Friday, November 2, 2018

Sweet Release

Do you know that feeling when the roller coaster ride ends, and you assess yourself and those surrounding you for damages and realize that you are okay? 

That momentary sweet release? 

The release I get each time I get a clean scan is much the same.  It's like finally being able to breathe after holding my breath for far too long.

This week has been terrifying, I feel like I am on a roller coaster ride all the time.  It is so hard for me to know that it is not just me on the roller coaster, but that I take all of you along for the ride too.

I have pneumonia. It was walking pneumonia, now its just pneumonia.  I went to an urgent care facility on Monday night.  I was just exhausted, and couldn't get a full breath.  One of the many tests that was ordered that night was an X-RAY. 

The X-RAY clearly showed pneumonia, but also something else, slightly more dense, higher than the other spots.  I think the words fell out of my mouth, I don't even remember stringing them together into a full thought, I just knew that I had to know, "Is it cancer?"

The doctor turned, and very calmly (not at all expecting the reaction that was coming) said, "It is something that is there, and I think your oncologist needs to look at it."

I felt the tears, hot and wet on my face as I put a plan in place.  I felt my body tremble and then go still.  I formulated a plan:


  • Step One - Pray, separate yourself from this situation and talk to God directly.



  • Step Two- Text Polly (that's my oncologist) to see what her thoughts are.  She immediately responded that we would order a CT scan.



  • Step Three - Call David.  Ugh - I can't even tell you how hard this call was.  To call my husband, after a month of beautiful pink ribbons everywhere and me giving inspirational survival speeches, to tell him that the cancer might be back.  To know that he would have to tuck our babies in with that knowledge, that fear looming.  That was when I made the very conscious decision not to call my parents. It hurts too much to be so afraid, and to not be able to do anything about the situation.  I hate seeing the fear in other people because of me.



  • Step Four - Contact the prayer warriors.  For me these are both the easiest, and the hardest calls to make.  I love the prayers, I adore them, and whatever your faith is know that I feel them wash over me.  The converse of this is that by contacting these prayer warriors I make them worry.  This is literally the last thing I ever want to do, I never want anyone to worry.  Again, that's why this time, for the first time, I didn't call my parents.  I *just* had a biopsy in August and took everyone along for the roller coaster.  I couldn't bring myself to do that again this soon.


Then I went home, to my husband and my babies.  I delighted in their presence, I wrapped myself in their sweetness.

There is a surreal quality to the days and hours following a "maybe" you have cancer again diagnosis.  Its hard to put words to, but everything has a keen sense of urgency, of possible lastness.

The following day I got two calls from the urgent care facility, the first telling me that the radiologist saw nothing - not even pneumonia, the second was from the doctor who treated me that night encouraging me to follow up with my oncologist.  I can't tell you how confused I was by this series of calls.  I knew I was sick, I knew I saw pneumonia and "something" and I knew that the doctor that treated me felt the same. I knew I was afraid and doing my best not to be.

I followed up the next morning with my primary care, he is a truly great man who cares about me and my family.  He has both laughed and cried with me over the successes and set backs of the last three years.  He walked in the room and the first thing he did after greeting me was to tell me he was ordering a stat CT scan.  Oddly, this filled me with a sense of relief- he saw something too, and we were going to check it out.  When I told him my oncologist had already ordered a CT he was relieved, and said that pneumonia or not we would all be able to breathe better once the results are in.  He also told me that I was no longer contagious from the pneumonia and could I could take the babies trick or treating and return to work.

The next morning I worked through all of my anxieties, literally.  There were about 80 emails waiting for me and I thrust all my focus into working so I couldn't process that the CT was just a few hours away.

Driving to the CT was hard, David called twice to see how I was.  I know this is the hardest part for him.  We are fixers, both of us, and with this situation we just have to let go and realize that we aren't in control. In his voice I heard all of my fears reflected.

I was surprised to see how fast the CT went. In my mind it was going to take at least an hour, that is undoubtedly what I remembered from past experience.  This one was fast, start to finish in under 45 minutes.  As instructed, I texted my oncologist and called my primary care to let them know I was done.

