Devon's Friend

A friend of Devon's recently went on a mission trip out of the country for a few weeks. She brought back bags of candy for all my kids. Devon got this little box full. Of, course the kids made a pretty big dent in the candy right away. Then I heard aggravated screaming coming from Devon's room. I went in to make sure a sibling wasn't the target of the screaming. It seems Devon had a little message written on the bottom of the box!

 I think my children's friends must be weird, unsocialized homeschoolers too!

One of THOSE Days!

Did you ever have one of those days? The ones where:

 You talk to your husband 14 hours after he left for work and he's not on his way home yet.
 The toddler refuses to take a nap and runs around like a maniac for the rest of the day.
 The septic tank backs up.
 Someone puts a pound of butter right next to the crock pot with dinner in it and the butter melts ALL over the counter.
 The preschooler who hasn't had an accident in 5 days has one, in the basket of formerly clean laundry.
 The toddler throws her dinner across the room.
 While you are cleaning up the dinner the toddler threw across the room, the toddler and her sister manage to shatter a plate in the laundry room (at least the shards landed in dirty not clean, laundry).
 Someone throws a hoodie in the wash with a bottle of black nail polish in the pocket and an entire load of laundry is covered in black nail polish spots.

I had one of those days yesterday. I'd say today can't get much worse, but starting out with an early morning, fasting blood draw for the pre-schooler isn't the best beginning!

Kids Clothes Sewing Week- Fail!

 So, I blogged HERE about participating in Kids Clothes Sewing Week. Sunday was the last day, and I'd love to show you all the cute kids clothes I created last week. Except, I didn't! I didn't actually finish a single project. I have one project that needs all the finishing done, including hems, cuffs, collar, buttonholes, and buttons. I have one project that is cut out and has a few parts pressed to start sewing, but I haven't started sewing it yet. I've probably made the most progress on the formal gown I am altering for Devon's friend. I have it all taken apart (lace and satin, so ripping out seams is a bit tricky) and the offending chiffon ruffle removed. I just don't have it put back together yet (with the lace mitered properly this time).

 The challenge for Kids Clothes Sewing Week is to sew (cutting, piecing, ripping out seams, etc. all count) for an hour a day. I might be alright with not finishing any projects if I had managed to sew for the requisite hour a day and just not had time to finish anything. Okay, I wouldn't actually be alright with it, but at least I would have still finished the challenge. I didn't manage that though. It doesn't seem like finding ONE hour a day to work on a project would be impossible, but this week it was. I didn't sew at all Thursday, Friday, or Sunday.

 It wasn't even like we had anything special going on. I just don't have the free time anymore. Since Owen started the Ketogenic Diet all of my free time has gone completely out the window. I guess I need to figure out how to become more efficient. I still think more than 5 hours of sleep (and not always consecutively) would help though!

Pumpkin Carving!

 AHHH! I had just finished uploading a whole bunch of pumpkin pictures and was starting the blog post when the internet cut out last night. At least the power stayed on. Then, Owen had another seizure that required the use of his rescue meds. to stop. I completely forgot to put gloves on him before he carved his pumpkin, so I don't know if that was the reason? I keep forgetting about things like soap, and play dough and alcohol swabs. They can all be absorbed through the skin. It's one thing to keep track of everything he eats. It's a completely different thing to keep track of anything he touches! Anyway, Here's some cute pumpkin pictures!

Yes, Brenna has a mohawk. She like to have her hair "done ".

 Brenna dug right into her pumpkin. Immediately scooping out the insides and putting them in the bowl. Then , suddenly for no explainable reason, she dumped the bowl on her head!

Owen wasn't actually stabbing himself in this pic. He was checking out the ridges on the blade.

 Owen was so proud about carving his own pumpkin!

Morgan did her own too!

 Duncan was so excited, I was even able to get pictures without him covering up his face!

 Cameron mostly stayed busy carrying pumpkin guts out to the animals.

 

Devon and Connor had to use the Saw Z All on their pumpkin!

Kristi and Simon came over to help too!

Brenna was not thrilled about being in the monster's mouth!

Even Morgan fit in the pumpkin this year!

When I asked Brenna what she wanted on her pumpkin, she said "duck"!

