Life With Miles

Gearing Up

As I begin this post, it is 1:50 in the morning and I’m having trouble sleeping. That’s why I’m up. I spent about an hour and a half in bed, just awake, brain on, with no signs of slowing down.

It was actually a night much like this one that got me writing this blog in the first place. I was just lying there thinking… and thinking… and thinking… about Miles, about the future, about the past, about the other kids, about whether or not a dog and a frog could actually truly be friends… (Hey, the mind goes where the mind goes…

So here I am again, only this night is a little different. It is the eve of Miles’ final hypospadias repair surgery. We are supposed to be at the hospital at 7:40 in the morning. I was told that Miles wasn’t supposed to have any food after midnight, which is standard — we’ve been down this road before — but they also said no liquid after two hours before, and this includes his liquid medications.

Miles is on three different liquid medications, which he takes a total of eight times per day: 3 in the morning, 2 at 2pm, and 3 at night. (We go through medication syringes like tissues in winter…) Before January, Miles was only on one medication, which he took at 7am and 7pm. His last surgery was two months prior to the super-increase of medication, and at that time we didn’t really have much of a problem. So I’ve been worried that I will sleep through the alarm I set for myself and miss the dose and what will happen if he has to go into surgery without having taken his medication?

TMI ALERT – The paragraph below contains TMI. Feel free to skip.

The weather today was gorgeous. We spent a good deal of time outside. I let Miles play in the sandbox in a diaper and t-shirt. Perhaps this was a mistake because when I went to change his diaper before dinner I noticed some red swelling… This is not something you want to see on a person the night before they go in for a surgery, especially when the surgery is to take place in the same location as the swelling.  I began freaking out a little bit. I took his temperature (normal). I put him in a warm bath with baking soda. Before getting him out we rinsed him off with the shower hose. I took his temperature (normal). I slathered polysporin on the affected area. I fed him dinner. I took his temperature (normal). Before bed I changed his (practically dry) diaper again. It looked better but was still swollen. I slathered more polysporin on and asked Ian if he thought we should call the urologist’s office and he said that we didn’t want them to cancel outright. He made the very valid point that, even if they cancel the surgery, they are the exact people we want looking to see if this is something to be more concerned about than I am sitting up typing this at 2:03am.

So I’m awake. Awake and thinking and nervous and tired but awake. And some neighbors just arrived home so the dog is trying to freak out in his sleep, which is kind of hilarious. So that’s something. Right?

Maybe I will get him up to leave and his swelling would have magically disappeared. I don’t want to cancel, but I don’t want to take unnecessary risks either.

Now those neighbors are just talking loudly outside the window and smoking. Gross.

I know I shouldn’t just wait until 5:40 when I can give medicine. I should chance it and take the 3 hours of sleep if they come. I’ll let you know how it goes.

All right. 2:11. See you folks later. To help us both, adorable pictures of adorable creatures sleeping:

 

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Life With Miles

Sometimes People Get It

Last week I wrote at great length, though not exhaustively, about the challenges we face as a family and gave you a run-down of what Miles has been through in his first four years. I got a lot of powerful and positive feedback, which I appreciate so much. Some people even stepped forward and shared some of their stories with me, which I think is just fantastic. If you ever want to share with me, or contribute as a guest blogger, feel free to reach out.

This week is to be a little more upbeat. You’re welcome. 🙂

I wrote last week about how hard it was to make friends. We had recently moved away from my favorite place I’ve ever lived, near family and surrounded by a community of close friends. On top of that,  I wasn’t working and cash flow was at an all time low, so going out and meeting people was just not something I was excited about. Plus, I was having all these issues and feelings and worry and strife, so I didn’t want to lay that all out there for every new person to have to deal with. Nothing says “You really don’t want to be my friend” more than being a needy and emotionally frail person-with-too-many-problems.

I did see people occasionally – we had “Birth to Three” (or early intervention) therapists come to the house a few times a week, and they were nice and stuff, and I really liked a couple of them very much, but they were professionals and, you know, boundaries and stuff.

At one point I tried making friends with a woman down the street who had recently moved in. She had a child a year or so younger than Verity and another child about a year older than Duncan and Miles. I am not a diagnostic professional, but the son was non-verbal and often in a stroller he was too big for and did a lot of yelling. I saw an opportunity to relate to another mother who might be going through some of the same issues I had been facing. I shared with her some of what I had learned while we were waiting for the bus one day and soon she became everything I was afraid I’d become. She needed me for everything you could possibly think of from “could you find me a lawyer” to “I’m bleeding, please come over and be with my kids.”

