Wednesday, September 11, 2013

I should write a book...

It's just become one crazy scenario after another around here. Lets back up to about 2 weeks ago. We thought Gavin's pupil situation was getting better then it came back. It has been more episodic than constant. Gavin's eye started swelling and he developed a rash like redness from under his eye all the way down to his chin line. He cried and rubbed his eye most of the day. He kept saying it hurt. The entire situation progressed after we went to the neighborhood splash pad. He thought he got something in his eye. That evening I decided to take him to urgent care so he could get some relief. We got to see our favorite NP Jill. She took great care of Gavin!! After consulting neuro & ophthalmologist it was determined that he had contact dermatitis. Steroids, Benadryl and hydrocortisone did the trick and it looked better with each day! (We go to ophthalmologist this Friday for follow up)
Now lets move on to last week. Gavin came home from school, a little cranky and tired. That night we get to a restaurant and right before walking in he pukes everywhere. He seemed to be fine the next day but I decided to keep him home to be on the safe side.
Thursday he was great so I sent him to school on Friday. That weekend my mom and I took the boys to Texas to visit family and take them to GWL for the day. We drove home Sunday and all was well. Until Sunday, middle of the night. Gavin woke up vomiting everywhere. I had taken Benadryl because I was dealing with nasal/allergy issues. It really knocked me out which scares me now because I don't remember much of the night. Thankfully Adam was home and got him showered and cleaned up. Gavin went back to bed. I got him up the next morning to shower and see how he was feeling. He got in the shower and vomited again. I was starting to think he had a virus. We took him back to our favorite urgent care and spent a couple hours there getting him to drink fluids to stay hydrated. We get home and our home health nurse came over to draw his usual INR labs. We started collaborating with cardio, home health and the urgent care. We started to wonder if it was drug toxicity from his Coumadin. We were worried his INR levels were high. At that point he became more lethargic and not interested in drinking. 
                     My pale boy :(
After further discussion Gavin was admitted for IV fluids yesterday. He continued to have diarrhea but perked up after fluids. Thankfully, all labs came back normal and same with stool samples. So he came home this afternoon. He drank some Gatorade and slept for 4 hours! 
Tonight he's back at it again. Diarrhea full force, but at least he's drinking and not so lethargic. Put in another call to cardio to make sure we were doing everything right. We will just keep a close eye on him for the coming days. 

Well of course we couldn't leave Brody out of this story! He joined in about 2:30 this morning with several vomiting episodes. I came home from the hospital to care for him while Adam cared for Gavin. Well after his last throw up session he perked up and started running laps around the house. He was eating and drinking and acting normal until this: 

Yes, that's staph infection! Just what we wanted to end this glorious day. Thankfully the dr didn't think it was contagious. But need to stay in for 24hours. We started oral meds, so we're ready for them to kick in! Hoping we're just getting all our sickness out at one time.

Back to sterilizing and laundry I go... Hoping tomorrow is not as eventful as today. In fact I hope it's boring, very boring. 

Thursday, August 22, 2013

FIRST GRADE!

Meet the Teacher Night:
The 3 amigos and their brothers

Miss. Williamson, Gavin loves her! We couldn't be MORE excited that she is his teacher!


First day of school 8.22.2013


Love this picture, walking to school.


Will & Gavin



Olivia & Gavin in the walker line


Lil' bro missed big bro while he was at school!


It was a great first day, I have a feeling it will be a GREAT year. Gavin has progressed so much emotionally since kindergarten. We will forever be grateful to his kindergarten teacher, Ms. Armstrong for helping him get through it. 

Update on Gavin

Before I post about first grade I want to give everyone an update on Gavin. Two weeks ago we had the ER incident. Gavin went to the neuro and the ophthalmologist for a check up. They do not think its Horners Syndrome & were hoping it would resolve on it's on. By the time we saw the ophthalmologist, his eyes were looking more normal. Well, now it's back, but more episodic. Some days you barely notice it and other days its more prevalent. Tomorrow will be the two week mark since we saw Dr. G last, so we will make another appointment with him to make sure all is good. 


