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Old 05-30-2008, 09:43 AM   #1
lizm100
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Angry Insensitive comments people say!

I'm sorry but I need to vent to someone who will understand. Wednesday night I was at a school function for my 11 year old and ran into an old collleague of mine. Now this colleague is a professional who I worked with in a hospital for a decade. She asked me if there's anything new and asked how I'm doing in general. She did not know the fact that I was diagnosed with BC in January and skin cancer in April so I told her what has been going on in my life.

After I told her my story, her eyes opened wide as she told me of another colleague of hers who just died of BC a few days ago. She said "Sara was in remission for 15 years..doing great and the BC came back with a vengence and she went down quick, I just went to her funeral yesterday". I felt sick to my stomach after this story, didn't enjoy the school function, couldn't sleep, still feel anxious and so on..... This story did not benefit me at all since I didn't know Sara because she started working at the hospital after I left.

Maybe I'm overly sensitive because I just finished radiation a week ago and still feel very unsettled about BC. I know with time it will get easier but shouldn't a professional person who works in a hospital know better than to say this to me?

I have had numerous other insensitive comments made and learned that people need to pay attention to what their saying or just not say anything if their not sure of what to say.

Thank you to those who read this....I just needed to vent.... Please feel free to share any of your stories, I would love to read them.

Liz
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Old 05-30-2008, 10:07 AM   #2
Leslie's sister
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I don't get it

Liz:

I just don't get people sometimes. And from a professional that works in a hospital.....

Something similar happened to my sister right after diagnosis. I was having a party at my house and my sister, myself and a friend were sitting at a table making small talk. Finally the friend decided that it was time to talk about my sister's recent diagnosis & started asking questions. My sister was fine with it and then out of the blue the friend starts talking about someone else she knows whose cancer came back, wasn't doing well and was probably going to die soon. My sister handled it very well. She just got up and walked away from the table. The friend had a puzzled look on her face, like hey what was that all about. Duh!

Lisa
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Leslie's Sister (Lisa)
Diagnosed 5/17/06
Left breast Stage II
5 cm. Her2Neu+++, ER-, PR-
1 positive node out of six,
double mastectomy 6/9/06;
TCH started 7/12/06
last chemo 10/25/06
herceptin ended 6-11-07
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Old 05-30-2008, 10:28 AM   #3
dlaxague
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people are just scared

Yeah, there are some doozy (doozie?) comments made. And there is silence, or turning away and avoiding eye contact. A rare few happen to hit it right, at the right time - and sometimes that's just luck, catching us in the right mood.

There is such fear around cancer. And there's such fear about saying THE WRONG THING. None of that is about us, or really, about them. It's about fear, and we should try not to take these comments personally.

I admire the person who tries to say something, no matter how it comes out. I give everyone credit for trying, and my take-away message from whatever awkward comment is made is that they cared enough about me to make the effort, despite their fear and awkwardness. Like in the song - "what they're really saying is ... I ... love ... you".

I think that one reason I was/am able to interpret interactions this way is that during most of treatment, I had an online community of breast cancer survivors and their loved ones who did understand, when I needed to vent.

Plus there was not a moment that I was unaware that people die from breast cancer, and that I could die. I cannot say that comments that re-state that fact bother me at all. Actually (thinking about it now), I probably appreciate that kind of comment more, because it acknowledges the seriousness of the situation. As opposed to dismissing it, as do the "rah, rah, you'll do fine, don't worry, positive attitude" kind of comments - which are far in the majority. But that's just me. And again, I quickly learned to focus not on exactly what they say but on the caring behind the comment.

I hope that venting has now helped you, too, Liz.

Debbie Laxague
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3/01 ~ Age 49, occult primary announced by large axillary node found by my husband. Multiple CBE's, mammogram, U/S could not find anything in the breast. Axillary node biopsy - pathology said + for "mets above diaphragm, probably breast".
4/01 ~ Bilateral mastectomies (LMRM, R 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 B-31's adjuvant Herceptin trial (no Herceptin): A/C x 4 and Taxol x 4 q3weeks, then rads. Arimidex for two years, stopped after second patholgy opinion.
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Old 05-30-2008, 10:28 AM   #4
Colleens_Husband
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Liz:

I am sorry you had to deal with such a ninny. Some people hear one thing and then the random synapsal firings of the brains connect things together and those thoughts just begin pouring out of their mouths without first checking in at the "should I be saying this" processing center. And other people are just dumb-asses.

