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
Thursday, August 16, 2018
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.”
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.
Sending you all love and light.
#fightlikeamommy
#itisstillmyfairytale
Thursday, December 14, 2017
On turning seven
“Mommy, I will be seven in four days!”
Your words instantly pulled at my heart strings and caused
an unexpected flow of emotion.
Those numbers, seven and four, that is how old you both were
when I was diagnosed with breast cancer.
Those numbers will remain forever ingrained on my heart.
Seven and four, that is when our little world was knocked
off of its axis. I look back at the
pictures before my diagnosis and see an innocence that is not present
anymore. I hate that my sickness took
that from you. I hate the little things
that it robbed me of. When I was
diagnosed we were watching Bubble Guppies and Star Wars Cartoons, playing with Little Tykes Toys and Cars, and then
suddenly you had outgrown those sweet playthings of childhood. I look at you both now and see tiny adults,
with your own opinions and personalities growing and expanding so quickly.
Cancer did give us many gifts, but I know that more than anything
it left a mark within your spirits that has changed all of us. It taught us the importance of love, faith, and
kindness. To never take anything for
granted, and to appreciate everything.
Seven in four days, wow. I cannot wait to see you grow into adults, raise children of your own - It is my deepest desire.
I am so lucky to be here, so lucky to see all of these beautiful
milestones. We had princesses come to
your party again this year. I imagine
that by next year you will want something a little more adventurous, maybe
Boomerang or skating. I am so very proud
of the beautiful little lady that you are quickly becoming.
______________________________________________________________________________
Sometimes I find myself lost in the wonder of survivor hood. I feel very guilty for not updating as often
as I once did. The truth is that I am indulging in living.
It warms my heart to have so many of you reach out to see
how I am. “Every day is different,” is
my go to answer. I still have an ache deep within my hips, sometimes it is hard to get up, harder than I would like to admit. Hard enough that I was given a handicapped placard for my car. At first I didn't use it, it made me sad to even look at it. Now I pull it out more often, especially after a long day.
I am elated to know that the pain is not cancer,
but instead the after effects of chemo that just make me achy from time to
time. I do my very best not to complain,
because I am here – living, breathing, loving.
I have a chance at life anew, and there isn’t a day that goes by that
that miracle is not lost on me.
There have been many wonderful occurrences since my last
update.
We are doing to Disney – and we are flying first class.
This is a true miracle, and one that I am breathlessly
excited about. As a family we have never
been on vacation, and the kids and I have never flown. We have never stayed in a hotel, or been
farther than a days drive from home (and our animals). I cannot wait to experience the pure magic
that is Disney with my family. It is going
to be amazing. I still need help booking
our fast passes if anyone is interested.
We got a puppy! His name is Sir Lancelot, and he fits into our family perfectly.
The kids are doing beautifully in school this year. Elayna won the Kindness award for the second
year in a row. Tommy has maintained
perfect grades and is excelling in all of his subjects. I am so proud to be their mommy.
As a side note, Tommy recently called me mom. When he realized he had said mom, not mommy it
brought tears to both our eyes. I took
him in my arms and told him that even if he is getting older, I would prefer to
be “Mommy” for as long as possible. He smiled, and said that he just wanted to hear how it sounded.
I am having surgery again at the end of the month. This procedure is purely cosmetic. If you have seen me in the past year or so
you know that my port scar is changing.
The best way to describe it is that it looks like a bullet wound, which
as I was reminded by a beautiful friend is stunningly accurate. Cancer hit me like a bullet to the chest.
Although that is an awesome conversation starter, I hate
it. I am not sure why it has spread the
way it did- almost into my body, but my plastic surgeon is willing to fix it
for me. Since I have met the deductible
for the year it won’t cost us anything out of pocket.
This procedure will just bring all of the skin flush, I don’t
think it will change the actual appearance of the scar (but I am hopeful). The other thing is that I will be awake! I was awake during my port removal – you may remember
that my amazing friend Courtney had them play New Kids on the Block for me
during the entire procedure. I wonder if
Dr. Stanwicks would be willing to do that for me too?
I cannot begin to tell you all how much you mean to me. From time to time I still receive get well
cards, and prayer cards. Sweet texts and private messages, they all mean more
to me that you could possibly imagine. This
year I have met many new warriors, too many.
My heart both swells and breaks each time I am introduced to a new
survivor. I am thankful beyond words to know
them, to be entrusted with their stories and friendships, but heartbroken that
they will need to endure the beast of cancer.
Continue to hold us in your hearts. Never forget to smile at strangers and hug
the ones you love.
