The Final Push!

t's been a BUSY summer at the Hawkins Household.  I didn't plan on taking a blogging break, but with buying a house, moving, traveling to Switzerland, baptizing our little lady, and spending time as a family. . . my blog was an easy thing to place on the back burner.  But now we're all moved in to our home, we've had loads of adventures, Joey's off to work after two and a half wonderful months home, and I'm ready to start reporting.

BUT first, I'm making one final push for the hydrocephalus walk.  We have recruited 50% of our team member goal and we've made 30% of our monetary goal of $3000.  Every little bit counts and I am so thankful for the support that we have received, but I want to do so much more!  I've never shared this on my blog, but one of my lifetime goals is to raise $135,000 for the Hydrocephalus Association.  Why that much?  Well, Aurelia's 10 day stay in the NICU/ICN cost $135,000.  That was just staying in the NICU/ICN (24 hour care, ventilators, monitors, medications, etc.).  That doesn't include the two surgeries, the anesthesia, the many consults before she was born, the trips to Duke, the twice weekly physical therapy appointments, the specialists we see, the list that goes on and on and on and is continually increasing.  I thought $300,000+ was a little more than I could chew so I went with a nice easy $135,000 10 day NICU stay.  Of course, we have insurance.  And although our medical bills are large, they aren't triple digits.  It is just staggering to me to look at the toll that this one little word, hydrocephalus, can cost one little person.

Here's why the Hydrocephalus Association (HA) gives me hope and gets my backing: They are the only group looking to eliminate the challenges caused by hydrocephalus.  For the rest of Aurelia's life, she will have hydrocephalus.  For the rest of my life, I'll worry about shunt malfunction.  For the rest of our lives, our family will live with the challenges of a condition with unknown causes and no known cure.  HA is working to improve the care available, researching causes and new care options, advocating and raising awareness, organizing support and education for families and individuals living with hydrocephalus, and so many other things.  And ultimately, they are looking for a cure.  All of that gives me hope in a sometimes frustrating and hopeless situation.

SO, here are two ways you can help:

1) Support our WALK team with a donation!  To donate to Team Hawk click HERE!  Then select either a specific team members name to enter a donation amount OR select General Team Donation to enter a donation amount.  We are grateful for any donations.  Every little bit counts!  And did I mention it's tax deductible?

2) Join our team as a member.  If you live in the Seattle area, you can walk with us on Saturday morning at Magnuson Park.  Click HERE for more information.  If you don't live in the Seattle area, you can join our team as a virtual walker.  To join our team, click HERE and select "Join Our Team."  Participation either as a virtual walker or real time walker is free.  We are encouraging team members to raise $50 to receive a WALK T-shirt (it will be mailed to you 6 weeks post walk).  I love the idea of all our friends and family wearing T-Shirts that say "Hydrocephalus Association 2011 Walk."  Anytime you get asked, "What's hydrocephalus?", you can tell them about sweet little Aurelia.

There you have it.  That's my final push.

Need some more practical application on why we need HA to eliminate some challenges?  Tuesday Aurelia was acting off all day.  She took two really long naps, she was fussy and lethargic, she threw up twice, and she had no appetite.  She had a low grade fever  by the end of the day.  Normal baby sick stuff, right?  Teething, or a little bug, or an ear infection.  Except that all of those things I listed are also signs of shunt malfunction.  While all parents have those moments when they think, "Should I call the pediatrician?"  Added to my list is, "And the neurosurgeon?  The neurologist?  Should we go to Mary Bridge?"  In the back of my mind, I kept thinking how it would be strangely fitting to miss the HA Walk on Saturday due to something shunt related.  In the end, I decided to monitor the fever and rock my miserable little girl through the night.  The fever broke at 5:30 and she's making her comeback to health.  But I know that every fever, every vomit, every off day will come with that little voice in my head. . . the hydrocephalus mom voice.

