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Old 02-08-2009, 07:19 AM   #21
Mary Anne in TX
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Hi Joy!
Please keep telling us how you feel, what you think and, well, whatever is happening with you. Your honesty is so helpful to us all. You speak of your experiences, but you also speak for all who are walking the same walk. Remember that love sees through love's eyes....seeing you only as beautiful, worthy, loveable, and so important.
I'm prayin' for this treatment to keep on working hard to destroy the bad cells and let our "cutie" Joy get back her energy, sparkle, and hope once again. Much love and belief, ma
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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!
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Old 02-08-2009, 07:39 AM   #22
Midwest Alice
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Hi Joy`, I agree with Mary Ann, what ever your thoughts and feeling are they are very important to us. I read your post and I just want to give you a hug. You're so strong and in touch with your feelings. Your teaching me that I am going to be OK.

Have a wonderful day,
Love and Hugs,
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Alice
04/08 age 50 III IBC Her2+++ ER/PR-8cm 14/14 Double M, Body and Brain CT/PET clear, ? on spine,Muga 53
06/08, 4 A/C, Neulasta
08/08, Herceptin/tax 12 every week
10/08, CT/PET clear, ? on pelvis, hips, MUGA 43, started Enalaprial for heart, Herceptin every 3 weeks
11/08 33Rads; 12/08 MUGA 48
2/09 MRI spine and bone scan, old mets to spine, Chest x-ray, blood work, IV NED,regular CPAP use,Zometa x6, first -flue like symptoms 2 days;Herceptin x3; stage 2 lymphoedema..sleeve and glove
4/09 Brain MRI - CLEAR; MUGA 54
7/09 chest ultrasound,
10/09 PET, brain and spin MRI NED Herceptin only. MUGA 59!!!
1/11 Hip replacement 7/11 Hip 2 replacement
4/12 4 years!! Herceptin
6/12 start reconstruction finish in 12/12
2/14 Herception - 6 years!!!

1 Corinthians 10:13 "No temptation has seized you except what is common to man. And God is faithful; he will not let you be tempted beyond what you can bear. But when you are tempted, he will also provide a way out so that you
can stand up under it."

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Old 02-08-2009, 07:39 AM   #23
nitewind
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Joy, there's really nothing more that I can add, the others have expressed my feelings so well. I was just delighted to log on and see your post. You are always in my prayers.
Hugs
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Susan
Age: 61
dx: 5/25/06
2 cm/ 0 nodes
Lumpectomy rt breast on 7/26/06
ER/PR- / Her2+++
A/C x 4
finished taxotere 2/07
finished 33 rads
Herceptin finished 12/07/07 Yippee!
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Old 02-08-2009, 02:00 PM   #24
karen raines hunt
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Dear Joy,

So sorry to hear about the high fever and pains. I hope those are gone forever!

You are the first bc survivor that I talked with in Fort Collins. You led me to this site. I don't post very often, but do read posts regularly.

You are a great mother and a great friend and I am confident you will feel better!

karen
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Karen Raines Hunt
Dx April 2005 at age 46
stage 3A, very large (12cm) tumor
2 positive axillary lymph nodes
ER+/PR+, Her 2 +++
Bilateral mastectomy, radiation, reconstruction, A/C, Taxol, Herceptin, Tamoxifen, Aromasin
5 yrs since diagnosis and NED
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Old 02-08-2009, 02:47 PM   #25
sally
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Hi Joy, I also had alot of pain in my forearms. I got it 2 hours after my last treatment. My Dr. said it sounded like I had nerve damage. I am currently on 4 tykerb daily and Gemzar. I have been having a hard time with the Gemzar and I haven't been NED in a couple of years now. I know what you mean when you feel your days are numbered. Good luck to you and getting the perfect cocktail. I always look forward to your posts. Hang in there and be strong. Sally
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Dx March 2004 HER2+ er/pr+ 8/16 + lymphnodes mets to the liver Stage IV / 6 cycles of TCH and 33 rads . NED Continued Herceptin 3 years w/ Femara. Tumor markers start to rise in Jan of 2007 and swiched to Tamoxifen. August of 2007 found more mets to liver and lymphnodes outside of liver. Went on Tykerb/Xeleoda--spots on liver gone found large mass between intestines. March 2008 started TCH. Stopped Carboplatin due to allergy. Still on Taxotere and Herceptin. Nov 2008 mass is gone. 3 new spot on liver and one on spine. Radiation on spine. tykerb/gemzar for liver mets. PET in April 09 showed shrinkage still a little activity, continue tykerb/gemzar until Aug 09. PET showed new spot on my spine more on my liver and a bunch of enlarged lymphnodes in upper chest. Start Adriamycin Sep 09. more radiation on spine . April 2010- Still on Adriamycin 3wks on 1 wk off and zometa every 28 days. PET -May 2010 showed progression. Starting Herceptin/Navelbine on June '10
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Old 02-08-2009, 07:50 PM   #26
Paty
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Sending you my love and prayers and big hugs. It was good to hear from you and hope that soon you will feel better.
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Dx. June 30th, 2006 at age 43
Lumpectomy rt breast
2.2 cm tumor, 13 nodes all negative
ER-PR+,her2+++
6 FAC
32 Rads
Dx. Lung fibrosis due to radiation
Ended 1 year herceptin in March, 2008
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Old 02-09-2009, 08:55 PM   #27
Debbie L.
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Joy, I am so appreciative of your honesty. Have you thought about journaling or writing in other ways that could help others dealing with cancer learn how to be clear about their feelings? You have a real talent for expressing yourself in a way that is not at all whiny but neither is it sugar-coated. That honesty and open-heartedness really resonates with readers. At least it does with this reader.

