Monday, July 7, 2014

Chemotherapy has started - let the fun begin!

Happy post Fourth of July!  I’m thrilled to report that almost two weeks into treatment I am feeling great except for the few days right after chemo.  I now feel better about making some summer plans but we are taking each day as it comes and working around treatment schedules.

No wig!  My new hairstyle for a few weeks
My first chemo treatment was Tuesday, June 24th.  Mike and I were at the Mayo Clinic almost all day.  My chemotherapy is called TC chemo which stands for Decotaxel (T) and Cyclophosphamide (C ).  It actually takes about 3 hours to intravenously inject but there seems to be many steps before it actually starts.  It was surreal to sit there with Mike and look around and see people of all ages who have to do this week after week; some without anyone at their side.  I am again reminded how lucky I am to have Mike, my family and all of you.

Monday, prior to chemo, I had my blood drawn to check my white and red cell count.  This will give doctors as my baseline throughout treatment.  The chemo, as you probably know, kills the cells as they are dividing, both good and bad.  So, there is about a one-week period where I am more susceptible to infection than other times.  The Monday, Tuesday and Wednesday of chemo treatments, I actually feel AWESOME.  They give you a steroid; which made me want to organize my house – my idea of FUN!  After, this first treatment, Thursday and Friday were pretty tough, but I rebounded Saturday and Mike and I joined friends at Steak44 for dinner.  So, it is basically and up-and-down, day-by-day, process.

My next three treatments will be July 15th, August 5 and the last one will be August 26th.  I will take a break after chemo before beginning radiation.  I think lots of progress has been made in regards to chemotherapy.  The doctors really try to help control the side effects as best they can with other drugs and suggestions on how to take care of yourself and your body at this time.  The day after each chemo treatment I will be given an injection called Pegfilgrastim, which helps my body make more white blood cells to fight infections.  YOU will not believe it, but this little shot alone costs $10,000!  It is crazy!  But, we are committed to following the doctor’s recommendations.

Okay, well I hope I answered some questions and also hope that you feel a little bit more educated about breast cancer and my treatment.  Thanks for reading!  xoxoxo



14 comments:

Monica said...

So happy everything is going well! You are one strong lady!! xoxo

Monica said...

So happy everything is going well! You are one strong lady!! xoxo

Unknown said...

Hey Katie,

Such super information and so glad you are feeling great! The sharing of your experience means the world.

Sherrie said...

Great mindset dearest Katie - true grit!!

Gee Gee Entz said...

One down and three to go.
I am thinking of you every day.
So glad to have your update and know your progress.

Dee Trent said...

Thank you for sharing your journey, Katie. We thank God you are doing well & Mike is by your side. Stay strong. Jeff & I send you love!

Karen said...

Hello, so glad you are feeling well!! Pat said you are considering coming to the wedding! So exciting! We will have a place for you even if you let us know the day of the wedding!!
Love, Karen

Sara Lee said...

Oh Katie..........praying for your health!!! You are an inspiration!! Love your new hair cut!!! XOXO

Terry and Sara :)

Karen said...

You can even just show up!

Kathy Petsas said...

Hi ! So glad to read your upbeat attitude is in full swing, as are your great organizational skills.Bill and I are thinking of you often and know your inner strength and great support will win the day. love to you and Mike. KP

Lucy Keough said...

Dear Katie,

You are a very brave woman to share your experience with your friends and family. I could never put into words what my husband and I experienced during his treatments. One thing I can say is that having Mike by your side every step of the way has it's own curative benefit. You are loved and there is no substitute for that. May God hold you and your family in his arms during this journey. Love and prayers, Lucy

Unknown said...

Hi Katie,

Just heard about your journey with cancer. Please know that you are in my daily prayers. Keep up the good fight!

Hugs and kisses

Gina Turiano-Arambula

Anonymous said...

Katie - you have courage to take on any challenge and a soul that beats with joy. We can tell that Bella knows this better than anyone. She is a lot like that too.
We want to help you, Mike and Bella in any way we could. Just ask.
May you feel the support and prayers that surround you,
Tom and Tammy

Unknown said...

Hi sweet friend! Thinking of you and sending love and support! Patti Green