It turned out Verity was suddenly old enough to walk herself home from the bus stop. Also, I stopped answering the phone. It was too much. They have since moved.

When Miles turned 3, he aged out of the Birth to Three program, which meant that he was eligible for the public preschool program. I honestly didn’t know how much this would heal me.

The program is a short-day (2.5 hour) program which is “reverse-mainstream.” Miles was referred to the program by his Birth to Three service coordinator. The teachers came to meet him, he was evaluated, and we had a big meeting about his eligibility and services he would receive. Duncan, as his twin, was automatically accepted into the school year program as a “model peer.” Miles took the bus to school in July after he turned 3 and then, because Duncan was not eligible for transportation, I began driving both of them in the fall.

Through the preschool program, I met parents of other kids who, though not quite like mine, had their own stuff going on. I got to bring the boys to birthday parties where I could see how they interact with the other children in the class. The children treated Miles as though he was everyone’s baby brother. Guiding him with an arm around his back, protecting him, and including him in whatever they were doing. Usually, Miles wasn’t quite at the same level as the other children, but they never seemed to mind, happily playing near him and asking him questions.

I met other parents at drop-off and pick-up. Though our stories weren’t the same, we shared some of the same pain of lost expectations and the realities of living in the Realm of the Unknown.

I met a mom whose child has some of the same kinds of seizures Miles has. She invited me to a monthly Epilepsy support group, so we started attending monthly. We carpool and laugh and rail about this and that, and then we laugh some more. I cannot say enough good things about the group itself — just having someone who relates, even just a little, to what you’re experiencing, or someone who has new ideas, or who has tried things you haven’t even considered, is like taking a weight off. Side note: the Epilepsy Foundation is pretty great. If you or someone you know has epilepsy, I highly recommend them as a resource.

I met a mom who has become one of our most vocal cheerleaders. I think she could write the book on advocating, and she always lets me know when she finds something cool (and cheap or free!) that the kids would like. Yesterday, on her recommendation, we took the children to a museum which has dedicated Accessibility Days once per month. On those days, families of children with disabilities are admitted for free. We took all three kids and they had a fantastic time! Miles tooled around in his wheelchair and showed me all kinds of tricks he’s learning; Duncan loved each new place more than the last, until he found his dream exhibit – the energy lab, where he played with water power and got soaking wet. Although she was kind of big for the museum, Verity had a great time anyway, trying stuff out, climbing where she could climb, and making friends with preschoolers. This mom also took Duncan on Thursday while I went to the endocrinologist with Miles.

I met a  mom whose daughter is, I’m pretty sure, going to marry Duncan when they get older. It’d be okay with me because I love them – both mom and child. When she has to leave school early for some reason, Duncan cries. They always want to play together outside after school and then, inevitably, one of them tries to climb into the other’s car to go off together.

I met a mom who is a special education attorney. I have yet to ask her about anything that has surprised her or that she didn’t have an answer for. And just when I think I’ve asked for too much free advice, she approaches me with follow-up questions and offers of assistance.

The teaching and therapeutic staff at the preschool is just wonderful. I have never felt like they were on anybody’s side but Miles’. The few times I’ve had to make special requests, they listened well and did everything they could to meet those requests.

So although I don’t have my amazing family right next door, or my “village” of friends and neighbors we had to move away from, I am finally building a community around myself and my family. I have missed that; it has truly been too long.

 


 

NOTE: Thank you so much for reading! I want you to know that, though I strive to publish every week, I will be taking this week off. School is out for summer, there’s a week before camp starts, and Miles is having surgery this week. Sometimes I just have to be realistic.

Life With Miles

Special Needs

If you know me, which you probably do because you’re reading this, you know that it is not always easy for me to talk about things that are difficult, particularly in an open forum or for any length of time. I put humor into it, or I slap on a happy ending, which may not fit into the narrative I have constructed. I use humor because I value it so much – a life without laughter is not a life in which I want to partake. I slap on a happy ending because, frankly, I always try to look on the bright side. In some instances, however, I realize that this may actually be a disservice to myself and to those who are trying to understand what it is my family and I are going through.

With that in mind, I am going to attempt to write about what life is like for us in a way that is a little more representative of how it actually is, without the silver lining.