I hope that having this forum as a place where you can be honest, and supported, is of some help.

I don't mean to minimize (at all), the enormous pressures that you are dealing with. It is difficult enough to face hard things when we are feeling well - but to add in fatigue is just so hard.

So (lecture of sort follows)- being in bed a lot with no energy is not what defines being YOU. Being YOU means you are fully "there" for your kids and your loved ones, when you are able. Your loved ones do not value you for your ability to get up and "do things". Your preciousness to them is not in the tasks you accomplish. It has nothing to do with that (although of course, they appreciate those things, when you are able to do them). They value and need you most for your loving presence. If you allow yourself to be distracted with concerns about what you can't do (which alas, you cannot control), you are a little less there for them. I know that it is very easy for me to say and very hard for anyone to do - but I hope that you can try to let go of your regrets about what is not - and focus on what is. What is, in your life, is (I gather from your other posts), a lively and wonderful connection to special children and adults. I encourage you to savor that and to cherish it. Savor it as if it were your last moment to do so (even though it is not). I wish that we could ALL do that - savoring this moment as if it were our last. How rich life would be. But daily stuff does get in the way, for all of us. Still - not a bad thing to strive for.

With love,
Debbie Laxague
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Old 02-11-2009, 11:47 PM   #28
harrie
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Hi Joy.....aka ms whiny pants....hahaha, that was cute.
You my dear are free to show all your highs and lows to all of us. That's what friends/sisters are for. Right??!!
Hows your WBC been? Are you feeling better?

If you feel like it, we would love to have you join us by the campfire. Its a great place to hang out and we all just breathe deeply and snuggly up together.

Much hugs, love, and peace to you my friend...
Maryanne

PS....and BTW, with that beautiful face of yours, hair or no hair, you are always beautiful. Really and truely girl!
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*** MARYANNE *** aka HARRIECANARIE

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

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

2007:
6 cycles TCH (taxotere, carboplatin, herceptin)
finished 1 yr herceptin 05/07
Arimidex, stopped after almost 1 yr
Femara

Last edited by harrie; 02-11-2009 at 11:49 PM..
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Old 02-12-2009, 02:06 PM   #29
Believe51
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Location: RHODE ISLAND (Ed getting me a latte on 2nd Cancerversary Cruise 2008) 'BELIEVE': To accept as true or real, To have faith in, To presume ALWAYS BELIEVE
Posts: 2,999
Talking

Joy, if you have not joined the campfire yet, please do. I have been looking for you and need you to drink up this iced latte before the ice melts. Come on over, I saved you a place right in the middle....this way no one fights over you!!>>Love>>Believe51
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9/7/06Husband 50yrs=StageIV IBC/HER2+,BoneMets10/06TaxotereX10,'H'1X wk,Zometa,Tamoxifen4/12/07Last Tax5/18/07Pet=Rapid Cell Activity,No Organ Mets,Lytic Lesions,Degeneration,Some Bone Repair5/07ChemoFail6/01/07Pleural Thoracentisis=Effusions,NoMalignantCells6/19/07+7/2/07DFCI
6/25/07BrainMRI=BrainMets,Many<9mm7/10/07WBR/PelvisRad37.5Gx15&Nutritionist8/19/07T/X9/20/07BrainMRI=2<2mm10/6/07Pet=BoneProgression
10/24/07ChemoFail11/9/07A/Cx10,EndTam12/7/07Faslodex12/10/07Muga7512/13/07BlasticLesions1/7/08BrainMRI=Clear4/1/08Pet=BoneImprovement,
NoProgression,Stable4/7/08BrainPerfect5/16/08Last A/C8/26/08BrainMets=10(<9mm)9/10/08Gamma10/30/08Met=5mm12/19/08Gamma5mets5
12/22/08SpinalMets1/14/09SpinalRads2/17/09BrainMRI=NoNewMets4/20/09BoneScan5/14/09Ixempra6/1/09BrainMRI=NumerousMets6/24/09DFCIw/DrBurstein6/26/09Continue
Ixempra/Faslodex/Zometa~TM now lower7/17/09Stop Ixempra By Choice9/21/09HOSPICE10/16/09Earned His Deserved Wings And Halo=37 Month Fight w/Stage 4 IBC, Her2+++,My Hero!!
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Old 02-12-2009, 06:34 PM   #30
naturaleigh
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Hey Joy,

When your mother named you, she knew what she was doing, she should have given you the middle name of inspiration because that is what you are, a Joy and inspiration!!

I love reading your post. You totally amaze me by how you can feel so rotten and still come here with happiness and laughter in your heart (whinny pants!!). That's a riot!!

I am praying for you daily and hope your treatments get better for you and you are back on your feet soon (but not too soon, make sure you don't overdo).
__________________
Anita

er, pr-, Her2+++
Stage 2b, grade 3
negative nodes
4 rounds AC
3 months of weekly taxol
1 yr of Herceptin
Finish Herceptin May 2007
35 rounds of Radiation
Reconstruction completed Dec 2007
Implant replaced due to infection Mar 2008
4 Years NED!!!
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Old 02-12-2009, 11:49 PM   #31
harrie
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Joy, got a new name for you......The Magnificent Warrior!! So please toss the Whiny Pants in the rubbish!!
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*** MARYANNE *** aka HARRIECANARIE

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

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

2007:
6 cycles TCH (taxotere, carboplatin, herceptin)
finished 1 yr herceptin 05/07
Arimidex, stopped after almost 1 yr
Femara
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