HonCode

Go Back   HER2 Support Group Forums > her2group
Register Gallery FAQ Members List Calendar Today's Posts

Reply
 
Thread Tools Display Modes
Old 08-10-2007, 04:23 PM   #1
KellyA
Senior Member
 
KellyA's Avatar
 
Join Date: Sep 2006
Location: Savannah, Georgia
Posts: 301
Is anyone ever afraid to make plans?

Is anyone ever afraid to make plans for the future, because your worried about recurrance? I seem to be having a lot of difficulty A). feeling motivated to do things and B). taking new risks because of the fear of cancer returning.

I work a very easy part-time job right now, and it has been nice. I have just been offered a chance at a new job that is full time and a little more demanding, but a wonderful find because it is at my children's school, is alot more money, and is just generally a big step up. Before cancer, I would have jumped on it in a second. Now all I can think about is, "would I be able to work this job if cancer came back? Will I feel the same bond that I felt with my current co-workers?" I know (because I have done it now) that I could work the current job if I needed more treatment. I feel "safe" in the current job. The new one seems very scary and I feel so insecure. I know that I have to go on, and live life to the fullest, but I am not that far out from dx, and still feel so unstable.

I notice that I feel this way really about so many things- just change in general, actually. Whether its about looking for a larger home (which we desperately need), making new friends, anything really. I've always been a creature of habit, but it's much worse now.

Is anyone else ever afraid to dream, make decisions, etc. because of what the future may hold?

Love, Kelly
__________________
dx'd 05/06, 37 years old
er/pr-, Her2+, grade 3
double mastectomy, immediate reconstruction- implants
Stage 2b, 2 tumors- 2.2 cm and 0.6 cm, 3/5 + nodes
all scans clear
genetic testing- negative
06/06 began dd A/C x 4, 12 weekly Taxols w/ Herceptin
30 rads
Herceptin weekly x 1 year
Herceptin completed 08/07
Port removed 12/26/07 MERRY CHRISTMAS!!!!!!
05/17/08 Two year anniversary NED

"We gain strength, courage, and confidence by each experience in which we really stop to look fear in the face... you must do the thing that you think you cannot do."

-Eleanor Roosevelt

KellyA is offline   Reply With Quote
Old 08-10-2007, 05:07 PM   #2
Grace
Guest
 
Posts: n/a
Yes, Kelly, I'm in the same situation. On Tuesday, we're buying a house ten hours away from New York City and I've been low for the last week about that change and also about finishing my herceptin treatment this week. I believe we've built up a sense of false security and are afraid of losing it. In the past I was always willing to follow my husband in any of his ideas and now I'm afraid to give up what I know even though it's not really what I want.

Nevertheless, we're going through with the purchase because I feel in my bones that it's the best thing for both of us. If you really think this job is right for you, I would suggest you take it. If you have a recurrence, you'll find the way, but don't stop doing what in your heart you know is best in the long run. And there is a long run.
  Reply With Quote
Old 08-10-2007, 05:27 PM   #3
Mary Anne in TX
Senior Member
 
Mary Anne in TX's Avatar
 
Join Date: Jun 2006
Location: San Antonio, TX
Posts: 2,357
Kelly, I bet we've all felt (feel) the same way! I live over 3 hours away from the treatment center and have labored over whether I should be closer. But changing anything it so hard. Moving a chair in the room is even hard. But I know that keeping on keeping on gives me the bestest life! It's just so hard to do.
I am finding that as I get into this 20th month and my mind is clearer (or at least I'm so far gone I think I'm clearer) and I have some distance from the surgery and chemo that it is easier to "think about" a "real life" again!
Probably having more energy and spending more time with my grandkids nudges me on. It's hard to stay stuck with little voices calling grandma and expecting to hear a "regular grandma" reply!
Good luck with your tiny to giant step process! You know that you are really wonderful and can do it! You decide! You did chemo...you can do anything! much love, ma
__________________
MA in TX.
Grateful for each and every day....