DISCLAIMER: As of the writing of this blog, it is my understanding that the terms for “special needs” and “neurologically typical” children are the most accepted terms to use. It is not meant to imply that a neurologically typical, or “typical” child is not unique or special in their own right, but simply that they developed more or less along a predictable and established (or “typical”) timeline and that they are about on par with their peers. Additionally, a “typical” child likely does not have medical needs and specialists beyond those of their peers. My personal definition of a child with “special needs” is: one who needs extra intervention on a regular basis just to navigate their home/the world/their school/their life.

A woman I was talking to once stated to me (sitting there with Miles, in his wheelchair,) that she didn’t like the term “special needs” because “don’t all children have their own special needs?” I was momentarily speechless, but I eventually said “Sure, all children are unique, but to me the term ‘special needs’ means something else.” I remember thinking “This is hard enough – do you have to take my adjective away?”

(A note of caution: adjectives are descriptors we use to help someone understand what we are talking about. We must be wary of the weaponized adjective: The Label. I try hard not to use labels because they imply a bias. As Ian has said: we need to use the words to help tell a story–not in place of a story.  It can be a fine line, but one we must strive to navigate with as much grace as Philippe Petit on the high wire.)

Even in the optimal situations, being a parent is difficult. Children are not trainable like puppies and they never behave as you might want or need them to… Make a list of things you need to accomplish during nap time and it’ll all but guarantee that there will be no naps. Your child only eats hot dogs? Buy the big case at Costco and he will insist that he doesn’t like them any more and only wants to eat macaroni and cheese. Need to be on time? She flushed her shoe down the toilet. They become preteens and then teenagers and grow moody and secretive and then they leave home and you have to hope and trust you prepared them well enough.

Right now I have a typical preteen and a typical three-year-old. Each of them is able to make me want to tear out my hair on a daily basis. If I had a dollar for every time I repeated something I just said ten seconds before, I would be a rich lady indeed.

And if that’s not enough for a parent, there are activities, sports, music, after school clubs, and everything. And everything costs money! Did you know children have to eat every single day? Not just the one time, either! They devour snacks like fiends and then, if you’re lucky, they eat food at mealtimes too. And if you want to put on a show and pretend they’re hungry dinosaurs eating tiny broccoli trees, they may even get an occasional vegetable in. And you have to cook it all, even if you know they won’t eat it, because they might actually eat that one time and if there isn’t enough they’ll let you know exactly how hunnnnngryyyyyy they are.

And you love them more than you ever believed it was possible to love anything ever. It even hurts sometimes.

Add into that mix a third child. This child is sweet and funny and wonderful, just like the other two are, but the frustrations he brings are different. They involve appointments, meetings, advocation, equipment, uncertainties, and worry.

We see two therapists a week and he has a bunch of specialists. Some months are busier than others. June/July is going to be particularly busy because we are going back to a developmental pediatrician and because most of the specialists see us on the same 6-month rotation. I have to find ways to occupy the boys – because Duncan always has to come too, and sometimes we have to bring Verity as well – through all the waiting otherwise they start going through all the drawers in the doctor’s offices.  Oh! And parking! I have to try to find a handicap spot so that I can take the wheelchair out and get Miles into it without much hassle. Sometimes I can’t find a handicap-designated spot and the building where we go for most of our appointments has a parking lot designed for compact cars so I usually end up parking our van like a jerk just to get the wheelchair out and hope that nobody blocks my ability to get it back in.

Miles has an ophthalmologist because his eyes took a long time to mature and it’s hard to tell if he has problems with vision. His next appointment is in July.

He had an infant nutritionist because he needed to be on special high-calorie formula so he would gain weight, and who helped us navigate some high-calorie first foods.

He has an ENT and audiologist because he doesn’t reliably respond to his name or to sounds and it was feared he had hearing loss. He ended up having several behavioral hearing tests before he had to be sedated and have brain analytics done. His brain responds, but he doesn’t always, and we don’t know why.

He has a urologist because he had a urinary tract infection when he was just a few weeks old AND because he had to have a surgical bilateral inguinal hernia repair at four months old AND because he has had to have three surgeries on his penis due to hypospadias. He has had to have testosterone injections prior to each hypospadia repair, except for the one next week, which will hopefully be his last.

He has a neurologist because when he was one year old he had a febrile tonic-clonic (or grand mal) seizure which lasted over 25 minutes and which caused him to “code” in the ER. I watched as they performed CPR, applied paddles, and injected his heart with epinephrine. As it was happening I started trying to figure out how to tell Ian that I watched our son die.

He has a geneticist because, once he came out of that horrifying scene, the doctors wanted to try to figure out what the heck happened and to find an explanation for his phenotype.

