She talked of them incessantly.
She went through radiation, chemo, another surgery, more radiation, more chemo, and finally last fall, had a chemo port put in her chest because her little veins were to beat up.
All the while comforting everyone who was worried for her and her family.
Never complaining. Just comforting.
Even though she had a headache for 5 years.
5 years. I start crying and demanding comfort and sympathy at 5 hours of a migraine.
That is the truth.
There were plenty of ups and downs from August 05 to May 10.
Remission, and then tumor growth, no growth, more growth. Tumor gone, and then back.
She wowed her doctors, and beat the odds.
All with the knowledge that nobody had ever survived this cancer.
Just imagine for a minute, raising your kids, and going about your daily life knowing you are going to die way before your time.
Watching milestones of your kids, and wondering if you will be around for the next one.
Talking to your kids, and prepping them for the days that will come without their mom.
Plays, awards, vacations, graduations, weddings.
And even more, the every day things.
Days that TT will come home from school crying because she had a fight with her friends. Tayland not being picked to play at the lunch time basketball game.
Everyday heart aches that inevitably come with raising kids.
She wont be there to be heatherjoish to them. Help them. Comfort them. Love them better.
How do you go on with your life with such an amazing disposition?
I don't think I could.
She did.
Last summer we took our girls to the Miley Cyrus concert.
We had such a good time.
The words to "The Climb" changed dramatically for me that night as I looked over to see Tt sitting on Heathers lap. Cheek to cheek, as her mommy sang the words in her ear.
Over the holidays 2009 she began to get worse.
Another tumor had popped up behind her ear, on top of one of her sensory nerves.
This made it hard for her to walk without motion sickness, and especially to be in a car.
Even then, she put how she was feeling aside to fly to New York with Bradford and Tt.
This was January of 2010
She wanted to take Tt to Broadway.
Memories. She wanted to make memories.
Im sure that was such a tough trip for her.
In April things got really bad. She was back to feeling the way she did before they initially found the tumor. Throwing up 30 plus times daily. Nothing could touch her headache.
On April 14th Hjos mom, Kathryn, called just as I was on my way home from work.
Bradford was at play rehersal, Kathryn had strep throat. With Heather being on such high chemo doses she didnt feel like she should be the one to help her that night with the kids.
She said she felt prompted to call me.
I immediately turned around and headed to Heathers.
I stopped and picked up movies, cheetos, and gatorade for the kids.
We had a great talk that night.
Mind you, she was still her. She was still lucid and sharp as a tack.
She just couldn't get out of bed much.
We laid on her bed and talked. She told me she knew the end was near.
She said she was tired, and that she felt like she was sick of being sick.
She asked me to be in her kids life forever.
To always make sure Tt knew what was fashionable. Also, to help her to become a strong independent female. She said she had always admired that about me.
She wants me to make sure that her daughter is not a door mat.
She asked me to make sure that we help Tayland if he wants to play sports. Ryan played major league baseball, and she asked if he would please coach him if he so desired.
Bradford is full of amazing talents. Sports are not one of them.
She wanted to make sure that Tayland had all the options he wanted for his future talents.
Just when you think all of your daily responsibilities are overwhelming.
Try being restricted to a bed delegating the whole lives of your children.
I tucked all 3 of them tucked into Heathers bed are started "Where the wild things are."
As I was leaving, little Tayland told me he wanted a snack.
I went out and got him the cheetos.
He told me that is not a snack.
Tayland had his top 4 front teeth knocked out last year when he feel against a cement wall.
He is not the easiest to understand.
He gets frustrated, naturally, when someone can't understand him.
Well I couldnt.
A cheeto is a snack in my house. Or a bowl of goldfish.
Heather fondly petted her sons head cooing for him to calm down.
She explained to me that a snack at their house is a plate of grapes, cheese cubes, and crackers.
How will anyone know that! How will anyone know what Taylands snacks are?
His mom was going to be gone soon, and nobody would be able to help him communicate what a snack is. I prayed to God to please let her stay here with her kids. They need her.
This is not to minimize Bradford. He is a wonderful dad. He really is. He is so good and patient with his kids. He is a really close second to a mother. The only problem is, Heather Jo makes him who he is too. What would he be without her? Could he still be his functioning self?
After I left that night I got this text from Heather.
Thank you for stopping by tonight, those efforts are really the things that make it all worth it.
Sorry for complaining so much.
She didnt complain once that night.
What an angel.
