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11-28-2008, 02:40 AM
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#1
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Guest
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Someone Please Help Me!!!!
Hi I am 33 years old, had stage 3c invasive ductual carcinoma R breast. CHemo-Hercep/carboplatin/taxotere. then had R side Mastectomy and Lymphectomy as I had 27 nodes removed they found 9 positive for cancer. Had 34 radiation treatments. And I am Her2 positive ER Positive and PR positive. no family history was diagnosed Jan 4 2007. I had the double tram flap reconstruction surgery and then a revision to that just 5 weeks ago.....HERE IS MY PROBLEM. I have found a lump at the inside top of my right breast and to me it feels just like the first three tumors I had that were cancer. My plastic surgeon thinks its just fat necrosis......Has anyone had a tumor come up relly fast...and or grow quickly..if so HOW quickly???? I am soooo freaked out right now. I have this ugly sinking feeling that this is just another fight coming. PLease if you have thoughts or suggestion or stories please talk to me. Everyone around me who by the way has never had cancer keeps telling me... "well you had chemo right?" "They took it out right?" "You did have radiation" I say I know I KNOW quite a few women that did all those right things too...and it still came back...same breast/breast area or to a new location all together. It happens all the time. I go this coming Tuesday for a removal of the "mass" and then they will send it to Pathology and then let me know. But PLease ladies and Gents....if you have anything to say please help me. Thank You All AND GOD BLESS!!!
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11-28-2008, 03:53 AM
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#2
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Senior Member
Join Date: Jun 2006
Location: San Antonio, TX
Posts: 2,357
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Good Morning! Welcome to our group. I know Tuesday must feel like years away right now. You are right that some on the board have recurred even after all their treatments, but there are also those here who had new places checked and found them to be necrosis or something with the healing process from surgery. I think they'll get on today and share their stories.
I don't have your experience, but I can send some prayers for peace and patience and best wishes for today!
God bless you. 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!
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11-28-2008, 07:31 AM
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#3
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Senior Member
Join Date: Apr 2006
Location: Wilmington, Del.
Posts: 1,126
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I don't have your experience, but agree with Mary Anne that chances are good that your lump is what your doctor thinks it is. I have scar tissue under my arm from the sentinel node that feels like three lumps. IMHO, one thing we all share here is post traumatic stress syndrome. A headache is brain mets, rib pain is lung mets.
Whatever you find out, you'll be able to deal with it. I look forward to hearing a sigh of relief from you. If there's a problem, we are all here for you.
__________________
MJO
IDC, Stage I, Grade 2
Oncotype DX Score 32
Her2++ E+P+, Node Neg.
Lumpectomy 11/04/05 Clear Margins
3 Dose dense AC (Couldn't tolerate 4)
4 Dose dense Taxol & Herc. (Tolerated well)
36 weeks Herceptin (Could not complete one year due to decrease in MUGA score)
2 years of Arimidex, then three years of Femara
Finished Femara May 2011
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11-28-2008, 10:01 AM
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#4
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Senior Member
Join Date: Jun 2007
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: 3,000
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I have no voice when it comes to your situation, but I do have a voice which to pray for positive results and I can send positive healing thoughts your way. We are right here for you and would appreciate your update when you find out what is happening. Stay strong Sweetheart, you are now in all our prayers.>>Believe51
__________________
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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11-28-2008, 03:04 PM
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#5
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Senior Member
Join Date: Apr 2008
Location: WA State
Posts: 199
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Try and not make yourself crazy over this. I know its hard but keep a positive outlook. I will be praying for good results and for you to have peace as you wait. Take care.
__________________
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 2024!
I am calling this my pink journey
Follow my journey into the pink at my blog here
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11-28-2008, 04:10 PM
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#6
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Senior Member
Join Date: May 2006
Location: Haarlem, the Netherlands
Posts: 835
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We've all been through that fear. And yes, it might be cancer, but it probably isn't.
As someone who's had benign lumps & cysts for 12 year before developing cancer, I've learned to rely on the doctors' "feeling". For 12 years my GP's were sure I had cysts Ultrasounds confirmed their diagnosis. I moved from one city to another, and my docs were always right. Then I developed a new lump. My new GP palpated my breast, and examined my "old" cyst. I smiled and told him that one was benign. He frowned and said: I'm not so sure. Then he examined the new, tiny lump and said that one felt like a cyst. So I went for a mammo & ultrasound. And whaddaya know? My doc was right. The old cyst had changed into DCIS and a small area of Invasive Ductal C. The new lump was B9.
There is nothing you can do until Tuesday. It's highly unlikely that a tumor would grow this fast. Your doctor knows how necrosis feels, but he can't be 100% sure, and you are freaking out (Like most of us would) so he's looking for confirmation.
When you get through this, you will be able to do something, make plans, take control. The waiting is the worst part. We've all been there. We are holding your hand, and hugging you, and telling you to take a deep breath. This too shall pass.
