Tuesday, July 22, 2014

The Summer When Energy Found Me

This summer, even amidst the grieving, something wonderful has happened in our family: my energy has begun to return. I still don't feel great, but I can say confidently now that I feel much better, better than I have in about three years.

This seems to coincide exactly with what the neuromuscular doctor told me to expect with the CoenzymeQ10 supplement: to notice improvement in about two months, with full benefits felt around six months. I've been taking CoQ10 for about three months. After six weeks I noticed the brain fog beginning to lift. My thinking felt clearer, less like I was moving in slow-motion and more like I was witty and ambitious again.

Within another two weeks I began to have short periods of time where I actually felt energetic, like I could wash the dishes and put in a load of laundry without needing a nap and a cup of coffee in between. It would only last an hour or two at first, but the energetic periods slowly became longer and more frequent.

Then I noticed that my legs actually began to feel like a weights had been taken off of them. Have you ever done the little slumber-party game where you stand in a doorway and press the backs of your arms out as hard as you can against the doorway for one minute, then when you step out of the doorway your arms begin to float upward? That's how my legs felt, like I was walking with so little effort now that they almost lifted too high, like the slightest amount of force made them just float upward now. I wondered if I might be able to lay on my back and raise a straight leg upward now, something I had been totally unable to do in December, and to my amazement my leg flew up with hardly any effort at all. I've been galloping through the grocery store lately (OK, not actually galloping, but it feels like it compared to the way I used to drag myself through stores last winter), and running up staircases for the fun of it.

About three weeks ago I noticed another completely foreign feeling: waking up feeling refreshed, like I'd actually had enough sleep, like I wanted to get out of my bed and do things: clean the house, take the kids to the swimming pool, or teach Toby to ride his bike. In fact, I've felt energetic and ambitious long before having that cup of coffee I used to cling to. And, at least in that way, it's been the best summer in a long time.

I got a pool pass for our family this summer, and we've gone now more times than I can count. Hannah apparently can hardly recognize me as her mother. When I told the kids we were going swimming for the second day in a row a few weeks back she gasped with wildly excited eyes, "Swimming again?! You've got to be kidding me!"

This summer:
-Hannah and Emma learned how to swim
-Naomi has grown to be quite a strong swimmer
-Toby learned to ride a bike
-Elijah has learned to play in the backyard and obey the boundaries I've set up for him
-The girls learned to make rubber band bracelets and set up a busy shop in our backyard where they sell  all sorts of rubber band accessories to the neighborhood kids.
-All the kids have made friendships with neighbors
-I took the four older kids bike riding on a nature trail while I attempted to keep up with Elijah in a stroller
-We took a week's vacation to visit my family
-We went to the county fair
-All four kids are on separate soccer teams, which means we have practices and games almost every day of the week.

And I'm actually enjoying it all. It's been really amazing to feel alive again. I remember how much of a struggle it was just to get up and get the kids out the door last year at this time, and how much I loathed any extra activities for that reason. I remember the dismay of knowing that no matter how many hours of sleep I got I would never, ever feel better. I remember the fear that something was seriously wrong with me when my arms and neck began to actually give out on me. And I am so grateful to be on the other side of those feelings.

I still get tired, but it's a much more normal tired, the kind that comes after a long day of activity and disappears after a good night's sleep like it's supposed to. I still struggle with weakness in my arms and neck, but even that is finally improving. Yesterday and today I have begun driving short distances without the help of my neck pillow--yes, holding my own head up against the movements of the van--and I'm able to do it for about five to ten minutes now, which is a great improvement.

All of this adds to the collision of emotions I've had in the last month: so much grief over the new BBS diagnosis, but so much happiness over the return of a good deal of energy and ambition. I've feel like this summer I want to give my kids the best summer they've had yet, to make sure that it is full of happy memories, and I feel that I'm achieving that goal and enjoying doing it, even with all the grief mixed in alongside.

Emma's endocrinologist called me today to tell me that Emma's enlarged thyroid is due to autoimmune thyroid disease, the same as Naomi has, but that her thyroid function actually looked a little better on this last test so she won't be put on medication right now--we'll just have to watch it closely. She also told me that Emma's hormone tests show that Emma's adrenal glands are definitely acting as if they are in puberty and Emma's pituitary is showing borderline high hormones as well--not scary-high levels or treat-it-right-now levels, but "we need to watch this closely" levels. Emma will be having a brain MRI in October to see if there's anything abnormal, such as a cyst in her pituitary gland.

