April 2, 2015

(Very late) Follow Up

Logan and I slept over Aunty Angela's place the night before so we didn't have to drive to DC from Owings Mills before daylight during rush hour. It was my first time ever driving in DC and believe it or not I didn't get lost or run any lights!

So we pulled into the parking spot at 6:30 am and with impeccable timing, Danny pulls into the spot right next to us.

So we get to the front desk, get our badges, and set out on our hunt for the MRI check in. They've done some construction in the hospital (which they warned me about) but I cannot for the life of me figure out why they erected a random wall blocking a hallway. So we had to go the long way around and then found out they moved the MRI check-in station. It's now in the MRI waiting room which does make more sense than its previous location. He was officially checked before 7! (when we were scheduled to arrive; I think it might be a record)

He gets called back and we talk to the nurse, radiologist, and anesthesiologist. They had the wrong papers at first. They were asking me when he had his last round of chemo and talked about putting in a port. Nope. Definitely not my kid. All of the papers were signed, we put all of his (and our) things in a locker and went back to the prep room. HE DID AMAZING. He didn't fight the mask or anything! He used to put up such a fight. I'm beyond proud of him.

He was wheeled off and I was given a beeper for when he was finished. I went over to the cafeteria (fasting is no fun, but it's only fair if your kid can't eat either). I ran into a nice family that I met in the MRI waiting room. Their child was also 7, autistic, and had brain surgery at Children's 2 1/2 years ago. Turns out the poor kid was a walking seizure, I can't even imagine. He had 1/4 of his brain removed, and even removed it was seizing. Crazy.

I got a phone call saying that he was in recovery, the beeper never beeped. Turns out they don't work in the cafeteria. Oh well. We go back to recovery and there he is fast asleep. The nurse comes in and tells us how it went. He was squirming and wiggling even after being sedated so they had to give him more. Doing so dropped the poor kids blood pressure to an average of 67/25. There were points when it was 58/something and something/20. Sigh. He slept it off for an hour and a half while attached to fluids. Usually he's in and out of recovery in half an hour to 45 minutes. We finally wake him up on our own, I think the recovery staff was getting a bit antsy and needed a room. We left with Logan in arm (quite literally, my arms) to go up and see Dr. Magge.

I carried that not-so-little boy through the now maze of the second floor, and up to the neurosurgery office. I get him all signed in and as soon as I do the little bugger is right back in my arms refusing to sit down, let me sit down, or to go to daddy. It wouldn't have been a problem if he helped hold his weight but he was still lagging from the anesthesia. So I held him for what felt like forever.

Finally get called back and wait in the room for awhile. Doctor Magge said the images look amazing! He can't explain why Logan was having headaches but if it starts again to call him immediately. He also said to put lotion on the incision because it may have been itchy and that could explain why he scratched at it. He then asked how Logan was doing with Doctor Dankner (eye doctor) and you know what, we haven't seen him in forever either. The first thing I did when I got home was schedule appointments.

Naughty little scab picker.

Sleeping it off.

See that tiny little speck that used to be a massive syrinx?!


The little dudes had dentist appointments today. They were amazingly well behaved. Both had x-rays done, both sat down and got their teeth cleaned. And most importantly of all, they're both members of the NO CAVITIES CLUB! Hooray for "excellent dental hygiene." I was concerned about Talon, he's a little sweets monster. 

We see the eye doctor in two weeks and then both the dentist and Magge in October. Let's see if I remember to update after his eye appointment. Someone out there reading this should hold me accountable. 

March 2, 2015

It's been awhile

I haven't written any medical updates and I'm going to let you know why

I dropped the ball.

Like...really really dropped the ball.

:(

Logan hasn't had a follow up since Summer 2013 when I posted last.

He was supposed to have a 6 month MRI and appointment at the end of January of 2014. Unfortunately, while that was scheduled, it was missed. The boys and I were still adjusting to living at my moms house, the loss of my Pop Pop, and my beginning work. The week that is was scheduled for was the week when the world exploded; my mom had a massive stroke. Her hospitalization and recovery overwhelmed our family for a long time. She's home and doing well now, but everything else was put on hold or overlooked and I'm so sad to say that Logan's follow ups were one of those things.

Well fast forward to last week: Logan started having headaches. They seem mild, and inconsistent, but headaches are headaches. So, here I am sitting wondering why I haven't heard about setting up an appointment this past January because they're supposed to be every January from now until forever. And then it hit me that we didn't even do last years (I COULD HAVE SWORN WE DID) but nope.

Regardless, the earliest date I could get for him is April 1st.

So guess who is getting up at 5 AM to drive through rush hour traffic to D.C. to be at Children's by 7 even though his appointment isn't until 8? Yep. This mom.

I can only wonder how he'll feel going back there since it's been so long. He's grown up a lot in a year and a half. Fingers are crossed for all good news. Let's hope that the syrinx is gone. Let's hope that the fluid is normal. Let's hope that the misalignment has settled itself. Let's just hope.

September 13, 2013

One year post op!

Happy surgeversary Logan!

Can you believe it's been a whole year? I can remember it like it was yesterday.

Well done my little warrior, well done. Thank you to everyone who has taken such good care of my little man.

September 6, 2013

Glasses

Logan has been wearing his glasses like a champ, all day every day since we picked then up. He wouldn't even wear the last pair for 20 minutes without an attitude.

August 21, 2013

MRI Update time!


Its just a sliver of it once was! The syrinx used to be wider than his spinal cord, now its hardly even visible! This is one of very few images that even showed it. The Doctor said he can resume normal little boy activities (still no roller coasters or touch sports though, shocking!) The craniocervical misalignment has corrected itself to within normal range too. We don't have to go back again for another 6 months and he doesn't even need an MRI then. 

My only disappointment is when I took pictures of him looking so super adorable today, the eye misalignment is getting worse and worse. Again. :(