Sometimes it helps to visualise a safe place. Create a mental picture of your perfect house. Set it in a lovely garden, that can be just the way you want. If you want a pool? Zip! There it is. You want a ski-slope on one side and a tropical beach on the other? Just dream it up. Anything goes. Just make sure it's a place you can feel at home in. Decorate the house any way you like. Add pets, books, music, whatever. But make sure you really "see" the whole thing in your minds' eye. Now go and sit in your garden, look at the flowers, the plants or trees. Listen to the music or the sounds of birds. Just focus on this picture and relax. You are completely safe here. Nothing can happen to you. If anything or anyone unpleasant tries to approach you, you take out a special little remote control and zap them out of your life. Just like that. They can come back when and if they are nice to you. When they are helpful, pleasant and supportive.
Try it. It worked for me. As soon as someone made a silly remark (like: Why are you dwelling on having cancer? They took it out. It's gone. Get over it) I'd imagine zapping them with my little remote control. It felt wonderful.
Please let us know how it goes. These are tough days, and we are here to help you get through them.
Hugs
Jacqueline
__________________
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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11-28-2008, 05:07 PM
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#7
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Senior Member
Join Date: Feb 2006
Posts: 1,014
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I have quite a few lumps in my breasts, they are all scar tissue, some are really big, others feel like the lump I found when I was diagnosed. I get regular PET/CT scans and my last scan they did an ultrasound also, all indicated scar tissue...so yes, it's very possible that yours is the same..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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11-28-2008, 08:03 PM
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#8
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Senior Member
Join Date: Nov 2005
Location: Northern Calif.
Posts: 981
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I know how scared you must be feeling. After having breast cancer it is really hard not to freak out if we feel a new bump or lump. It's a good thing to get it checked out right away. But, I am really hopeful that it is just some scar tissue.
Hang in there sweetie. I am saying a prayer for NO cancer.
Lexi
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11-28-2008, 09:14 PM
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#9
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Senior Member
Join Date: May 2006
Posts: 3,142
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Someone Please Help Me !!
I would get it checked out with an ultra sound, a biopsy or another appropriate tests. No matter what the results are, you will have piece of mind knowing you did all you could. If it is only scar tissue you will be more relaxed. If it is not good news it is better to find out sooner rather than later.
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11-29-2008, 06:17 AM
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#10
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Senior Member
Join Date: Sep 2005
Location: france
Posts: 1,648
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Take a deep breath and try to relax. It's probably fat necrosis since it's come up so fast. I think all of us who have had recurrences would advise it's best to be absolutely sure so a more thorough test than a mammo or sonogram would be a good idea - MRI? PTscan? That way you'll feel more confident that you're not in danger.
I had a recurrence but it was years later and originally I wasn't given any chemo or radiation or herceptin because it was back in "middle ages" and originally my cancer wasn't invasive.
Worry won't help but do demand whatever you feel will make you feel secure even if it means a second opinion.
Waiting for news is the worse.
stay calm and positive, you'll get through this.
hugs and love
Sarah
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11-29-2008, 09:52 AM
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#11
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Senior Member
Join Date: Oct 2005
Posts: 3,519
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I can't offer any more help than has already been offered, but all the best as you move forward and try to determine what is going on.
Please join our group officially, too - instead of being unregistered. We would like to keep up with you!
__________________
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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11-29-2008, 12:03 PM
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#12
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Senior Member
Join Date: May 2006
Posts: 3,142
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Someone please help me !!
I vote for calmly getting a second opinion. We should listen to our bodies. I also vote for you joining our group.
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11-29-2008, 08:48 PM
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#13
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Senior Member
Join Date: Nov 2007
Location: Connecticut
Posts: 2,077
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My thoughts and prayers are with you. Holiday weekends seem forever when something like this is going on. Please keep in touch.
__________________
For Nicola
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11-29-2008, 11:28 PM
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#14
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Senior Member
Join Date: Jun 2006
Location: san luis obispo, ca
Posts: 1,150
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I am praying that it is just scar tissue. I had chemo, then a mastectomy in 2004. 6 weeks later, I had a new tumor at the scar line and yes, it was the cancer. they had gotten clean margins and removed 19 nodes in which 6 were positive. The difference is that I had not yet had radiation. So I will keep you in my prayers and thoughts with the hopes that it is something else. By the way, I am going on 5 years (unbelievable, with my diag.of 3c also) Just know you are loved and cared about here at this site. Hang in there and please let us know how you are after Tuesday. Much love, Vickie
__________________
Love and Hugs, Vickie
Life's not about waiting for the storm to pass,
It's about learning to dance in the rain.
Feb 04 IBC IIIC/IV er-/pr- her2+++
3/04 TCH X4
7/ 04 MRM 9/04 Taxol/herceptin wkly 1 yr 33X rads
11/04 skin mets 33x rads,10/05 Avast/Herc. 11 mos.
8/ 06 PET mets lymphs, neck
9/ 06 Navelbine/herceptin
11/ 06 PET NED
2/ 07 skin mets, 4/07 Xeloda, 5/07 add Tykerb
2/ 08 Tykerb failed. Doxil /Herceptin 6 months
8/08 PET skin mets, 8/08 Abraxane/Avastin
11/ 08 PET prog., skin mets
1/09 PET/CT progress, 1/09 Ixempra, 2/09 add Xeloda and low dose Naltrexone
2/09 off Ixempra/Xeloda
3/09 navelbine/herc/cytoxin 4/09 PET shows regress.7/09 start Topotecan. Failed.