On August 4th I will be taking Naomi and Emma to see a pediatric ophthalmologist to begin the process of assessing the condition of the girls' retinas and watching their degeneration, an appointment I am simultaneously anxious for and dreading.

But today, today they are well. Today they are "healthy." Today is what we have. So you know what I did today? I took the kids to the pool and we had a glorious time. Naomi passed the pool's swim test and got up her courage to jump off the diving board, then decided it was so much fun she jumped off ten more times while we laughed and cheered her on. This is an amazing accomplishment for a girl who three years ago couldn't stand the feeling of any water on her face.

Tonight we went to soccer practice and had a lovely time there as well watching Toby ham it up in front of all his new friends. I'm so glad that I am now able to give this kind of day to my kids, and I'm hoping to do it again tomorrow.

Monday, July 14, 2014

Bravery

I watched you tonight
In the golden evening
Surrounded by girls
Leaner, stronger, faster
And I saw in you strength
Those girls will never have

I watched them flit with ease
But you concentrated
With you whole being
They glided
You fought
They never tired
You tired
And ran on

Girl after girl showcased
The reflexes of a gazelle
You took a ball to the face
And chose to stay
In the line of fire
Even when reflexes failed you

They danced on ankles
That have never turned
Your ankle betrayed you
For the thousandth time
In your short life
Leaving you behind
Yet again

When I saw the tears well up
When I went to meet you
You sighed
Wiped your eyes
Stood up
And began your plans
To practice harder at home
That's when I knew
You were stronger
Than all of them

I watched you tonight
In the golden evening
Beauty
Courage
Determination
And my greatest sorrow
Was knowing the others
Didn't see it

I wish that I could gather them up
Players, coaches, parents, fans
Wish I could explain
Everything you had overcome
To be where you are
Wish I could give them eyes to see
Your bravery

But I stood silently
And marveled
And thanked your maker
That out of those twelve girls
You were mine

Thursday, July 10, 2014

The Ache

I wanted to come out fighting when we were told our girls had Bardet-Biedl Syndrome. I wanted to be the mom who makes the best of a bad situation.

I took notes like a madwoman at the BBS conference. I didn't miss a session, or a word. I came home on a mission. I e-mailed doctors and more doctors. I checked into insurance coverage for specialists. I marched myself into the special education headquarters and talked with their director to find out how to get the girls the best educational opportunities. I wanted to fight. I wanted to be thankful for what we have and hopeful for the future. I didn't want to ache.

But somehow the ache has found me.

And I've realized that it's better to meet the ache, to give it a long look and a deep sigh, to unchain it and acknowledge that it lives here now--not just an occasional visitor, or even a frequent guest; this ache is a part of my story now, a part of me.

The ache finds me as I watch my kids play in the backyard: Hannah and the rest of the neighborhood running circles around Emma, who waits patiently to join in the game.

It finds me when the nurse asks Emma how she's doing today and Emma stares back blankly, not sure what the nurse is asking; and when that nurse interprets her blank stare as mental disability, gives up talking to Emma, and talks to me instead.

The ache wells up when Emma runs into a pole on her left side at church, her sister on her right side that evening, and falls flat on her face tripping over a curb five minutes later. She cries that she didn't see the curb as I wipe her knees. And now I know. I know that she didn't see it. And it breaks my heart.

I am heartbroken.

The ache finds me when she gets up, dusts herself off, and smiles again. It wells up when she giggles.

I ache when she comes grinning with her hands hidden, "Mommy, geh wuh I ha behine my back! (Mommy, guess what I have behind my back!)" and reveals three droopy dandelions with all the pride her heart could muster. I kiss her forehead, find the perfect vase, send her back outside, and I ache.


I don't ache from despair or because there's no hope; I don't ache because there's no beauty left in life. I ache because there is so much beauty and so much sadness all woven together in our life now. And as far as I can tell language fails for that emotion.

Watching Emma makes me ache like a sunset, full of mournfulness and grandeur all intertwined; like a wolf's howl on a still night, so haunting and yet breathtaking that you don't cry or smile, you just stand, and stare… and ache.

If you see me fall silent at one of Emma's soccer games this summer, staring quietly at her while she swipes for the ball. Please don't tell me that everything will be OK, because you and I both know that in a way it will and in a way it won't. Just stand beside me, and if you want you could whisper, "It's like watching the sunset, isn't it?"