Being a person of the male persuasion, sometimes I let fly without thinking, especially around my wife. She just gives me the "I don't want to even think about cancer, especially now, possibly never. If you want to talk about the 'C' word, go outside and talk to the cat." look. Thats fair enough. However, if someone other than the immediate family tries to talk about my wife about some Terms of Endearment thing, I feel it is my duty as a male person to be the jerk and say something like, "Are you sure this is the kind of thing you want to be saying to someone who is in a fight for survival"?

Mind you, it hasn't actually worked. They give me the stink eye and finish their story but at least I tried. What can you say? Some people are dunderheads.

Lee
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This happened to Colleen:

Diagnosed in September 2007
ER-/PR-/HER2 Neu+++ 2.1 cm x .9 cm spicluted tumor with three fingers, Stage 2B
Sentinal node biopsy and lymph node removal with 3/18 positive in October 2007
4 TAC infusions
lumpectomy March 2008, bad margins
Re-excision on June 3rd, 2008 with clean margins
Fitted for compression sleeve July 16, 2008
Started the first of two TCH infusions August 14, 2008
Done with chemo and now a member of the blue dot club 9/17/08
Starting radiation October 1, 2008
life is still on hold
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Old 05-30-2008, 10:41 AM   #5
NanaKaren
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I had a similar situation happen to me that left me rattled. I too, work in a hospital and a co-worker is in the middle of her treatment. I ran into her one day and asked how she was doing. She explained that she was doing OK, but that her mother had just died of breast cancer. But that her mother was Her2 and she was SO glad she wasn't. I told her I was Her2 and of course she couldn't apologize enough. It still left me shaken and upset the rest of the day. It is such a great comfort to come to this site and feel like you are not alone. As always, all my love..Nana Karen
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Old 05-30-2008, 10:46 AM   #6
lilyecuadorian
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Thumbs down

stupid old colleague !!!
__________________
Lily
Diag April/06 5 months after give birth my son Max
stage IV mets on liver (5 tumors) 38 year old,
her2+++ and ER+PR+ from32 nodes 4 positives
mastectomy right breast chemo before surgery herceptin/carboplatin/taxotere ,clear and surgery have radiation 20, `& then herceptin and tamoxifen
NED until Aug/07 body only then 'n June 04-06-07 .1 lesion of 1.6 cm on cerebellum ...novalis ,open sugery
5m.m brain met again novalis, 4mm.In the liver. Waiting 2 months now 3 tumors enroll on T-MCC trial start first infusion Nov 5/07 at Dec 17 scan show one tumor despair the 2nd and 3th diminish Doc said great results until March/08 ct scan show progression
03-05-08 start tykerb & xeloda
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Old 05-30-2008, 11:00 AM   #7
chrisy
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I stand by my earlier opinion..

That people are just ignorant and clueless! Now I can add scared, too. People don't know what to say. But they feel like they should say something and end up saying something COMPLETELY wrong.

I've had my share of people saying really stupid things - often they are really good friends who I know love me and are just trying to be kind.

My top 3 favorites:
(3) From a newly diagnosed acquaintance: "Well, I'm going to be very aggressive with my treatments because I don't want to end up like you" (with mets!)
(2) A really good friend sent me a beautiful flower arrangement upon hearing of my recurrence. The card with the flowers said "with sympathy"! That one made me laugh, and I had to tell him that usually the sympathy cards are for AFTER you're dead!

And still holding the #1 spot on the stupid things people say wall of shame....TA DAAAA..

"I was trying to put myself in your shoes and how I would feel. You know, I've always wanted to die first (before my husband), too!"

This last one was a very very dear friend and although I knew she was trying to speak out of love, I just hung up the phone and was shaking and crying as I told my hubby what she had just said! BTW, she and her husband (both still living!) are STILL very dear friends...

In fact, that last one I told to my business/personal networking group which is like my extended family. They were so upset when I told them my cancer had recurred, but then were also afraid THEY might say something stupid! So we made a deal: I told them that I knew they loved me, and if they ever unwittingly said something wrong, I would just say to them "I know you meant that out of love" and then we would laugh together.

