Thursday, July 14, 2016

Last Game Before Surgery


So, cleaning fish tanks or aquariums is not for the faint of heart. I can tell you that from my newfound personal knowledge. Recently, on the Fourth of July my husband, my office manager and myself spent six hours cleaning a dried-out, gross saltwater aquarium. It was utterly disgusting!

We had taken the salt-caked rocks out, soaked them over the weekend and then on Monday, we hand washed them-one by one. The smell was like stagnant water and I will admit it, I gagged once or twice. Once the rocks were clean, we left them to dry in the glorious sunshine and attacked the gravel and tank.

My husband, Ed, hooked up the hose, pulled it around to my office window and handed it in. Mylinda and I had poured some water on the insides of the glass while Ed was hooking up the hose, oh the stench! It was ten times worse than the rocks! This was dehydrated filth assaulting our senses. We donned industrial strength gloves and Mylinda started loosening the gunk that was stuck on the glass. While she was doing this, perched on a step stool, I climbed to my perch. We noticed that the small amount of water we had added to the tank had been absorbed by the dead greenery,(that suddenly didn't appear so dead) and I started picking it up gingerly and discarding it in the trash. It now felt kind of rubbery and even through the gloves, caused waves of nausea.

I think Mylinda held her composure much better than I did as I threatened the owner of the tanks life on more than one occasion. Mylinda kept me laughing throughout and helped us stay on task. Anyway, after we picked out as much slimy goo as we could, we filled the tank. We had purchased a large gravel vacuum at the local pet store and started sucking out the putrid water. Most of you know how a siphon works. You use a hose, place it in the container to be drained, apply suction and then place the other end of the hose in a receptacle well below the height. Normally, you suck on the tube to get the process started (yuck) but this vacuum had a hand pump, yay! After getting it started, I was managing the vacuum and Mylinda was scrubbing away. Ed would take the tube and move it from bucket to bucket and then empty them. We made it through the first tankful then disaster struck, Ed had gone to dump a bucket and the vacuum tubing came apart! That nasty water spilled on my carpet. I looked at Mylinda and we both cracked up. Water had spewed everywhere and it was going to smell so bad. I told her it would be okay, I would bring my steam cleaner in and fix it right up.

Ed came in, looked at the two of us, and just shook his head. The pump wouldn't work much after that and Ed had to use electrical tape to hold it all together and I, (much to Mylinda's disgust) had to go old school and suck on that tube to get it started. Yes it was gross, but the tube was clear so I was able to detach before the nastiness got to me! We filled and emptied the tank three times that day and felt the filtering system would do the rest. So, moral of the story is - don't let your aquarium dry up in the first place!

On our other front, I've been sharing our journey after our teenage daughter was diagnosed with Papillary Thyroid Cancer, inadvertently, after an injury playing softball. It was an absolute shock. Cheyenne was hurt on March 7, 2015 and was formally diagnosed on the 20th. Now it seemed like we were on a rollercoaster with no brakes.

Last time, we were heading into the Friday night softball game on the 27th. Earlier that day, I received a call from Dr. Athanassaki, Cheyenne's endocrinologist.

She asked how we were handling things and then said, "I wanted to let you know the tumor board met and we would like to schedule the surgery for Good Friday. Will that be okay?"

'Boy, they aren't playing around,' I thought. "Yes, my office manager said we would work around anything and school will be out for the holiday anyway. We said this had been a God thing and Good Friday fits right in."

She went on to tell me that they would also be scheduling Chey for another ultrasound before the surgery at the radiologist’s request. "Alright then," she said. "Alli will call you with all the details" and with that, we disconnected.

As usual, Alli called back promptly later that day, and gave us all the details for the upcoming appointment. We were to arrive in Houston on April 2 and we would meet Chey’s surgeon, Dr. David Wesson, have the ultrasound and then the following morning she was going to surgery. Oh my little heart was going pitter-patter, pitter-patter again. Chey had surgery before, on her foot, but this was a totally different ballgame and I was frightened. I started making a mental checklist of things to ask the surgeon, how long would it take? Would you be able to tell if it had metastasized? What happens if there was other disease in her neck? What about her vocal chords? I had to tell myself to stop, just write down the notes and ask the doctor when you see him. These were things Dr. Google couldn't tell me. I called my husband to inform him and we decided we would tell Cheyenne after the softball game that night.

After work, I met my husband and we hauled it to Eastland for Chey's last Friday night softball game. They were due to have another game the next Tuesday but when we got to the game Cheyenne informed us that game had been moved to a later date. So we had to tell her this was her last softball game.

"They've scheduled surgery haven't they?" She asked me.

I said "Yes, next Friday on Good Friday."

I could see the instant fear in her eyes as she quickly looked down to the ground, she took a deep breath and waddled back to the dugout. She was already in her catching gear, minus the helmet. I did what I always do, I got my books and went up to the announcers booth and got all the names of the other team and their lineup. I waited for Coach to give me ours. Then I sat down and tried to absorb every moment, every movement, every sound, every smell of this night. I watched Chey warm-up wondering how would she play knowing this was her last game, what would happen?