Thursday, July 3, 2014

To Whisper to the Dark

I came tonight
To where the crescent moon glows
In deepest blue
Over brightest copper
Behind the dark outlines
Of age-old pines

I came because here
Nothing has changed
When everything has

I came to watch tiny lights bob carelessly
Over the rising grasses
And listen to the lonely train whistles
Miles away
And to breathe again

I was a little sick to my stomach
As we drove to that quiet room
Knowing it was coming
Yet shell-shocked when we left
Despite all efforts to be prepared

I was too busy to feel much
Too much to learn
Too many people to meet
Sandwiches to pack
Hours to drive
Holding my breath
Until now

I came tonight
To where the crescent moon glows
In deepest blue
Over brightest copper
To breathe again

Today I fought for them
I scanned reports
I e-mailed specialists
I knocked on offices
Today I put my hands to boulders
And my axe to trees
To clear a way for them
But tonight I came to breathe

To let out the ache
That begs for air
To lift my eyes
To the depths of the universe
And whisper that this hurts

I've come to sort emotions
Tangled beyond recognition
The grief from hope
The relief from sorrow
The immeasurable pride
At the maturity with which
She's taken this news
From the horror that any ten year old
Should have to be so mature

I came tonight to watch the grasses
Lit by the streetlight
Long after the sky is nothing but dark
To let the ripples settle a bit
From the latest stone
Tossed into my heart

Today they rode bikes
In the golden evening
Eyes bright
As if nothing had changed
And I can't decide whether that
Is beauty
Or tragedy

I came tonight
To where the crescent moon glows
In the deepest blue
Over the brightest copper
Behind the dark outlines
Of age-old pines

Because here nothing has changed
When everything has
I came to let out the ache
To whisper to the dark
To settle the ripples
And to breathe

Sunday, June 29, 2014

The Diagnosis that was Ten Years in Coming: Bardet-Biedl Syndrome

Ten and a half years ago Matt and I sat bewildered when our OB told us that our prenatal ultrasound showed our little baby girl had unusually bright kidneys. We began our search for answers ten and a half years ago, but all we found were more questions, that is, until last Thursday.

Naomi was born with club feet, a distended abdomen, and kidneys that functioned poorly. She grew into an intense, demanding, and draining baby, and then toddler. Then her eyes crossed. Then we were told she had a heart murmur. When our third daughter, Emma, was born with a similar condition both girls were given the diagnosis of Autosomal Recessive Polycystic Kidney Disease and Congenital Hepatic Fibrosis, called ARPKD/CHF for short, and we added the concerns of liver disease to our list of diagnoses.

We learned everything we could about ARPKD/CHF, but were still left with questions. Children with ARPKD/CHF have kidney and liver disease, but do not normally have crossed eyes, heart murmurs, and general developmental delays (unless it is delays from long hospitalizations due to illness). My girls had multiple neurological problems including: difficulties with balance and coordination, severe stuttering, severe speech apraxia, slowed mental processing times, eyes that were overly sensitive to light, nearsightedness, and decreased white matter volume on brain MRI. These problems, the experts told us, were not a part of ARPKD/CHF and must be purely coincidental.

We were told we knew for certain that the girls had a "ciliopathy," meaning a defect to a gene important for the proper functioning of the cilia (or tail-like structure) on many cells of the body, and that ARPKD/CHF was the one ciliopathy they shared the most features with. When Naomi began to struggle with obesity that no doctor could explain to me I had had enough. I researched every ciliopathy that had been documented so far in human history, looking for clues. What I found both shocked and scared me. I found Bardet-Biedl Syndrome (BBS).

BBS is also a ciliopathy that can cause polycystic kidneys and liver fibrosis, but can also cause a host of other conditions in children, including problems in almost every system of the body. It can cause neurological and developmental delays, it is often associated with severe speech problems, it can cause heart murmurs, crossed eyes, social communication issues, sensory-processing problems, and autistic-like traits. It can also cause morbid obesity. These findings were almost a relief to me: we had these issues already so finding a cause would have been a cause for celebration if it weren't for the main symptom of BBS: retinal degeneration inevitably leading to blindness.

