Monday, January 18, 2016

He's Amazing

My husband, he is amazing.
He has a very important roll at Nationwide.
He is a father.
He is my husband.
He takes his personal time to pursue a 'acting career'... :)

On the 23rd, he has his opening night of "Caucus: The Musical"....
He's playing a Presidential Candidate.
It's advertised on the big screen outside of the Civic Center.
This is a big deal people....a big deal.

He comes home from a stressful job.
He eats dinner and checks on me and Mary.
He heads to rehearsal.
6 days a week for the last few weeks.

I'm so proud of him.
It takes a confident person to enter the world of entertainment.
He takes it very seriously, but has so much fun.
In August he did The Soldiers Play.
It was amazing.
He did sooooo awesome.

Now he's doing Caucus, and even though completely different then the last play he did, he's enjoying all of it.
Mary and I miss him.
It's hard when he is gone so much, but I know when we see him on stage, singing, dancing, enjoying all of it, it's totally worth it.

My husband is amazing.
I am continually proud of him, admire him and have his back.

I hope everyone takes the opportunity to go see the play.
It's going to be awesome!

Image result for caucus the musical 2016
http://www.desmoinesperformingarts.org/events/other/489-caucus-the-musical/

Sunday, January 10, 2016

Guest Post from Jerry Jr - My Trip with Dad

My Trip with Dad
By Jerry Brantley, Jr.

Sometimes you think you are doing something to help someone.  Sometimes you think you are called
upon because people need you.  I feel that way often.  My wife needs me, my daughter needs me.  I am there to help my friends when they call, I will be there for family, etc.

Today I took my dad to Iowa City to visit with Medical specialist to discuss how they are going to treat his cancer because I thought he needed me. He had called me a couple of days ago asking if I was busy Thursday morning and to tell me his wife could not take him and wondered if I would go.  I told him let me check my schedule and I would call him back.  Now you may be thinking what kind of asshole tells their dad that they have to check their schedule, but I am that kind of asshole.  I honor my commitments, and I wanted to make sure that I hadn’t agreed to do something in that time frame.  My word is my bond!  I got home looked at my calendar saw it was open, and called Dad immediately and said I will be there. 

Last night before leaving I had a bad feeling, I kept thinking there is something I don’t know, something Dad is not telling me, he doesn’t usually ask for stuff like this.  I am wondering if he wants to use the 2 hour drive to tell me something.  I wonder if there is something that he knows that doctors are going to say that he needs me to hear first hand.  I told my wife this and she said, well make sure to go and ask a lot of questions and hopefully you will get answers. 

We left at 6:00 am this morning, and made the drive from Des Moines to Iowa City.  The drive was
smooth, not a lot of traffic and Dad and I talked the whole way.  About Sports, about life, and he also for the first time let me in on the things he goes through battling his cancer.  It has given him lesions on his skin, that itch terribly, to the point where he has to take sleeping medicine (that doesn’t work) to get to sleep through the night without itching.  He still wakes up itching, and also the skin growths fill up with puss, that will leak on to his pillow or hand, so he sleeps with a rag in is hand so that he is not leaving puss everywhere.  He also has these lesions in his ears and can’t reach them, there other more gruesome things I will leave out.  I wouldn’t describe my dad as vain at all but he has always taken pride in his appearance.  So much so that two years ago when I showed up to his house at 33 yrs of age, and I had on brown wingtip shoes that were scuffed I got a 30 min lecture, and spent the next 20 mins shining my shoes.  To this day I now don’t wear my wingtips outside to avoid scuffing them.  One of the things about his disease that affects him the most is the fact that he doesn’t like what he sees in the mirror.   It’s easy to tell someone that you don’t care about how they look, that you love them and just want them to be healthy, but in saying that we forget about the person actually suffering.  I had said that before to my dad, and I apologized on our ride up.  Not because he was upset, or even pointing out that it bothered him, but because as I reflected on it and put myself in his shoes, I would get tired of people saying Jerry we don’t care about how you look we just love you.  I would be thinking the whole time well that’s nice but I F&*CK*&G CARE ABOUT HOW I LOOK!!!

We got to the hospital and started walking into the Cancer Center.  This as I said earlier is the first time Dad had asked me to come along, so it is the first time I got to make this walk.  I will tell you when I saw the words “Cancer Center” a wave of emotions went through me.  I felt my stomach drop like I was on tip of a roller coaster that was heading downwards.  I wanted to tear up, but I fought it back.  Brantley men are tough, and I was there for my dad.

We got to the office and were called in.  A very helpful nurse came in and took information.  She gave him a gown and asked him to change.  When she left he asked me not to be too grossed out from the things all over his body.  I thought you are my Dad you could have a second head growing out of your belly button and I will still love you.

