/2008!
Herceptin for 1 year
Radiation starting in 9/2008
MUGA score 61.9 on 9/04/2008
33 Rads with boost - Done 10/13/2008
MUGA score 58 on 12/01/2008
MUGA score 59 on 3/16/2009
Herceptin for 1 year - Done 4/27/2009
MUGA score 64 on 6/22/2009
All scans - NED 6/24/2009
MRI - NED 11/10/2009
All scans - Still NED 8/25/2011
Still NED 2017!



I am calling this my pink journey
Follow my journey into the pink at my blog here

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Old 06-03-2008, 08:10 PM   #8
Soccermom
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Today is a Gift thats why its called, "the Present"!
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Old 06-03-2008, 09:19 PM   #9
LAURIE
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I am actually thinking that I have post traumatic symptoms from all of this. I cannot go 15 minutes about fearing about reoccurance. (this is even happening during my extermely busy workday)The nasty lymphedema I have is also just a constant reminder. I started taking xanaz to hep me calm down. I am seriously thinking about talking to a psychiatrist about it. Though I don't want to take drugs they are the things that are helping my thoughts get manageable. I would of thought being 6 months out treatment I would not of been so scared. I am going to be this scared until I am 2-? years out? I also feel nauseous and very dizzy when I am in a building with a very a high ceiling, or overly crowded room, with lots of people. Before I could handle anything. what has happened to my psyche? STRESS I guess (post traumatic and current)
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Laurie
Diagonsed 8/10/06 (found own lump)at 35
Her 2 +++, er-/pr-
4 A/C 8-29-06 to 11-06
Lumpectomy, node dissection- 11/30/06
Pathology report stage IIIC
1 tumor 3 cm
10 of 15 nodes +
12 Taxol 12/18/06-03/06/07
Herceptin 12/18/06- 12/11/2007 done!!! yeah!!!
33 rads started 3/22/07, done!! yeah!! 5/07/07
Lymphedema diagonsed 2/1/07
BRCA1/BRCA2 negative
port out 1/10/08
pregnant after 6 yeas of trying- due mid feb.
Ryder David Kessel Hunter born feb.6th 2009

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Old 06-03-2008, 11:28 PM   #10
hutchibk
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The trauma of cancer dx and treatment can really wreak havoc on your nervous system. Your "sympathetic" nervous system can easily get stuck in the 'fight-flight-freeze' mode and your "para-sympathetic" isn't able to kick in and play it's role of 'rest and digest'... and it can cause a degree of underlying depression that results in a "tape loop" playing over and over in your head. I learned this recently from my counselor. If you haven't considered going to a counselor, I highly recommend it from my experience. And maybe do some reading up on Somatic Experience as a possible way to activate your 'para-sympathetic' nervous system. In my humble opinion, anti-deps and anti-anxiety meds are a god-send to cancer patients, as long as you find a psychiatrist who is a skilled artist at finding the right one for you at the right dose.
__________________
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."
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Old 06-04-2008, 06:42 AM   #11
Sheila
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Alyce
Unfortunately this is life...none of us has a guarantee against any disease....you begin by taking and savoring every day....you must always be vigilent, but not to the extent that you do not enjoy the life you have....no of us know....its like before diagnosis...yes there is always a chance, but I do not focus on the negative...there is too much positive influence around to focus on!!!
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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 06-04-2008, 06:58 AM   #12
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Same boat

I think there's something about having the technicians get bug-eyed and say, "Holy Crap" when they put your first ever mammogram on screen (the first one was "diagnostic") and they mammogramed your shoulder because there was nothing on the breast mammogram...they're shocked by the image of cancered lymph nodes that are fixed and matted to your chest wall that looks like a big bird hocked up a well-chewed rat...that creates a bizarre sense of unreality that follows you your entire life.

Then, when you have a biopsy, the surgeon comes in and says, "I've never seen anything like this. I've called all over the country."

We just cannot forget "Holy Crap."

Yup.

I get it.

