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Old 05-15-2009, 05:12 AM   #21
WomanofSteel
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Marie, I am glad to hear that Ed finally got a treatment. I hope that he experiences little or no side effects from this. I am sorry that you have been given such a full plate lately. I have been there many times. Remember to take a deep breath and relax and try to get some time for you from time to time. Don't let yourself get run down it is easy to do. Hang in there, we are all praying for you and Ed and Dad.
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dx aug 03
invasive dcis 1 cm
er/pr/her2+
bcs 8/4/03
bcs 8/21/03 0/16 nodes
tx 4x ca 36 rad tam
postmenopausal 06 aromasin
sept 07 biopsy node in neck
muga/pet/cat/bone mets to lungs nodes and liver stage iv
tx hki-272
tx not working switched to taxol herceptin
Taxol not working switched to navelbine
navelbine is causing bad neuropathy
starting gemzar
gemzar quit on me now on Ixempra due to increasing number and size of liver mets
another progression starting tykerb/xeloda
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Old 05-15-2009, 06:09 AM   #22
schoolteacher
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Believe,

So glad to hear that the Mighty Oak got his treatment. Yeah! Did you get to see your outside buddy?

I will call you this afternoon after 7 p.m. I will be finished working by then. I started to call at 7 a.m. but decided to wait.

Sending blessings and prayers to you and the Mighty Oak.

Amelia
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Old 05-16-2009, 02:34 AM   #23
Kavy
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Marie,
I am so sorry to hear about your mother-in-law and your dad. You are going through too much. When enough is enough?
I am glad that Ed had his treatment, and I pray that the side effects will be mild for him.
I am on Ixempra/Herceptin since October 2008, and the 3 tumors in my lungs are shrinking. My doctor is very excited, he says that all his patients on this new drug have a good response, I hope this will also be true for Ed.
Ixempra is not an easy drug, as you already know, but it is doable and it works.
My side effects are hair loss, I lost my hair for the 3rd time, but it is coming back fast. No nausea or vomiting, sometimes change in the taste for the first few days, then it goes back to normal, but I do not lose my apetite. Sometimes I have mild constipation ( I use prune juice) or mild diahrrea in the first few days. I have neuropathy (numbness in hands and feet), and on the first night of treament I few a little tired, on the second day I few normal, on the 3rd day I feel very tired, and stays like that for a few days, then I go back to normal. Tell Ed to drink lots of water, and rest, rest, rest.
On this past treatment something interesting happened, I did not get very tired at all. The nurses and I are trying to figure out if the order of treatment has anything to do, I mean, for the past 6 months I have been taking Herceptin first, then Ixempra, but last time, I got Ixempra first, then Herceptin in 40 min drip. So today I had treatment, and we did exactly the same thing Ixempra then Herceptin, and so far so good, I hope it will stay like that. What drug did Ed get first?
If you have any questions, please PM me that I will be happy to help.
You and Ed hang in there. I will pray for all of you, and for this combo to be Ed's magic bullet.
Hugs,
KarlaV.
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Old 05-16-2009, 04:16 AM   #24
Mary Anne in TX
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Such good news Karla on your Ix. treatment! Marie, I'm so prayin' that it does the same for Ed.
Marie, don't you dare thing that you're not going to be strong enough for whatever comes at ya.
You are always strong enough, brave enough, and awfully wonderful too, to handle what comes. You have an army of "family" who love and support you and will be there for you.
Take some time to "fill your cup", Marie. time to take care of the one who has taken such good care!
Much love to ya, 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 05-16-2009, 05:40 AM   #25
Lien
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Dear Marie,

I'm echoing your words: enough is enough! You need time to heal.

Hugs & good vibes & healing energy coming your way.

Love

Jacqueline
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Diagnosed age 44, January 2004, 0.7 cm IDC & DCIS. Stage 1, grade 3, ER/PR pos. HER2 pos. clear margins, no nodes. SNB. 35 rads. On Zoladex and Armidex since Dec. 2004. Stopped Zoladex/Arimidex sept 2009 Still taking mistletoe shots (CAM therapy) Doing fine.
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Old 05-16-2009, 03:58 PM   #26
Joan M
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Marie,

I'm glad that Ed finally had his treatment and I hope he'll be feeling okay.