The home health nurse came off and on for several days, Gavin had 4 lab draws in one week! His poor veins were sick and tired of all the poking and prodding. His levels have finally dropped to a more normal range, so we get to go two more weeks without a lab draw. The cardio office is trying to get us an INR home test kit, so we can just prick his finger instead of getting lab draws. Even though Gavin takes the sticks like a champ, it's hard for a six year old to understand why he is having to do this so often.

Gavin finally got outside to play with his friends and ride his bike. He was exhausted after a couple of hours. Thankful he had the energy to get out and play!


A couple of weeks ago we lost a dear friend, Larry Seidel. It's only appropriate that I pay tribute to him on Gavin's blog. When Gavin was born, we lived with the Seidels in Edmond. They took us in their home, fed us, washed our clothes, and treated us as family. They never hesitated to welcome us in their home, even when Gavin had appointments and other surgical procedures. Their home was Gavin's first home. A couple of years ago the Seidels moved to Texas to be closer to their children and grandchildren. So I put their Edmond house key in Gavin's baby book. We will never forget their loving home. We will forever cherish the memories we had with Larry.


Wednesday, August 7, 2013

Today

Today Gavin had lab work and an appointment with the neurologist. I would say Dr. Siegler is his favorite doctor. Gavin always says, "I just love him, he makes sad kids happy!" He truly is a great doctor, brings a lot of laughter out of Gavin when we spend time with him. Dr. S consulted with Gavin's ophthalmologist during our appointment today. They decided to run some more tests, so we will see Dr. Groves in the morning. Hoping for good news!

After the appointment with Dr. S, Dr. O (Gavin's cardiologist) called and said that today's labs showed that Gavin's INR levels were higher. He said to stop the Coumadin tonight and we will do a smaller dose tomorrow. In the meantime, we need to keep him in a bubble so he doesn't get cut or bruised. Not an easy task with 2 boys! Home health will come on Friday to draw more labs and we will go from there. Hoping things level out before school starts, that will just be an added stress... Thank you all for the continued thoughts and prayers! We feel
them! 

Gavin's stash of daily meds! 

Tuesday, August 6, 2013

ER adventure

Well it is 2:30 in the morning and we're heading home from the ER. Gavin's pupils haven't been symmetrical. As in the left pupil is way bigger than the right. After sending a picture to our nurse and medical friends, it was apparent we needed to call the doctor. Put in a call and thankfully Gavin's cardio was on call. He said to email the picture. So I sent him the email. He called me and told us to take Gavin to the ER immediately to have a CT scan done. Once we got there they had the hardest time getting a stick for the contrast. His poor little veins are blown and they had to poke around twice to get it in. And it still wasn't the best stick, they had to pull it out a little during the CT to get the contrast to go in. Gavin finally teared up in the scanner room and asked if he "could just fall asleep?" I said of course, and he fell asleep. I felt so bad for him tonight I just wanted to take his pain away. I would trade places with him if I could. 

It looks like Gavin has the symptoms of Horner's  syndrome. The two stents were placed in his jugular vein. It looked like it was swollen in the area which could cause his pupils to dilate "unequally." He still needs to be seen by his neuro, so we will put in a call to him tomorrow. Home health will come on Wednesday for more lab draws, pray for good veins!! Feeling thankful tonight. It could've been a lot worse. Thankful for great medical friends and for an amazing cardiologist that takes such wonderful care of our son! God is good, ALL the time!!

My poor baby.

Sunday, August 4, 2013

Great News!

Today we went to children's to get Gavin's labs drawn. We just received a call from the cardiologist. His INR levels were great so we get to stop the injections until Wednesday. Home health will come and do another lab draw. If his levels stay the same we get to quit the injections all together. Which is super!!! Poor G is already looking beat up from injections, IV's and lab draws. 


The boys relaxing today. Trying to keep a 3 & 6 year old from wrestling and injuries is no easy task! 

Saturday, August 3, 2013

Blessed

Gavin wants to thank everyone for all of the gifts, cards and well wishes!! He received packages in the mail from his aunt, uncle & cousins in Tennessee. A bag of things (to keep him occupied in the hospital) from his favorite kindergarten teacher. He got lots of goodies in the hospital from his great grandparents, grandparents and family friends. He came home to more treats, like yummy donuts that were left on our porch. Today, he got a balloon guy & candy from the Weedens. He wanted me to help him thank everyone for the special treats and gifts that put a big smile on his face! He loves you all!