People really are good, they're actually God's best things. But sometimes we're just dumb!
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Chris in Scotts Valley
June 2002 extensive hi grade DCIS (pre-cancer-stage 0, clean sentinal node) Mastectomy/implant - no chemo, rads. "cured?"
9/2004 Diag: Stage IV extensive liver mets (!) ER/PR- Her2+++
10/04-3/05 Weekly Taxol/Carboplatin/Herceptin , complete response!
04/05 - 4/07 Herception every 3 wks, Continue NED
04/07 - recurrence to liver - 2 spots, starting tykerb/avastin trial
06/07 8/07 10/07 Scans show stable, continue on Tykerb/Avastin
01/08 Progression in liver
02/08 Begin (TDM1) trial
08/08 NED! It's Working! Continue on TDM1
02/09 Continue NED
02/10 Continue NED. 5/10 9/10 Scans NED 10/10 Scans NED
12/10 Scans not clear....4/11 Scans suggest progression 6/11 progression confirmed in liver
07/11 - 11/11 Herceptin/Xeloda -not working:(
12/11 Begin MM302 Phase I trial - bust:(
03/12 3rd times the charm? AKT trial

5/12 Scan shows reduction! 7/12 More reduction!!!!
8/12 Whoops...progression...trying for Perjeta/Herceptin (plus some more nasty chemo!)
9/12 Start Perjeta/Herceptin, chemo on hold due to infection/wound in leg, added on cycle 2 &3
11/12 Poops! progression in liver, Stop Perjeta/Taxo/Herc
11/12 Navelbine/Herce[ptin - try for a 3 cycles, no go.
2/13 Gemzar/Carbo/Herceptin - no go.
3/13 TACE procedure
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Old 05-30-2008, 03:19 PM   #8
harrie
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I know exactly what you are saying. That use to drive me NUTS! There were a fair number of people that would immediately tell me of someone they knew that died of cancer. I would get SO irritated, but I suppose it was just their way of relating. They did not have a clue.
How much nicer it would be to hear of someone they knew that survived...and for a really long time!! But I guess they don't make as much of an impact on people as the ones that died. Who the h- knows...
__________________
*** 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 05-30-2008, 04:05 PM   #9
kcherub
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Funny...it seems that people loooove to tell me about their mother, sister, aunt, grandmother, friend, second cousin twice removed who died of BC. Every time someone gives me that "look" and tells me something like this, I grind my teeth and think "WTF?" I actually have a blog where I talk about what NOT to ask me after my BC.

Then, I realize--they want to say something. They want me to feel/know that they have been touched by BC, although in a totally un-PC way.

Having been a part of the PG. loss community for many years, people say things like this in all sorts of uncomfortable/scary situations. It's not fair, but I like to think that they aren't trying to scare me, or seem uncaring. It just comes out totally wrong. Who knows if I have said anything inappropriate over the years before PG. loss and BC? I shudder to think...

That being said, I understand how your feelings were hurt and you were offended. Just take in stride, and know that you would NEVER make the same mistake. Especially now.

Take care,
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Krista
Diagnosed 3/29/2007 @ age 34
Stage 1, Node Neg. (SNB), Grade 2, 1.4 cm. IDC
ER/PR 90%+ HER2 +
6 TCH started 5/25/2007, ended after #5 due to steroid "reactions" and neuropathy in feet and hands
BUT--#6 CH w/o Taxotere
Begin Herceptin alone 9/28/2007
30 rads completed 12/19/2007
Finish Herceptin 5/9/2008
Stopped Tamoxifen early--HATED it.
Married 17 years
13-year old son
3 embies on ice (from 1999)
GA, USA

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Old 05-30-2008, 04:11 PM   #10
Sherryg683
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I get offended when someone acts like it's no big deal. I've had so many people say "Oh', you're lucky it isn't anything more serious they have so many cures for breast cancer now".. I always feel I have to say.."well, I'm stage IV and there is no cure". I always hear the stories about the aunt, mother that has been living 30 years with BC. That's nice to hear and I"m glad, but we're not in the same boat. Oh yea, my sister in law does the annual cancer candle light walk thing they have here...she emailed me a picture of my candle burning in the bag, it said in big letters "IN MEMORY OF SHERRY GAUTREAU"...lol...Hell last time I looked I was still kicking and kicking better than her...lol...sherryg683
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Sherry

Diagnosed: December , 2005 at age 44
13+ positive lymph nodes
Stage IV , Her2+, 2 small mets to lungsChemo Started: Jan, 2006
4 months Taxotere, Xeloda, Hercepin
NED since April 2006!!
36 Rads to follow with weekly Herceptin indefinately
8 years NED now
Scans every year