I know what you mean about needing strength.

Prayers for Ed to get well.

Hugs,

Joan
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Diagnosed stage 2b in July 2003 (2.3 cm, HER2+, ER-/PR-, 7+ nodes). Treated with mastectomy (with immediate DIEP flap reconstruction), AC + T/Herceptin (off label). Cancer advanced to lung in Jan. 2007 (1 cm nodule). Started Herceptin every 3 weeks. Lung wedge resection April 2007. Cancer recurred in lung April 2008. RFA of lung in August 2008. 2nd annual brain MRI in Oct. 2008 discovered 2.6 cm cystic tumor in left frontal lobe. Craniotomy Oct. 2008 (ER-/PR-/HER2-) followed by targeted radiation (IMRT). Coughing up blood Feb. 2009. Thoractomy July 2009 to cut out fungal ball of common soil fungus (aspergillus) that grew in the RFA cavity (most likely inhaled while gardening). No cancer, only fungus. Removal of tiny melanoma from upper left arm, plus sentinel lymph node biopsy in Feb. 2016. Guardant Health liquid biopsy in Feb. 2016 showed mutations in 4 subtypes of TP53. Repeat of Guardant Health biopsy in Jana. 2021 showed 3 TP53 mutations, BRCA1 mutation and CHEK2 mutation. Invitae genetic testing showed negative for all of these. Living with MBC since 2007. Stopped Herceptin Hylecta (injection) treatment in March 2020. Recent 2021 annual CT of chest, abdomen and pelvis and annual brain MRI showed NED. Praying for NED forever!!
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Old 05-16-2009, 05:27 PM   #27
Jean
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Thinking of you & Ed. Sending you strong warm hugs.

Jean
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Stage 1, Grade 1, 3/30/05
Lumpectomy 4/15/05 - 6MM IDC
Node Neg. (Sentinel node)
ER+ 90% / PR-, Her2+++ by FISH
Ki-67 40%
Arimidex 5/05
Radiation 32 trt, 5/30/05
Oncotype DX test 4/17/06, 31% high risk
TOPO 11 neg. 4/06
Stopped Arimidex 5/06
TCH 5/06, 6 treatments
Herceptin 5/06 - for 1 yr.
9/06 Completed chemo
Started Femara Sept. 2006
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Old 05-18-2009, 11:26 PM   #28
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
Thanks for keeping us in your thoughts and prayers, it has given us the courage to make this happen.

Kavy, thank you so much for the post I can not tell you what it did for us both. Ed is currently taking the Ixempra alone but I am contemplating adding Herceptin to the mix. With his particular genetics I am not sure it will do any good. Seems like Herceptin did not protect him as well as we wished but I would like the 'idea' that it may do something. I will surely pm you soon, appreciate the offer.

I will make a special update post for others to be able to follow the Ixempra journey. I will put details in it for everyone too. I have heard and seen many wonderful things that this drug is doing. Sharing is caring and I am sure our posts will certainly help others as they search for their magic bullets.

I so appreciate you all>>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 05-19-2009, 08:26 AM   #29
Shobha
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Marie,

You really are such a tower of strength and positive attitude. Please know that Mighty Oak and you are in my thoughts and prayers everyday. May God put Ed on the path of recovery with this regimen.

hugs,
shobha
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DX: 06-30-2007 - left breast -stage IIIB, Her2/Neu 3+++, ER weakly positive, PR-
Taxol+herceptin weekly for 3 months
FEC+herceptin every 3 weeks for 3 months
BRCA 1 and 2 - Negative
Jan 2008 - Bilateral mastectomy, prophylactic Rt. side.
Radiation for 5 weeks
Completed my yr of herceptin on 07-14-2008
Brain MRI - 3/2/09 Clean
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Old 05-19-2009, 03:32 PM   #30
juanita
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keeping both of you in my thoughts and prayers! you're such an inspiration!
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dxd 9-04, lumpectomy,
st 1, gr 3, er,pr-, her2 +,
2 tac,33 rads,6 cmf
1 yr herceptin,
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