Diag. 12/05 at age 60
Stage II, Grade 3, 4.5 cm primary tumor
ER/PR- Her2 +3 strongly positive
Her2 by FISH 7.7 amplified
vascular invasion
Ki67 20% borderline
Jan - March '06 Taxotere/Adriamycin X 3 to try to shrink tumor - it grew
April '06 Rt Modified Radical Mas, 7 of 9 nodes positive
April - Aug. '06 Herceptin/Taxol/Carboplatin X 8 (dose dense)
Sept - Dec. '06 Navelbine/Herceptin x 8 (dose dense)
Radiation & Herceptin Jan. 22 - March 1, 2007
Finished Herceptin Dec. 10 '08! One extra year.
Port removed August, 2012.
8 1/2 years since diagnosis! 5 1/2 Years NED!
Mary Anne in TX is offline   Reply With Quote
Old 08-10-2007, 05:40 PM   #4
dberg
Senior Member
 
Join Date: Sep 2005
Posts: 52
Oh yes! I understand that feeling. I told my husband I was no longer contributing to my teacher retirement account until further notice! I was ready to spend my IRA for reconstruction too. Somehow, dear girl, you move on though. I am 3 years out from dx, hardly out of the woods, but feeling like I might be. I had a bone scan Friday and told my onc I really didn't WANT one because I didn't want to know if anything was there. Only people with bc would understand that. But today, I spent about 6 hours getting ready for my first grade classroom. You just have to move on and at some point you will feel like you can.
dberg is offline   Reply With Quote
Old 08-10-2007, 06:30 PM   #5
juanita
Senior Member
 
juanita's Avatar
 
Join Date: Dec 2005
Location: indianapolis, indiana
Posts: 1,544
About 6 months after I was diagnosed I totalled my car and had to get a new one. I felt so guilty having to because I was sure I was going to die and not ever get to drive it.
__________________
dxd 9-04, lumpectomy,
st 1, gr 3, er,pr-, her2 +,
2 tac,33 rads,6 cmf
1 yr herceptin,
juanita is offline   Reply With Quote
Old 08-10-2007, 06:38 PM   #6
Becky
Senior Member
 
Becky's Avatar
 
Join Date: Sep 2005
Location: Stockton, NJ
Posts: 4,179
Dear Kelly

I am just a few weeks away from my third cancerversary. The only thing I am afraid to move on from is my employer. I moved in February, 2006 (18 months out from dx) because I NEVER liked the house I was in and swore I wasn't going to die there. It was exhausting to move (I was still on Herceptin having been one of the lucky ones who could receive it "late"). My husband and I went on an alone vacation - the only one we've had since having our daughters and it was planned and paid for 7 months in advance.

My problem with my job is many fold. I got a new assignment which isn't really what I want to do. I could leave but there are many things to consider. These include that I get a pension at this company (many companies (including this company) do not give pensions to new employees - they might match more 401K $ but no pension), I have been there and get short and/or long term disability if I should recur (a new company would give you this after you have worked there a year - what if I leave and recur quickly?), and lastly, I have great benefits in which I do not need referrals and they've denied me nothing so far (I wouldn't leave without benefits that didn't cover pre-existing conditions). But I would much rather be in sales (I was a sales mgr - rather just be a rep) and now I am in marketing (ughhhh).

So, we all have our fears of change - I will probably not leave as in 6 years, I can retire (they have this age and years of service thing) and I will still be young enough to do my own thing.

You need to weigh the job's benefits to the chance of recurrence but the other perks of the new job. You are younger than me (by 10 yrs) so you don't have 23 yrs at the company you are currently at. However, you have decades to live and earn a living (and to buy that bigger new house you need NOW). So, start small - get the house. You and your family need a bigger house and will need it regardless of your situation. And its fun to get and redo your way (new paint and wallpaper - maybe furniture too). The job could come later except for the fact that this job is available now. But it is one job and there might be dozens that are also perfect for you too.