He has an endocrinologist because, during that seizure his blood sugar was low and he was consistently unable to get his little body on the growth chart. (Except his head. That was always 50th percentile.) We will see her on Thursday.

He has a gastroenterologist because, at my sister-in-law Llama’s diligent suggestion and my advocation, he was screened for celiac disease and lo and behold, we found it.

He has an orthopedist because he turned two and wasn’t walking. He is seen every six months still. We go back in two weeks and I am excited to see if anything changes now that Miles can cross a room on foot.

He has an epileptologist because about nine months ago he started suddenly losing focus in his eyes and dropping his head, sometimes banging it. Hard. or he would just stare off for several seconds at a time. In January we had an overnight electroencephalogram (EEG) and it showed he was having hundreds of seizures, both absence and atonic every single day. He was diagnosed with Epilepsy.

He has a developmental pediatrician, who is helping us try to figure out the best way to meet him where he is and help him learn. 

We had a hematologist because Miles had chronic anemia, requiring re-admission to the NICU, two transfusions during that time, and then another transfusion right before the hernia surgery mentioned above. Also because his white blood cell count was elevated and remained elevated for several months.

We had a cardiologist because he was born with two holes in his heart. Thankfully, they appear to have closed and we have been discharged from cardiology.

He has weekly speech therapy, both in school and as outpatient, to try and find ways to communicate with him.

He has an hour of physical therapy at school every week and a half hour every other week as outpatient.

He has occupational therapy weekly at school and every other week as outpatient to try to gain dexterity and improve functionality in his fine motor skills.

He has a soft helmet he wears because, despite ten doses of medication every day, he still has dozens of atonic (drop) seizures every day. Mostly, the helmet keeps him safe, but now that it’s summer, golly he heats up good. 

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Cutie in a helmet

When he outgrew a stroller, we got him a wheelchair so that I don’t have to carry his 33 pound body everywhere. We chose a wheelchair instead of a special stroller because we wanted him to learn to move around in it on his own. He’s getting pretty good.

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Cutie in a wheelchair
When he outgrew his crib, we got nervous that he was going to fall out, so I put him in a pack and play to sleep. He *did* fall out of that. Onto his head.  We were able to get a hospital bed with netting to keep him safe at night. It is entirely white, giving it an impersonal and sterile feeling. I change the white sheets a lot because I can see everything on those things.

As he continues to grow, I can’t help but think: if we are lucky, he will grow up. He will likely not live an independent life. He will grow out of the cute small child phase. He will hit puberty and may be very confused about what is happening. Will he learn to shave himself? Will he ever hold a job? Will he talk to me? Can we have a conversation? When he was a baby in the NICU I consoled myself by dreaming of the future time when I could tell him the story of his harrowing newborn period and he could take some pride in being born small but becoming the soccer star / computer programmer / whatever the heck he wants to be.

On holidays or even regular days Ian and I often discuss the possibility that we are unlucky. How many more holidays do we get? Is it possible to capture the moment of hearing his giggle, of seeing his wonder, of smelling his wee head, so that we can relive it when we don’t have it any more? As I write, he is asleep in his bed. I can see him in the video monitor sprawled out on the mattress trying to keep cool on this hot night. I want to go in and scoop him up and hold him close to me as he sleeps, although I know it would be unbearably hot. Moments like these I just yearn to pause time. I ache.

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Sleeping and hot
Special needs for us means all of this stuff. It means I can’t work a typical job because I have a fantastic balancing act to perform on a daily basis. Starting friendships, a super-power of mine, has become incredibly difficult because I find I can no longer relate to others as well, or rather I don’t know that they can relate to me. Touching upon all of the aspects of caring for Miles, as I have here, seems daunting to think of all at once, but it’s always there, all at once. Every day. Parenting without special needs is a difficult job. Everyone has their story, their past, their pain. This is a peek into ours.

 

 

 

 

 

Invent-ery Shop

Invent-ery Update: 6/5/17

Remember last week when I posted that there was not a whole lot of progress in the shop? Well this week was very much the same. I actually took two days off by myself to celebrate my sister in law and get a little sleeping accomplished. I’ve been working pretty fiercely on end-of-year gifts for teachers – between therapists, teachers, assistants, and volunteers, my sons have eight teachers.

The Smiles for Miles t-shirt orders closed last night, but I haven’t placed the order yet, so if you’re kicking yourself for not getting an order in, shoot me an email at Smiles4milesy@gmail.com and I can maybe add one for you. They’re $20 in two styles, two colors each style. Sizes XS-3XL.

