Our Quiverfull

Aug. 22, 2009

stranger than fiction

Posted in Noah Updates
Noah's broviac is, as I had guessed, un-fixable.  We don't know why or how it came apart the way that it did - in fact, the doctors keep saying that they have never seen anything like this before.  (Leave it to Noah!)

As discouraging and sad as it is to lose a central line after just 3 1/2 days, I figured we would come in, start an IV, pull the line, and get a new broviac.  Nope.  In a twist that would make Hollyworld screenwriters proud, there is a national shortage of broviacs.  The hospital only has neonatal sized lines (like the teensy one in Noah) and all of the others are on backorder.

How surreal is this?  How does something like this happen??  Wouldn't you think that demand for central lines would be pretty stable and predictable?  It's not like broviacs are the hot new Christmas toy and manufacturers just can't keep up!  Jeff used to work in management in a manufacturing environment and is utterly baffled by this as well - how on earth do manufacturers of central lines just fail to make enough?

The amazing doctors here have been working very hard and brainstorming and researching what to do for Noah.  It looks like there are three options:

1) Put in a port instead of a broviac.  This is a central line that does not stick out of the skin and has to be accessed with a needle.  These are usually used for things like chemo, but not usually used in situations like Noah's where it would be accessed all of the time for TPN.

2) Try to hold off until the hospital can get a more appropriately sized broviac in stock.  This would probably mean a PICC line.  Noah sustained a lot of damage to his blood vessels during his last visit and I'm not sure that they could even get a PICC line in (this was a matter of discussion a few last week) - plus there is concern that scarring from a PICC would make a future AV Fistula harder to place.

3) Find another hospital that still has larger broviacs in stock and transport Noah by ambulance to have his surgery there.

This whole thing seems just incredible to me.  I'm just thankful beyond words for our team here and all that they are doing to figure out the best plan for Noah.  It is such a blessing that they were able to start formulating plans even late on a Friday night.  I'm not sure when we will know which route we'll be taking, but I will update when we have information.

Please pray for wisdom for the right plan (each has very real pros and cons) and for safety in carrying out the plan.  Also please pray for his new IV to hold as long as possible.  It was truly heartbreaking to have to take Noah back in to the treatment room for another IV last night, and I am thankful for Noah's loving and skilled nurses.

***Please take a minute to visit Eithene's blog (link on the right) to pray for her and leave a comment.  Sweet little Eithene is in the hospital even more than Noah is, and is really having a hard time right now.  This whole family is very precious and needs your prayers for Eithene to feel better and for her dad Sean to find a teaching job in the next couple of weeks.

Blessings,
Kate
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Comments

Aug. 22, 2009 - Untitled Comment

Posted by narnialover95
I'm praying for you guys!
Blessings,
Taylor
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Aug. 22, 2009 - Untitled Comment

Posted by nachoaveragegirl
*jaw drops* A NATIONAL SHORTAGE ON BROVIACS??? Whoa. That is...how does that happen? I mean, seriously peoples, come ON! It's so weird it's almost funny!
Leave it to Noah.

Love you,
~Hannah Grace, who is still stunned and amazed.
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Aug. 22, 2009 - New Broviac

Posted by Carla
Praying hard, Kate, for the best and wisest solution for sweet Noah. Admittedly, I like Option No. 3 and will be praying for a local hospital to have exactly the right Broviac Noah needs. God, you, Jeff, the docs. . . they all know what the best option is for Noah. Praying for the right decision and then peace. . . and of course, healing and comfort and no fear for Noah. I will go over to the other child's blog and pray now. Hang in there, Mom. I wish I was 1/100th as tough as you are, Kate!
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Aug. 22, 2009 - Wow!

Posted by Anonymous
That's one post I never even thought could happen! A shortage! It makes me wonder now just how many people actually uses them. Wow! I'm praying for guidance for all of you in this decision. Couldn't a hospital that has the right one for Noah just give it to the hospital where Noah's at? Obviously I'm not very familiar with how it all works but that's the first thing that came to my mind.