Owen's Story Part 2

 Today marks another important milestone in the Life of Owen the Miraculous! You can read part one of Owen's story HERE. I've actually posted parts THREE and FOUR already. I briefly referred to Owen's 2 hour and 40 minute seizure in these posts, but since today marks the 2 year anniversary of that, I decided it was a good time to do that post. (Pictures are from our Yellowstone trip at the end of August 2 years ago since I didn't take my camera to the hospital.)

 On October 27th, 2011, Owen had gone two weeks without using his feeding tube! We were starting to discuss how long to leave it in with his doctors and therapist. He was still extremely picky about what he ate, but he had at least one or two items in each food group that he would eat consistently. He was maintaining his weight and drinking enough to keep hydrated. He wasn't taking any medications at all. We had discontinued his phenobarbital at 6 months old and he'd been off his reflux medications for a few months. His development was right on track for his age other than the few lingering food issues. We thought we were in the clear. Everything was going to be fine, our special needs child wasn't going to be special needs any longer. We decided to keep his tube in through flu season to make sure he could get through an illness all right and then in the spring we would pull the tube and be done. We were convinced that you would never even know that he'd had such a rough start and been through so much.

 That morning Owen woke up with a stuffy nose and a slight ( 99.4 F) fever. At first, I panicked. I didn't want him to get sick when we were just getting his eating under control. Then I decided it would be a good test of whether he would be able to maintain hydration. That was our main reason for keeping the tube in after all. We wanted to see if he would still eat and drink when he wasn't feeling well.

 I helped Owen with his breakfast and got him some juice, then I set Cameron to watch him and got in the shower. The minute I got out of the shower, the older kids were telling me that Owen had gotten hot, really hot. I threw on some clothes and rushed out with the thermometer. In less than an hour Owen had gone from barely having a fever to running 103.8F. I gave him a dose of Tylenol and starting sponging him down with a cool cloth. Two hours later the fever had come down to 101 and Owen fell asleep. I figured sleep was the best thing and put him to bed expecting that he would wake up just in time for another dose of Tylenol.

 I started the older kids making sandwiches and ate one myself. Then I went back in to check on Owen. It had been about 15 -20 minutes since I put him down. When I went in the bedroom Owen was seizing! His left hand and the left side of his face were twitching. I hollered for the other kids to get me the phone and suddenly the twitching stopped. Knowing what we know now, we are pretty sure he was just in a brief tonic phase and that the seizure wasn't actually over. Since the twitching had stopped (he was still clenched), I called the doctor's office. Just as the nurse picked up, Owen started twitching again and I told the nurse he was having a seizure. She told me to hang up and call 911 immediately. I called 911 on my cell phone and handed land line to Connor to call Daddy. Devon had the kids cell and I gave her a list of relatives to call until she could find someone to stay with them( Devon was 14, but I didn't want her to be left with all the kids for very long). Cameron locked up the dogs and cleared the shoes out of the entryway. Connor couldn't get through to Rod (it turned out that he was out of cell range that day) and headed down the driveway to guide the ambulance.

 Within about 7 minutes, the guys from our local fire department started showing up. The local ambulance arrived a few minutes later. Our county has this program where the Bellingham fire department handles all paramedic services and is the only ambulance who transfers to the hospital. The decision was made to have our local ambulance transport us to the Medic One ambulance rather than wait for Medic One to get to our house. I grabbed my phone, my wallet and Owen's diaper bag (which somehow managed to get left on the sidewalk next to the driveway) and we loaded into our first ambulance of the day. We only drove about a mile before meeting up with Medic One and switching to our second ambulance of the day. The medics immediately started Oxygen and began trying to get an IV in Owen so they could give him medication to stop the seizure which was just getting stronger and stronger. We were only about 5 minutes from the hospital (we're about 20 minutes away at ambulance speeds) when they finally got a line in him (Owen unfortunately inherited my cruddy veins) and gave him the first dose of Ativan which unfortunately did nothing.

 Owen had been wearing a sweatshirt I had made for Devon before Connor was born that had been worn by all of my children up to that point. They had to cut it off him. I quickly pulled off the handknit longies he was wearing so they wouldn't cut those off too. It's so weird when I remember this incident what things stand out in my mind and what I have completely forgotten. I can still see that sweatshirt in pieces on the floor of the ambulance, but I can't remember if they gave him a second dose of medication or if he got that once we were already at the hospital.