Beyond that, I ordered business cards! So when you order from us from here on out you can expect to get one of those with your order, which I find endlessly exciting. 🙂

Keep your eyes out for more stuff we have in the works and we will post again next week!

 

Life With Miles

Hindsight Blog #3: The NICU Part II

The NICU at Massachusetts General Hospital is amazing. We were set up in a private room. Miles had his own incubator bed thing and the nurses wheeled in a little newborn crib thing for Duncan. (They wrote a sign for it and everything. It said “My brother Dunkin’s bed.” We made no complaint about the spelling.)

In the beginning he was on heavy antibiotics and was visited by X-ray technicians every few hours and by surgeons lurking in the shadows waiting to be called into action should the antibiotics fail. If required, they would go in and cut out a section of dead colon. He hoped fiercely that they would not be required. We willed the surgeons away with our stares like a person wills away vampires with a cross. 

While Miles worked to get better, we visited whenever we could find someone to stay at home with Verity.  My parents stayed in a dorm room in the boarding house for a couple of weeks and we would pack – because of course we were moving to another boarding house – and whenever we could, we would take Duncan and go to the NICU. Ian’s mom would also come when she could, after work, during the whole of her only vacation, and on the weekends to help. We couldn’t hold Miles, but we could try to arrange his wires and we could change his diaper and put it aside for weighing. I would pump as often as possible so that when he was able to eat he would have a smorgasbord awaiting him. Well, there was only one thing on the menu, but it would be the perfect food.  We had a little cushioned bench by the window, next to the sink where we could wash out the pump parts. We also stored labels and containers for the milk in the cupboards. It often seemed that Duncan would sense when I was about to pump because he would wake up demanding to be fed.

At one point, listening to Miles’ heart, they noticed a murmur. An ultrasound showed he had a hole between the two atrial quadrants in his heart, called an ASD. This is usual in new babies, and generally closes quickly. In addition, he had another defect in his heart, called VSD, which is a hole between the two ventrical quadrants. This is not as common, but his was small so they just listened and recommended follow-ups with a pediatric cardiologist.

They had to put him under anesthesia so they could install a central line down by his groin. This would keep them from having to change his IV so often. You see, an IV can only hold out for so long before the vein gives out and they have to prick him again. The first line didn’t take, so they had to try again in the other side.  He still has little white scars on the insides of his thighs as a reminder of his first anesthesia and how sick he was.

Honestly, there wasn’t much we could do for Miles at first, except listen to the updates from the doctors and nurses, will the surgeons away, and listen to the beeps, alarms, and other ambient NICU noises. (I used to joke that they should include a CD of NICU noise with the discharge materials so that the babies would feel more at home after transitioning.) Although we might have felt useless, we still felt the need to be there every day, so we would go at all hours of the day and night – whenever we could get away – and just hang out near him, in the room, Duncan often sleeping as well.

We brought along an iPad for watching Downton Abbey and an occasional movie while we sat in the room with our new babies nearby. Sometimes we would get hungry – I was allowed a meal as a nursing mother, but at the best times we would stroll down to the cafeteria to partake of the amazing salad bar down there.  (Seriously, if you ever have occasion to be at MGH: salad bar. So many options. So many wonderful greens, purples, reds, oranges, seeds, dressings, proteins… so good. And, of course, at the end of the salad bar were the desserts. Because why not, right?) We weren’t allowed to eat in the room with Miles so we ate in the little family lobby that was always showing one of three things: an infomercial for the Insanity workout videos, an infomercial for some cleaning product, or, when we were super lucky, episodes of Wipeout.

For some reason, Wipeout was the perfect relief from the stressors of NICU life.  Let me describe Wipeout to you, in case you are uninitiated:  People of all levels of athletic ability run through a ridiculous and near-impossible obstacle course, mostly made of inflatables, where they get very muddy and wet and fall down a lot. The falls are spectacular and it’s dumb and it was perfect.

Meanwhile, Miles slept. A lot. His little body fought hard. I don’t know if I have ever fought so hard for anything in my life. And he was just over three pounds and a few weeks old.  And at a few weeks old, he was still behind, having been forced to deal with a bad placenta and umbilical cord in utero.  In essence, I had two babies who were conceived together, who shared a uterus, and who were born on the same day, but one was a full-term baby and one was a preemie.