I brought my findings up to several doctors who told me with certainty that my daughters did not have BBS. These doctors thought you had to be born with extra fingers and toes to have BBS (in actuality only 80% of patients with BBS have extra fingers and toes). They told me my girls weren't obese enough to have BBS, (but they wouldn't take into account that Naomi had had celiac disease for the first six years of her life and I had worked very hard to control the obesity after that). They told me that my girls would be mentally retarded if they had BBS (a very common and unfortunate misconception made by doctors who didn't understand that slow mental processing time is not the same as being stupid). And so I let the idea rest for awhile.

Last January, with Naomi's kidney function worsening, we saw a new nephrologist (kidney doctor). She told me with in no uncertain terms that my girls did NOT have ARPKD/CHF. Their kidneys were small instead of enlarged, and their blood pressure was not elevated as you would see in ARPKD. She believed their kidney condition was either Cystic Dysplastic Kidneys or Nephronopthisis, two kidney conditions that can be seen on their own, or as a feature of BBS. She didn't want to jump to the conclusion that the girls had BBS, but it was enough evidence for me.

I came home and joined the Families of Bardet-Biedl Syndrome Facebook group, where I found that there was an upcoming BBS convention in Iowa and that I could send in my children's blood samples for free genetic testing ahead of the conference if a doctor suspected they might have BBS. We sent our samples off in March and waited and tried not to think too much about it in the meantime.

-------------------------------------------

Last Thursday Matt and I met with a researcher from the Wynn Institute for Vision Research at the University of Iowa and she told us that Naomi and Emma do, in fact, have Bardet-Biedl Syndrome. After ten and a half years the genetic mutation has been found and we have a concrete diagnosis. She handed us papers that I wanted to just stare at stating:

A homozygous ATG>AGG nucleotide substitution resulting in an amino acid change of Met390Arg is present in the coding sequence of the BBS1 gene of this patient. This finding is consistent with the diagnosis of Bardet-Biedl Syndrome (BBS).

I read it over and over in the following days, because with that finding, everything changes.

What does this mean? It means Matt and I both carried the exact same mutation in one copy of our DNA and Naomi and Emma each happened to inherit that mutated copy of the BBS1 gene from both of us. Two mutated copies of the BBS1 gene means that the instructions to make the BBS1 protein are all screwed up and that protein is made incorrectly in both girls. The major problem is that this protein is needed (as Matt and I learned at the BBS conference this weekend, following the diagnosis) in nearly every cell of the body in order to help traffic other proteins up and down the cilia of the cells in order to send and receive messages from other cells. It's like having all the taxi cab drivers in the city drunk at once, which would severely affect the traffic flow in the city and may eventually crash the city completely. In addition the BBS1 protein also seems to somehow help the "garbage man" of the cells to collect the trash. When the "city" of the cells cannot effectively move traffic or take out the trash, they at first function poorly and eventually die.

It is this mutated BBS1 protein that causes cystic kidneys, liver fibrosis, poor neurological signaling, heart defects, skeletal defects, endocrine abnormalities, obesity, and eventual retinal degeneration leading to vision loss. We were told that Naomi's extreme sensitivity to light and Emma's near-sightedness are early signs of retinal degeneration and that they need to get to a pediatric ophthalmologist who is familiar with BBS as soon as possible for further, in depth testing including Optical Coherence Tomagraphy and Electroretinograms to evaluate the condition of their retinas. Unfortunately at this point in time, there is nothing they can do to slow the degeneration. Apart from a miracle of God or modern medicine, the girls will slowly go blind, probably over the next 10-20 years of their lives.

But here is where the good news comes in: that miracle of modern medicine may not be many years away. The University of Iowa has been given an enormous sum of money by a man with a similar retinal degeneration disease for the purpose of ending genetic retinal degeneration. They have built facilities and hired researchers and have begun trials of gene therapies that have had good success with other types of genetic retinal degeneration. Multiple children with genetic retinal degeneration have been treated in these trials with gene therapy and have had some vision restored. They told us at the conference that they believe gene therapy for the retinal degeneration of BBS is only single-digit years away from being a reality. And so we are sober, yet hopeful.

We met many other families, including adults with BBS this weekend. The conference center was full of white canes and guide dogs, but also full of smiles, laughter, and friendships. We learned from the few experts in the world working on BBS everything there is to know right now, and we in turn offered our insights to them so that they can further the research. We are hopeful.