Life is not about avoiding the thunderstorms, it's about learning to dance in the rain!
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Old 05-30-2008, 04:19 PM   #11
harrie
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High 5 Girls!!
__________________
*** 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 05-30-2008, 04:22 PM   #12
Sheila
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OH but I have one to even top this stupidity
Last week, I received a phone call from a former co worker....she was so glad when I answered the phone...OK, I haven't talked to her in a couple months, but gee....then she said...I had to call you because I got a call from someone today who said you had passed away. I was shocked...so I said, well why are you calling then...she of course said she knows me well enough to know that I would probably find the humor in this situation...we talked for an hour, and ended with...if I was going to die, I'd surely let you know friend!m Later that night, I got another call from a girlfriend I had worked with (all within the same construction company)...she calls occasionally, we do lunch when she is in the area...she started the phone call off with idle chit chat....I had to stop and ask her if she was calling to see if I was still alive. She was silent....but then admitted she had heard the same rumor, and called to verify it....at that point I was upset, mad, hurt....what would make someone do that? Then after talking, we figured someone had heard about another man who works with my husband whose wfe died last week from cancer....a simple mistake of mistaken identity? I hope so...but as an added bonus to my pain and suffering, I asked her to please announce to her coworkers that in lieu of flowers, I would prefer cash donations that I could send to my favorite charity...I am still awaiting the funds!
__________________
"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 05-30-2008, 04:23 PM   #13
Barbara H.
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comments

I know how bad off I am, but still feel fortunate to be here. For some reason, these kinds of comments do not bother me. Nevertheless, I can understand why others are very offended. I am much more upset when people tip toe around me and are afraid to inform me of such issues because they are afraid it will make me upset.

I guess I compare it to this website. I am very upset when a member here is having a difficult time, but I would feel worse if we were protected from knowing what is going on.

I hope that makes sense.

Best wishes,
Barbara H.
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Old 05-30-2008, 04:26 PM   #14
Sherryg683
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Shelia, I like that cash donation thing....sounds like a good idea to me...lol..sherryg683
__________________
Sherry

Diagnosed: December , 2005 at age 44
13+ positive lymph nodes
Stage IV , Her2+, 2 small mets to lungsChemo Started: Jan, 2006
4 months Taxotere, Xeloda, Hercepin
NED since April 2006!!
36 Rads to follow with weekly Herceptin indefinately
8 years NED now
Scans every year

Life is not about avoiding the thunderstorms, it's about learning to dance in the rain!
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Old 05-30-2008, 04:27 PM   #15
Sheila
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Sherry...I could see expensive shoes in my future!!!!!
__________________
"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 05-30-2008, 05:20 PM   #16
lilyecuadorian
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well I forgot to said that every time someone said something stupid ....I go and said "Oh do you have your mammogram yet ???, the rate of breast cancer is too high?, doesn't matter what age you are ??? my suggestion is for you to go and get a mammogram? .....that way I felt like it I pass the "worried ball" to them ....

....
__________________
Lily
Diag April/06 5 months after give birth my son Max
stage IV mets on liver (5 tumors) 38 year old,
her2+++ and ER+PR+ from32 nodes 4 positives
mastectomy right breast chemo before surgery herceptin/carboplatin/taxotere ,clear and surgery have radiation 20, `& then herceptin and tamoxifen
NED until Aug/07 body only then 'n June 04-06-07 .1 lesion of 1.6 cm on cerebellum ...novalis ,open sugery
5m.m brain met again novalis, 4mm.In the liver. Waiting 2 months now 3 tumors enroll on T-MCC trial start first infusion Nov 5/07 at Dec 17 scan show one tumor despair the 2nd and 3th diminish Doc said great results until March/08 ct scan show progression
03-05-08 start tykerb & xeloda
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Old 05-30-2008, 06:20 PM   #17
Chelee
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Liz, I can certainly understand your need to vent. You would think a professional person that worked in a hospital would know better then that. I know some people are good at not letting these comments bother them but I know I'm not one of them.

Since being DX over two years ago I too have heard all the stories about someones friend or family member that had cancer and is now passed away. (Is that to cheer me up?) Why don't people use their heads before speaking. Long before I was ever DX with cancer I was very careful to choose my words when someone told me they had cancer...so I'm sorry but I just don't understand half of what comes out of these people's mouths?