8/09 extensive mets rgt brst, back and torso. starting Pazopanib clinical trial.
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12-01-2008, 11:47 PM
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#15
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Guest
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Update
Thank you ladies for all your thoughts and prayers. I saw my oncologist today and he was very concerned that it may be cancer...He said had I come in like this before surgery he would have instantly thought cancer, but since I had surgery he said too many things were at play.uugghh He was worried that tomorrow when I go for a biopsy that if it is cancer they will not remove it all as it is very large. My Onc would like chemo started before surgery but no for sure way to tell what it is until they do a biopsy. So tomorrow we drive to Woodland Hills, Ca and I have surgery at 4pm. THey said I should have the results from pathology by Thursday. Once again thank you all so very much. I will come and update this post as soon as I know something more.
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12-02-2008, 04:39 AM
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#16
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Senior Member
Join Date: May 2006
Location: Haarlem, the Netherlands
Posts: 835
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Ouch, that sounds scary. Perhaps my mothers' story will give you some hope. She had had an ovary removed at age 38. 2 months later she had a growth in her womb the size of a 5 month pregnancy. Her gyn/onc was convinced she'd developed a malignant tumor, so he planned the surgery asap. Turned out it was entirely benign.
I will be thinking of you!
Sending you good, healing vibes.
Love
Jacqueline
__________________
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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12-05-2008, 02:23 PM
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#17
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Senior Member
Join Date: Jun 2007
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: 3,000
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Hello Again
Just wanted to let you know that we are here for you and awaiting your results. Continued pleasant thoughts for you as you filter out what is happening. As soon as you find out please post what you know.>>Believe51
__________________
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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12-05-2008, 09:12 PM
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#18
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Senior Member
Join Date: Oct 2006
Location: I live in Christmas, MI - located on the shores of Lake Superior.
Posts: 606
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If you read the postings on this site for hours you would see that people face things and the results can be different than what is anticipated.....it is so complex and can be scary. Perhaps they are trying to prepare you for the worst? I don't know your doctor. I certainly cannot tell you what to do.
We are all hoping for positive results for you.
__________________
Barb
10/03 Radical Mastectomy 3 cm tumor - 1/17 Nodes Stage II B, Her 2 +++ ER-/PR- 11/03 4 AC 4 Taxol 12/05 Stage IV - Lung met , Bone mets - Carbo, Taxotere, Herceptin 9/06 - 2 cm brain tumor 10/06 - Tumor removal surgery - Herceptin Halted 12/06 gamma knife tumor base.1/07 Navelbine/Herceptin 4/07 Rads to R femur 5/07 Stereotactic - new 2 cm brain tumor 4/07 Start Xeloda 5/07 Tykerb added 7/07 Brain MRI clean 10/07 .055 cm brain met found. 12/07 Stereotactic -1 cm brain tumor Start Tykerb 11/07 Abraxane/Herceptin 5/08 Cisplatin, Gemcitabine/Herceptin 6/08 Stereotactic to 1cm 9/08 Stereotactic repeat (growth). 11/08 Pet Scan Good but new tiny met on L lung/dead Brain surgery (no cancer cells found/scar tissue) 1/09 Chemo restarted 2/09 Pet Scan Bad - R larger very active/active L active lymph nodes both sides of chest MRI- mets slight increase 2/09 Start Doxil/Tykerb Treatment
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12-06-2008, 04:34 AM
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#19
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Guest
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update #2
Well Ladies I am soooo very happy and excited to report to you. My surgery went well he removed half of the mass as he said if he took all the mass out it would leave a "dent" in my breast. The great thing though was all Pathology reports came in and its all Benign.....PRAISE GOD!!!! My Dr. actually said that when he started slicing open the healing scar that lots and lots of puss came oozing out everywhere. So I ended up haveing a major infection and some fat necrosis. He put in another drain to help get that infection out ...did I mention it was all benign??? YIPPIE I AM SO HAPPY SO RELIEVED. So I am on clindamyacin for 10 days taking 8 every day. SHould get this drain out in the next few days and then off to heal again!!! I am so happy that I was given the chance to stay in the mental fight and NOT in the physical one again. LOVE AND PEACE AND HEALTH AND HEALING GOD BLESS ALL OF YOU STRONG BEAUTIFUL WOMEN..... WHERE EVER YOU ARE IN THIS FIGHT. AS WE ARE ALL STILL CONNECTED> GOD BLESS AND THANKS FOR HELPING ME THROUGH ALL THIS!!!
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12-06-2008, 05:05 AM
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#20
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Senior Member
Join Date: May 2006
Location: Haarlem, the Netherlands
Posts: 835
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You just made my day!!! Wonderful news!!! I had an abcess in my sentinel node scar too, and it healed beautifully. And you know what, the old internist I saw a few months later, told me that having an infection is often a good thing. It helps clean up any residual cancer cells in the area.
Love
Jacqueline
__________________
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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