I didn't want to wait on everything because I figured that if I did, I really would die in my old house - of old age, frustration and boredom. Lots of people thought I was nuts (probably some on this board as I reported my massive packing project) but it was one change that has made the world of difference to me. Next stop, job hopping maybe.
__________________
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"
Becky is offline   Reply With Quote
Old 08-10-2007, 07:41 PM   #7
Sherryg683
Senior Member
 
Sherryg683's Avatar
 
Join Date: Feb 2006
Posts: 1,014
Yes, I go from feeling why the heck bothering to buy new clothes for myself, to going on a shopping frenzy to make myself feel better. I always tell my sister that she will have one heck of a wardrobe if I go. Lately, I've been into redecorating the rooms of my house, sort of like at least if I go, things will look good for awhile. As far as work, I've slowed down major on that. I am an artist and have a business on ebay that I devoloped and did very well with over the last 7 years..now Im lucky if I list an item a week. My priorities have changed major..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!
Sherryg683 is offline   Reply With Quote
Old 08-10-2007, 07:59 PM   #8
CLTann
Senior Member
 
Join Date: Oct 2005
Posts: 476
Once you are diagnosed with bc, the dark cloud is over you regardless what stage you are classified. I think all of us have this concern of making major decisions. Deep in our head, we know we must take the possibility of recurrence as a factor in making sound judgment. In your case, you have a near dream job that means a great deal for your career and income. I would consider the health insurance as one of the major factors in accepting or rejecting the offer. If the new job will pay for pre-existing conditions in future treatment, I would think you should accept it. Also keep in mind that the most likely period of recurrence for HER2 patients is 12 to 18 month after dx. This is another factor to consider. Wish you best of luck.
__________________
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.
CLTann is offline   Reply With Quote
Old 08-10-2007, 09:05 PM   #9
Angela
Senior Member
 
Join Date: Apr 2006
Location: North Carolina
Posts: 45
I know how you feel

My husband wants to take me on my dream vacation which is to go to New England in the fall. I have order information and looked up places to visit on the website but I can't bring myself to make any reservations. I am so afraid that I won't feel good and it will ruin our vacation. I am still on herceptin and some days are great and some days it is all I can do to get dressed and sit on the couch.
__________________
Hugs and Smiles,
Angela - NC

Dx May 2003 at age 39
Lt mastectomy, no nodes
DCIS, PR- ER- Her+++
4 rounds AC
Recurrence Dec 2006 Rt lung
2/07 - 3 Brain mets - Radiation
3/07 -
Carboplatin and Herceptin
8/07- mets stable. Finished Carboplatin-remain on Herceptin
12/07 - Herceptin only
5/08 - Lung mets grew - tykerb and Navilbene. Reaction to Tykerb -9/08 Herceptin again
12/08 - Lung mets growing - xeloda.
8/09 - Given Zometa for precaution
10/09 - Lung mets back plus new ones. - Put back on Xeloda.
1/10 – Began short-term disability

2/10 –Lung mets growing - Gemzar
9/2010 – Scan show tumors in lungs growing. Put on Ixempra (every 3 weeks). MRI of the brain showed a brain bleed but it had stopped bleeding.


Angela is offline   Reply With Quote
Old 08-11-2007, 04:46 AM   #10
sarah
Senior Member
 
Join Date: Sep 2005
Location: france
Posts: 1,648
I'm not afraid of near plans - adopted a dog (my husband would love and look after her so that's the only long term commitment I've made), changed houses, built a garden and building a pound and plan to plant fruit trees but.....I bought a CD series to learn Italian and soon after was diagnosed with my recurance. since then I haven't been able to start it. I feel as though, if I start it, something again will happen. In the meantime all my friends and m husband considered me "cured"!!! and of course I've put on 15 lbs in chemo so I do look very healthy!!!!
I think we're all afraid to tempt fate. It's the old saying "If you want to make God laugh, make plans." but that said make short term ones and believe.
stay strong and of course you know you are not alone
sarah
sarah is offline   Reply With Quote
Old 08-11-2007, 05:06 AM   #11
michka
Senior Member
 