Later a Resident of the facility came in.  She said she had read the chart but asked dad the main reason he was here today.  This as you may understand irked him a bit.  He has been suffering with this rare form of cancer for years.  He has seen many doctors and had been misdiagnosed with Eczema, Psoriasis, and MRSA infections.  Finally when nothing was helping he went to an ER Dr. who sent him to Iowa City where they finally figured out it was a cancer - Mycosis Fungoides Lymphoma.  This is a very rare disease which is why it was not diagnosed properly.  So he has had many trips to Iowa City, has had pictures taken, biopsies taken, been poked and prodded and whatever you could imagine.  So when the young resident asked why he was here today, he grew a little agitated.  He explained a story that I could tell he has told time and time again, and ended by saying, “I am here because I want to get some answers on treatment, I am a little tired of being poked and prodded and not hearing anything.”  She assured that when we left today they would prescribe a treatment.  She was going to go talk with the other doctors, a skin specialist and a Hodgkin’s Lymphoma specialist, to put the game plan together. 

At this point my dad and I both relaxed.  The two doctors came in later accompanied by the resident.  The first doctor had my dad go through his story again, to be thorough and make sure they understood the full picture.   Dad told the story less agitated this time because he knew that something was going to come out of this.  I can’t imagine how painful his wait has been to get a treatment.  The doctor explained the reason it took so long is because they had to get all the facts, and really look at the puzzle to make sure they fully understood what Dad has and the best way to go about.  How severe it was, what “flavor” of cancer it was (which was his fun way of saying what are the cells doing and attacking), which dad asked “So do you think strawberry or watermelon!!” and ultimately the best way to fight it.  The second doctor had not said anything really but his foot had not stopped tapping the whole time he had been in there.  So the first doctor turned it over to the second who was the specialist with Lymphoma.  His first words were “since reading your charts and now seeing you I have been chomping at the bit to get to you.  I can tell you are in pain and I am confident that we can treat this and control it.  It is not curable, but it is controllable.  There is something comforting about a doctor that’s excited to get you taken care of; who realizes that you are suffering and wants to help.  I also appreciated the word “controllable” in that sentence because to me that meant it was not life threatening. 

Since I heard my father had cancer, and the doctors thought it could have spread in his body, I had been consumed with the thought of losing my father.  How I would make sure my little brother and sister were ok, what would I need to do to take care of family, basically writing his eulogy in my head.  I know if he goes I am the patriarch of the family, and that is a duty I don’t take lightly.
It had been on my mind so much, that without knowing I think it closed me off a little to family and
friends.    I cried the day I heard about it, but then really didn’t want too afterwards.  I didn’t talk about it a whole lot because that made it more real.  One of my best friends even called me out saying “you haven’t said boo about your dad since you told me he had cancer.”  I simply said I wasn’t ready to talk about it.  I even found myself down a little at Christmas, I thought it had something to do with not feeling like I gave my wife and daughter enough this year, but now I know that was not it.  I couldn’t fully enjoy the holiday not knowing what my dad’s fate was.

 My dad was prescribed a pill form of Chemo; that will hopefully help.  I say hopefully because being a specialist he let us know that the treatments prescribed may or may not work on different patients, and they have no way of knowing until they try.  “We will try X and it doesn’t work we will try Y, if Y doesn’t work we will try Z, but we will figure it out.” My dad and I were both excited about the prospect of him getting this treated.  We thanked the Drs. and were on our way. In the car ride home we stopped at the diner, we talked more sports, Dad shared stories about watching me play football in high school and college, and how proud it made him.  We talked about marriages plural as we have both been married multiple times, and we talked about leadership and life lessons.  He said one of the things he appreciates about me is that I am a consummate professional, I need things scheduled, which is why he was never mad when I told him I would check my schedule…”you have
always been that way.  When you were a kid you were never late, you always did what you said you
would.  I have always appreciated that about you.”
He also told me something that hit me like a 100 lb weight.  Truth be told I had been worried Dad had
not been as aggressive as I would like getting answers, I told him before I left Christmas night, that if he didn’t have answers by Jan 4th, I was taking him to the Mayo Clinic in MN.  I am not defiant or
authoritative with my dad.  He is and has always been my hero.  But this time he said he could tell I was serious and he wasn’t going to fight me.  So during our drive home he told me “son thank you for driving me today.  I knew this would be a good trip for both of us.  I hear how serious you were at Christmas and I wanted you to meet the doctors and see the people working with me, and know that I am getting good care, and I knew if you heard it yourself from them it would make you worry less, which would help me worry less".  WOW!  My dad fighting cancer, going through stuff that as he described he would rather have four hip surgeries then go through, wanted me to take him not because he needed it, but because I needed it. 