I told you earlier the girls had been struggling. At the last game they played hard and together and they lost by one run. It was tough, but they played well and we wanted to see if they could put two games together and they did. Chey had a pretty good game considering everything she'd had to deal with - an injury, a cancer diagnosis, an impending surgery and all the hell going on with the school in the grievance. She went two for five with two RBIs, one run scored and eight putouts. Not bad at all! We went into the bottom of the sixth tied up at four each. We got the first two outs but then after a couple good hits on their part, and three untimely errors on ours, they went up by four. We had our half of the inning to try and tie it up or better yet, win it!

We started the inning with a double to left, followed by a base on balls. Then Chey pushed their pitcher to six pitches and bombed one to deep left field. The left fielder was playing way back after the previous double over her head and made a great running catch for the out. Chey had already rounded first and was nearly to second. She slapped her hands together, knowing most of the time that would be at least an easy stand-up double. The next batter hit a blooper to the short stop and we were down to one out with two on base. All of us were on our feet cheering as KK came to bat. Now this kid had always had the potential to be an outstanding hitter and is an awesome first baseman, but sometimes she got into her own head. She was in that place none of the girls (or anyone else for that matter) wants to be in, down to the last out of the game. She worked the count to one ball and two strikes when BAM she hit a rocket to left field. There was no doubt she had gotten all of that ball and just like that, she had her one and only HOME RUN! We all were on our feet cheering like crazy people as her dad ran down the fence to grab that ball. The dugout emptied and the girls were standing off the third base line.

KK crossed that plate (I was already bawling at this point) and she turned and ran straight at my little girl, hugged her neck and said, "That was for you Chey."

They were both bawling and my heart just melted. What a class act. Chey actually carried a bruise on her cheek for several days after that, Kay's facemask had popped her during the hugging but Chey was very proud of it. She talks about that one moment fairly often, it's probably the kindest thing anyone had done for her in a long time. Thanks KK, I'll never forget it either!

The girls ended up losing by one, but they had finally gotten it together and ended up making the district playoffs. Chey didn't get to play in any more games but I don't think there were any regrets.

Next time, Surgeon Extraordinaire.

XXOO Make Everyday Count,
Bonnie

Tuesday, June 28, 2016

Cancer Sucks


I'm not a good Christian. I have a real problem trusting and forgiving, but I work on those issues every day. I say bad words sometimes and I think really bad things about people sometimes as well. Then again I work on those things every single day too. I see those people that profess to be such good Christians and then I see them in action and those actions are anything but Christian-based. I have to work really hard on not judging. I guess what I'm getting at is nobody makes me do these things, it’s up to me to change them. Life is about attitudes, and the only attitude that really matters is your own and getting that attitude in the right place. Then maybe, just maybe, you are able to show others by your own example that their attitude is what makes them happy or makes them miserable. With that we will continue our Journey.

Earlier in the day on March 20, 2015 I received a call from Cheyenne's endocrinologist, Dr. Athanassaki, and she had confirmed that this beautiful young woman had papillary thyroid cancer at the tender age of seventeen. We were lucky that we found it, period. Cheyenne had been injured in a softball game a couple weeks prior while sliding back into second base. She hyper extended her neck, which led to an ER visit and inadvertently showed a nodule on her thyroid. This Discovery would change our lives forever. I had been hoping for a diversion for the evening, something that would take time and thought so I could put off the inevitable - telling my child she positively had cancer.

Usually, on a Friday night, we would be going to a high school softball game to watch Chey tear it up but it was Spring Break - my dumb luck! I went home and had nothing else to do but spill it all. I told Chey and her father everything Dr. A had said. I really thought that Cheyenne would crack. To be honest, I was scared to death that this would finally be the thing that would push her, completely and forever, over the edge.

Instead she sat there for a minute and simply said, "I told you."

And with that, she stood up and excused herself to take a shower but first she turned and asked, "What's for supper?"

I was flabbergasted, flat out. She was far stronger than anyone I had ever known. Again, thanks Dublin ISD, you gave her that metal jacket! The rest of the weekend was pretty uneventful, we tried to have the house and our belongings ready in case we would be traveling soon. Monday came and went, and Tuesday we were finally back on a softball field. The season had been plagued with an enormous amount of rain, so the home game against Breckenridge was swapped and we traveled. The girls had been on a horrible streak and had been outscored 63-4 since the beginning of the month. We felt terrible for them and Chey felt guilty for not being on the field contributing.

That night Chey played with complete abandon and the team was as one. They ended up losing 11-10 but they played one heck of a game! Chey was very emotional, so much so that after the game she told us how after reaching second on a double the tears just started to flow.

"The umpire and the players were asking if I was okay. I told them yes, just get away," She let on as it had finally hit her.

The realization that this could very well be her last time on a field and how much she would miss this game had just hit her like a ton of bricks. (Thank goodness I didn't know that at the time or I would have totally lost it.) As it played out, she would get one more game in the following Friday.