michka's Avatar
 
Join Date: Feb 2007
Location: Paris, France
Posts: 858
Post

I am happy someone talked about this horrible feeling.
I feel the same. It is difficult to think of new plans. I have a very demanding job but it helped me survive chemo. I went in every time I could and it prevented me from going crazy. But is was so difficult!
Now, I would like to drop it and work less but who is going to hire a 50 year old women with a cancer? And anyway, I do not have the strength to go start something new. I need a job and I am stuck. I don't feel like seeing friends, going out, or even looking at television. It doesn't interest me. I feel destroyed. I am still suffering. In my body and in my head.
Maybe with time...
Micka
__________________
08.2006 3 cm IDC Stage 2-3, HER2 3+ ER+90% PR 20%
FEC, Taxol+ Herceptin, Mastectomy, Radiation, Herceptin 1 year followed by Tykerb 1 year,Aromasin /Faslodex

12.2010 Mets to liver,Herceptin+Tykerb
03.2011 Liver resection ER+70% PR-
04.2011 Herceptin+Navelbine+750mg Tykerb
06.2011 Liver ned, Met to sternum. Added Zometa 09.2011 Cyberknife for sternum
11.2011 Pet clear. Stop Navelbine, continuing on Hercpetin+Tykerb+Aromasin
02.2012 Mets to lungs, nodes, liver
04.2012 TDM1, Ned in 07.2012
04.2015 Stop TDM1/Kadcyla, still Ned, liver problems
04.2016 Liver mets. Back on Kadcyla
08.2016 Kadcyla stopped working. mets to liver lungs bones
09.2016 Biopsy to liver. no more HER2, still ER+
09.2016 CMF Afinitor/Aromasin/ Xgeva.Met to eye muscle Cyberknife
01.2017 Gemzar/Carboplatin/ Ibrance/Faslodex then Taxotere
02.2017 30 micro mets to brain breathing getting worse and worse
04.2017 Liquid biopsy/CTC indicates HER2 again. Start Herceptin with Halaven
06.2017 all tumors shrunk 60% . more micro mets to brain (1mm mets) no symptoms
michka is offline   Reply With Quote
Old 08-11-2007, 06:31 AM   #12
KellyA
Senior Member
 
KellyA's Avatar
 
Join Date: Sep 2006
Location: Savannah, Georgia
Posts: 301
I so appreciate everyone's responses and thoughts on this. It's funny, but I am still always so amazed at how deeply breast cancer affects one's life, even in situations that seem unrelated. I feel sometimes as if I have been robbed on the deepest level.

The job that I am thinking about would have no bearing on my insurance, or on pre-existing conditions, as we are very lucky to have a great policy with my hubby. It's funny because some of you mentioned "testing fate" and although I've never been a superstitious person, I find that I feel that way often. I worry that if I stop doing this, or don't do that, that "it" may come back. I worry that if I change this or do that, "it" may come back. Last year when things were going very well for us, prior to being dx'd, we broke down and splurged, and bought a nice car- 2 weeks later I got dx'd and was just sick about doing that. I walk around on a daily basis feeling like a ticking time bomb and to make things worse, feel like many people are looking at me the same way. It's so overwhelming at times that I just want to take the easy way out and sit home and wait it out. Sometimes I wish for the two or three year time frame to go by very quickly, so that I can feel a little more comfortable (never safe, of course). Then I remind myself that any time I have now my be my only time and not to wish it away.....

I was always a very structured, controlled person. Actually a would even say a go-getter (except for laundry and household chores :-) ), and now I don't even know who I am. I feel lazy, unambitious, and weak. For someone who has always had control issues ( I grew up and lived with an eating disorder for 20 years), I am the WORST person to handle something like this. It has definitely been a rediscovery of who I am and I've had to take a long look at myself, that's for sure. Some days I am so pissed off that I feel like I could take the world by storm. Other days I just want to crawl in a dark corner and hide. Some days I am so happy for what I have and so grateful to be alive, that's all that matters.