Again I was rushed with emotions, but I didn’t tear up… Brantley men are tough. 

Our ride home was great, Dad and I had not spent this much time together in a long time.  I dropped
him off he thanked me again, and this time I thanked him.  He walked into his house I backed out of the driveway, and I cried.  I cried for 25 damn minutes on my way home, I am crying as I type this right now.  At first I thought why am I crying, and smiling at the same time?  Well sooner or later the emotion you hold in makes it way out.  It has been knocking at the door for a couple months now, and finally I let it out.  Happy tears, because my dad is ok, tears because I am in awe of a man going through cancer who has enough love for his son to bring him on this trip to help him see.  Sad tears because I know I haven’t been the Husband, or father that I could because my mind was preoccupied.  I blamed it on being busy, work, life etc.… but really it was because I just hadn’t been happy.

So I thank my Dad.  Thank you for asking me on this trip, thank you for knowing your son.  You will never have to fight this alone, I will always have your back, and I hope to mean to my child or children what you do to me.  He said to me that as men grow older we grow in wisdom.  We look at things differently.  I can honestly say, I took a trip today, which changed me forever.

Wednesday, December 30, 2015

5 Years

It's been five years since I've heard your laugh.
I think that is the hardest part.
That laugh was... original.
Entertaining.
Infectious.
It wasn't a sound I thought about until it was gone.

5 years is a long time.
Lots of things change.
Life goes on.

However, I do not think a day passes where I don't have at least a moment that I think about you.
It may be brief, just a slight flutter in my brain.
Or a whole car ride home by myself.
I have come to the conclusion that you will never leave my mind.
I used to try and force you out.
Mad at myself when you entered.
Then I realized, ignoring those thoughts, was just a try at controlling an uncontrollable situation.
Grief.

It's been five years and I believe I'm past the stages of grief.
Denial.
Anger.
Bargaining.
Depression.
Acceptance.

Denial: When you first died, I was sure it was some kind of practical joke.
You'd show up any minute at the bar and say something stupid like "YAHTZEE!"

Anger: WHAT THE FUCK WERE YOU DOING!!!??? This one hit hard. I was already mad/disappointed you hadn't come to my 30th birthday party. You died when I was mad. Goes to show, you never know what might happen, never hold on to anger.

Bargaining: I begged you... BEGGED you to show up in my dreams. I said I would move on. I'd do good things, I'd be a better person... I  just NEEDED to see you. I am not a religious person.... but I know I attempted to make deals (bargins) with God to just have you back....

Depression: I suffer this bitch anyway... but it was deep. I changed. I cancelled plans. I drank constantly. I disappeared into the grief and didn't want to come out.  In the grief I was closer to you.

Acceptance: I know you are gone. I know I won't see you. I know you will always be apart of me though, because in your own fucked up way, you taught me so much about myself during the 7-8 years we were friends, roommates.

So here I am... 5 years later, remembering VIVIDLY the phone call telling me you had died.

I know....
I will never listen to certain songs again. (Dirt Road Anthem, Over You...)
I will never enjoy Southern Iowa, 4-wheeling or dive bars like I used to.
I will always miss you, that smile and that laugh.

I miss you and I always will.





Thursday, December 24, 2015

Merry Christmas Eve!

It's cold.
It snowed.
The ground is covered in white.
The PERFECT Christmas Eve.
Sitting in the living room with my husband and my dogs.
Mary is with her mom on Christmas Eve....

My Christmas gift from my parents is in the basement.
A treadmill they gave us money for a few months ago.
I bought on Craigslist, it's pretty nice actually.
I've used it... a few times... since August.

My gift from Jerry is on my finger.
He took a ring of my Grandma's and had it reset for me.
It's an opal.
It.Is.Beautiful.
I held back tears when he gave it to me.
It is a birthday and Christmas present.
So we sit here on Christmas Eve, looking at the presents under our tree.
There is not a lot.
Mary got a few things from Dad and Holly, some expensive, some not.
Jerry has a few gifts from me, but his main gift is a new smoker/grill, which we do not have yet.
As I said, my gift is on my finger.
I love it
I love it.
I LOVE MY RING!

We look at our tree, with very few presents under it,  thinking we should have bought more.
But...
There is thought.
There is love.
There is need/want in those gifts.
Even though the tree is not as full as we are accustomed to; it has gifts under it.
Some people don't even have that.