It blew my mind though, that not many of the parents even asked about Chey's diagnosis. I can't imagine not asking what I could do for another family in the same situation, so I try and believe that maybe, just maybe they didn't know what to say. It bothered me then, and it bothers me now - Lord knows I'm still working on that one too! People that we had known since kindergarten didn't seem concerned about a child, yet her employer of less than a year was organizing a fundraiser to support her. How messed up is that? But even with all of that, what bothered me more than anything was wondering about how Chey dealt with it. If it bothered me, how did she, a seventeen year old girl, go through every day acting like it was normal for people to behave in that manner? As a nurse, I know it had to affect her both physically and emotionally, and as a mother that just crushed me. The only answer was, as I said before, she's a strong kid. Oh well, maybe it would be different on Friday night, and tonight I pray.


Next time, Last Game.

XXOO Make Everyday Count,
Bonnie.

Wednesday, June 15, 2016

The Call That Defined Time


My commute to work is usually a time for reflection, making plans and dictating this blog. I have the basic Sirus XM radio in my car and just like when I watch television, I surf channels. Things do not hold my attention very long. I have 70s on 7, The Blend, On Broadway, Love, 60s on 6, The Highway, Symphony, Classic Rock, Prime Country, The Bridge and Radio Classics preprogrammed. I flip back and forth through them all, most days, and others just depends on my mood. Yesterday, on my way to work, my favorite song came on. You can ask my husband and he won't know it. He will know my favorite movie but probably not my favorite song. Now, if you ask Chey, she'll tell you Don McLean American Pie. I've loved that song since I was a little girl and when I hear it now, as an adult, it brings back so many memories. I remember having my hair brushed by my older sister while singing this song, as well as, Seasons in the Sun, Take Me Home Country Roads and many others. I flash forward a few years and I'm in a car on my way to high school singing this same song with Tommi, a girlfriend from school, and I hear the skating rink and smell the smells of that wonderful place and time stands still briefly. There is popcorn, cotton candy and dirty socks. I remember Tuesday night was wheat penny night. Really, your entrance fee was a single wheat penny. I wonder what the Staton's did with all those pennies?

Anyway driving to work yesterday when my favorite song came on, instead of singing, I just started bawling. Sometimes this happens too, no rhyme no reason just hits me out of the blue. I don't know if it's sorrow of how things could have been or how things are? Sometimes it means I'm coming down with something or just plain tired. Haven't decided which it was yet.

When we last left off in our story, Chey and I were headed to tuck in for the night before the long drive home from Houston. We had met Chey's endocrinologist after some testing in the morning. Cheyenne was injured in a softball game eleven days before, and a nodule had been found on her thyroid by CT scan. To date, she's had ultrasound, nuclear uptake scan, fine needle aspiration, labwork and numerous physical exams-all in eleven days! That's a lot to wrap your mind around, especially for a seventeen year old. We had spent the afternoon unwinding at the zoo after learning Chey, most likely, would be diagnosed with cancer.

The drive back to Dublin is about five hours, give or take, and sometimes it's grueling. I was dreading it this time. I was thinking, 'Where is Chey mentally today?' My child keeps things very close to the vest, generally. Over the last couple years of dealing with a grievance against her high school, that vest has become a metal jacket. She's really hard to read but I can usually tell by her actions and requests. So far today, she hadn't shown me anything. I was worried and tired, she had talked most of the night, in her sleep which made me wary. We loaded up and headed out, soon I found out where she was. 

"Momma," (there it was) "how bout we have a Disney Marathon on the way home?" She was looking at me, grinning ear to ear while clinging to her stuffed red panda she'd gotten at the zoo. 

I furrowed my brows thinking, 'Five hours of Disney songs, crap' but told her "Sure, no prob!"

So the marathon began. We are all proud of our children, or we should be, and I'm no different than the next parent. Well okay, maybe a little different but I am proud and blessed by my kids. Now Cheyenne has a God given gift, she has a beautiful singing voice, speaking isn't too bad either. Even though she had needles probing her thyroid the day before, she just started belting the tunes. It wasn't long until I had joined in. We had to be a sight, not unusual for us as you've discovered , driving down the highway singing songs from Disney movies. I have to admit, it made for a pretty good time burner and secured that my child was still sane and dealing with her emotions. We stopped along the way, yup you guessed it, so Chey could read some historical markers and in some little bitty towns to stretch the legs before finally making it home.

Friday, May 20th started like most others. Chey went to school, it was her senior year, and I went to work. I talked with my office manager, Jeanette, and filled her in on all we had learned. She just sat and listened while I rambled, only giving words of encouragement along the way. She is a really good listener, Thanks J. I went on about my day and heard an overhead page. 

 I expected the call to be work related and was caught off guard when I heard that Greek accent. "Hello Mrs. Holt, it's Dr. Athanassaki."