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2 boys, 1 shirt

He fought so hard the surgeons stopped having to come around every few hours – the antibiotics were – slowly – doing their job.  After a week of waiting we were finally allowed to hold him.  I was so scared, he was still so fragile, but when I finally got him on my chest I never wanted to go anywhere or do anything else ever again. He was so small, frail, and sick, but he was also just so perfect.

There were times when holding him wasn’t so blissful, however, as it was still another nine days until he was able to even attempt eating, so when he was hungry and snuggling so close to food, he would get quite upset. His little cry was so small and desperate and hungry and heartbreaking. He was receiving IV nutrients, but that’s not the same as filling your belly.

When we finally did get to feed him for the first time in the NICU, it was only 3 cc’s. There was no bottle – they put it into a nipple only and it took a real long time to get it all into his little body – he just didn’t know how to do it.  But he was able to slowly increase the amount over time. We would have to hold him up right next to our ear to burp him, because otherwise we couldn’t hear his tiny little burps. His burps, like many other things, have improved a great deal since then.

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First feeding

Somewhere in there, Ian and I managed to move us into a new apartment on campus… This was something we could not have done without the incredible community that we lived in. The Operations crew would finish whatever they were working on or just come by for a box or two when they were on our side of campus. Local students, colleagues, family, and friends would pop by and take care of whatever odd job was needed at the time. People came out of the woodwork and showed up with food.  It was amazing and we will never forget it.

Finally, he started looking good enough to transfer to a special care nursery. We had a tour of the facility at MGH, but were also told that, if Emerson had space, we could transfer back there.  We told them that was what we wanted, if it was possible. They began making arrangements. They took his central line out. Silently rejoicing, Ian and I left the hospital for the night.

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This is one of my favorite pictures of all time.

The next day we visited again, ready for the discussion about transferring him back near home. When we walked in, we saw that he had a new IV.. We were told to sit down and the doctor came in to talk with us. “The nurse noticed he wasn’t behaving like himself,” he said. “He has developed a fever and we need to run some tests to determine the cause.” We sat up straighter, listening harder, as though our will could fix it, or figure it out, or at least cause the doctor to suddenly understand what was causing the fever.

They inserted a catheter to collect a urine sample. “We are hoping it’s a urinary tract infection (UTI).” They took more blood, which showed elevated white blood cells (a sign of infection) and anemia (which had persisted from the beginning and would continue to persist, but that’s for another post, I think). They needed to send blood and urine to culture as well, which can take days to develop. Additionally, they said they needed to check his spinal fluid. This meant doing a lumbar puncture, or “spinal tap,” which is where they insert a tiny needle in between the vertebrae in the lower back to collect a sample of fluid and the drummer dies

Protip: Do not ever agree to stay in the room at a teaching hospital where a doctor-in-training is about to do his or her first delicate procedure on your offspring. Especially with a curtain closed where you can only listen to the continued encouragements of “no, you’re doing great” and “sometimes that happens,” punctuated by the confused weak cries of your tiny baby. Elect instead to partake of the aforementioned salad bar. Or Wipeout in the lounge. Or walk the streets of Boston looking for the cookie truck. Or go pluck out your eyelashes one by one… Or anything really… If you happen to be a doctor in training or a teaching doctor – Ask the parents to leave. Tell them it’s hospital policy, even if it’s not, because I assure you, you do not want them to listen, even if things are going well.

Miles’ spinal tap went well, but as you may have guessed, it didn’t seem like it was going well from our side of the curtain. From behind the curtain it seemed like it was going  to eleven. And although that’s what you may want in an amplifier, it’s not good for spinal stuff in a three pound baby.

While we waited for the test results to come back, Miles was given a new broad-scope antibiotic. We learned that it was, indeed, a UTI, which brought in another specialist, a pediatric urologist, who also talked with us briefly about Miles’ hypospadias, which would eventually need surgery or surgeries.

They couldn’t re-install the central line, so they had to use an IV, which they kept having to move because his little veins couldn’t take it. One day we walked in to an IV on his forehead. That was alarming, but apparently there was a really great vein up there. Fortunately, it was the last vein they had to use, and after another week or so he was well and able to be transferred back to Emerson where he could practice eating and growing until he was healthy and plump enough to come home. With relief, we filled out all the paperwork and cuddled wee Miles – I was even able to nurse him, hold him and Duncan together, and even try nursing them together! Things were finally looking up.

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Multitasking
Invent-ery Shop

This Week in the Shop 5/28/17: Introducing: The Invent-ery!