She had an MRI 2 days later. April 16, 2010. They gave her days to live. The cancer was everywhere. They would be managing her from home with hospice.
On April 27th I woke up to this Hjo text
Dude-I love you and havent mentioned it yet today.
How lucky I am to have such a friend in my life.
Bradford limited her to just family. I am eternally thankful to him for considering me as such. I love both of their families. They are awesome.
Eclectic and awesome. The most talented bunch of people around.
Heather Jos mom is in the Mo Tab.
Let me tell you about her.
Kathryn
She was married and had two daughters.
Her first husband died of a heart condition.
She remarried and had Heather
When heather was 12 her sister Lisa unexpectedly died of the same heart condition.
Her sister died of cancer (Kathryns)
Her oldest daughter April has the same heart condition
And now Heather Jo. Given days to live.
You would never know she has endured so much loss. She has white hair down to her waist.
Big white teeth that are always showing because she is always smiling
Her skin looks like that of a 20 year old.
She is a woman of god and emulates it wherever she goes.
No wonder she raised such an amazing daughter.
The week of May 10, Hjo geared up for a final trip with her family. She was in a wheelchair by this time, and her cohearency was a little comprimised. Just a little.
They went to Vegas to be pampered by her wealthy uncle.
Their suite had a hottub on the balcony.
They made more memories.
On May 12 Bradford sent out this text
Four little Garrisons sitting out under the stars and palm trees singing lullabys, laughing and eating cheesecake. We will remember this forever.
Again. I am so grateful to be considered privy to these precious moments.
After her last awful diagnosis, we spent I spent a lot of time with her. We had a lot of fun.
We went to the mall. Had dinner. Manis. and took our kids to one last dino land visit.
We went out for our favorite melting pot visit.
We layed in bed and reminiced.
On Sunday May 16 Billee and I saw our sweet little Hjo for the last time.
Nobody should see someone they love like that.
She had deteriorated so fast from the prior Tuesday that we had spent at the mall.
She couldnt see.
She was laying flat down.
She was so thirsty, but couldnt keep anything down.
The liquid morphine given to her burned her mouth, only to be thrown back up minutes later, giving her no headache relief.
It was awful.
She didnt make sense all of the time, but was able to share a few old memories.
We laughed.
Although through wet, snotty tears.
When we all worked together at The Springs, we would play this game when we were slow.
We would say, "pretend you just found out you have herpes". Then we would make a face, and take a picture with our camera phone. They were always halarious pictures. She wanted to play that game on this Sunday. The pictures were still halarious.
She started to become obviously fatigued. We told her it was okay, that she could go to sleep.
She said she didnt want to, because she knew it would be the last time she saw us.
It was.
On Monday May 17 Hospice put her on a morphine patch.
She went to sleep.
On Tuesday May18 I received this text from Kathryn
Our dear sweet Heather Jo slipped peacefully away at 830 this evening. It's finally over.
She went just the way she wanted to. Peacefully. At home. With her family.
I went to visit Bradford and the kids the next day.
Death is the weirest thing. It is so so hard to know what to say, how to act. Even how to feel.
It is still weird to me that she isnt here. I think I still feel her around, but again, thats a weird thing, and its hard to know. I sure miss her, and her sweet texts though.
Her memorial concert was held at Hale Center theatre. A theatre in the round.
It was very intimate
It was held on Tuesday, May 25, 2010.
Her 29th Birthday.
It was amazing. It was chalk full of her talented inner circle
Every song was hand picked by Heather.
A gift that she orchastrated for her family and friends.
One last act of compassion and kindness.
Pianos, guitars, acapella solos, slide shows and comedic acts.
I would like to think I would have been asked to be a part of the concert, but I dont actually have any talents. :)
They had HJo's body creamated so that they could take her with them wherever they went.
On her Urn it says this
You are the pearls I could not buy
You are the trip I did not take
You are my piece of forgien sky
You are my blue Italian lake.
She picked that out. Beautiful huh?
Since then, I have still been blessed to be a part of Heathers life.
I am in contact with Bradford almost everyday.
Over memorial weekend, we took Tt to Mesquite with us.
Made cookies and crafts with Grandpa
(we established shared grandparents long ago)
Tatum taught her how to swim.
She taught Tatum manners. (or tried hard anyways)
She won the dance contest at the pool.
She was patient and funny with my step dad and uncle who only call her Jo.
She answers only to that when around my family. Embracing anything that comes her way.
If someone called Tatum a boy name, she would freak the freak out.