"Oh hi, Dr. A. I didn't think we'd hear from you so soon," I told her, with my heart suddenly racing. In fact, to be honest, I had expected to hear from Alli, not the doctor!

Dr. A. continued, "We got Cheyenne's pathology report back and, it was as we expected. She has papillary thyroid cancer." (It still really does amaze me how she can make those words seem pretty when she says them in her accent.)

My stomach jumped into my throat and I asked her to hold on for a second. Yes, I put the doctor on hold. Then I ran to Jeanette's office. I closed the door, bent over and put my hands on my knees and choked out that my child, my baby girl, had cancer. 

 I sobbed for a short time, pulled it together and went back to the phone. "Sorry about that Dr. A., I've got it back together so please continue," I said.

I grabbed a pen and a sticky pad to write on because those damn bees were buzzing around in my head. Dr A. told me that the tumor board would meet the next Wednesday, as she had explained in the office. She said she would have Alli get all the appointments set up and let us know as soon as the decisions were made. 

"So, she will definitely have surgery?" I asked.

"That is my recommendation, to have complete removal of the thyroid. We don't usually see any metastatic disease until after the thyroglobulin level is greater than 100, (Chey's was 76) so I don't expect anything more invasive. We will look at all the information and call soon." 

That was pretty much it, and then she said it would be okay and hung up.

I sat at my desk for a minute before going back to Jeanette's office crying, sobbing actually. I thought I would be okay when they confirmed it, but you just can't imagine how horrifying and final those words are until you really hear them. All the hopes and dreams you've had for your child just seem to disintegrate and you can't think of anything past taking the next breath. Jeanette hugged me and kept saying how sorry she was and then said that it sounded like we were in good hands. She was always able to see the good side.

I can't remember much more about the rest of that workday, it's all kind of blurry. I do remember trying to figure out how I was going to tell Cheyenne and the family. I sure was wishing this was a Friday softball night instead of Spring Break...

Next time; Strong Kid.

XXOO Make Everyday Count,

Bonnie

Tuesday, May 24, 2016

Detour: Cancer and the Zoo


Nearly everyday, Facebook shows me my memories. Most of the time they're pretty neat, they make me laugh or make me thankful that we are where we are. Others though, totally tick me off, period. All those feelings of seeing my child abandoned by her so-called friends and being targeted by adults come boiling up again and I just get furious. I look at how decisions were rendered to adults and then not complied with. How a child that didn't know if the didn’t evene know if her future held life or death, became even more of a target and my blood boils, I mean really boils. I think of vengeance and then God waves his magic wand and in the room flows that angel.

She smiles and hugs me and says, "I love you Mom, isn't it a beautiful day?" The anger just vanishes, she's right, it is beautiful because she's here and I smile.

Over the last several weeks, you've been learning about our journey after Cheyenne was hurt in a softball game and a nodule was found on her thyroid. We had just left the doctor's office after meeting Dr. Athanassaki (Dr. A) and her staff for the first time. Chey had also undergone an FNA (fine needle aspiration) earlier that morning. Dr. A had informed us it would be a few days until the results would be available. Ugh. The two of us walked hand in hand out of the office and across the lobby to one of the many lab draw areas in the hospital. While Chey was in getting her blood drawn, I called her father and explained all the details. He didn't have much to say. I mean really, what is there to say when you are told your child most likely has cancer? He did ask how I thought the result would be though and I told him that I agreed one-hundred percent with Chey, it's cancer. We hung up and I remember standing there waiting for Chey to return asking God, ‘What the hell? She is going through all this crap with the school district, (that's going to be book fodder one of these days) why are you doing this? Hasn't she been through enough? What is she, or we, supposed to be learning?’ Then it dawned on me, I guess that is what people call an epiphany, I thought, ‘Maybe she has gone through all this hell with that damn school to prepare her for the real battle, Cancer.’ Maybe, He had been preparing us all along, making our skins thicker in order to fight this animal.

Chey finished in the lab and walked out. We interlocked arms and started toward the elevators.

"Momma, let's go to the zoo. We need a pick me up. I probably have cancer and might not get a chance to go later," she said as my voice just stuck in my throat.

I couldn't say anything. She was so nonchalant and didn't seem fazed, at all about the words she had just uttered.

I handed her my purse and said, "Man, I gotta go, hold this."

Then I bolted. I got to the bathroom and the sobs just exploded. I was so glad there wasn't anyone in there, not that it would have changed my outburst, and I kicked the door. Then I ran to the toilet and vomited. Hot and violent, then I told myself, ‘Stop, she's out there, get it together!’ So with my insides rolling, I splashed my face with cold water and rinsed my mouth, dried off and hauled by butt out to my child. If she could tell I was upset, she didn't show it.

She simply handed me back my bag, tipped her head and said, "Zoo?"

Well, as usual, you guessed it. We headed off to the zoo. Houston is really not a hard city to navigate, outside the medical complex that is, and the zoo was easy to find. Parking, not so much, which seems to be my bane.

We drove around and around, I looked over at Chey, "Everyone must be at the dang zoo today, you sure you want to go?"