Yet we are sober. This diagnosis has been an enormous collision of emotions for us: relief at finally knowing; sadness and fear for what is ahead. But that is still not all. The University of Iowa would also like blood samples from our boys. You see, Hannah, who was tested for BBS and found to be a carrier (one bad copy of the BBS gene, and one good copy) also has small kidneys and the same heart murmur as her sisters. Toby, who does not have cystic kidneys, has one small kidney that is out of place. Carriers for BBS do not normally show symptoms of the disease, which leads the U of I researchers to believe that there may still be another mutation, perhaps in a more kidney-related gene, that may be complicating our family's health picture further. These researchers will now be sequencing the entire exomes of all of our five children (some 20,000 genes each) in an effort to see if another genetic mutation is shared by our children that would explain why four out of five of our kids have unusual kidneys. This information will help them better understand the interactions of genes in the human genome, and it will help our family better understand the health of our children. It will be several months before we get results from all of this.

This is all very difficult for us to fully digest. When we return home I will have to begin the process of connecting our girls to the correct eye doctors and low-vision resources. I will have to argue with our school system until they conceded to teach them braille while they are young instead of waiting until they are blind, because while the potential of gene therapy is thrilling, it is not yet a reality we can count on. I will be working to connect with the Foundation Fighting Blindness and other resources which can help us on this journey. I will be working to implement more stringent dietary plans for both girls to control their weight and hopefully lower their chances of developing type II diabetes (though this may develop in BBS even with proper weight control). I will be taking Emma for further evaluations to determine the proper cause of and treatment for Emma's early puberty. And I will be sending copies of the girls' genetic testing results along with information on BBS to their geneticist, pediatrician, nephrologist, cardiologist, endocrinologist, GI doctor, speech therapist, and physical therapist.

And then, in the quiet moments, I will be grieving this new challenge that has been heaped upon more challenges in two little girls' lives.

Thursday, May 29, 2014

The Chemistry of Meltdowns

It was the first concert we had been to in ten years, since the spring that I was pregnant with Naomi. Matt's favorite guitar player was in town, his mom and dad were watching our kids, and we were enjoying a marvelous performance together. We had just settled back into our second-row seats after the intermission when Matt's phone vibrated.

He didn't recognize the number. They called again and left a message. Then my phone vibrated with same number. Again they called twice and left a message. I hated to disrupt the entire second row and everyone behind them, but I was pretty sure this message was important. As soon as the song ended I made my way past applauding people, apologizing as I swiped their knees and stepped on their toes.

In the lobby I retrieved the message. It was Matt's dad calling from a new cell phone number we didn't recognize, but I didn't so much hear him as I heard the shrieking. Wild, panicky shrieks came one after another; hair-raising, blood-curdling screams of terror that made me want to drop everything and fly home with superhuman-mama speed. The volume was so loud that I hurried outside, worried that the screams now echoing through the empty lobby would make their way through the double doors and into the concert hall.

I recognized those shrieks, only they were older and more violent than ever, terrifyingly so. It had been over three years since I had last heard them. I was at the same time angry with Naomi and filled with compassion for her, sorry that Matt's parents were dealing with this, and embarrassed that it had happened again. I erased the message and dialed my home only to hear the continuing cadence of panic and anger, terror and rage ringing out so loud I had to shout to be heard over the phone.

I asked them to give the phone to Naomi but she swiped and punched and kicked with such force that they couldn't get near her. I asked them to put me on speaker phone and I tried to out-shout her, "Naomi! It's Mommy! NAOMI!! Calm down and listen to me!!" But I might as well have been shouting down an erupting volcano. Naomi was gone. She wasn't in that kicking, flailing, red-faced, shrieking body anymore. I knew, because I had fought that demon before, and that girl was not my daughter.

Matt's dad was bewildered. He had asked her to come inside for bed. That was all. And she had had plenty of warning. But she had dug in her heels. It started as stubbornness and anger. She was culpable for that wrong response, but the downward spiral that followed without warning I recognized as something far beyond her control. They had had to drag her inside as the whole neighborhood looked on, and they barely got her one-hundred-pound frame in the back door before she collapsed in her violent tantrum of nuclear proportions.

I asked to talk with Matt's mom. "Try talking to her gently," I coached, "Ask her if she thinks she's having a reaction. Tell her you think she'd feel better if she had an epsom salt bath."

I couldn't say much more because it was nearly impossible to yell loud enough to be heard. I thought about driving straight home, but I knew Matt would be worried, not knowing what had happened. I'm not terribly tech savvy, and forgot I could have sent him a text message. I decided to slip back in at the next applause, and I handed Matt a written synopsis on the back of a ticket stub, "Naomi is having a horrific meltdown."