Within minutes I got a text from my oncologist.

No cancer.
A little pneumonia.

Soon after I had a tearful message from my primary care telling me he had never been so happy to tell someone she had pneumonia, pneumonia and nothing else.

I truly have the best medical team.  I am eternally thankful for their knowledge, faith, and grace.  I am such a lucky lady.

I am savoring the sweet release of knowing that I am okay.  I have come to the realization that this roller coaster ride, it is my normal.  This is my truth.  No matter how unpleasant, this is my roller coaster.  A diagnosis of HER 2 + cancer means that this is the ride I will be on, until I am not. 


I am sending you all so much love.  Thank you for loving me through it.  Thank you for understanding my need for chemoflauge.

Smile at strangers, hug the ones you love, be the change in the world.

#fightlikeamommy
#itisstillmyfairytale








Thursday, August 16, 2018

Preliminary Results

You guys are so amazing,  I truly have a community of love.

I have been blessed with more phone calls, text messages, messenger messages, comments, and hugs than I can count.  My church is dedicating a rosary for me tonight, I have been told by so many of you that you have added me to your prayer lists.  I am more thankful than you could possibly imagine.  Each and every prayer means so much to me.

I know that I was wrapped in prayer because I was able to continue to place one foot in front of the other, I could literally feel the love pouring over me.

This afternoon, while I was having lunch with my precious children my surgeon texted me. 

"The preliminary results are in, the lymph node was reactive - but shows no sign of cancer."

I can breathe, my husband can breathe - it's truly a big beautiful sigh of relief.  My mom cried, right in the middle of getting her oil changed.  My daddy and Pat are celebrating in joy.  I have delighted in the texts and messages from friends.  I am so truly thankful.

Cancer is a war that is not won with one battle.  My fighting did not end when chemo ended, and will continue.  I will continue to be an advocate and an informer.  I will continue to share my story with transparency in hopes of educating and inspiring others.

I am sending you all love and light.  Please continue to keep us in your hearts, please pray for a cure for all cancers.  Keep my beautiful mermaid Sawyer in your prayers, she is at St. Jude now.

This week has been terrifying, I am grateful to all of you for loving me through it.

Please also keep my sweet Tommy surrounded in love and light. He is having surgery tomorrow and I pray for the surgeon to have skilled hands and the healing process to be quick and painless.

I truly cannot thank you enough. 

Go be the change in the world.  Give smiles, love, and laughter whenever possible.  Tell the people you love how much they mean to you.

#fightlikeamommy
#itisstillmyfairytale

Tuesday, August 14, 2018

My Yearly Checkup




We could call this the “before” picture.  I snapped it moments before my lovely surgeon and her medical student came in for my yearly exam.  I was super excited to post it when I left the appointment this morning declaring another wonderful checkup.

But, that’s not what I’m doing, at least not yet.

Dr. Stephen's found a small lump, on my cancer side. Uncomfortably close to the previous cancer site.

With surreal speed she rolled over the ultrasound machine and passed it over my breast to show both the student and I what she felt, an enlarged lymph node.

An enlarged lymph node could mean anything, really and truly anything – and it could also mean THAT THING. 

So, we did a Core Needle Biopsy.  She took two samples and placed a clip so she could find the area later.  Hopefully, we will know results on Friday. 

I am not kidding when I tell you that the waiting is the worst, like truly the worst.  The pain is also not much fun.  

I laughed a little when I re-read the aftercare instructions.  They read that there may be “some tenderness,” this is much like the Neulasta commercial saying that you may feel “some bone pain.”

For right now we are all in a little state of shock, this is not at all what I thought would come of today’s appointment. 

You are all my prayer warriors and my well wishers, and now that this news has settled in and the waiting begins I wanted to update you so you can keep all of us in your thoughts and prayers.  

Tommy & Elayna do not know, I don’t want them to worry unless we need to.

Go be the good in the world, hug your babies, tell the people you love how much they mean to you. Go to an animal shelter or rescue organization. Find your tribe, love them hard.  Most importantly, know your body.  Early detection saves lives.

Sending you all love and light.

#fightlikeamommy
#itisstillmyfairytale