The next couple of hours are a bit of a blur. I remember incidents, but I'm not entirely sure of the exact timeline. Owen ended up getting 11 doses of at least 5 different medications. I only recognized  Ativan, Valium ,and Phenobarbital.  After a couple doses of medication had been administered, they informed me that we would be transporting down south. Children's was full, however, so they were trying to find a hospital that had room probably Harborview or Mary Bridge. I remember the nurses discussing the different hospitals and throwing half of them out as not being able to meet Owen's needs. One nurse's exact words were "Oh no, He's too sick for there!" They decided to do a chest X-ray to check for aspiration from his feeding issues and to look for a possible cause for the high fever. I had to leave the room then since I was nearly 12 weeks pregnant with Brenna. That's when I finally got  hold of Rod who was still over 30 minutes away. They wanted to do a spinal tap on Owen to check for meningitis, but couldn't because he was still seizing. His pulse ox dropped to 70 and he had to be intubated which required 3 more doses of medication. I remember the ER doctor coming into the room, pulling at his hair and yelling at the nurse about why transport wasn't ready yet. The nurse replied that transport was ready and waiting , but we didn't have anywhere to send him. At one point we were all (I don't think there were ever less than 8-12 people in his room) just standing around and watching him seize while waiting for the pharmacist to hand carry 3 vials of medication to his room. I don't have  a clue what was in the vials, but the pharmacist mixed them in the room with us and injected them into Owen's IV and FINALLY the seizure stopped.  2 hours and 40minutes was the final tally not including however long he had been seizing before I went in to check on him.

 We finally got a call that Children's had been able to make room for Owen after all and we would finally be transporting. During the time we had been waiting for an ICU bed in Seattle the helicopter had been used for another transport so we were taking a plane, which meant I could go with Owen. The helicopter doesn't have room for a passenger, but the plane did. Rod finally got to the hospital just as they were getting Owen ready to transport and had a chance to catch up on what was going on. When they switched Owen to the stretcher, he started seizing again and had to have another dose of Ativan.

 Rod headed home to pack for a hospital stay of undetermined length and Owen and I got into our third ambulance of the day. Owen remained stable on the ride to the airport and we loaded onto the tiniest, most adorable, little plane I've ever seen. I was issued a set of earplugs and a barf bag ( I don't usually get airsick but being pregnant we decided not to take any chances, no I didn't need it). Under better circumstances the ride would have been a lot of fun. We were going over the sound just as dusk was setting in, it was absolutely gorgeous. Thanks to the earplugs and the fact that Owen was finally stable it was a nice to have a bit of peace after several hours of extreme trauma.

 We finally landed in Seattle and loaded onto our 4th ambulance of the day for the ride through Seattle traffic to the hospital. The ambulance driver warned me before he turned on lights and sirens that it didn't mean that Owen's condition had gotten worse. It was just that with it being the tail end of commute time and Owen being intubated we weren't going to fight traffic anymore than we had to. I rode in the front seat on that leg of the trip. I'm not sure how many traffic cameras snapped my picture during that ride, but it was a lot. We entered Children's through emergency, but were just waved right through to ICU. I later got a lecture about that from security when I went down to get my name badge, I guess I was supposed to stop and get my badge even though Owen was waved right through. Once we settled into ICU, they performed an EEG. I was told that it didn't show any seizure activity, but that didn't really mean anything because it did show that he was EXTREMELY drugged. I overheard the technician asking how many drugs you can give a kid this size before the drugs kill him.

 Rod got to the hospital around 10:00 and I finally got something to eat and had a chance to get my official name badge. Our dear friend Bridget happened to be in Seattle and we were able to get special permission to let her visit Owen even though visiting hours were officially over. I ended up staying in Owen's room that night while Rod slept upstairs in one of the special parent rooms the hospital has. Early in the morning they were able to extubate Owen and start feeding him. Owen was like a newborn baby. He couldn't hold up his head. He couldn't sit up, he couldn't use his hands properly. He hit himself in the head trying to bring a toy close enough to play with it. So, we ended up giving him formula through his feeding tube. Two weeks with no feeding tube at all and here we were on a continuous drip feed. Owen had never had formula before. I had given him breastmilk through his tube and then transitioned to blended diet as he got older and would have started solids.