If you're not familiar with autistic meltdowns you might assume I am a lenient parent, that I encourage tantrums by not disciplining them or by giving in to them. So let me quickly say: please educate yourself. Naomi has never once been rewarded for a tantrum: quite to the opposite, we dealt very strictly with them when she was little, before we understood them. The autistic child does not tantrum to get their way. Though it may initially begin as stubbornness, it quickly escalates out of their own control. They tantrum because they must. And no, a spanking will not cure it.

I sat, bewildered and worried, through the last four songs of the concert. I watched the fingers move and heard the notes, faintly, but my mind was racing through every food Naomi had eaten that day, any new chemical exposures she may have had. We knew these meltdowns were usually caused by exposure to foods containing large amounts of phenols, a chemical found naturally in many fruits and vegetables, but in especially high doses in artificial colors and some preservatives such as sodium benzoate.

Three years ago, when Naomi's diet had been full of "fruit" snacks, yogurt, Nestle Quick, fruit loops, soda, and other dye and preservative-containing foods these violent meltdowns often happened multiple times a day. She had been plagued by terrible headaches that were only worsened by Tylenol. She had had stiff, sore joints. She had been a miserable child, overwhelmed by the world around her, in constant pain or discomfort, withdrawn into a world of her own, then suddenly lashing out with violent, unpredictable force at the tiniest of disruptions.

But we had cracked that code. We had pinpointed phenols as the culprit. We had eliminated all artificial food dyes, sodium benzoate, Tylenol (which is itself a phenol), and even some natural foods high in phenols such as red wine vinegar. And she had vastly improved. The headaches disappeared, the joint pain subsided, and the angry, violent tantrums ceased completely. The dark bags under her eyes disappeared. She slept better. Just like that she was a different child, and every medical professional I mentioned this to looked at me like I'd grown three heads. The humored me, but I knew I was right.

Then tonight it reappeared, the child who might as well have been demon possessed. What went wrong? There was nothing, nothing new that she had been exposed to. She had eaten the most bland, tried and true foods. We hadn't gone swimming (chlorine exposure causes the same symptoms), she hadn't tried a new sunscreen, a new lotion, a new deodorant, nothing.

I was at the peak of mental frustration when I looked up at that guitar player in front of me and the idea crashed into my brain like a freight train: what if she's unable to process the chemicals released by her own anger? What if the only catalyst for her meltdown was her anger itself?

When we arrived home Naomi was almost back to her normal self. After 45 minutes of flailing, wailing, and shrieking, when Matt's mother had suggested to her that she might be having a reaction, she began to calm herself. She sang songs to her pet gerbil while she calmed down. When the epsom salt bath was ready, still feeling a bit stubborn, she claimed she didn't need it. She remained a bit on-edge the rest of the evening, arguing with Grandma that she ought to be able to sleep in her dirt-smeared pants if she wanted to. But by the time for tucking-in she gave her Grandpa a hug, told him she loved him, and shed tears of remorse when I explained how her tantrum had affected our evening out.

She didn't remember much of the tantrum itself, only the anger that led up to it. She said she just felt like she had to scream, like she had to kick and fight, her body compelled her to. She didn't feel like she was in control of it at all. Looking back she felt ashamed.

More determined than ever to find answers for my daughter I have spent the last few days at my computer like a madwoman giving myself a crash course on biochemistry, the degradation pathways of catecholamines, and the three phases of liver detoxification. And I think I've found it. I'm almost sure I have.

-----------

We know that Naomi, and many children with Autism lack the proper metabolic pathways to excrete phenols efficiently.

From Wikipedia: "Rosemary Waring a reader in human toxicology at the School of Biosciences, University of Birmingham, was the first researcher to produce scientific evidence suggestive of abnormal sulfur metabolism affecting people with autism spectrum disorders. Her findings suggest that people with autism present with consistently lower levels of circulating plasma sulfate and higher than normal levels of urinary sulfate than non-symptomatic controls (reflective of excessive 'dumping' of sulfate into the urine). Follow-up work has suggested that people with autism also present with higher than normal levels of other sulfur-related compounds, including sulfite. Waring found that most people with autism conditions have a deficiency in a key detoxification pathway involved with sulfation. The enzyme involved is phenol sulfur-transferase (PST), which is essential to the process of breaking down and removing certain toxins from the body. Waring postulates that symptoms arise from an inadequate supply of usable sulfate ions, rather than from a deficiency of the metabolic enzyme itself."