One things that I always know and that NEVER changes, is how grateful I am to have found this site and found all of you. Thank you.

Love, Kelly
__________________
dx'd 05/06, 37 years old
er/pr-, Her2+, grade 3
double mastectomy, immediate reconstruction- implants
Stage 2b, 2 tumors- 2.2 cm and 0.6 cm, 3/5 + nodes
all scans clear
genetic testing- negative
06/06 began dd A/C x 4, 12 weekly Taxols w/ Herceptin
30 rads
Herceptin weekly x 1 year
Herceptin completed 08/07
Port removed 12/26/07 MERRY CHRISTMAS!!!!!!
05/17/08 Two year anniversary NED

"We gain strength, courage, and confidence by each experience in which we really stop to look fear in the face... you must do the thing that you think you cannot do."

-Eleanor Roosevelt

KellyA is offline   Reply With Quote
Old 08-11-2007, 12:47 PM   #13
IRENE FROM TAMPA
Senior Member
 
IRENE FROM TAMPA's Avatar
 
Join Date: Oct 2005
Location: TAMPA, FL
Posts: 568
Smile This is how I feel

Kelly ....

I know how you are feeling about making future plans,,,,I felt the same way and must admit I still have thoughts of what if....

but let me tell you ladies - I have been fortunate enough to be here after 11 1/2 years and living with active cancer. I would think about Xmas and then tell myself, if I am still here. Then I would want to put up a new front door,,, then I would think, I won't be here to get that "little project done" well I installed the door about 7 years ago,paint the house, well that was 10 years ago, plan a trip... took them and made it through with wonderfu experiences AND the best have seen 5 more grand children added to my list.

SO ladies I say GO FOR IT and try to get past the worries of what COULD happen, instead plan for what a good time you WILL have. If I had not done so, I would be sitting around "waiting" for the day, which I refuse to do.

Good luck to everyone and God Bless..
__________________
Irene from Tampa
1996 - INFILT DUCTAL CAR.W/ LYMPH NODE INVOLVEMENT. ADRIA/CYTOXIN/5FU
1999 - RECURR. TO AUXILA AND 2 TUMORS IN LIVER
TREAT: STEM CELL REPLACEMENT/HERCEPTIN.
2002 - RECUR TO LIVER
TREAT: NAVELBINE, THEN GEMZAR, THEN XELODA.
2004 - TUMORS STILL IN LIVER
TREAT: RFA TO LIVER
STABLE UNTIL
2004 - TUMOR PROGRESSION IN LIVER.
TREAT: RESECT HALF OF LIVER.
2005 - RECURR TO LYMPH NODE OUTSIDE OF LIVER.
TREAT: TAXOL/CARPO/HERCEPTIN. FAILED ON
THIS TRIO. STARTED ON ABRAXANE.
2006 - PROGRESS WITH 2ND TUMOR GROWTH.
TREAT: AUG. BEGAN ON TYKERB/XELODA
TRIAL. CONSIDERED STABLE TO DATE.
2007 - TAKEN OFF OF TYKERB/XELODA TRIAL DUE TO
PROGRESS STARTING TYKERB/AVASTIN.
NOV 2007 - SCANS SHOW PROGRESS TUMOR GROWTH
IN ABDOM. AND TWO NEW TUMORS IN NECK AREA.
BEGAN HERCEPTIN/AVASTIN/TAXOTERE
Feb 08 - Ixempra/Xeloda
June 08 - Her/DM1 trial

"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 is offline   Reply With Quote
Old 08-11-2007, 12:51 PM   #14
StephN
Senior Member
 
StephN's Avatar
 
Join Date: Nov 2004
Location: Misty woods of WA State
Posts: 4,128
Wink It does get better

Just when I was trying to get over the idea that it was ridiculous to buy new clothes or shoes except what I needed to get by with, plan a trip, etc., the bad news came.
My mets came so fast after my initial treatment that I hardly had time to get started again, if you know what I mean. I felt like I was sucker-punched. Once I got through the next ordeal, I did decide to move on a bit. Then the brain mets. Not as hard of a punch as the liver mets, but still a punch. Then the problems with my head afterwards last year. Those 2 surgeries really sapped me and I am still trying to get over the side effects of those and the new port placement.