 We were transferred to an isolation room on the medical floor later that day. Everyone had to gown and glove before coming into the room because we still didn't know what horrible disease Owen had that caused the fever. Owen refused to sleep in his crib, so we took turns sleeping on the parent bed with him. Children's has a rule that the child can't sleep in the bed with a parent unless one person is awake in the room, so they come in constantly to check on you and wake everyone up (this will be important later). The neurologist on duty started Owen on Keppra to prevent more seizures and they continued to test for various illnesses with no success. Owen ended up having horrible stomach pains and diarrhea from the formula, so I finally convinced the doctor to give us baby food to put through his tube instead. Owen was still groggy and had an extreme lack of coordination. At first they assured me it was due to the medications. After a couple of days they started suspecting it was from the seizure and told us he might not get back to normal.

 On day four they finally discovered the cause of Owen's illness. The evil, dreaded Rhinovirus, AKA the common cold. All the other tests had come back negative. All that was from just a cold. Meanwhile we are in the hospital doing absolutely nothing. Rod and I started pressing the doctors about when we could go home since they don't have any treatments for the common cold. We needed to know whether to send Rod home so he could work and take care of the other kids or if we'd all be going home. We only had Rod's work truck with us so if Rod left, I had no way to get Owen home without someone making a 5 hour round trip drive to pick us up. The doctors kept putting us off. Owen wasn't back to normal, so they weren't sure if they should send us home. The Attending finally said that we could probably go home tomorrow, so we decided to have Rod stay after all.

 The next morning the resident came in and explained that they still weren't sure if we should go home, but they didn't have any idea how long we might be staying. I BLEW up! Keep in mind that I was 12 weeks pregnant and hadn't slept for 4 nights. I told her in very stern language that even the cable company can give me a 4 hour block of time, the hospital should be able to also. I told her I was angry that we were still here when they really weren't doing anything for Owen. I didn't have a safe place to set him down to play, only the hard, dirty hospital floor( he still wasn't sitting up very well). I couldn't feed him properly since the hospital while having a premier feeding clinic that exclusively does blended diet wouldn't offer it to him and he wasn't tolerating the formula. His IV had failed, but that was still the only way we had to give him rescue meds in case of another seizure even though they wouldn't be able to give it that way since the IV had failed and they hadn't been able to place a new one. And, most importantly of all, none of us were getting any sleep due to their ridiculous rules! Then I calmly told her that if we were staying, I wanted a plan for Owen's care so I knew why we were still here. I wanted blended diet for him prepared according to my specifications with appropriate whole foods for him to start trying. I wanted a different form of rescue medicine ordered and the failed IV removed. I also wanted a plan for all of us to get some sleep even if I needed to sign a waiver form for Owen to sleep with us. If they couldn't do that, then I wanted to be released immediately. 

 The resident left the room to go work on my list of demands and Rod followed her out so he could get us some food. The resident informed him that I was the nicest mean person she'd ever had to deal with. She came back a few hours later with a prescription for Diastat, followup appointments and discharge papers.

 Rod dropped the prescription off at the pharmacy and went to go buy a carseat, while Owen helped me pack. The nurse came in and removed Owen's IV and instructed  me on how to use the Diastat.  By the time Rod came back from buying and installing the car seat, I was all packed and ready to go. We picked up the Diastat  from the pharmacy and headed home.

We got to Grandma and Grandpa's house where the other kids were staying just in time to pop Owen into his Halloween costume (which the other kids had packed just in case) and go trick or treating! Owen had a blast even if he couldn't talk or walk without sounding and looking like a drunk. Although, he was Iron Man that year so maybe the drunk look was a costume enhancement.
 The next day we had a follow up at our normal Dr.'s office. She was torn between the effects being from the drug or the seizure and decided we'd just have to wait a week or two longer. After 2 weeks Owen was back to about 95% of normal. After 1 month he was eating 100% orally again. After 6 weeks we switched medications due to the horrible side effects from the Keppra. Over the next year we tried 5 different medications and /or combos of medications and kept having seizures every 2-8 weeks. That pretty much brings us up to PART THREE.