Tammy Lou...diagnosed January 2005
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Old 06-04-2008, 01:50 PM   #13
CLTann
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Although the question is asked by all of us, yet there is no potential test method that can detect the micro cancer cells. All people have cancer cells in their bodies and we rely on the healthy cells to destroy them. Therefore, even if there is a sure way of testing, all of us will get a positive report. The circulating cancer cell is a test being actively studied, but I don't think it will be quickly adopted.
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Ann

Stage 1 dx Sept 05
ER/PR positive HER2 +++ Grade 3
Invasive carcinoma 1 cm, no node involvement
Mastec Sept 05
Annual scans all negative, Oct 06
Postmenopause. Arimidex only since Sept 06, bone or muscle ache after 3 month
Off Arimidex, change to Femara 1/12-07, ache stopped
Sept 07 all tests negative, pass 2 year mark
Feb 08 continue doing well.
Sep 09 four year NED still on Femara.
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Old 06-04-2008, 02:47 PM   #14
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Alyce,
I know exactly what you are talking about; ever since completing my chemo in January, I can't stop thinking about it coming back. Every cough, every bone ache, every twinge in my breast makes my head go directly to the bad place. Since my doc doesn't do scans unless there are symptoms, I haven't had any. I don't know when this will stop, but it's terrible...can't sleep most nights worrying. I am going on with my life...working, planning a wedding, exercising...but it's always there. Can someone explain to me when it will feel better????
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dx 07/20/07 with IDC
left MRM with expander 08/07
2.2 cm er/pr-, her2+ all nodes clear
2/08 BRCA negative
4 AC dose dense 09/06/07-10/18/07
12 weekly Taxol/Herceptin 11/01/07-01/18/08
Herceptin 1 year/done 10/31/08!
2/08 reconstuction
port out 12/4/08
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Old 06-04-2008, 03:53 PM   #15
DanaRT
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Alyce,

I asked a 3-year survivor I met a few months ago this exact question. She did say over time it gets better. I sleep well at night thanks to Ambien. It's the mid-day nap that I wake in a panic, I nearly cannot breath. Hoping the tiredness will go away once rads are complete---I need to quit napping!
Where in Ohio are you from? Your onc practices the same protocol as mine in Fort Wayne...no scans unless there are symptoms.

Take Care,
Dana
__________________
-Dana-

]
Diagnosed - Nov. 2, 2007 at 45
Lumpectomy - Nov. 13, 2007
Tumor 1.2 cm
Stage 1 Grade 3
ER/PR - Her2 +++ (3.8)
Taxotere/Carboplatin/Herceptin- 6 rounds
Neulasta
Radiation 33 treatments - will be done 6/6/08
Herceptin through 12/08
12/07 MUGA 61%, 4/08 MUGA 60%, 7/08 MUGA 64%
three wonderful daughters, a terrific husband,
Life is Good
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Old 06-04-2008, 05:09 PM   #16
Mary Jo
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One more thing........

After reading Laurie's post I have one more thing to say.................

to Laurie and anyone else feeling like her........Laurie you first had your port removed 1/08 - it is now 5/08. Not very long at all "away" from treatment. I SOOOO remember being 6 months past treatment. I was a WRECK. Like you, I constantly thought of recurrence and EVERYTHING scared me to death. I thought everything was cancer.

The reason for my post was to reassure you that it does get better. It does!!!!! I am approaching my 3 year "cancerversary" (July) and just recently - I'd say, the last 6 months to a year (I don't even think a year) is when I really started feeling "better." I think it's when I really started putting things in a little better perspective and trying to TELL myself how unsure life is for anyone and really started believing it.

It is a hard process. It is! But, you will get through it and you will start trusting your body a little bit more. Eventually you will be able to put some of this behind you. Does it ever go away for good? Of course you know the answer is a solid no but I think it starts getting easier and life starts feeling alittle more normal as time goes on.

Just give yourself time. And most definitely get some help dealing with these new found emotions if you need it.

Love to you Laurie and to the rest of you...

Mary Jo
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"Be still and know that I am God." Psalm 46:10

Dx. 6/24/05 age 45 Right Breast IDC
ER/PR. Neg., - Her2+++
RB Mast. - 7/28/05 - 4 cm. tumor
Margins clear - 1 microscopic cell 1 sent. node
No Vasucular Invasion
4 DD A/C - 4 DD Taxol & Herceptin
1 full year of Herceptin received every 3 weeks
28 rads
prophylactic Mast. 3/2/06

17 Years NED

<>< Romans 8:28
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Old 06-05-2008, 08:59 AM   #17
Jackie07
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Having breast cancer means that we are more likely (compared to other people who have never had cancer) to have another kind of cancer, according to one of my neurosurgeons.