F.A.Q. The one I don't want to answer

A month or so ago, I posted some F.A.Q. that I can answer.  But there are a lot of questions about Aurelia that I can't answer.  I know people have good intentions.  And I know that they don't realize certain questions cause a little internal grimace, or wince, or tear.  Some of the questions I get asked I don't want to answer or think about.  Some of these questions I just can't answer.  And here's my disclaimer: If you've asked one of these questions, don't feel bad because the nature of frequently asked questions points to you not being the first person to ask the question.  You're not the only.  I've probably asked the same question too.  And now I'm going to try and answer some of the F.A.Q. that I don't have answers too.

Grimace

Do you know what caused it?

Believe me, I've asked myself this question many times (more on that another day).  The dry, medical answer is no.  The doctors we have talked to about causes can only hypothesize since there was no clear, "aha" moment that points to how Aurelia ended up with hydrocephalus.  There was no infection, no drug use, no genetic reason.  One thing that has been brought up repeatedly is whether there was any intrauterine vascular trauma.  From what I've read, we're talking a baseball bat to the tummy type trauma.  And I had no stair falls, no car accidents, no bumps or bruises (except the ones from Baby Hawk on the inside!).  The reason they bring this up is along with the hydrocephalus, she had a small hemorrhage in her brain and other areas of her brain that are getting less blood than they should.  This could reflect trauma.  The answer to this questions contains words like "could" or "might" or "maybe" or "possibly."  Ultimately, it's just one of those things and we don't know what caused it.

Wince


What are babies doing at 8 months? OR Is she rolling over, sitting, crawling, waving, high fiving, talking, walking, signing, singing, reading, solving math problems yet?
I have a feeling that most mothers get this question in some form.  And it's probably not a difficult question to answer for mother's of neurotypical babies.  This question usually comes from people that don't know our situation.  And I have no idea how to discreetly avoid opening the can of worms that is the answer to this question.  I mean, does the lady in the grocery store checkout line really want a 15 minute explanation to why my 9 month old isn't doing things a 3 month old can do?  Do I answer with what neurotypical babies are doing?  Do I answer with what Aurelia's doing and brace for more questions or hope they're clueless on baby milestones?  Do I say that my daughter has special needs?  I usually take the route of avoidance.

Tear


Does your baby have issues? OR Is everything alright with your baby?
Honestly, people usually ask these questions because of the helmet.  And these people are usually complete strangers that have no tact and think that Macy's is an appropriate place for clueless questions.  But that doesn't take away the sting.  And how in the world do I answer?  Seriously, I'm taking suggestions from the gallery.  I want to show poise and grace, but I also want to let them know there are more appropriate ways to ask things.

Are you still planning to move overseas?
Most of you are aware that before we had Aurelia, we lived in Central Asia.  And our plan was to go back, or to someplace similar after she was born.  These plans were formulated before words like hydrocephalus, CVI, and early intervention were part of our daily vocab.  Before we had biweekly physical therapy appointments and a billion different specialists.  Actually, hydrocephalus entered our world one year ago next Thursday.  Things seemed a lot more black and white before.  And we grieve the loss of "our plans" to a degree.  We also celebrate that God has far greater plans for us!  And we also rest in the unknowns and wait on a known God.  It would be safe to say that our plans are delayed. . . not cancelled, just delayed.  Our medical team has said we need to stay put for 3 years at the least, 5 years more likely.  And if and when we do head out, it will be someplace with a pediatric neurosurgery unit and great health resources for our little lady.

BUT we are going to Switzerland on Sunday!  So, I should close this out and pack!

Recently. . .

We've been busy lately.

We took the train . . .

. . . to Portland.

Lots of Stumptown, Powells, and food carts.

And then the Todds came to visit and to celebrate their 30th birthdays!  We lived next door to the Todds in Texas (the first time we lived down there).  I think we had dinner together four nights a week.  The other three nights a week we were probably in class or working.  We haven't seen each other in four years, but some friendships are so easy to simply pick up where we left off.  They are some of our favorites and it was too much fun having them here.