She just opened those baby blues wide and said, "Please?"

So, of course, I drove around for another fifteen minutes then Chey had an epiphany of her own. "Mom, people are coming out, let's stalk someone," she said in typical Chey fashion.

She's such a funny kid I thought before adding, "Great idea!"

So we idled and then two women with a couple kids came out. We slowly followed them, row after row.

Chey started giggling when they started looking back at us and I said smartly, "Crap, it's not funny, we are in Houston and they're probably going to shoot our butts."

She just giggled harder and slid down in the seat. As is my way, I pulled up to them, rolled down my window and told them we'd been driving around for nearly an hour.

"Please tell me you are leaving and we can have your spot," I said and they promptly just looked at me and kept walking as the lady reached into her purse.

Chey screeched through clenched teeth, "You're right, they're gonna shoot us Mom, roll up the window and drive!"

Then, the lady pulled keys out and just kind of pointed, with an extremely long nailed finger, to a Cadillac.

I yelled Thank you to them and turned to my now upright daughter, "Yay, Chey. We get a spot!" We waited while they loaded up and then we parked, moved our essentials over to a string backpack and headed towards the gate.

I was, and am still, amazed at how resilient God makes kids. We both knew, deep in our bones, that this beautiful young woman was about to fight the biggest battle of her life. Yet, here we were, giggling like two school girls as if nothing was out of the ordinary. We spent a fantastic afternoon wandering through the grounds. Chey enjoyed herself as much as she had the first time we went to a zoo. She climbed in and out of exhibits, read all the place cards and involved the younger kids that were around her. I watched her, soaking in every single moment. Absorbing how she moved, how she felt when I touched her hand. I imprinted it all to my memory, how the light shown on her hair and the way the youngster ‘ooh'd’ when she shared some magical knowledge with them. I spent the whole time just being amazed by her, period.

The stress of the day finally began to take its toll and when the light rain began to fall, she wrapped her arm around me and leaned her head on my shoulder as she hugged her stuffed red panda and said, "I'm done Momma. Thank you, it was great."

And with that, we headed back to the hotel to rest before the long road home tomorrow.

Next time, The Call...

XXOO Make Everyday Count,
Bonnie.

Thursday, May 12, 2016

Hugs All Around



Do you ever have days where you feel like you could stay in the shower until the lake runs dry? Today was that day for me. My alarm went off and I hit the snooze button, which I very rarely do. It feels like I didn't even sleep 10 minutes. I laid there for about 10 seconds and it dawned on me ‘You have to get up, you have to go to work Dummy.’ So I bolted up and gathered my clothes for the day before jumping in the shower. Usually I'm in and out, it doesn't take me very long to shower, but today I just wanted to stand under the water and let it run. I started thinking about this blog post, today's the day you all get to meet Dr. Athanassaki and Alli.

We were at Texas Children's Hospital in Houston meeting Cheyenne's endocrinologist for the first time. We were here because doctors had found a nodule on Cheyenne's thyroid after a softball injury to her neck and the subsequent testing required due diligence and a full work up. Earlier in the morning Cheyenne had undergone a fine needle aspiration, she had cells removed from her thyroid to be read by the pathologist. Now we were heading for the Clinical Care Center, floor 11.

On the way there, we ran into a huge cow standing in the lobby of the elevator and stood in amazement. "Wow, that's so cool," Chey exclaimed!

I had to agree, it resembled a Cow Parade collectible -only it was life size! It was beautiful, so colorful and it just made you smile which was welcome in the face of what my daughter would soon be going through.

We loaded into an elevator with a number of other people. There were people everywhere, doctors, nurses, patients; it was unreal compared to our little country hospital for sure! We finally arrived at our destination and neither of us seemed to want to get off the elevator. I could see the trepidation on my child's face and my own heart was pounding. I reached down and took her hand in mine and out we marched.

Each area at this hospital has a sign on a stand giving you instructions to wait at a certain point several feet from the reception desk until you are called. (It's like waiting to be seated in a restaurant.) Yes, HIPPA that's exactly the reason behind it. We stood in line quietly waiting our turn and we both took in the scene before us. The waiting area was enormous and it very kid friendly. The area behind the receptionist was like a tree house that the kids could climb on. There were display cases with models of ships, bead mazes, books and movies playing on TV screens. These people obviously were all about the kids, that was for certain!

One of the receptionists called us forward and I realized Chey was still holding onto my hand, or I was, either way we walked hand in hand up to her desk and went through the process of signing in. After the paperwork was completed and I had my insurance card in hand, (I have a bad habit of leaving my belongings all over creation) we were directed to take a seat and wait for the nurse to call us back. We sat side-by-side and Chey commented on the children in the lobby. Many were being transported in wagons and several in strollers. There was a little girl that appeared to be maybe two. She had a tube in her nose and an IV with one little tuft of hair sticking up on the side of her head - she was absolutely beautiful. Cheyenne watched her for a bit and then excused herself to go to the restroom. When she came back, her eyes were red rimmed and I knew she had slipped off to cry for this sweet child. She sat down next to me and laid her head on my shoulder and whispered, "I love you Momma." God had to be sitting there with us because I was able to just pat her leg and hold back my own tears that were attempting to flow. Luckily, that was when we were called to the back.

