This is not MY story, it is the story of my breast cancer. My breast cancer is but a part of my wonderful and exciting life. I was a survivor even before I was diagnosed. I won't EVEN consider the alternative.... :) Now I realize I am also a Warrior.

Ta-Ta-411

My photo
Diagnosis Date - 31 December 2007; Invasive Ductal Carcinoma (IDC) & Ductal Carcinoma in Situ (DCIS) Lumpectomy - 14 December 2007 Re-excisions - 31 January & 6 March 2008 Stage 2, Grade 2 Lymph Node-, HR+, HER2-, BRCA- Treatment; 4 cycles of chemotherapy; Cytoxan (cyclophosphamide) & Taxotere (docetaxel), every 21 days. Chemo completed July 2008. 6 and 1/2 weeks of daily Radiation completed at the end of September 2008. Left radical mastectomy with tram flap reconstruction August 2009.

Thursday, January 31, 2008

2nd Lumpectomy & Sentinal Node Biopsy



It was the morning of surgery. We got up at 0 dark thirty (seriously, 0400 - that's 4:00 in the blessed morning for you non-military time folks!) and headed to Walter Reed, Will & I in 1 car and my mom & dad in theirs. My report time was 0600. The actual time of the surgery wasn't known but the first procedure (dye injection) was supposed to happen at 0700, and the surgery somewhere around an hour later.

The wait time was borderline miserable for all of us. We were in an overcrowded, 60 degree pre-op waiting room. I expected the O.R. to be cold but the waiting room?! The staff was sympathetic though and brought us all blankets. My sister Alisa met us at the hospital after she had gotten Coley off to day care. I was SO very fortunate to be surrounded by so many people that love me (here after referred to as my entourage!), and I knew that so many more people were with us in thought and prayer.

Close to 7:00 my trial nurse (Angie) brought me the magic cream I had agreed to "test". The purpose of the cream was to numb the injection site where the radioactive die would be placed for the lymph node trace. It was a 50/50 chance whether the cream was an actual numbing agent or a placebo but I was sure mine was the real deal. Even it it wasn't, I refused to think otherwise. I convinced myself that one way or the other, even if it was only because of the power of positive thinking, I wasn't going to feel that needle. After about 20-30 more minutes Angie came for me again and escorted us all down to Nuclear Medicine. It was comforting that she stayed with me the entire time and allowed my family to go everywhere with me.

Up to that point I really hadn't been very nervous, although I don't think I can say that for Mom, ;0) but when I entered the room and they paged my surgeon I literally felt my heart rate increase. I told her I thought that the injection would be the worst part of the day at that I was happy to be getting it done & over with. Honestly, it really wasn't as bad as I had feared. Yes, it was definitely uncomfortable, but it wasn't excruciating. I truly believe that a lot of that had to do with the cream. How else could that not be terribly painful? Angie said I didn't even flinch!

The injection itself took a few minutes. Once the injection was complete I was placed in a scanner/mri for about a minute and then went back to the waiting room to greet my entourage. Seriously, they all looked so much more fearful than they needed to be and I wished they had known just how o.k. I was.

Within minutes I could feel the warmth of the dye start to run through the left side of my chest and up towards my neck and arm. I had heard from a couple of women who had the procedure done just how painful it was and I was surprised that I found it to be merely uncomfortable, again not unbearable. There were a few minutes of stinging & burning over the next 15 minutes or so but it came and went pretty quickly, never lasting more than a few minutes at a time.

Angie came back for the 3rd time, this time to place me on my gurney and take us all to the operating room/waiting area. I was ready to get this done! Enough of the waiting already! They allowed 2 people at a time to sit with me in the prep area. Mom & Dad took the first shift while Will & Alisa went to the new (but not improved) waiting room. There was so much action happening in that little area with all the staff & equipment. There were 3 or 4 separate conversations occurring at any given moment. Patient after patient lay behind each curtain, all with their own team. Everybody was moving so quickly and efficiently that I thought I might be put to sleep without being able to say "goodnight" to everyone or even give Will a chance to come back. I must have asked the anestethiologist 3 times if they would give me plenty of notice before knocking me out and wheeling me away.

I opted for a spinal block and also agreed to have additional blood taken for trials so that added to the already busy prep. Within a few minutes of being on the gurney in the midst of the chaos I asked my dad to trade places with Will, just in case they really didn't give me enough notice. That was what I was concerned about most! Will came back and he & my mom watched every move the staff made. I won't get too graphic but around the time the I.V. was being inserted I could tell I was doing much better than my mom. When they started marking my spine for placement of the block injections I knew it would be best to do the hug and kiss thing sooner rather than later (partiularly for Will & mom, o.k., mostly for mom ;0).

My bartender (anesthesiologist) was ready to serve me the first of my 2 margaritta cocktails. He offered me 4 but I let him know I was a light weight and that after 4 I would surely wake up with a headache and sick to my stomach! I also asked him to use only the best ingredients. ;0) Almost the very moment he added the 2nd one in my I.V, while still sitting up I was out! I don't even have the faintest memory of receiving any injections.