Tides for Nate's birthday

The Crab Pot for Dara's birthday

We spent some time at the cabin.  I love that place.

And besides that, we've been looking at houses (yep, homeownership appears to be in our near future), preparing for Switzerland, enjoying the few sunny days, and being negligent with things like blogging.  

Quick Aurelia update:

We've had a few appointments here and there over the last few weeks.  She still isn't growing, and she's also struggling to gain weight.  She's been hanging out around 15 lbs for quite awhile now.  We're doing some different things to help her gain like adding formula to her solid food to up it's calories.  She is not a fan of the formula, but she's slowing getting used to it.  She's also taking iron supplements because her most recent blood tests reflected that she was anemic.  BUT despite these "setbacks", she is a happy baby.  She's moving forward (not literally).  She even rolled over from back to tummy on her 9 month birthday!  Way to go Aurelia!  We are so proud of our little lady!

F.A.Q. The ones I can answer

I get a lot of frequently asked questions/statements about Aurelia.  Some I feel comfortable answering.  Some don't have answers.  Some catch me off guard.  Some make me feel uncomfortable.  Some questions are a little scary.  Some are questions that I've asked myself.  And I really don't mind the questions, even the ones I don't like.  But I do feel a bit like a broken record at times, repeating the same answers over and over again.  I thought I'd address some of these questions in the next couple posts.  Maybe we'll all find some answers.

Hydrocephalus
How long will she have the shunt?
This is the most frequently asked question.  And the answer is simple.  She'll have the shunt forever.  There is currently no cure for hydrocephalus.  Unless one is found in the near future, Aurelia will always need the fluid drained off her brain.  In very rare cases, people have had their shunts removed because their hydrocephalus has become "normal pressure."  There is also an alternative procedure called an endoscopic third ventriculostomy (etv) where a small perforation is made in the ventricle to allow the fluid to bypass the blockage and drain into the normal CSF space (the interpendicular cavity).  I suppose this may be a possibility for Aurelia, but it doesn't appear to be that common and has it's own set of complications.  That's the long, medical answer with the different possibilities.

Where does the fluid drain?
The fluid from Aurelia's brain drains into her abdominal cavity and is reabsorbed by her body.  Here's an illustration:

Aurelia has a VP Shunt, meaning it goes into her abdomen.

Is the shunt working?
The simple answer is yes.  We thank the Lord that our baby girl hasn't had any infection or shunt malfunction.  The big issue or fear with the shunt is that is has a 50% failure rate, meaning there is a 50% chance that it will malfunction at some point.  But I'm a glass half full kind of mom, so there's a 50% chance that it will never malfunction.  She will have to have a revision at some point to add to the tubing in her abdomen.

The Helmet
Why is she wearing a helmet?
I only get this one from people that don't know us and I get it a lot.  Kids love to ask about the helmet.  Adults are curious about it and either just stare or ask.  I've even had people ask me where they can get one 'cause their kid is always bonking his/her head on stuff.  Now that we've put a bird on it, most kids just want to talk about the stickers.  But just in case you've missed the last posts, the helmet is a cranial molding helmet to round out the flat spot on her head.

How long does she wear the helmet each day?
23 hours.  She gets an hour break for a bath and play time.  We get lots of helmet free snuggles during that hour (but only after the bath, 'cause that thing makes Baby A smell funky).

How long will she have the helmet?
Anywhere from 3 to 12 months.  The longest she would have to wear it would be until she's 18 months, but that's unlikely.  Most kids seem to wear them for about 4-5 months.  I'm guessing Aurelia will be in her's a bit longer because her plagiocephaly was pretty severe and she isn't growing much.  But she's so cute in it, I don't really mind.

Yes, she is wearing Patagonia.  Baby Girl's got style and Uncle Zach.