I know as kids we got a lot of toys and things, probably more than what my parents should have gotten us.
But it seems to be the universal symbol, that a Christmas tree is not REALLY a Christmas tree unless the gifts are PILED up beneath it.
The 3 gifts I  remember most are:
1. Red Rider Wagon (metal, not that plastic shit. Still have till this day.)
2. Chris Mutt (holiday animal Target had every year. Still have till this day.)
3. Mr. Cart.... a cart with three 'levels' that I pushed around the house (and still have till this day.)

But I don't remember much else when it comes to gifts.

I remember the scents, the people, the warmth.
F--- the gifts.
Give me those memories, the family together, the good food, the happiness that comes with the holidays.
I rather have a tree that is bare of gifts, then a house with no family.

Can I get an Amen?

 Merry the Eve of Christmas.
And please know, that the lack of gifts, never has to mean a lack of love.
Image result for the grinch who ville


Monday, September 21, 2015

F#ck Cancer

I got an email from a good friend today that an old co-worker of mine passed away last night.
I hadn't seen him in a few years.
Hadn't seen him since he was diagnosed with cancer.
My friend is obviously upset, as this guy was pretty awesome.
He was a dad, husband, friend and one of those co-workers that was always smiling.
I didn't know him well.
But I know he will be greatly missed by everyone that knew him.
Image result for cancer sucks
A old friend and co-worker was diagnosed with colon cancer years back.
She is having to have surgery again to remove some questionable looking spots. (from what I understand)
As she wrote on FB "Going to be a little more tricky than the first time as he will have scar tissue to work with and because my organs have been previously operated and disturbed. He says he'll ultrasound the entire liver to make sure he got everything."
She is the mother of two, married to a great guy and an all around good person.
We aren't close, but I care for her.
Image result for cancer sucks
A friend I worked with in my early 20's (who I haven't seen in years)...her teenage daughter is battling cancer.
This is her FB post from earlier:  "Without a successful surgery, Kenzy's life expectancy goes from below 20% to 0%. This is the ugly truth about Osteo when there is recurrence. We are not looking at statistics cause Kenzy proved all the doctors wrong last time."
Image result for cancer sucks
W.T.F?

This all came across my email/social media today.
I can't even imagine what ANY of these situations would feel like.
All I know is I am hoping and thinking of those that are fighting and those that have been left behind.
I know it's set me back emotionally - thinking of all these wonderful people.
Makes one think.
Image result for cancer sucks

Sunday, September 20, 2015

There Is No Place I Rather Be... (LAMBEAU!!)

My aunts and uncles (and a couple cousins) are at Lambeau as I type this blog.
They are watching the greatest team ever: The Green Bay Packers.

In November my Grandpa passed away.
It was a little expected....
But it's never easy.
My Grandpa was a very intelligent man.
Loved his beer.
Loved his Packers.

He would always give us a dollar and walk us to the corner store when we visited in Texas.
We would buy candy cigarettes.
It wasn't frowned upon then... and they were yummy.

My mom and dad, her brothers and sisters, with their significant others (and a couple cousins), are at the game tonight to say "Goodbye", to my Grandpa.

I know he's happy that his kids are gathered together, in Green Bay, cheering on the Packers.

I hope the Packers take the win.
But if they don't... I still know the power behind the Frederick family, the memory of my Grandpa and the night game at Lambeau is one that my family at the game will remember and cherish forever.

I know, sitting on my couch in Iowa, that I will always remember it also.

I love you, family.
I love the Packers.
Lets do this! GO PACK GO!


Friday, September 11, 2015

A Few Random Things

To start out, I love my new job.
I notice so many things about kids.
How they act.
Behave.
Tell tall tales... constantly.
And pick their noses...constantly
I never thought I was a patient person, but I have proven myself wrong.
One of my students calls me Mrs. Crazy (or Mrs. Cray Cray - and it's just between us).
She thinks I'm so funny, silly and, well, crazy.
Which I like, because she still respects me, we have fun with her school work and we still follow all the rules.
Today I didn't feel the best and when taking her to the bus she looks at me and says,
"I know you said you don't feel good today, but I hope Mrs. Crazy is back on Monday, ok?"
And she left me with a big smile.
I'm making an impact.
Image result for big smiley face pictures

I'm teaching Mary about the important things in life.
Need To Breathe, my favorite band.
We listen to it in the car and she likes most of the songs, sings a long to a lot of them.
It makes me happy.
We have started watching the first Harry Potter movie - and she is actually into it!
Loves all the magic, the mystery, the what if's...
I love that she likes it.
There are actually a lot of great life lessons in Harry Potter... besides just learning how to ride a broom and play quidditch.
Image result for harry potter quotes
She watched Captain America 2 and The Avengers... she thought Avengers was a little boring.
I am slowly, but surely converting her to a nerd.
And I'm SOOOO proud.