However, I told myself a long time ago that I HAD to accomplish something EACH DAY, no matter how hard it was to drag my fanny around. This meant that for at least a few minutes a day I had to ignore those nagging feelings and doubts. Then I began to take on small projects and that was a lift in itself.

Fighting this beast means finding a way to "tame the dragon" and get out in the sun a bit. I will never be the same person as before cancer (BC) and I have only a few friends who understand at all how hard a fight it has been. Not only with the cancer, but with the psychology that comes with it.

Kelly - try to take the new position. It may be a way of helping you over this "hump." It may be a blessing in disguise.
__________________
"When I hear music, I fear no danger. I am invulnerable. I see no foe. I am related to the earliest times, and to the latest." H.D. Thoreau
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.
StephN is offline   Reply With Quote
Old 08-11-2007, 06:13 PM   #15
Patricia
Senior Member
 
Patricia's Avatar
 
Join Date: Oct 2005
Location: San Francisco, CA
Posts: 96
Hi Kelly,

I definitely understand about the fear of plans. It is nice to have a conversation about it - sometimes I think everyone here has it all together much better than I do - so this conversation makes me feel more like the rest of you. When I was dx I had just started a new job. I was there for less than 1 mo and then went out on disability for surgeries and chemo for 6 mos. I felt so guilty, but what could I do. Then as I was planning on coming back, my group did a re-org and they asked me to help plan it. I felt ridiculous making all these plans feeling certain that I would not be there in a year so what was the point. I left that job after coming back from disability for 8 months. I decided that the stress that had been so normal for me (hyper growing start up software co) was completely overwhelming for the new (much slower) me. I found a job doing the same thing but in a very established, slower growing company that is 10 mins from my home. The change was terrifying because again I felt like a fraud, selling myself through interviews but feeling like I wasnt sure if I would be there very long before a recurrence. I had terrible chemo brain and I felt a fraction of my old professional self. Well, I made the change and it has been very good for me. I eventually settled in and felt more confident in my value to the new company, I deal with chemo brain (i just don't debate as much as I used to) and I truly let things just flow off me a lot more and now I have a much more sustainable work life. I also found a wonderful friend in a co-worker who is a 5 year survivor and has a husband who is a 10 year survivor of esophegeal cancer. We both feel lucky to have found each other and to be able to work together.

I really think the pshycological aspects of cancer are not talked about nearly enough and that most of the people around us really have no clue the challenges that we face. I have talked with my therapist about it that it feels like there is an alternate (but parallel) universe for those that have faced their mortality. Almost like we are in a tunnel that we can't get out of, you just keep moving forward through life in this tunnel. My HIV+ friends are the only ones that I have found without cancer that 'GET IT', if you know what I mean.

Best of luck with the job decision. Sounds like a nice opportunity to have come along unexpectedly. Kind of like the bulbs in spring - enjoy!

Hugs,
Patricia

ps. I was very supersticious about removing my port and finally got up the nerve to get it out last week while I was out for oopherectomy. I am now very happy that it is finally out and am glad I waited until I was emotionally ready to let it go.
__________________
age 37 @ dx 7/21/05: IDC 1.5cm, grade III, Stage 1c, ER /PR+, HER2+,
7/29/05: Partial Mastectomy
dx 8/15/05: Papillary Thyroid Cancer
9/15/05: Total Thyroidectomy
A/C X 4 DD, 11 weekly Taxol + Herceptin, + 9 mos Herceptin Alone, 36x Rads, Lupron, Aromasin
7/29/07: 2 years NED :)
8/6/07 Oopherectomy (Lupron no more! :-)
Aromasin & Estring plus Synthroid and supplements
Patricia is offline   Reply With Quote
Old 08-11-2007, 06:40 PM   #16
Mary Jo
Senior Member
 
Mary Jo's Avatar
 
Join Date: Aug 2006
Location: Sheboygan, WI
Posts: 2,582
I have a different take on this subject..............