Like most offices, we were taken into a room for Cheyenne's vital signs, weight and height to be taken before we were moved to an exam room. The room was average with an exam table, a couple of chairs and a computer on a desk. There were also educational posters on the wall showing the anatomy of the thyroid and endocrine system. We waited a very short time and a young woman entered and introduced herself as a doctor doing a fellowship. I think her name was Amy and she explained that she was going to be a fertility specialist (reproductive endocrinologist) and was doing a rotation here. She explained that she would take Chey's history and then Dr. Athanassaki would be in after. She did so, left and shortly she returned with Dr. Ioanna Athanassaki MD (Dr. A) who introduced herself and shook our hands. Dr. A is Greek. She has a very light voice with a very pleasant accent that is also light. She is a small woman with an affectionate smile and dancing eyes. You just can't help but like her immediately. She sat down on her stool and began to review what she had been told by her understudy, when there was a soft knock at the door and a smiling young woman with dark hair walked in with a chart in her arms. She immediately apologized for being delayed and started to introduce herself. There was no need, from her first word I recognized this was Alli and I practically jumped out of my seat in my haste to hug her. I had warned her previously that we are huggy people so she wasn't completely taken back. I croaked out her name and the tears started at this point with smiles at the same time. I actually think this exchange made us all much more comfortable and we just sat down and talked.

Dr. A informed us that she was aware we had more knowledge than most of her new patients.

She said, "We don't usually recommend our patients visit the Internet, but your situation is a little more unique."

Obviously, Alli had told her about my friend Dr. Google but it was alright.

She went on, "In your case, it makes it easier because you both have a good understanding of the possibilities so we don't have to necessarily spend time on those explanations ."

I told her we tell our patients the same thing, "Don't talk to Dr. Google" but it's just not in my DNA. They all laughed and she asked how the procedure went earlier.

Cheyenne spoke up and said, "I have it, they didn't make extra passes they didn't need to because they had enough cells to tell."

For about half a heartbeat I was afraid how they would react but Dr. A simply leaned in toward my child and said, "It is very indicative of Papillary Thyroid Cancer (PTC), yes, but we really have to wait until the pathology report is given. Right now I would like to examine you if that's alright."

Cheyenne said "Of course, sure."

She stood up and moved to the exam table, stepped up and sat down. Dr. Athanassaki donned gloves and told Chey that she would be gentle. She tried to feel the nodule but couldn't, she said Chey had been very lucky to have had the accident and that they call this an "incidentaloma." She said it is when a tumor is found by coincidence and with out symptoms. When Dr. A finished the exam, she motioned Chey back to her seat and sat down herself.

"Well, as it does appear to be PTC, let us discuss what would happen next," she sais as she rolled her stool closer and leaned over toward us. "We have a group of doctors that meet on Wednesdays to discuss the cases. There are surgeons, ENT's, oncologists, endocrinologists and radiologists present. We will go over the results of the fine needle aspiration, as well as all the other data. Then we decide what the best course is. Usually with papillary thyroid cancer (she can really roll that off her tongue by the way) the recommendation is to remove the entire thyroid."

I interjected, "But, we have to be careful about the parathyroids right?" (The parathyroid glands control calcium levels in our bodies. They are situated behind the thyroid gland and can be damaged during surgery.)

She sat straight up, put her hands on her knees and smiled broadly, "Yes we do, you really have done your research."
Chey said, "She doesn't know any other way, that's how she deals with things." I guess my daughter knows me pretty well too.

Dr. A continued speaking to Cheyenne, "We will do more lab work and possibly another ultrasound before setting you up an appointment with surgery. Right now, we will wait and see."

She asked if we had any other questions and Chey only said, "How long for the result?"

Dr. A answered and said, "Hopefully very soon."

We all gave hugs all around, to multiple giggles. We thanked them over and over again before they asked us to hold on and Alli would get us notes for school and work.

We sat down and Chey said, "I really like her, she knows what she is doing and I feel safe."

I agreed and shortly Alli reappeared, all smiles, she gave us notes and directed us to the lab. "Dr. Athanassaki decided to go ahead and get these done today. Don't worry and we will be in touch soon."

She wrapped us in a group hug and led us out into the hall. The fear was still there but now it was veiled by the feeling of hope, glorious hope. We both walked out of that office like we were wearing wings, it was such an uplifting feeling and I knew we were in the right place.

Quick note before I leave you, with summer around the corner posts will likely start coming out every other week! Enjoy the sun and thanks for reading!