This week was not a huge week for production; Although we sold a few more jewelry kits, we spent most of the time planning, talking, and organizing. Unfortunately, this does not make for much of an interesting read, so I am going to just take a moment to give you a peek into something we are working on and also tell you that we named our shop!

Back story: When Ian was creating a work area for his thesis machine, we were talking with Verity, who was 8 at the time, about something she was reading. She read the word “inventory,” but pronounced it “invent-ery.” We fell in love with the new word she had inadvertently invented. Like Hogwarts’ Owlery is where Hedwig chills out with her friends and a nursery is where you grow plants or children (or both?), the invent-ery is where creativity blooms.

XCarve

CNC Close-up
The CNC in action

As Ian switches from graduate school to working life and we get into a routine, we will be updating with more of our designs and projects and showing you what’s going on.

There is one week left to order a Smiles for Miles t-shirt from CustomInk. We need to sell one more to print, so hope on over and get one. They cost $20. Money earned from all sales (of T-shirts and our creations) go to help us make ends meet while I can’t work a traditional job and we have heaps of student debt to repay and all these mouths to feed…

Coming up: pictures of some pre-ordered stuff we are hoping to finish up over the next couple of weeks and hopefully starting some work on stuff we have come up with. We will see how we fit it in alongside Ian’s work schedule.

PandaPreview
A little preview of a stool we are making…

Please feel free to follow us on Facebook or email us with any special requests. We have a lot on the docket and are excited to get to it, but we want to hear from you as well!

WritingBuddy
Writing is always better with a buddy. 

 

Life With Miles

Meet Milesy

This week I have started writing at least half a dozen posts and none of them were right. I haven’t been quite in the zone for going into the details of the NICU. Then, this weekend, I had the opportunity to spend a lot of time with just Miles, and I realized that HE is what I want to write about. I want you to know Miles, who he is now, not just the sum of his history and what we as parents have gone through. So here we go: all that I can think of to tell you about this wonderful, sweet, amazing little guy. I will include some of the medical stuff, but will avoid going deep into it because although it’s all a part of his life, it is not all of who he is.

Miles is funny. Laughter is all it takes to get him to laugh. He wants to be in on the joke.  The laughter you prompt him with might be fake, aimed at the singular goal of getting him going, but once he starts going you will find yourself in the most fantastic feedback loop.  He responds amazingly well to his bedtime ticklefest and sometimes will laugh when we have no idea why. He particularly enjoys spotting Elmo and Cookie Monster in unexpected places and delights in the picture of Louis Armstrong at Uncle Bill’s house.

Miles is sweet. Apropos of nothing he will climb up on me, stick his thumb in his mouth, and snuggle up. He will find something the dog likes to chew on (whether an approved chew toy or not) and follow the dog (“Sprocket”), arm outstretched, trying to give the object to him. Sprocket is quite patient with him, sometimes taking it and chewing, sometimes taking it and putting it down, and sometimes just turning his head and walking away. Miles, determined to share, will follow Sprocket to his next destination and keep trying. He has also taken to feeding me his snacks, which is just delightful. He gets a look of concentration on his face, aims for the mouth (my mouth) and goes for it.

Miles is determined. Whether he’s trying to feed the dog or reach an object, he will find a way. We often say he has Go-Go-Gadget Arms. For example, at the dinner table, we may wonder where our forks have disappeared to. Miles will be sitting there grinning, trying to use all the forks his little hand can hold to pick up his food. He has discovered a way to move his high chair so he can get to whatever he is lacking.

 

Miles is able. He may not use words to communicate, but he can tell you with clarity what he wants, whether he likes something or not, and where he wants to go.  If it is too far to walk on foot, he will use his knees to walk or if he’s in his wheelchair, will propel his wheels by himself. When I take him out of the bathtub, he reeeeeeeaches his leg back, trying to hook the side of the tub with his foot. When we went to a birthday party at a play gym, he made it absolutely clear that under no circumstances was he to play anywhere but the ball pit. 

Miles is curious. He will take the thing. He will lift it, turn it, mouth it, try to open it, bang it on the other thing, pull it out, push it in, or stack it on top. He loves connecting duplos and figuring out how the train tracks go together. He enjoys the sounds that dumping out the bin makes and may even put some of the things back in, until something else piques his interest. Much to Duncan’s chagrin, he wants to see exactly what is going on with whatever Duncan is doing. This often results in a crash of some sort, and two incredibly different sets of emotions.

Miles is happy. He will hum as he plays. Even when he has an atonic (“drop”) seizure he will go right back to playing and vocalizing as soon as he recovers, which is usually rather quick. Sometimes it seems he gets more upset when we comfort him after a particularly nasty bonk because he wants to get back to playing.