In other words, phenols must have a sulfate attached to them by certain enzymes in the liver in order to make them water soluble, and excretable by the kidneys. If the phenols aren't properly sulfated they will build up in the blood. I'm not completely sure what they do there, but I think they may want to bind with organic acids where they are able to react with them, which might conceivably affect the krebs cycle or glycolysis pathways. This is one area I would like to research more. Whatever these excess phenols are doing in the body, it isn't pretty to watch a child with phenol toxicity suffer from headaches, joint pain, dark bags under the eyes, inexplicable fevers, irritability, and irrational tantrums of nuclear proportions.

But is it possible that anger itself, and that well-known fight-or-flight response can trigger phenol toxicity? Yes, I am almost certain of it, and here's why.

The chemicals released in a fight-or-flight response are called Catecholamines. Dopamine, epinephrine (adrenaline), and norepinephrine (noradrenaline) are the three major catecholamines released in fight-or-flight, and they are all phenols. These phenols are then degraded within a few minutes by Monoamine Oxidase and Catechol-O-Methyl transferase down to other forms of phenol abbreviated MOPEG and VMA as illustrated below from Neurotransmission: The Autonomic and Somatic Motor Nervous Systems.


Ultimately, these phenols (MOPEG and VMA) need to have a sulfate added to them by enzymes in the liver in order to be excreted by the kidneys just the same way that phenols from diet do. Without adequate sulfating, these phenols will build up in the blood.

If I'm correct here (and I'm no chemist so I'll admit I might be wrong), this does not just mean that the child will suffer from excess phenols, but that build-up of these phenolic metabolites will slow down the further degradation of these catecholamines. This would mean that dopamine, epinephrine, and norepinephrine themselves would stay at extremely high levels for long periods of time in a child who is not able to excrete their degraded forms quickly and efficiently.

While these catecholamines might be degraded and excreted within a few minutes in a healthy individual, for a child with impaired sulfating, these fight-or-flight chemicals may stay at extremely high levels for forty-five minutes or an hour. If this is true, this child very literally cannot calm down.

No amount of discipline or reason will calm the child in this physiological state. They must yell, they must fight, kick, scream, thrash, and shriek as these chemicals increase their heart rate, their blood flow increases, their blood pressure rises, their energy stores are released, and their attention narrows.

Akathisia "is a syndrome characterized by unpleasant sensations of inner restlessness that manifests itself with an inability to sit still or remain motionless." According this Wikipedia article, "It was discovered that akathisia involves increased levels of the neurotransmitter norepinephrine, which is associated with mechanisms that regulate aggression, alertness, and arousal." And again, from this article, "Severe akathisia can become a very harrowing experience. Jack Henry Abbot (1981) describes the sensation:

...[It comes] from so deep inside you, you cannot locate the source of the pain … The muscles of your jawbone go berserk, so that you bite the inside of your mouth and your jaw locks and the pain throbs. … Your spinal column stiffens so that you can hardly move your head or your neck and sometimes your back bends like a bow and you cannot stand up. … You ache with restlessness, so you feel you have to walk, to pace. And then as soon as you start pacing, the opposite occurs to you; you must sit and rest. Back and forth, up and down you go … you cannot get relief …"

I cannot say for sure if my daughter suffers from an acute, hour-long akathisia due to norepinephrine overload, but it sounds hauntingly familiar. She says she must scream, she must kick, she must fight, no matter how ashamed she feels later; she has no control over it. And I think I am finally beginning to understand why.

Rosemary Waring demonstrated that many children with autism lack adequate sulfating pathways. She saw that children who ingested phenols in the form of food additives suffered symptoms that some have called phenol toxicity. She suggested that limiting dietary phenol intake in these children would improve symptoms. I have found this to be true with my daughter.

Though some research has touched on the roles of catecholamines in autism, like this study which found increased levels of catecholamines circulating in the blood of people with autism, and this study which found altered patterns of excretion of catecholamines and their metabolites in autistic children, and this rather frustrating study from as recently as 2013 which concludes that "neurotransmitters might play a key role" in autism and suggests that further research is needed, I cannot find anyone who has suggested that it is the phenolic properties of catecholamines and impaired sulfation that may underlie their altered metabolism.

