Just another journal entry…

It’s quiet in my house, and that means I have too much time to think.  I’m waiting on the girls to get home from the beach with Nonnie.  They left yesterday morning and are due back any minute.  Mom wanted to take Mary Clare to the Mermaid show at Ripley’s Aquarium.  She said MC sat in awe and completely mesmerized throughout the show, while McCanless kept rolling her eyes, telling her that mermaids were NOT real.  (Although, she told Nonnie after the show that she had the best day ever.)  Typical.

They had a fun evening last night at the aquarium and then hit the Pavilion rides at Broadway.  Today, the ocean was a bit rough, so they didn’t stay out long.

Even though it’s only been one night, I miss them terribly.  Although they drive me nuts some days, I miss them so when they aren’t around.  It’s almost 9 pm, so I’m sure Nonnie will need tomorrow to re-coup.  Good thing it’s Labor Day.

I’ve been reading Lucky Duck Hits Speed Bump a lot recently.   It’s truly remarkable how much better I feel just reading about my new blogging friend’s journey through breast cancer diagnosis and treatment, and still being able to be a mommy to two young girls and a wife to her hubby.  She is very open and honest and takes her treatment on full-steam ahead with humor and laughter.  She makes it clear that she understands how it’s a sensitive matter and some don’t feel comfortable being open and tongue-in-cheek.  It’s how she deals, though.  It’s how I deal.  I’m go glad to have her.

It’s easier for me to explain everything up front and tell my story once, right here.  I, like my friend, want to get it out in the open.  Why be ashamed?  Why leave an elephant in the room?  Cancer is a big deal, but it’s all around.  It evokes so many emotions and so many different reactions.  It’s interesting; I’ve learned who is curious about facts, who is sensitive, who only wants to know dates, who I can joke with, etc.   I love being open and answering questions that I know.

And if you want to know, but don’t want to ask, here’s what’s on my mind right now…

-Right now, I’m mostly thinking about my girls.  I so wish I would have been able to have the surgery/radiation route.  It would have been much easier to keep them from worrying about me.  Obviously, loosing my hair will be a pretty drastic change in my appearance.  They will notice that.  (I know that both of my girls aren’t really detail oriented, but if they miss that, I’ll have to call Ms. Irene, for sure, and get to work on that ASAP.)

-I’ve been very honest with both of them.  We’ve been talking about cancer and chemotherapy for a few weeks.  I’ve explained every detail and every step to them.  They know that the medicine that will kill the cancer will also make me tired and will make my hair fall out.  As I explained this to Mary Clare one night, she looked up at me with a smirk, laughed, tugged my hair, and said, “It’s not going anywhere, Mom.”  Needless to say, we’ve got a bit more convincing to do with her.  I just don’t want it to be a shock.

-My biggest fear is that I’ll not have the energy to be the mom I want to be.

-My second biggest fear is that my girls will be afraid of me.

-You know our generation of parents is so accommodating and is so paranoid of “screwing up” our children.  Count me in.  I just don’t want this to change who they are for the worse.  I know it will be a huge part of our family’s story.  It will change each of us.  I just hope I can help them through it all and that the impact it will have will not be a negative one.  Sometimes, I feel that McCanless grew up way too quickly as she watched, lived through her baby sister’s journey with a half-heart.  She learned tough lessons the hard way.  She learned to understand things beyond her years.  She became independent and understanding at a young age.  She learned that sometimes, life isn’t fair, but we keep going.  And again, that’s what we’ll do.  We’ll get through this, and we’ll keep on truckin’!

3 Comments

Angela  on September 5th, 2011

Good Morning Kerri 🙂

It’s Angela….and I’m so glad you posted your thoughts.

I want so badly to appear right in front of you right now to tell you so much…especially these things:

1-Your girls are going to be amazed by you! Not afraid. They are going to marvel at how you handle everything. You, your husband, and your girls will be stronger and better because of this journey that you’re on. There is not one ounce of doubt in my mind about the fact that you are already handling this in the way that your girls will feel front row and center and comfortable knowing that their mom is brave and strong.

2-You will be able to do more than you think during chemo….proof is on my other blog:
http://macandcheesetwins.blogspot.com/ Don’t get me wrong, I definitely have needed and asked for help, especially days 3-6 of each treatment cycle….but it is not as horrible as I had imagined….(had my low points and frustrating times) but still was able to take my girls places and enjoy them very much.

3-I think it is so smart of you to involve your girls and let them know anything they’re curious about. In fact, as I’m typing this, I am thinking that if you think it would be helpful for them to meet a baldy baldersox lady like me with two little girls to help them prepare, I would totally love it. …and you have something big going for you that I didn’t….you’re beautiful, cute, cool, hip and any hat, etc., that you wear is going to look awesome on you! You’re going to definitely make bald look COOOOL….

Which reminds me of another thing I want to share with you…. There’s a teenager in Properity or Newberry who is going through an amazingly difficult journey…he has some cool shirts that he designed for “bald chicks”…I bought myself one a while back… http://www.hamboneshope.com/bald-chicks-shirts.php His story is amazing and humbling.

I’m sorry to go on and on. I just want to share so much with you.

I think you’re doing GREAT and I’m here for you in any way I can be.

Much love,
Angela

chaarlow  on September 5th, 2011

You are just amazing. Your girls will be as awesome as you are when they grow up and will know they can do anything, because you are so strong! It is time for you to lean on your family, as you have done so much for yours so far! Love you sister!!

ann  on September 5th, 2011

I can assure you, they will, given the opportunity, rise to the occasion. If they are shielded and protected, they will learn to desire and expect that treatment. They will also tell you exactly what and how much they need to know – example, I was ready for a big explanation, I had books, plans, etc. (this was a leg amputation in grandfather for diabetes complications) Then 3yo daughter asks “where’s Grandpas leg?” I began with – it was sick and the doctors had to cut it off, it’s called amp….” She was gone to play – no need for the big. I would have messed up if I had gone with my plan, and not listened to her. They’ll let you know what they need! You are intuitive and know them so well. You’ll know just what they need – when I was recovering from a broken ankle, they enjoyed a lot of lying in bed and reading with me – it can be a good thing – and you know exactly how to do that.