Although I couldn't agree more on the uncertainty of our future's I have a different take on this subject...........................

Although the thought of recurrence in my life (because at this point I have had no recurrence) is unsettling at best, I try to keep those thoughts and the thoughts of all of our uncertain futures at bay. You see, I try to look at life this way..................none of us knows what our tomorrows will bring us. None of us. I often comment that the only difference between me and my husband who has never had cancer is this..............I had my mortality slapped in my face and he hasn't. I've had to look at life differently - or chose to - because like you all said, uncertainty is a part of our future. BUT, it is also a part of every single persons future. Cancer or otherwise. That is what keeps me striving forward each and everyday. I look at each new day as an adventure. Each new purchase and decision a purchase or decision I have made for today. And only for today because I don't know what my tomorrow holds BUT (I hate to keep plugging away at this point) neither does anyone else.

People on this board have shown each of us that living with active cancer for years and years is definitely possible.

So, although I do understand what you are all saying (as I think of that day where I may experience a recurrence as well) I also understand that life is here for us to live. Life is here for us to enjoy and to do all we can with what we are while we are still here.

Cancer may rob us of many things but I refuse to let it rob me of a life I WANT to live. A life I WANT to enjoy. And, the WONDERFUL life God has given me.

Thanks for "listening" to my 2 cents worth.

Hugs to all,

Mary Jo
__________________
"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
Mary Jo is offline   Reply With Quote
Old 08-11-2007, 06:53 PM   #17
Brenda_D
Senior Member
 
Join Date: Jan 2007
Posts: 368
I told my husband I don't know whether to plan for the future or my funeral.
It this point I am planning for next spring, as far as gardening, planting, etc, but as much as I'd like to go on a vacation this fall, I'm afraid I couldn't stand the trip from a "pain and fatigue point of view". I don't know from day to day if it's going be a decent day, or a bad one that I'll end up sleeping most of the day.
__________________
12/12/06- IDC Stage III, 4x A/C, 35 rads, Herceptin 1 year
Brenda_D is offline   Reply With Quote
Old 08-12-2007, 09:50 AM   #18
Kim in CA
Senior Member
 
Kim in CA's Avatar
 
Join Date: Sep 2001
Location: California's Gold Country
Posts: 404
I tend to feel the same as Mary Jo. None of us on this earth know when our number is up. Just think of the poor folks on the bridge that collapsed with absolutely no warning. You just can't let this disease keep you from living.

Strange as it seems, I feel like my disease has been a blessing in disguise. Many of the things that I was saving to do "later on" when the kids were grown and we had our retirement funded, I am doing now.

I do admit to having feelings (big feelings) of doubt sometimes, but after having my little pitty party, I have to kick myself in the butt and remember that I'm just burnin daylight by engaging in such thoughts.

I'm over 10 years since diagnosis, and six years stage IV, and life is just too interesting to not keep pursuing it.

There is one thing however that I haven't had the nerve to do yet. My husband and I spent a week in North Carolina last August looking at horse properties and thinking of making a major lifestyle change. We actually almost made an offer on a place. Then we decided we had better not do anything to hasty.

Now that we've been back home and thought through the logistics of such a move, we've cooled off. I do still find myself dreaming of the little horsefarm in Carthage, but then I can't imagine leaving my doctor and the great care I receive here.

So for now, I just keep dreaming about it..... But who knows!

Kim
__________________
Diag. Feb 1997 4.5cm IDC <10%ER+, PR-. 5 out of 36 nodes +. Mastectomy followed by 3 rounds Adriamycin/Cytoxin.


5/1997 Hi Dose Chemo w/ Stem cell rescue. Spent 4 weeks in isolation ward. Then 6 weeks radiation.