The surgery took longer than anticipated (What a surprise! this is ME we're talking about!) because they had a tough time capturing my tiny and elusive sentinal lymph node (the one the dye had flowed to the first). After about 3 hours I was wheeled into recovery, having hopefully left all the cancer in the O.R

Thursday, January 24, 2008

Tammy's Personal Update (sent via email)

Hello everyone.  I wanted to take a few minutes and let each of you know that I am thinking of you and I thank you so much for the care, positive thoughts, support, prayers and love that you have already provided me.   I am doing very well, in spite of or maybe even in a sense because of my recent  breast cancer diagnosis.  It is a fact and my motto that it is a part of me, but not me.  I will not let it consume me in any way, physically or emotionally.   Please, those of you who love  me (who is every single person reading this email!), please do not let it get the best of you either. 

My surgery for the second lumpectomy is scheduled for next Thursday, the 31st of January.  It will be at Walter Reed Medical Center.   I have a fantastic and experienced team of doctor's and have every confidence in them.  I will also have a great "nursing team" that will help me out at home afterwards (Thanks Will, Mom & Dad! :)   I'll have to stay overnight but only because I have volunteered for a case study and have agreed to have a pain relieving catheter in place for a couple of days.  It will administer pain relief directly to the surgical areas - how could a girl pass up an opportunity like that?!  Pain reduction AND on the cutting edge?!  

I am getting a little anxious the closer the surgery date gets but not out of fear of the surgery, but due to impatience about hearing that they got it all and what stage they determine it to be, and of course whether or not it is in the lymph nodes, and if chemo will be required.  As you probably know, I should start radiation in March (5 days a week for 6 weeks, which is the standard).  Keeping up with a schedule like that may be the toughest thing I have ahead for me!  The surgery itself is not very complicated and I will be out of work for 2 weeks starting the healing process.

I believe this is more than just positive thinking but I know that with time, treatment and prayer I will be completely ok from this.  I have said that my life is too good and too busy for me to have b/c so I have to hurry and get it out of me and get healthy.  I have many  many more wonderful memories to make with the incredible people in my life and the adventures I have yet to discover!

OK - for the technical parts of it I don't know what has been shared so far so this is the most current.  What they do know so far is that I have IDC - infiltrating ductal carcinoma, (moderately differentiated, grade II and III), and DCIS - focal ductal carcinoma in situ, grade 2.
They don't know what stage yet until my lymph biopsy results - that won't be until the end of the 1st week of February.  It is hormone positive (which is good considering I had a hysterectomy years ago and will stop my hormone replacement therapy after surgery to help prevent growth/recurrence.)  It is HERR2 negative, which I found out yesterday and don't really know what that means yet other than what drugs they choose to treat me with.  The did not get it all, but think it is small and so probably still in early stage.  The goal is to get it all out next Thursday.

The first procedure is set for 7am when they will inject the radioactive dye into my left breast.  From there is will flow to my lymph  nodes and be able to determine which ones are reached first.  At some point after that (I'm guessing probably an hour later) they will start the surgery, do the lumpectomy and remove the 1st (up to 3) nodes that the dye has reached. 

I definitely want to get this over with.  It s an important step in the right direction heading to complete healing.  In many ways this is not yet real for me and I think that it may only become more real as each step is taken.  I am a true believer that that is the way things happen - as they are meant to,  when they are meant to.  That has truly been the testament of my life and it has worked out pretty darn good so far!

I am working on a web page to keep people posted and also to use it as therapy for myself to write it out.  Talking doesn't really seem to help yet because sometimes I feel like I am stuck in the cancer/patient mode and as I said, I do not want it to consume me in any way.   I have been writing a lot the past couple of days and it has helped.  Even this, so again, thank you for being there to read it.  

I will keep you posted.  I hope no one minds that this was a mass email.  If you do, then you are officially elected to compose all of my personal emails from here on out!  :0) 

The most important things I can ask any one to is, if you are a woman, PLEASE - DO REGULAR SELF BREAST EXAMS, get annual exams, and get you mammo's.  If you not a woman, tell every woman you love to do it.  Also, as you are holding me close to you hearts, please hold yourself in prayer and take care of yourselves.  Especially those closest to me.  This (as many things do) has a way of touching so many more people than solely the person in lingers in.

Much love to you all,


Tammy :)

As an after thought, NOT that I am expecting flowers or a fruit basket or anything like that from anyone, SERIOUSLY, but it you feel compelled to and simply can't stop yourself (I'm that type too!) please don't send the dollars on anything like that.  Save the $$$ for the time when I and/or my team (Tammy's Ta-Ta's) will be asking you to support us in the Breast Cancer Walk (Avon in May and/or the 3 day in October).  Thanks!  :0)

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Inspirational Quotes & Thoughts

"There is no medicine like hope, no incentive so great, and no tonic so powerful as the expectation of something better tomorrow." - Orison S. Marden

Dancing in the Rain

I came across this one evening while "researching" cancer info. I found it to be so inspirational. I found just what I needed. I can only hope to have such an amazing attitude throughout life. Here's to "Dancing in the Rain." TTFN