Miles is amicable. He will go on several errands, in and out of the car, his wheelchair, a cart, whatever, and – as long as he’s well-fed – be happy just being.  In the car, he doesn’t complain when I want to listen to NPR and he likes all the same music as I do. He loves music. In his rare times of distress, a little bouncing and singing goes an awful long way.

AppointmentTime
Third appointment of the day: Time to see Miss Amy for speech therapy!
Miles EATS. His celiac disease may restrict him to a gluten-free diet, but otherwise, this kid will basically eat anything.

SmilesyPasta
The messier the better!
Miles is ambitious. He will crawl up the IKEA shelves if they don’t have toys on top. (Frankly, he may try even if they do…) We had to get a special safety bed because he climbs on everything without fear. One night, fearing he would fall out of his crib, we tried a toddler bed. We watched on the monitor as he climbed out, got up on Duncan’s bed, and climbed across Duncan’s head in an effort to get to the curtains so he could play with them.

Miles is a miracle. Three separate times in my life – while pregnant, when he was a neonate, and when he was 1 year old, I thought I would lose him. Right before he turned two we got a diagnosis that made us believe that his time with us would be short. He keeps defying odds and expectations. As his epileptologist put it “Miles didn’t read the book. He doesn’t follow the rules.” As my sister-in-law Carin put it “Miles doesn’t know what his diagnosis is or what it’s supposed to mean. He’s just being Miles and doing Miles things.”

Miles is a life saver. I mean this in the most literal way it is possible to mean anything. Because of Miles’ major status seizure when he was one, he acquired many of the specialists he has now. One of them was a geneticist. Because of Dr. Zhang I learned that he has a rare genetic mutation in the BRCA1 gene, which increases the chance of developing breast and ovarian cancer in women. I was able to take steps via preventative surgeries to reduce those risks so they are now practically non-existent.  Additionally, this past summer in a search to find out why he wasn’t gaining weight or height, and prompted by Auntie Llama’s vigilant suggestions,  Miles was tested for and diagnosed with Celiac Disease, which is, it turns out, also genetic. A few months later I brought it up with my doctor and found out I was also afflicted.  Duncan and Verity also have been tested and carry the genetic marker, but are not diagnosed. They may never develop it, but now we know to watch for both that and its best pal, Type 1 diabetes.

Miles is a natural educator. He has taught me so much about what it is to be a mother, a person, a patient. Like many young people, I put far too much stock in what other people thought of me. This past year I was surprised to learn that I just didn’t care any more. I am doing everything I can and yes, sometimes I may fall short, but I have learned much of what is truly important, what just looks important, and what I can control.

Finally, Miles is challenging. He has had four surgeries and is scheduled for one more. He has epilepsy that we can’t seem to get completely under control. (To be fair though, he went from having hundreds each day to just a few dozen or so…) Though he’s getting physically stronger, he doesn’t generally walk more than 50 steps at a time. (Although 50 steps at a time is amazing!) He needs a wheelchair when we go out. He has a dozen medical specialists, and that’s not hyperbole. He needs weekly PT, OT, and speech therapy. He generally does not respond to his name and he does not say any real words. He doesn’t seem to understand safety concerns or changes in tone of voice when we try to alert him to danger. When Duncan gets frustrated that Miles will probably knock down his tower/building/whatnot, he’s probably right, and when he gets upset about it, Miles thinks it’s a hoot and laughs. It’s hard to explain to Duncan why that’s okay. And it’s currently impossible to explain to Miles why it’s not okay.

DuncanTower
Duncan’s doomed tower of dino-thingies
His challenges add to our life-as-a-family-challenges. We need room in the van for his wheelchair at all times. When we go to his appointments there is rarely enough handicap parking to maneuver his wheelchair so I have to park like a jerk in the compact-car sized parking spots in the rest of the lot. I have never been good at asking for things but I have learned and continue to learn to be an advocate. It’s a work in progress. We have all had to learn to balance and prioritize—sacrificing some things that meant so much before, but that now seem trivial.

Walkies

Despite the challenges inherent in being Miles’ mother, I find that being Miles’ mother is the easiest part of the job. He fills me with so much joy, and each gain feels like we’ve conquered a new mountain. He has long since decided that he wasn’t going to follow anyone else’s instruction manual, but instead that he’s writing his own story. I am so blessed to be able to read along.

Miles&Mum
Miles and Mommy