Just recently my step-daughter that lives up North from me calls and says, "Guess what, I'm coming down in June to see you so whatever you do DON'T die before I get there". (Its NOT that far away till "June", I'm pretty sure I can hang in there till then. ) In all seriousness it really did upset me. I couldn't believe she said that to me.

Then since my mother passed away last August my brother & I have been at odds over her estate. So I'm on the phone with my Aunt telling her how my own brother thinks he's entitled to everything and I'm to get nothing although the will says "share & share alike". I was telling my Aunt how my Brother is all I have left out of my imediate family so I just want us to get along. I explained to her all the offers I made him where in the long run he comes out ahead. I was making sure he could keep the house but pay me some rent or something. After she hears all my offers to my brother she says, "Oh Chelee I can't believe he didn't take you up on any of those offers. After all you have cancer so he will eventually end up with everything anyway". Then she followed it up with even more remarks about me recurring and dying since I'm a stage III. She let me know my brother isn't very smart not taking me up on my offeres since basically I WON'T be here. (I swear...I'd had enough lately.) (Liz...seems your not the only one that needed to vent.) lol

Chelee
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DX: 12-20-05 - Stage IIIA, Her2/Neu, 3+++,Er & Pr weakly positive, 5 of 16 pos nodes.
Rt. MRM on 1-3-06 -- No Rads due to compromised lungs.
Chemo started 2-7-06 -- TCH - - Finished 6-12-06
Finished yr of wkly herceptin 3-19-07
3-15-07 Lt side prophylactic simple mastectomy. -- Ooph 4-05-07
9-21-09 PET/CT "Recurrence" to Rt. axllia, Rt. femur, ilium. Possible Sacrum & liver? Now stage IV.
9-28-09 Loading dose of Herceptin & started Zometa
9-29-09 Power Port Placement
10-24-09 Mass 6.4 x 4.7 cm on Rt. femur head.
11-19-09 RT. Femur surgery - Rod placed
12-7-09 Navelbine added to Herceptin/Zometa.
3-23-10 Ten days of rads to RT femur. Completed.
4-05-10 Quit Navelbine--Herceptin/Zometa alone.
5-4-10 Appt. with Dr. Slamon to see what is next? Waiting on FISH results from femur biopsy.
Results to FISH was unsuccessful--this happens less then 2% of the time.
7-7-10 Recurrence to RT axilla again. Back to UCLA for options.

Last edited by Chelee; 05-30-2008 at 06:23 PM.. Reason: Corrected spelling.
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Old 05-30-2008, 07:12 PM   #18
Becky
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Well, what a thread this is. My father (who has been gone over 17 years) used to remind me that "God didn't make everyone smart, Becky. Always remember that".

And not everyone is smart - maybe not rock dumb, but certainly not smart. Or they have the social skills of a 5 yr old (remember when you had a new boyfriend and your little cousin asks "Are you going to get married?")

Well, I finished chemo and radiation. As many of you know, I got Herceptin late because it wasn't available when I was on chemo. So, after I could get it, I go into my (then) boss and tell him that I am going to take Herceptin for a year and will leave work early every 3 weeks. I explain everything, the trial results and that it will be standard care for newly diagnosed - articles and that all is well but Herceptin will throw things in my favor that all stays well. And he says, "Are you going to die?"

Well my heart sank but for once in my life I was quick on my feet and told him, "Why of course and so are you. Everybody dies one day." And that was the end of that.

Like my dad said, not everybody is smart and we just have to get used to 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 05-30-2008, 07:57 PM   #19
Bill
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Good Lord, I don't have enough cyber-ink to comment individually to y'all, but I cringed with each post. One time Nicola and I were eating in a restaurant, and a woman approached our table, and said,"excuse me, but I noticed that you're wearing a scarf, and don't have any hair. Do you have cancer?" She meant well, and invited us to her church, but still it bothered us.
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Old 05-30-2008, 08:19 PM   #20
lizm100
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Posts: 141
Wow!

Wow what a response! Bill you took the words right out my mouth... so to speak. All of you are great...it's nice to have all of you here. I do feel better after venting and am glad to see that I'm not the only one this has happened to. There are those out there who don't fully understand breastcancer and how it changes your life forever and those who have good intentions but just don't know what to do or say...I'm sure it will happen many many many more times. Your stories made me laugh and cry at the same time, thank you for sharing them. Anyone else...please feel free to add your story too.

Hugs to all,
Liz
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