Pictures from the MTM Conference (July 29)

We made it back safely to Seattle.  Lucas was exhausted by the time we got off the plane, picked up our luggage, ran to get the van, and finally made it back home after 10 pm (midnight Minnesota time!)  But he did great and everyone was relieved to be home, and inspired by the trip.  We’ll write more about the conference soon but wanted to share a few more of our pictures from the trip in the meantime:

29th July, 2013 This post was written by burke 3 Comments

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Wrapping up, heading home (July 28)

This morning we woke up in our hotel room at the Best Western in Minneapolis to the sound of Lucas moaning and calling out for help.  After a half hour of suctioning, nebulizer treatments, and more suctioning, we started to face the reality that Lucas was getting sick.  Our plans for another powerful day of family conferencing – not to mention our return flight to Seattle – flashed before our eyes.  We started making contingency plans and bracing for the worst.  And then all of a sudden Lucas smiled and said “you want to play the I Spy game!”.  Just like that he was back to normal and we were off to breakfast.

It’s hard to describe how important being at the myotubular myopathy conference has been for us and all the other families here this weekend.  Sure, there was lots of fascinating and groundbreaking medical research presented to the group as part of the rather remarkable progress that has been made towards a treatment for x-linked MTM.  But most importantly for us, being at the conference was about connecting with, sharing, and learning from other families of kids born with MTM.  Being parents of a child with a disability can be very isolating, even more so when that disability comes from an extremely rare gene defect that causes the child to be medically fragile.  There’s just a lot of stuff you deal with that no other parents can really understand or relate to.  And then you walk into the 2013 MTM family conference and look at the wheelchairs rolling all around, and hear the whirr of multiple suction machines and the annoying beep of an errant pulse odometer… And, as conference organizer Erin Ward said during the opening, it feels like home!

As we watched another couple switch out an oxygen tank – gracefully and in perfect sync with each other – or a father gently suction his son’s trach while carrying on a conversation, or a mom expertly pick up her 2 year old with low muscle tone, taking care to maneuver around the vent circuit, we thought “that’s us!”  Discussions about highly specific technical and medical information felt completely natural and often totally exciting, and we learned as many tidbits from other families as they hopefully learned from us.  In a conversation on Saturday afternoon that we facilitated, moms, dads and siblings talked about challenges and triumphs related to travel, school, nursing, family relationships, and other topics.  At every step of the way, the connections we made felt deep (especially given how little  time we had known people) and empowering.

We went through some ups and downs over the course of the weekend, and dealt with tough emotional and logistical challenges.  But in the end we are so grateful to have been able to attend the conference as a family.

Lucas sings “Take Me Out to The Ballgame!” (He got a little nervous…)

28th July, 2013 This post was written by burke 6 Comments

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MTM conference in Minneapolis (July 26)

20130726-230247.jpgYesterday Lucas flew on an airplane for only the second time in his life. We were understandably nervous – about forgetting some vital piece of equipment among other things – but in the end it went really well… Despite some nasty traffic going through security that had Krista ready to tear someone’s head off.

There are few things in the world that could convince us to take Lucas and all of his equipment on an airplane but the MTM family conference is definitely one of them. This is the third time families of kids with myotubular myopathy have gathered for a conference – the first was around the time Lucas was born in 2009 and Krista attended the second conference alone in 2011. The opportunity to meet other families and kids, learn from doctors and researchers, share stories and build community with people that have something very big in common with us was too much to pass up.

We’ll write a lot more when we return but for now we at least wanted to share a few pictures and day one highlights… Like a visit to the Sea Life aquarium in the Mall of America (across the street from the conference center) where we also ran into Burke’s old high school friend Erin. Lucas wasn’t that into the Mall but he did perk up when the conference got rolling in the afternoon and balloons and party packets were distributed. He had a break down right as our family was about to introduce ourselves to everyone, but after some time resting in the hotel bed (which he refers to as “Minneapolis”) he made a comeback and ended up hanging in the bar with us until close to 10 pm watching the Mariners-Twins game and chatting with the locals.

We’re looking forward to another big day tomorrow!

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26th July, 2013 This post was written by burke 3 Comments

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Thanks, and Flip the Chicken (July 12)

Thanks to everyone who’s replied to our last post with solidarity, support, and willingness to be in the Lucas book club, near or far.  We couldn’t pull this off without you.

We also wanted to give a quick update on Lucas’s health.  He was sick for a solid week, but on Wednesday he turned a corner and got up into his wheel chair for the first time in days.  We took him to the doctor, and they found a minor infection in his trach, but nothing serious.  So he got to go to two days of his summer school this week, which made him happy.

He doesn’t have school on Fridays, so this morning Susie came over and we took him to the amazing Seattle Children’s Playgarden.  Lucas met the baby chicks there a month ago, and he was really excited to be reunited with the now awkwardly adolescent chicks.  One of them even jumped right up onto his chair’s headrest!

