Thursday, November 26, 2015

I'm Moving

Hi Friends!
I am moving. I am now the proud owner of www.cathykhayes.com. So head on over and continue to follow my story there.

XO,
C

Monday, November 23, 2015

Through All Of It


Every day, fighting breast cancer becomes a little less scary. I have already made it through my first chemo topped with a dose of Strep Throat and I am still going. The only other side effect that I am experiencing right now is dry cracked lips. I could barely open my mouth to eat this morning without pain. After calling my oncologist this afternoon, her solution was Lansinoh, something I used for dry cracked nipples while nursing my babies! So weird, but she was right and it's working. I am so thankful to feel good other than this small annoyance. I am not even scared of loosing my hair anymore. I have the date set for my buzz cut, as my hair will begin to fall out after my next treatment on December 3rd. I am sure it will be emotional, but I am not afraid.

 There is always something to be grateful for. 

I was able to be loved on again this past weekend, to spend time with my (SOFLO) south florida girlfriends. Of course I always want to get away, but I didn't realize how much I needed it until I got there. I laughed, I cried and I danced...and it felt good. I shared my heart and that felt good too. Many times my eyes aren't open to my own behaviors and habits until I hear them back from my friends. The friends that love me the most. This weekend I told them about my fears of going through chemo without my spouse by my side. I cry when I see a husband holding his wife's hand in the waiting room, I tear up in the valet when I watch a husband open the door and buckle his wife in the car safely. I told my friends I wasn't looking forward to the holidays because everything will be so different this year. My ideals are wrecked and everything that I have had in the past is gone. I have to accept a new normal, and find joy in that all while fighting breast cancer at the same time.

Something else I am learning:
Don't ever assume that what you feel in your heart is the same as what someone else feels for you.

I talked about how I wish I could be harder, less giving of my heart and less needy of a partner and emotional support. They reminded me that I can be needy right now, but I need to depend on the right people. God first and safe people like my family and friends who want to help. They also told me not to change, to keep my heart soft and open to loving and giving to others...BUT to put up some DARN boundaries and stop letting people take advantage of me! I made a small step toward that on Sunday and it felt good, letting go of something that I really never had in the first place.

I would be a fool to think that there won't be more pain coming, but I refuse to let it steal my joy one more minute. I'll give my heart, but I'll give it to friends and family that will protect it. I will accept that the holidays will be different this year and enjoy every minute that I have with my children, friends and family. I will release my ideals and pray that God will replace them one day with something so much more than I can even imagine. It really is the only way, He's been here through it all of it. Take a minute to watch and listen:






Monday, November 09, 2015

153



153...the number of cards I have received since my breast cancer diagnosis. When I see these cards they remind me of the unconditional love that is surrounding me and supporting me. Even when I feel so alone that I can barely breathe. This has been such a painful rollercoaster ride. Waiting on a plan and having the plan change multiple times. I am emotional and irrational 98% of the time, but I am amazed that I'm not in a psychiatric ward after everything I have been through over the past six months.

I have a confirmed plan now. This Thursday I will start chemotherapy to attack my HER2 positive breast cancer and make sure that there is not one cell left in my body. Four rounds of a triple whammy consisting of Taxol, Carboplatin, and the targeted drug Herceptin. My infusions will be every 3 weeks. I'll be done with the chemo by January and then I will finish out the year with Herceptin infusions every three weeks. It'll be no picnic. I am still terrified no matter how many people tell me I can do it. I don't want to, but who does? So many amazing women have gone through this before me, how can I stop fighting now?

I lived in a tad bit of denial this weekend. I went to New York, to pretend like I didn't have cancer. It was fun, but on the drive back home from the airport I lost it. It felt good to escape and feel normal and not sick, but coming back to reality felt empty and scary. After surgery, I kept praying the plan would change again and I wouldn't need poison pumped through my body. That didn't happen, so I didn't want to think about it. I just wanted to have fun...and I did, but reality was still waiting on me when I unlocked my car to drive home. It didn't make the cancer go away, and it didn't cure my loneliness.

I was able to regroup early this morning. I prayed instead of denying my situation. I asked God to show me how to handle the cancer with grace—and to use him instead of running toward distractions. After all, I am learning that the distractions aren't there for me when I feel low afterward. Reality will always return, and I have to accept that this is my life right now. I have to learn to lean on those that I know really care about me and what's best for me. Those who love me to the fullest no matter what I am capable of giving them in return during this season.

When I was praying on the way home, this song came on. It spoke to me and I wept. He his my revival, not distractions or denial. XO, Cathy