Next time: Test Results

XXOO Make Everyday Count,
Bonnie

Wednesday, May 4, 2016

Here You Go Paula


As I'm driving to work today the sky is cloudy and overcast. I, as well as many others are just trying to get through the workday. Get there, get it done, get home. I watched Chey drive off this morning and with only one-week left of school, she's going to have her freshman year of college under her belt. She was a little feisty this morning, too much going on, too little time and I know she's tired but she'll gut it out like she does everything else. That's the attitude that got her through our first day at Texas Children's Hospita over a year ago. We had ended up there after an inadvertent discovery of a nodule on my teenage daughters thyroid eleven days earlier. Cheyenne had been injured in a softball game and a CT in the ER started the dominoes falling into place. We had driven down the night before, it's about a five hour trip.

We got up the next morning and had a light breakfast before heading to the hospital early. I'm not the best on directions and my little Tom-Tom is a lifesaver but sometimes even Tom-Tom can't get me where I need to go. That's not necessarily Tom-Tom's fault, sometimes I can't figure out where left is because there aren't good enough signs on top of there being too many distractions. Anyway, after several trips around the complex we finally found our parking garage and guess what? It was underground. Well, let's just say I started off the day embarrassing the fire out of my child. When you turn and go into this parking garage there's a lane in and a lane out and they are both really small! Once you navigate in, the in lane splits into two lanes and there are these little boxes on posts on the left in each. I could see the people ahead of me doing something but I was not sure what they were doing. I was praying it was going to be like the ones in the metroplex that print a little card out but nope, not so lucky. I pulled up into my spot and I couldn't figure out what I was supposed to do. It was so damn frustrating, all these people lined up behind me and no card. There was a slot like I should put money in it and a blinking green light but no instructions. What the heck? Cheyenne was in the passenger seat, already stressed out and of course, I look over and she's sliding down further and further and further in the seat so I do the only sensible thing.

I get out of the car and with my arms up I start asking the people behind me, "What do you do?"

By this time, Chey was just writhing in her seat "Mom, Mom, get back in the car!"

Luckily, the nice lady behind me motioned that you just push the button. I did and ta-da, a little yellow chip came out. You hold onto the chip until you leave and that's how you get charged for your time parking. So once we parked, and Chey climbed out of the floorboard, we looked at each other and just busted out laughing, we just rolled! Here we are, small-town America in the big city and can't operate a parking box, thing. I don't know what to call it, kiosk, I guess? It was a riot.

We eventually gathered ourselves up, got the instructions Alli had sent and headed in. We, okay I, was worried about finding our way back so while we were walking, I was taking pictures of our elevator, our parking area, the building... while trying to figure out where we were going. Once again, Chey was like "OMG Mom," and shaking her head. You’d think she would be used to this by now.

Texas Children's Hospital in Houston is like many other hospitals, being made up of multiple buildings that are connected by enclosed walkways. We had parked under the Clinical Care Center and were due in the Interventional Radiology Department, in the West Tower, for Chey's FNA, (fine needle aspiration) at 0800. The hospital was very overwhelming the first time we were there but they color-code everything and there are plenty of information desks, which helped immensely. We arrived at our destination and checked in and shortly we were escorted into a room. It was kind of like an ER bay, several rooms separated by curtains. A nurse came in and took Chey's vital signs and a medical history. She was very nice and put us both at ease (Pretty much the norm there.) She explained how the procedure would go and allowed Chey to ask questions. Chey only asked about the needles used for the biopsy. The nurse told her they would use a really small needle to extract the cells from her thyroid and then place them on a slide for the pathologist to look at. She said that one pass is usually three specimens.

Chey's face lost some color then and the nurse immediately added. "They will use numbing medicine so you won't feel much, and don't worry if they take several passes, that means they aren't finding much so they are checking more areas."

She handed Chey a gown to change into and a bag for me to carry her clothes in before leaving the room.. Soon there after, the doctor came in. He was so young! He was really tall and skinny and he had braces! I was thinking, "You've got to be kidding, I've got uniforms older than this kid." Then he started talking and I knew - Doogie Howser M.D! He was very knowledgeable and very personable. He was from India and Chey would just love him. He went over everything the nurse had said, had me sign consent forms and then we headed down the hall.

It was like a maze as we twisted and turned down back halls until we came to a little waiting area, for me. I sat down and watched as my daughter left for the most important test of her life. The hall was like a refrigerator and I was shivering. I had brought a book to read but I couldn't seem to get past the first paragraph. I tried but all I could do was keep looking at my watch and the door that had consumed my child. I remember praying over and over, "Please, let him take lots of passes." It seemed like an eternity that she was gone and sitting alone in that little, deserted area made it longer. In reality though, she was gone well less than an hour. I had leaned my head back and pulled my arms inside my shirt when I heard their voices, laughing.

They walked down the hall toward me and the doctor smiled and said, "She is really brave and she's funny too."

All Cheyenne said was "I've got it, I know it because he only did one pass plus one." The doctor, as they are trained to do, told her she needed to wait on the pathology results and led us back to the original room so Chey could change.