9/2001 widespread mets to liver. 8 mos Taxotere/Herceptin brought me almost to NED. Stop Taxotere & add Femara .

11/2002 liver resection to remove spot that turned out to be necrosis. Officially NED!

7/2003 Tumor markers rising add Xeloda Disastrous reaction, 8 days hospital, but tumor markers came back to normal!

June -Dec 2004 UW Vaccine Trial.

7/2005 MRI single 11mm brain met
8/2005 Gamma Knife.

Brain MRI @3 months NED!

2006-2011 brain/body still NED

8/04/11 Taking Herceptin break, will monitor with tumor markers.

6/20/12 Tumor markers begin to rise. CA15-3 is 31.3 and Her2 Serum is at 17.1 Decide to repeat in one month.

7/23/12 CA15-3 now 49.3
Her2 Serum 26.8

8/6/12 Back on Herceptin
CA15-3 now 76
Her2 Serum now 49

11/7/12 Add weekly Taxotere for 4 cycles

2/2013 Stopped Taxotere added Perjeta. MRI shows approx. 50% reduction liver mets. CA15-3 still elevated @ 55. Will continue on just Herceptin & Perjeta.

November 2014 Continuing on Herceptin, Perjeta, and
Femara indefinitely. Guess I'm NED again, but watching those tumor markers carefully!

Dec. 2015 PET scan reveals mass in perirectal area of abdomen.biopsy confirms. Still Her2+, but no longer ER+. Bye bye Femara

Jan 2016 Begin Kadcyla

March 2016 PET scan shows tumor now barely visible, still NED everywhere else.
2016/2017 continue Kadcyla

November 2017 brain MRI reveals small focus of T2 hyperintensity with possible 4mm enhancing nodule. Short term follow up MRI suggested. Stay tuned...
Kim in CA is offline   Reply With Quote
Old 08-12-2007, 10:23 AM   #19
Patb
Senior Member
 
Join Date: Oct 2006
Location: Louisville KY Naples FL
Posts: 665
Images: 2
Yes to what everyone has said. I guess this is the new normal. One day
I buy a new car, the next I say no I shouldn't buy anything but its good
to know others are also adjusting their sails and we will survive this and
be stronger for it.
patb
__________________
patb

Diagnosed June, 06, Stage I, Grade3, ER+PR- Her2positive, No Nodes. A/C X 4. Radiation 33 with boost, Herceptin every two weeks until Nov.
07, Arimedex for 5 years. Mugas and Echo and chest xRay. Bone scan of whole Body, and Back of Brain and spine MRI.
CT scan of Lungs every six months
due to two small places. December
2009, bone scan due to bone pain.
Follow up test in 2010.
Patb is offline   Reply With Quote
Old 08-12-2007, 10:38 AM   #20
AlaskaAngel
Senior Member
 
AlaskaAngel's Avatar
 
Join Date: Sep 2005
Location: Alaska
Posts: 2,018
What we do and why we do it

To some degree it depends on where you stand. I feel like it would be presumptious as a NED stage I to have any genuine idea of how it feels to consider this question realistically in other people's shoes.

I don't have much fear of making changes, although I am much more tuned in to the practial genuine need to hang onto whatever health care benefits I have.

I think that a big part of the problem is that the sheer fact of loss of hormonal impetus gets ignored, not only by the doctors but US as well. When we had lots more hormones we had more drive. I think we need to "allow" ourselves a lot of credit for making the most of whatever we have left. I believe that the loss of hormones does actually change who we are to some degree -- our personality and our motivations -- and we have to find some way to learn to live and make new choices with the new person that we have become.

AlaskaAngel
AlaskaAngel is offline   Reply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

Forum Jump


All times are GMT -7. The time now is 05:08 AM.


Powered by vBulletin® Version 3.8.7
Copyright ©2000 - 2024, vBulletin Solutions, Inc.
Copyright HER2 Support Group 2007 - 2021
free webpage hit counter