Vision
She seems to see really well.
Sometimes she does.  Sometimes, not so much.  The thing with CVI is that her vision is "fine", as in her eyes work properly.  The issue is the way that her brain processes what she sees.  So when that little brain is processing well, she sees great.  When she's tired, working really hard on something else (like tummy time or eating), frustrated, or just having an off day she loses a lot of her vision.  For example, this morning at physical therapy she appeared to have no vision by the end of the hour long session.  After a short nap, she was engaging and looking around again.

Odds and Ends
What do you do in physical therapy?
Yes, it is strange to think of such a little person being able to do much in physical therapy.  Afterall, Aurelia doesn't roll over, sit up, crawl. . . there doesn't seem to be much to work with.  But there is a lot to work on (like rolling over, sitting up, crawling).  Physical therapy looks more or less like play time with some pretty cool toys.  She does tummy time on an exercise ball.  She plays with different visual toys.  She works on tracking.  We practice movements and rolls.  We work on strength and flexibility (she's a very, very stiff baby).  And she swings in a lycra hammock, which is her favorite thing to do.  We do a lot of these therapy things at home too.  When we move in a couple weeks (more on that later), she'll have her own hammock at home and loads of other cool sensory and strengthening toys.

Do you have good insurance?

We see A LOT of doctors, therapists, and specialists.  And all of these come with bills.  Our insurance is good, but no insurance would cover it all.  Aurelia's 10 day NICU stay came with a $135,000 price tag.  That's a staggering number, that's a mortgage, and that's just for NICU care, not for her surgery, my surgery, or any of the subsequent follow ups.  Our insurance covered MOST of that bill.  We also have a complex case manager with our insurance company that calls and checks in on Aurelia once a month.  She's really great and I truly feel like she has Aurelia's best interest in mind, not just the insurance companies interests.  She gets our referrals approved and recommends different care ideas.  It's also nice to know who to call when I have questions about our policy or any bills we receive.  So, yes, I think our insurance is good.

When does Joey get home?
Joey gets home in a week!  He's gone a lot for work.  And yes, it's awful that he is gone a lot.  I miss him more than it's possible to imagine.  Solo parenting is really tough work.  But in the glass half full mentality, I'm so thankful that he has a job that he enjoys.  I'm glad that I'm able to stay home with our baby, take her to appointments, be the main point person on her care team.  I love that when Joey's home, he's home 24/7 for a long stretch of time.  And I'm thankful that I have a loving, supportive husband who makes me feel loved and supported everyday, even when he's away.

How are you?
I guess this is a F.A.Q. that everyone gets, right?  But it deserves an answer too.  I'm fine.  I'm happy.  I'm tired.  I'm averaging about 5 hours of sleep a night.  I have seasonal allergies.  I'm soy and dairy free.  I miss chocolate and cheese.  I'm ecstatic to have Joey home.  I'm looking forward to moving in a couple weeks.  I'm looking forward to Switzerland.  I'm dreaming about many more trips to many different places.  I'm wondering what in the world I'm doing with my life.  I'm attending conferences on differently developing children.  I'm using words like differently developing.  I'm Mama Hawk (that's still new to me).  I'm ready for bed.  And that's how I am doing at this moment.

Good Friday Thoughts

Fitting that my reading this morning should include Isaiah 53.  Fitting to read these words on Good Friday:

But he was wounded for our transgressions; he was crushed for our iniquities; upon him was the chastisement that brought us peace, and with his stripes we are healed.  
Isaiah 53:5

A lot of emotion comes with contemplating the significance of this day.  Many men and women more eloquent than I have written words of wonder, amazement, grief, and gratitude.  These are some of my favorite:

My sin, oh, the bliss, oh the glorious thought, 
My sin, not in part, but the whole, 
Is nailed to the Cross and I bear it no more, 
Praise the Lord, Praise the Lord, oh my soul!
-Horatio Spafford


And as my precious little gift calls out to me from the other room that nap time is officially over, I'll carry these thoughts with me as I go about this {sunny, beautiful} Good Friday.