She told me quietly, "Momma, he did the first pass with three samples and the pathology lady was right over from us in a little room. The girl in there with us carried the slide into her and then came back and said she only wanted one more straw. I HAVE to have it, the other nurse said it was better if they took more."

What do you say to that? The room that had been so cold suddenly became like a sauna and my mind was whirling again. I was thinking the exact same thing but I told her we would just wait to see the doctor at 1100. Chey seemed very matter of fact about it and after she dressed and we cleaned the residual betadine from her neck, we left and she told me what had transpired in that room.

She was really kind of giddy and her eyes were huge and glassy. I think she was scared to death and talking was her way of working through it. She described how the room was like any other X-ray bay and they had asked her to lay on the table. She said they positioned her just like for her other ultrasound, on her back with a roll under her neck to hyperextend it and then they cleaned it with "that orange stuff that burns a little" and numbed it. She said he described the procedure to her again while they waited for the numbing and then while using the ultrasound as a guide, he took the samples and then the tech carried them to the pathologist. She said they waited for the pathologist to look at the slides.

Then she started giggling and said, "He asked what I wanted to do in college. I told him Ag/Comm. He had no clue! The guy in there with us was in FFA too and we tried explaining about showing animals and such. He couldn't believe I walked pigs!"

She said they talked about his home too. The pathologist was in a room adjacent to theirs and it only took about fifteen minutes for the decision and then the doctor told her, "We only need one more straw." He took the sample, cleaned her up and that was it.

We spent the next hour walking around the hospital just taking in all the sites, it's like several mini museums spread throughout to take your mind off of where you really are, I think. Soon enough however it was time as we moseyed on over to the Clinical Care Center towards Chey's destiny, Dr. A and Allie....

Next time; Hugs all Around.

XXOO Make Everyday Count,
Bonnie

Tuesday, April 26, 2016

Houston or Bust


After my discussion with Alli, the intake Coordinator for Texas Children's Hospital's Thyroid Tumor Program, I said I was able to sleep without terror but that doesn't mean sleeping without fear. It also doesn't mean I didn't have fear every waking moment.

I had been doing enormous amounts of research since being informed of a nodule on my daughter’s thyroid by an ER physician after a softball accident and ensuing CT scan. The information was unending and somewhat unnerving even for me, a 20 year-plus nurse. Through the research, and my intuition, I knew we needed to do further testing and we did. Cheyenne had an ultrasound, a thyroid uptake scan and lab work. Ultimately, we learned the nodule had the potential to be very serious, it had a blood supply, was solid and had "micro-calcifications." So, yes I was scared to death for my child.

We've talked about the diagnostic exams, but not much about the lab work. Chey's family doctor is an internist and initially he ordered labs to check the thyroid. He also ordered an antibody test that could show if cancer cells were present. I had forgotten about the tests until Alli called Friday (the 13th go figure) and asked if we could get them drawn in Comanche. She was quite surprised to learn that they had already been drawn. I promised to fax them immediately. Well, of course, this had to mean the labs were significant and Momma Bear came roaring back and pounced. The regular thyroid panel was normal but the antithyroglobulin antibody test showed a "low positive." Crap, normal is negative (no number) and she had one, low but it was there. I talked to our doctor and he said it was really low and to wait until we consulted with Dr. Athanassaki as well as the results of the other portion of the test.

So, here we go nail biting, sick stomach time again! We waited all through the weekend and finally on Tuesday we got the thyroglobulin (ICMA) result. It was 76. All I could think was Damn, Damn, Damn. Another piece falling into place against us, we couldn't get a break. I didn't tell my husband or Cheyenne this result but I spent time talking with my office manager. She was very supportive and allowed the mom in me to bawl like a baby before settling me down and telling me to wait and not jump to conclusions, no matter how bad the picture seemed. I swear, I was like Jekyll and Hyde those days, but she helped me keep my sanity. Thanks Jeanette, it meant the world!

All this time Chey was on Spring Break so she wasn't missing school but she was missing her beloved softball and that was so gut wrenching to watch. On one hand it was good for her to rest, but I wish the kids would have visited, this would become the norm though in the long run. I think it would have helped her deal with the emotional battle more effectively. She would cry out in her sleep mumbling about cancer and statistics nearly every night, way too much baggage for a seventeen-year-old kid to handle! In the waking hours though, you'd never know and I, to this day, don't think she had any recollection each morning.

I took off work early on Tuesday so Chey and I could take the drive leisurely. She has a thing about historical markers, so we stopped many times for her to read. It was calming for her and sometimes during the drive, I would get glimpses of the Chey before the "C" word. She was laughing and playing all the Disney songs on her playlist while we sang and acted out parts to each one. We had to be a site, if anybody was looking that is. We pulled into Houston in the early evening, checked into the hotel (thanks Jodi) and had a light dinner. Chey's defenses kicked in and she became very solemn and begged for an early night. Even though there were two beds, she snuggled right in with me and that was fine by me!

Next time; The Incredible Dr.A and Alli Too.

XXOO Make Everyday Count,
Bonnie