I propose (as I cannot see anywhere else on the internet that this has been proposed, if I am wrong, please let me know) that children who lack adequate sulfating pathways also suffer from not only phenol overload but catecholamine overload when the fight-or-flight response is activated and these chemicals are not efficiently excreted because of impaired sulfation pathways. If I am correct, this is a plausible explanation of the chemical basis for the autistic meltdown.

My experience with Naomi seems to bear this out. When sulfate is absorbed into her skin in an Epsom salt bath, the readily available sulphates make it possible for her to quickly and efficiently excrete phenols. Twenty minutes later, she emerges from her bath as a new child: no headache, no joint pain, no stomach ache; not irritable or irrational, but bright and sweet and healthy as could be. This is equally true whether she is experiencing phenol toxicity from FD&C red dye 40, or from her own fight-or-flight meltdown.

There are many more questions to ponder here: why exactly do so many children have impaired sulphation? Has something made the enzymes sluggish? Are they wasting sulphate in the urine so that it is not available for the enzymes to use?

Beyond this, I know that my daughter adversely reacts (big time) to many common drugs that are not phenols, but are processed in phase one liver detoxification through an enzyme called Cytochrome P450 3A4 (CYP3A4). I have personally witness violent meltdowns in response to:

-Midazolam (Versed)
-Fentanyl
-Dexamethasone (Decadron)
-Diazepam (Valium)
-Acetaminophen (Tylenol)
-Lidocaine
-Dextromethorphan (cough suppressant DM)

All of which are processed by CYP3A4 in the liver. I don't know whether she has a genetic modification of this enzyme, or whether the Pregnane X Receptor which is supposed to cue this enzyme into action is the problem. Looking into things that downregulate PXR, which would ultimately lead to poor processing of these drugs is also fascinating, including inflammation. Let's not get into everything in our environments that could cause inflammation.

And so I have a lot left to think through, but I think I know this: my child who cannot tolerate dietary phenols also cannot tolerate the natural catecholamines released during the fight-or-flight response. Adding sulphate to her blood stream as epsom salts absorbed through her skin gives her almost immediate (within ten to twenty minutes) relief of all symptoms. I would also like to look at other ways to help her cope: dietary supplements, deescalating conflicts, calming techniques, and such, but understanding the chemical reactions are the basis for all of this, and something that is all too often overlooked in the study of autistic meltdowns, at least as far as I can see.

I need to add that Naomi is known to have both kidney and liver disease (polycystic kidneys and congenital hepatic fibrosis) that are not currently well understood in the medical world and are caused by a genetic mutation that had not yet been identified in Naomi. It is possible that her particular metabolic challenges are a result of her genetic defect and could not be applied to the autistic community as a whole, but if Dr. Waring is correct that a majority of autistic children have impaired sulfur metabolism, then I think it is reasonable to conclude that impaired catecholamine degradation may lie at the heart (or at least be a part) of the autistic meltdown.

While I am not a chemist, I did talk this through with my dad who holds a PhD in Chemistry, and he believes this is plausible. If anyone out there who has a background in biochemistry would like to challenge or confirm my musings, please do so, we could only both benefit from your insights.

Wednesday, May 28, 2014

Backyard

In the corner of the goal
Not wanting to be hit
In the shade of great walnut trees
Just bursting into leaf
She stands, arms crossed
Smiling a little at the boys
Running full-on towards her
With the pink community soccer ball

Across the dusty field
Her sister comes leaping
To guard the goal
That's not quiet guarded
Nimbly swiping the ball
From boys twice her size

A third sister giggles
At her good fortune
from the other side of the goal
She was jointly
Not quite guarding

In a corner of the dust field
Two brothers sit
Convinced they've found a sandbox
Developing roads and railroad tracks
And chasing down ant holes
With their newfound friend

She speaks no english
They speak no spanish
And no one minds
They understand just fine

The littlest brother peeks up
Catches my eye
And runs with joy-filled eyes
Towards me yelling
"Mama! Mama!"
To find a hug
And the assurance
I'm always watching

His friend follows
Explaining something exciting
In spanish
And when I explain
That I don't understand
She smiles, shrugs,
And somehow convinces
both of my sons
Without a word
To gather piles of last year's walnuts
To feed the squirrels
That she doesn't at all
Find a nuisance

When my littlest one
Sees the biggest boys
Jumping bicycles on ramps
He watches, mesmerized
Toes on the edge of the road
He knows he must not cross
Wishing I wasn't calling him to dinner
When there's so much to do
Outside