#fightlikeamommy
#itisstillmyfairytale
Friday, July 21, 2017
Remembering My Final Chemotherapy Infusion
It occurred to me yesterday morning that I had never posted the bulk of the pictures from my last chemotherapy infusion. I have been so open and honest about my journey with cancer, but these pictures are different. These pictures speak to my soul in a way that is difficult to put words to, even now it is hard to see through my tears to see the computer screen.
There is immense joy in these pictures. Look at us laughing and smiling through tears of absolute joy. I cherish the joy in all of our smiles, even when there are tears making our eyes sparkle. I made it through 17 chemotherapy infusions and five surgeries, I promise that I could not have done that without your help, without your love.
Cancer is hard. I didn't have any tangible experience with Cancer until it was me going through it, it was like all of life's true struggles - you just kind of get thrown in. There isn't a pause button, or time to stop and catch your breath. From the moment of diagnosis there is one goal, to survive. For me that drive was so strong, and re-enforced each and every time I looked at my babies.
They were so young when I was diagnosed, Elayna was 4 and Tommy was 7. My biggest fear was (and is) that Cancer will steal me from them, that they wouldn't remember me. I remember spending hours in the beginning of my journey with cancer trying to conjure up my first memories, the earliest ones to test myself and see if I could recall anything from their ages. I found that my memories were all fairly scattered and blurry until about age 10. That struck a terror in me that I never talked about, but that I am sure was apparent to anyone who was watching. I did my best to fill our days with love, laughter and magical memories, just in case.
It was about halfway through my infusions that I got the notion that I wanted to dress up like a princess for my last treatment. I mentioned the idea to my sweet friend Christine and immediately a plan flew into action. It is pretty spectacular to have someone like Christine in your life. She set a a series of events into motion we invited everyone to come celebrate dressed as a princess, or dragon slayer, or just as themselves to celebrate my victory. My last chemotherapy treatment.
I remember explaining my idea to the nurses at the Virginia Cancer Institute, I can remember them smiling and saying that it was okay. I don't think they had any idea just how big the celebration was going to get.
There is immense joy in these pictures. Look at us laughing and smiling through tears of absolute joy. I cherish the joy in all of our smiles, even when there are tears making our eyes sparkle. I made it through 17 chemotherapy infusions and five surgeries, I promise that I could not have done that without your help, without your love.
Cancer is hard. I didn't have any tangible experience with Cancer until it was me going through it, it was like all of life's true struggles - you just kind of get thrown in. There isn't a pause button, or time to stop and catch your breath. From the moment of diagnosis there is one goal, to survive. For me that drive was so strong, and re-enforced each and every time I looked at my babies.
They were so young when I was diagnosed, Elayna was 4 and Tommy was 7. My biggest fear was (and is) that Cancer will steal me from them, that they wouldn't remember me. I remember spending hours in the beginning of my journey with cancer trying to conjure up my first memories, the earliest ones to test myself and see if I could recall anything from their ages. I found that my memories were all fairly scattered and blurry until about age 10. That struck a terror in me that I never talked about, but that I am sure was apparent to anyone who was watching. I did my best to fill our days with love, laughter and magical memories, just in case.
It was about halfway through my infusions that I got the notion that I wanted to dress up like a princess for my last treatment. I mentioned the idea to my sweet friend Christine and immediately a plan flew into action. It is pretty spectacular to have someone like Christine in your life. She set a a series of events into motion we invited everyone to come celebrate dressed as a princess, or dragon slayer, or just as themselves to celebrate my victory. My last chemotherapy treatment.
I remember explaining my idea to the nurses at the Virginia Cancer Institute, I can remember them smiling and saying that it was okay. I don't think they had any idea just how big the celebration was going to get.
I am so very thankful to be here a year later writing this post to you. I have poured over these pictures for the last two days remembering being cloaked in so much love and kindness. I am so blessed to be counted as a survivor. Thank you all for your love, for your friendship, for your words of encouragement, for your prayers, and most of all for your kindness towards my family.
Today was breathtaking, it was a spectacular anniversary of my last chemotherapy infusion. The kids finished the week at Vacation Bible School. If you have been following our journey you may know that it always seems that VBS weaves its way into our lives in the most magical of ways. This week Tommy and Elayna had to look for God Sightings. God Sightings are when you see God in your life. My beautiful, brave little six year old stood before an entire congregation and told them my story. I wasn't there, so I don't know what her words were - but I do know how proud her brother was of her for talking about it. He was beaming when he told me.
She made this to go on the display for all of the parishioners at church to see this week.
Please continue to spread light and love in the world, be the change that you want to see.
#fightlikeamommy
#itisstillmyfairytale
Special thanks to Rachel Kurtz for the amazing pictures, you truly captured the essence of the day!!
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