Thank You for the cross.

Let's take a walk

The 1st annual Seattle Hydrocephalus Walk is Saturday, July 30th in Magnuson Park.  Aurelia and I will be there, and we hope you'll be there too!  Our Team Hawk goal is to raise $3000 and recruit 30 walkers.  Of course, we'd be happy with a larger team and a larger fundraising amount, but this is where we'll start out.  Gig Harbor Crossfit has already said they're in if they can run it for time.  Those guys are hardcore.

Here's our little team blurb:
Baby Hawk was diagnosed with congenital hydrocephalus when Mama Hawk was 28 weeks pregnant. The last year has been a whirlwind of tears and triumphs for Team Hawk. So many friends and family have walked with us as we've journeyed this sometimes rocky road. Now we ask our friends and family to WALK with us as we raise money and awareness for hydrocephalus! 


You'll be hearing about this event a lot in the next few months.  And I look forward to many of you joining us!  For more information, click on the links above or contact me in the comments section or on facebook.

Progress Report: Part 2

A few weeks ago I detailed our goals for Aurelia's Individual Family Service Plan.  In short, our hopes is that Aurelia would explore, tolerate tummy time, eat, and sleep.  Here's where we are with each of those goals:

Explore

A picture's worth a thousand words, right?

This may not look like much, but Aurelia just started reaching and touching things in the last two weeks. She's very tentative with her reach, she rarely looks at the things she's reaching for (this is typical of CVI), and her favorite color to reach for is yellow.  These are the first steps towards exploring her world.

Tolerate
Sometimes I feel like our apartment looks like a physical therapy gym.  We have an exercise ball, a tummy time surf board, mats, and all kids of equipment to encourage Aurelia to tolerate tummy time.  As we learn more about her vision and sensory needs, we adapt to help her.  For example: Aurelia gets overwhelmed when there is too much to process.  If she's working on tummy time, it's hard for her to work on vision.  Therefore, I never put Aurelia on her tummy on anything that's not a solid color (she prefers bright blue).  I only offer her one toy that is either black and white or a solid contrasting color.  And she loves tummy time on the exercise ball.  She fully extends her arms, has great extension, and even laughs.  Again, we're on our way towards achieving our goal!

Eat
This is where we're having the biggest strides towards goal accomplishment.  After I figured out the texture, temperature and taste that Aurelia prefers, she no longer chokes on her food!  We have a nice little routine that we do every time she eats, and that has helped her anticipate the spoon (which she can't always see).  She's still figuring it all out, but she's figuring it out quickly.  Oh, and she loves pears.

Sleep
Ok, confession time.  We found a loophole in the sleep goal.  The actual goal states that Aurelia would sleep in her crib for 5-6 hours at a time.  Two weeks ago she fell asleep in our bed and I didn't have the heart or energy to move her (this is what comes of 7 months on 2 hour increments of sleep for Mama Hawk).  She slept for 7 hours.  Since then, she's been sleeping in our bed for most of the night.  The past few nights she's been getting up 3 times again, so I think I'm ready to transition her back to the crib.  This would be the goal that seems the least attainable to me.

Summary
I feel like every week I'm amazed at how far this little lady progresses.  She's doing so well at working towards her goals.  She's also getting closer and closer to sitting unsupported (she loves to arch back when she's sitting up, but it's getting better).  She is on track verbally with all kinds of consonants.  She babbles b's, m's, d's, y's, g's, and I think I heard a p today.  Joey is convinced she said "Dada" to him over skype the other day, and I'm pretty sure that will be her first word.  She loves blowing raspberries and making noises with her mouth.  Her specialty therapist and I did a milestone assessment for children with visual impairments and moderate disabilities yesterday and she does almost all of the 0-3, about half of the 3-6 month milestones, and even a few 6-9 month things.  It's nice to look at milestones on a scale that better fits her needs and takes the CVI into account.  All in all, I feel like we're making lots of forward movement.