Lynn in FL
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Aug. 22, 2009 - Option 4????

Posted by Croy8forJesus
Hi Kate,
Is it not possible for a hospital with the correct size Broviac to send it to you? This way Noah, himself, would stay put and the Broviac would come to him and the team who is most familiar with his care.
We are earnestly praying...
With Deep Love (1 Peter 1:22),
Dennis & Linda Croy and family
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Aug. 22, 2009 - Crazy!

Posted by Anonymous
How crazy is that to be short on a line??? Last summer when I was pregnant with our sixth baby, I was on Heprin, and there was a national shortage of it and I couldn't get any for a month, so I had to be on a different blood thinner. How crazy to have a shortage of anything life saving in the medical community!
We will be praying for the best outcome for Noah. And for much better IV's than last time.

Amy
http://insearchofnormal.blogspot.com/
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Aug. 22, 2009 - Untitled Comment

Posted by adoptionmom
I'm sure there is a logical reason this can't be done, but couldn't they find a hospital with a broviac and transport the broviac to your hospital? It wouldn't even require an ambulance.
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Aug. 22, 2009 - Untitled Comment

Posted by Anonymous
Port. I had a strong, positive feeling about Noah having a port. I don't know why. It was sudden, and the day of his surgery.
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Aug. 22, 2009 - Untitled Comment

Posted by Anonymous
It seems like getting a broviac to the child would be easier than getting the child to a broviac. But then, I'm not a doctor.

Thinking of you all and I hope you get some answers soon.
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Aug. 22, 2009 - WOW!

Posted by Tami
That is unbelievable! Another option would be to find a hospital that has a broviac in stock and asked them to send to you. Or if it is within driving distance maybe one of your blogger friends would be close enough to a hospital and could bring it to you. I am within range of driving to Winston-Salem or Charlotte. It seems that it would be easier to get a broviac to Noah than to transport him to a different hosptial.

Let me know if I can help in any way!

Love, Tami
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Aug. 22, 2009 - Untitled Comment

Posted by cancrrider
Why can't another children's hospital that has a larger sized broviac in stock send it to Noah's surgical team to implant at his current hospital? It seems a much simpler solution and far less costly and traumatic than sending Noah to another hospital for his broviac placement surgery.

Praying for the best solution for Noah and all of you.
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Aug. 22, 2009 - Pray without ceasing!!

Posted by Anonymous
I have and will continue to pray for Noah. I pray for him along with my little girl who is still in the hospital. I understand the daily battles, and the, "Leave it up to Noah or leave it up to Alana. Some of my friends have ask me how Noah is doing. I let them know as you update. Keep strong. God is right there with us.

Hope
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Aug. 22, 2009 - Robin In OHIO

Posted by Anonymous
Praying for clear direction and the quickes path there...the hospital where I work just had a shortage on the nuclear isotope that is made a plant in Canada had flooded and there is only two plants in the world that make it it lasted for a long time and it was nationwise it amazed me about that
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Aug. 22, 2009 - Untitled Comment

Posted by Kate
My son has a port and I love having it ~ if Noah can't get a new broviac, I hope a port would work for him.

Many prayers.
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Aug. 22, 2009 - I don't even know what to say about this...

Posted by Anonymous
Seriously?!? OUT of broviacs? Yes, that seems beyond bizarre. The closest thing I can think of is last summer when our huge regional hospital ran out of Neocate- the most common elemental formula... but this is far beyond a neocate shortage!

Kate, I'll be praying the drs can figure out the best plan for Noah. We frown on PICCs- they permanently damaged E's veins and cost her most of her central line access. I hope you don't have to go that route. :(

God has a plan!

And, thank you so much for thinking of us and sending prayers our way. We love you guys!

PS- the surgical service here was DROOLING over your broviac vests... they want them!

Jessica :)
www.fromthebanksofjordan.blogspot.com
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Take a look at our sometimes crazy but always blessed life as we homeschool our eight children, run a homeschool business, and serve God as He leads us. You can also follow our baby Noah as he struggles with some serious health issues - we covet your prayers for him.

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