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1st Chemo Wednesday

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TysMom View Drop Down
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    Posted: May 03 2010 at 7:43pm
I got my diagnosis 4/15/10.  I had a lumpectomy on 4/12/10, my mammogram showed nothing and my ultrasound only showed a cyst.  I work with doctors so my surgeon friend said if I wanted the lump out he would remove it.  Thank God he did. 
I was diagnosed with DCIS, LCIS, and infiltrating adenocarcenoma triple negative.
MRI, CT, bone scan all came back good.  The only thing that showed was "a few lymphnodes that are minimally enlarged".  Lump and lymphnodes are on my right side.
 
I am taking part in a research study at Missouri Baptist Hospital in St Louis. I will have 12 weeks of weekly Taxol with Avastin added in every other week.  Then I will have AC every 2 weeks for 4 cycles with Avastin added to the first 3 treatments.
 
I fully intend to beat this this thing.  We have a 14 year old son at home that I need to be around to raise.
I am so glad I found this site.  I had not been able to find anything about TNBC.
 
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123Donna View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote 123Donna Quote  Post ReplyReply Direct Link To This Post Posted: May 03 2010 at 8:28pm
Hi Tysmom,

I'm from St. Louis also. 

Have you seen this brochure about TNBC?

http://www.lbbc.org/data/media/LBBCunderstandtriplenegative.pdf

Donna





Edited by 123Donna - May 03 2010 at 10:21pm
DX IDC TNBC 6/09 age 49, Stage 1,Grade 3, 1.5cm,0/5Nodes,KI-67 48%,BRCA-,6/09bi-mx, recon, T/C X4(9/09)
11/10 Recur IM node, Gem,Carb,Iniparib 12/10,MRI NED 2/11,IMRT Radsx40,CT NED11/13,MRI NED3/15

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Post Options Post Options   Thanks (0) Thanks(0)   Quote 123Donna Quote  Post ReplyReply Direct Link To This Post Posted: May 03 2010 at 9:16pm
I forgot to ask you if you've had your Vitamin D3 level checked?  Most of us with TNBC have very low levels of D3 at dx.  Ask your onc for a Vitamin D3 test.  They can do it at the same time they draw blood for other testing. 

Here's a thread talking about the importance of D3:

http://forum.tnbcfoundation.org/vitamin-d3_topic5338_page1.html

Also, the EDGE-CAM at no surrender website has thorough research about the importance of D3, especially with TNBC.  Here's the link:

http://www.nosurrenderbreastcancersurvivorforum.org/post?id=4698965&trail=20#1










DX IDC TNBC 6/09 age 49, Stage 1,Grade 3, 1.5cm,0/5Nodes,KI-67 48%,BRCA-,6/09bi-mx, recon, T/C X4(9/09)
11/10 Recur IM node, Gem,Carb,Iniparib 12/10,MRI NED 2/11,IMRT Radsx40,CT NED11/13,MRI NED3/15

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Post Options Post Options   Thanks (0) Thanks(0)   Quote TNBC_in_NS Quote  Post ReplyReply Direct Link To This Post Posted: May 03 2010 at 10:17pm
Tys Mom:
 
Welcome to our TNBC Family!  I am sorry you have be here but it is so good you found us!
 
You were so fortunate to have pursued your treatment rather than let it go as a cyst!  Thanks be!!
Sounds like you will have a great combination of chemo.  You didn't mention radiation?  That will get any swimmers that are missed in the surgery and chemotherapy.  Also, you can do a search on this site to find various questions you might have.  Denise has sent you information on the brochure so read that and the vitamin D is so important!
 
Take care and know you are not alone now.  We are here for your questions, concerns, good stuff, not so good stuff, whatever you need, we are all here for each other. 
Your sister on the journey, Helen in NS
Diag@57TNBC04/092.5cm Lquad 05/09 TCx4Radsx30CT03/01/10 FU03/31/10ClearBRCA- 01/2011 RTNBC BMX 06/14/2011~2013 clear
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Toodlybug Quote  Post ReplyReply Direct Link To This Post Posted: May 04 2010 at 8:31am
I'm curious about the CT's etc.  I had my surgery on Jan 28th.  Was unable to start chemo until last Tues, April 27th due to wound healing.  There were 2 of 27 nodes positive.  I thought they would check to see if there was cancer anywhere else before chemo, but the oncologist said only if there was labwork to indicate spread.  Insurance doesn't pay for it otherwise I guess.  Did your insurance pay for scans, etc?
Toodlybug
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Lillie Quote  Post ReplyReply Direct Link To This Post Posted: May 04 2010 at 3:35pm
Dear Toodlybug, (What a cute name)

I am sorry you needed to find this site, but glad you did since you have questions.
You mention wound healing. Did you have a lumpectomy or mastectomy? Was there infection? What size was the tumor? What chemo regimen are you on? Sorry to be asking so many questions but it helps us understand where you are if we know more of your history. You will notice that most of us post this information in our signatures at the bottom of posts.

Between my surgery (mastectomy) and the beginning of chemo I had a CT scan of my neck, lungs and liver. My oncologist told me he needed a baseline of everything before starting chemo. He told me that he did not like to depend totally on x-rays. My insurance did pay for these scans.

You might want to bring the subject up again with your oncologist if it is something that bothers you. Scans can be done between chemo treatments.

Love in Christ,

Lillie
Dx 6/06 age 65,IDC-TNBC
Stage IIb,Gr3,2cm,BRCA-
6/06 L/Mast/w/SNB,1of3 Nodes+
6/06 Axl. 9 nodes-
8/8 thru 11/15 Chemo (Clin-Trial) DD A/Cx4 -- DD taxol+gemzar x4
No Rads.
No RECON - 11/2018-12 yrs NED
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Lillie Quote  Post ReplyReply Direct Link To This Post Posted: May 04 2010 at 3:45pm
Dear TysMom,

What a blessing that you opted to have the cyst removed. I am sorry it was malignant, but still a blessing that it was found sooner than later.