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12th July, 2013 This post was written by admin No Comments

Interdependence Day (July 8)

(Krista writing)

I’m a bit obsessed with reading about disability these days (please keep recommendations coming!)  I just took a break half way through Far From the Tree, the giant brick of a book based on the author’s 2000+ interviews with parents of children who are “different.”  The parents’ stories of allowing themselves to be transformed by their wildly unexpected parenting journeys helps me feel like I have a tribe out there.

But it’s the political disability community – the older-guard disability rights activists, and the younger, more idealistic disability justice crowd – that talks about the experience of disability in a way that regularly blows me away.  Their poetry, theory, music, and performance resonate with my experience of parenting Lucas, but they use new frameworks and new language.   For example, they talk about this false notion in our society that disabled people are “dependent” while able-bodied/non-disabled people are “independent.”  Who said that needing help with tasks like growing your food or making your shoes counts as “independent” while needing help putting the food into your body or getting the shoes onto your feet makes you “dependent?”  Why the line?  Wouldn’t it make more sense to recognize all of our interdepence?  It makes sense to me not just for political reasons, but also because it is a view of the universe that nurtures my soul.

I write all this as a preface to my day yesterday, when things went to hell for me.  Lucas was sick.  Burke was out of town.  I won’t bore you with trying to describe how it took me all of three hours to get Lucas and myself out of bed, fed and dressed for the day, but it has to do with the fact that Lucas somehow lost all ability to entertain himself, even for 15 seconds.  He chanted “Mommy, mommy, mommy” endlessly while I prepared his food.  And while I walked from the kitchen over to his side to see what he needed.  And while I went to the bathroom.  I’d tune the chanting out, except that when he’s sick sometimes he actually needs me to clear his airway ASAP, but he doesn’t necessarily change his tone of voice from the “Mommy, mommy, mommy” chant that means he wants me to sit next to him and ask him “what kind of dinosaur is that?” about every last dinosaur in his dinosaur sticker book.

Another hard element of the morning was that yesterday was the anniversary of my dad’s death.  It’s been long enough that I don’t feel the sharp sadness every year, but since we moved to Seattle his being gone has felt a little bit more raw.  We’re so close to where I grew up – he could have been here helping us love and care for Lucas.  And to top it off, I was starting to worry about Lucas.  He’s had a lingering cold for over a week now, and while it hasn’t been too serious, it has tired him out to the point that he’s been sleeping lots and hasn’t left the house in days.  It’s likely that he’ll get over it with a round of antibiotics, but inevitably we worry when a cold knocks him out.  For kids like Lucas, a common cold can turn into pneumonia or some other illness else that could be life threatening.

All that mess of emotion – grieving, fear, worry, grumpiness about being alone for the day (one whole day!) – got the better of me, and I found myself sobbing as I sat next to my lovely, endlessly demanding son who was now prompting me to ask him another set of predictable questions.  “How do you spell cat?” he’d say.  And if I didn’t ask, he’d repeat with just a little more volume, “How do you spell cat?”  We’ve been through this enough that he knows that I know that he is feeding me my line.  Maybe he was trying to get me to toughen up, or change the subject.  But the truth is that Lucas isn’t too worried about other people’s emotions – as far as I can tell – so I think he was just moving forward with the day and letting me know that I needed to come with him.

Usually I am grateful for everything about his quirky, curious, determined personality, and it helps me through slumps.  But yesterday the slump was too deep, and the many, many hours of the day – with him and the laundry to be done (his bed smelled strongly of pee) and the dishes to be washed and the medicine to be given and the games to be fetched and the books to be read – looked like too much for me to handle.

And so I remembered that I don’t have to do this alone.  I remembered that, even though I grew up with a father who believed his main job as a parent was to teach me to be independent, I can be interdependent.  And even though Burke is on the road for work, and family is out of town, and our lovely friends in Seattle don’t know Lucas like the people who saw him grow up from his tiny, original four pounds in Washington DC… I could still ask for help.

I wrote an email to two sets of friends, grossly understating the urgency by saying I was feeling a bit overwhelmed.  Asking for help is hard for me, and the universe rewarded me for going outside my comfort zone.  Within an hour they’d both called me.  One promised to be over before Lucas’s nap to read books, the other would come over in the afternoon with her new puppy.

I’m not sure how to talk about this without clichés.  I felt like I’d won the interdependence lottery!   It was better than a locally-brewed ginger beer float with vegan horchata ice cream on a hot day. (Which, Dan, Andy, and Stef, I will take you out for any day.)  Even before they came over, what had looked like a thousand uphill miles ahead of me transformed into a do-able day.  I could sit and play the spelling game for an hour, knowing I’d be relieved soon enough.

Burke and I both want to do more of this – we want to be available to do these kinds of things for friends and neighbors, and we want to keep getting more comfortable asking for help when we need it.  A while back we thought about creating a formal care team for our family – and I’ve read about some cool ones – but we’re often not exactly sure what we need, since so much of our medical needs are covered.  This weekend having book-readers was an urgent need, and I’m sure other needs will come up.  So if you’re interested on being part of an on-call book reading Lucas team, let us know!  Or if you have ideas, models, or needs for your support team, we’re happy to offer our skills, time, and love.

 

8th July, 2013 This post was written by admin 9 Comments

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