So, the question is not "will it happen" or "when will it happen again". The question is "Do we accept us as who we are?" We are cancer survivors. The fear is real. But we continue to live life to the fullest, so our effort for survival will be our mark left on this earth when we are gone.
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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
Erythema Nodosum 85
Life-long Central Neurocytoma 4x5x6.5 cm 23 hrs 62090 semi-coma 10 d PT OT ST 30 d
3 Infertility tmts 99 > 3 u. fibroids > Pills
CN 3 GKRS 52301
IDC 1.2 cm Her2 +++ ER 5% R. Lmptmy SLNB+1 71703 6 FEC 33 R Tamoxifen
Recc IIB 2.5 cm Bi-L Mast 61407 2/9 nds PET
6 TCH Cellulitis - Lymphedema - compression sleeve & glove
H w x 4 MUGA 51 D, J 49 M
Diastasis recti
Tamoxifen B. scan
Irrtbl bowel 1'09
Colonoscopy 313
BRCA1 V1247I
hptc hemangioma
Vertigo
GI - > yogurt
hysterectomy/oophorectomy 011410
Exemestane 25 mg tab 102912 ~ 101016 stopped due to r. hip/l.thigh pain after long walk
DEXA 1/13
1-2016 lesions in liver largest 9mm & 1.3 cm onco. says not cancer.
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.
"I WANT TO BE AN OUTRAGEOUS OLD WOMAN WHO NEVER GETS CALLED AN OLD LADY. I WANT TO GET SHARP EDGED & EARTH COLORED, TILL I FADE AWAY FROM PURE JOY." Irene from Tampa

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Old 06-05-2008, 06:26 PM   #18
Becky
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Posts: 4,179
The first year out is a difficult time. Treat your with care and ensure that everyone else who loves you pampers you too. Besides the fact that it is one year or less since your whole life changed, you are also not even looking like you. Your hair is extremely short, probably not the same texture or color you are used to. Maybe you were lucky to have lost some weight but unfortunately, you probably gained (which I think is really unfair). You wonder if you will see your children or grandchildren grow up. And I will say what I have said here before, LIFE IS GREAT but not everyday is good. You will be here. My daughter just graduated college 2 weeks ago and she was just packing up to go when I was diagnosed. And I saw her graduate. And next year my youngest daughter will graduate high school and she was just going into 8th grade (that will be a traumatic and tearful one for me).

It is hard to get past treatment quickly because you aren't yourself in many ways - physically, emotionally, spiritually. It's not even a "Why me" thing - its just so much is different and it will never be the same. But that does not mean it won't ever be good, great, better than before because it will. It will be a new normal and it will be more relaxed than you can imagine! Boss screams at you, child breaks curfew, broke another "good china" dish - none of these things are the worst thing that ever happened to you - no way. Relish that one. Find great places to go and survive in - restaurants, parks, malls, islands (whatever your pleasure). It takes some getting used to to learn how to really live but you will have the rest of your life to get used to your new normal. Have fun at it.
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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 06-05-2008, 06:28 PM   #19
CLTann
Senior Member
 
Join Date: Oct 2005
Posts: 476
Earlier, I was looking for an article showing the recurrence rate versus time. I just ran across the following article having the data to show the high recurrence rate at about one year after first diagnosis. Please read the following:
http://breast-cancer-research.com/content/9/3/208
The authors use the term dormancy to characterize the delay of recurrence.
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Ann

Stage 1 dx Sept 05
ER/PR positive HER2 +++ Grade 3
Invasive carcinoma 1 cm, no node involvement
Mastec Sept 05
Annual scans all negative, Oct 06
Postmenopause. Arimidex only since Sept 06, bone or muscle ache after 3 month
Off Arimidex, change to Femara 1/12-07, ache stopped
Sept 07 all tests negative, pass 2 year mark
Feb 08 continue doing well.
Sep 09 four year NED still on Femara.
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Old 06-06-2008, 03:15 PM   #20
goops
Senior Member
 
Join Date: Jan 2008
Posts: 305
In the not to distant future - it appears that there may be a blood test that could be used to diagnose and to monitor cancer patients.

http://www.cbsnews.com/stories/2007/...n3633108.shtml
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May 2007 - Stage 3A, 12 positive nodes, her2 positive
July 2008 - Stage 4 - Liver Mets

Help my city grow:

http://goopsville.myminicity.com/ind/
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