It sounds a though you have a good chemo regimen lined up. Also, taking part in a research study helps you to be more involved in the knowledge of what is what. I did a clinical trial and I felt as though I got the best "standard of care" at that time, plus some. I hope your experience is the same.

Yes, that 14 years old son needs his mother and you WILL BEAT this thing.

Love in Christ,
Lillie
Dx 6/06 age 65,IDC-TNBC
Stage IIb,Gr3,2cm,BRCA-
6/06 L/Mast/w/SNB,1of3 Nodes+
6/06 Axl. 9 nodes-
8/8 thru 11/15 Chemo (Clin-Trial) DD A/Cx4 -- DD taxol+gemzar x4
No Rads.
No RECON - 11/2018-12 yrs NED
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TysMom View Drop Down
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Post Options Post Options   Thanks (0) Thanks(0)   Quote TysMom Quote  Post ReplyReply Direct Link To This Post Posted: May 05 2010 at 3:23pm
Got home about 20 minutes ago.  Everything went well, the fear of what to expect was much worse than what went on. 
The nurse I had was incredible!!!
Today was Taxol and Avastin.  1 down and 11 to go for these 2 drugs.Thumbs Up
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Allybat Quote  Post ReplyReply Direct Link To This Post Posted: May 05 2010 at 3:27pm
I have not had surgery but will begin my neoadjuvant chemo cycles next Thursday of Taxotere and Cytoxan.  I was dx on 4/19/10.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Allybat Quote  Post ReplyReply Direct Link To This Post Posted: May 05 2010 at 4:22pm
Please keep us posted...I'm a newbie also.  Glad to hear all was well and not what you feared.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote specksmama Quote  Post ReplyReply Direct Link To This Post Posted: May 05 2010 at 4:32pm
I too am doing the neoadjuvent course of treatment, I was started with adriamyacin/cytoxan every other week for eight weeks, then taxol every other week for eight weeks. I really didn't have much trouble with any of my treatments. I had very mild nausea which they gave me meds for. I did get tired while on A/C, fell asleep on the couch most nights and took naps during the day. Taxol did give me some bone and joint pain, but nothing that couldn't be fixed with a few pain killers. I think the fear of the unknown is always worse than the actual thing we have to do. I was just convinced that I would be so sick that I would be bed ridden - well that was certainly not the case. I am now very nervous about my surgery exactly three weeks from today - Yikes. But I think it will all go well. I am being treated at Mayo Clinic in MN, they have given me the best care I could ever hope for, I never have to wait more than a few minutes for any appointment there and all the doctors and nurses treat me like a person with feelings and not just a number.  Good luck to all of you that are just starting out - it is sometimes a tough road, but not something we can't do - we are women after all, we can do anything!
Diagnosed 12/09 IDC triple neg
2cm tumor
1 of 11 nodes positive
Chemo until 4/20/10
Surgery 5/26/10 No viable cancer left in breast
1 mm of cancer in one lymph node.
Radiation 6/28 to 8/9
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Post Options Post Options   Thanks (0) Thanks(0)   Quote TysMom Quote  Post ReplyReply Direct Link To This Post Posted: May 06 2010 at 12:09pm
Allybat  you and I will get through this together!  Being diagnosed so close together I have a feeling we will be going through a lot of the same things at the same time.  We can do this! Handshake
 
 
 
 
123Donna what area of St Louis are you in?  Who are your docs if you don't mind me asking?  I work with a lot of doctors at MoBap which is how I wound up there.  The first day I met Dr Lyss he said he had already had calls from 3 doctors about me besides my surgeon and he was glad to finally meet me in person.  I am very lucky to have the support that I have there.  Smile
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Post Options Post Options   Thanks (0) Thanks(0)   Quote trip2 Quote  Post ReplyReply Direct Link To This Post Posted: May 06 2010 at 5:35pm
Hi Tysmom,
 
Good for you for persuing the "cyst"!
 
I'm very sorry that they found cancer and you have to do chemo.  We have some "chemo Tips" in the TNBC News/Resource forum that may be helpful.  Also clicking on the "resource" link at the top of the page will have info you might want to read.
 
It's good to hear your first treatment went well.  Keep us posted on how you are doing.
 
Has your doc said anything about being tested for a brca 1/2 mutation?
This website, http://www.facingourrisk.org  is a great place to learn more.
 
It might be advisable for you to see a Certified Genetic Counselor to see if you qualify for testing.  This could be important informaton for you if you are positive.  Many brca 1 women are TNBC but most TNBC do not have a mutation.
 
Best wishes,Heart


Edited by trip2 - May 06 2010 at 5:37pm
Stage 2 2003
Stage 1 2007
BRCA 1+
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Carol (Tenn) Quote  Post ReplyReply Direct Link To This Post Posted: May 07 2010 at 5:41am
Good Morning !!
Many prayers for all of you in treatment. I would expect that you all figured out how lucky we are to have Pam here with us. She is so knowledgeable and kind and helpful and uplifting and I could go on and on. We have so many wonderful sisters (and brother) here. It's a wonderful place to come together....we are not alone....beside our heavenly Father, we have each other. What can be better than that?
Love and Prayers,
Carol
St 2 Gr 3, A/C/T, DD
Radiation x35
Rec chest wall 07/09
Radiation x28
NED 10/24/11
NED 10/5/12
NED 03/15/13
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