At the last minute, angels swept in, did the blood draw the midnight before school started, and Bo walked into school with all the other kindergarteners. I cried. I did not think I would, I'm sure my cry was very different from other parents', but I did, I cried. To see the school district's head nurse, Bo's schoolroom nurse, our good friend (also a nurse), and Bo. It was overwhelming to see and feel so much support. So many people who helped in so many ways, both visible and invisible, to achieve something that so many said was impossible.
And today, the first weekend after the first week of school, Bo's infection is officially clear. I am back to laundry and facebook. Bo is back to Lego's and libraries. We are as back to normal as we will ever get.
I have deadlines, and surprises at work. Jose has plans and art to create. Ahn has yogurt and rice to splatter across the house.
We get another tomorrow, together.
Bo was born on 6/3/07 with the rare congenital disorder currently known as Microvillous (Microvillus) Inclusion Disease. It took 2 hospitals and 5 weeks to diagnose. He became the 61st baby in the US to receive Omegaven. His nutrition is 100% TPN/Omegaven. We believe there will be a cure for this in our lifetime, and that a transplant is NOT the best option for this disease. This is our story.
Saturday, September 8, 2012
Monday, September 3, 2012
detour
Vancomycin levels were lower than the surgeon wanted, so the pharmacy will compound new doses and deliver tonight. Instead of the 1st day of kindergarten, Bo will get to go to the hospital for a blood draw. The laboratory studies from this will: ascertain that the new level of antibiotics are strong enough to kill the bacteria (and not Bo), that the other components of his blood are stable, and that there are no longer pathogens living in his circulatory system. I guess that is a little more important than standing in line for the bell to go inside.
Saturday, September 1, 2012
First the Pinch
As you apply pressure with the needle, first there's the pinch, then the tug.
The stitches. Each pinch remains a surprise, in its inevitability, in its staccato repetition. With multiples of these filigrees, suddenly these ephemeral wisps bind together with a certainty.
Bo is on the 2nd day of a (hopefully) 7 day course of IV antibiotic treatment for the 1st confirmed line infection since starting Omegaven. He had one before. While I know this is a VERY low rate of infection compared to what the literature suggests, it is no less life-threatening.
So before your freak-out. Remember, we live this every day. The very real and imminent threat, and the very normal. Bo, for better or worse, is acting well and has no obvious signs of illness. No fever, no lethargy, no real change in demeanor. Something was a little off, and we had cultures run. As it turns out, he has MRSA(!). But it is currently vancomycin resistant, and we are hoping that the vanco does the trick.
Last week Bo was in a fashion show with 2 of his surgeon's kids. I stayed home with Ahn, who was napping. But we had not seen Dr. L since Bo's last line breakage over a year ago. And as it happens, Jose was able to chat with Dr. L as another dad at the Chalk the Walk. Then a few days later, we are asking him to allow us to treat a line infection from home, call the infusion company at 4:45pm on the Thursday of a long weekend.
Between his antibiotics and his TPN, he still has a 4 hour window of unconnected time. Which is exactly as long as the kindergarten day lasts. So he will start school on Wednesday. Hopefully he will finish his antibiotics on Thursday.
We were disappointed to learn that labs must be run on Sunday, cutting short any plans to visit my family across the state for the long weekend.
But we will be able to go to a friend's 5th birthday party, visit some friends at their lakehouse, and maybe even go to the local Pow Wow.
The stitches. Each pinch remains a surprise, in its inevitability, in its staccato repetition. With multiples of these filigrees, suddenly these ephemeral wisps bind together with a certainty.
Bo is on the 2nd day of a (hopefully) 7 day course of IV antibiotic treatment for the 1st confirmed line infection since starting Omegaven. He had one before. While I know this is a VERY low rate of infection compared to what the literature suggests, it is no less life-threatening.
So before your freak-out. Remember, we live this every day. The very real and imminent threat, and the very normal. Bo, for better or worse, is acting well and has no obvious signs of illness. No fever, no lethargy, no real change in demeanor. Something was a little off, and we had cultures run. As it turns out, he has MRSA(!). But it is currently vancomycin resistant, and we are hoping that the vanco does the trick.
Last week Bo was in a fashion show with 2 of his surgeon's kids. I stayed home with Ahn, who was napping. But we had not seen Dr. L since Bo's last line breakage over a year ago. And as it happens, Jose was able to chat with Dr. L as another dad at the Chalk the Walk. Then a few days later, we are asking him to allow us to treat a line infection from home, call the infusion company at 4:45pm on the Thursday of a long weekend.
Between his antibiotics and his TPN, he still has a 4 hour window of unconnected time. Which is exactly as long as the kindergarten day lasts. So he will start school on Wednesday. Hopefully he will finish his antibiotics on Thursday.
We were disappointed to learn that labs must be run on Sunday, cutting short any plans to visit my family across the state for the long weekend.
But we will be able to go to a friend's 5th birthday party, visit some friends at their lakehouse, and maybe even go to the local Pow Wow.
Saturday, August 25, 2012
Finally!
Kindergarten starts the Wednesday after Labor day. Bo will be in the AM class at the school down the street. There was no fanfare in that announcement from the school district. Just a matter of fact letter stating that we lived too close for bussing.
Send in the clowns.
I started the process for Bo's placement in January. We had 3 meetings, countless emails and several terse phone calls. I consulted a lawyer, other special needs kids' advocates/parents, and sent reference literature.
There will be a 504, and IEP will be written if needed, a nurse will be in the room. We will get an emergency medical supplies kit to have on campus.
We will start going to bed earlier and waking up with more structure. I am still a little dazed.
Send in more clowns.
Send in the clowns.
I started the process for Bo's placement in January. We had 3 meetings, countless emails and several terse phone calls. I consulted a lawyer, other special needs kids' advocates/parents, and sent reference literature.
There will be a 504, and IEP will be written if needed, a nurse will be in the room. We will get an emergency medical supplies kit to have on campus.
We will start going to bed earlier and waking up with more structure. I am still a little dazed.
Send in more clowns.
Thursday, August 16, 2012
The Unsettled Indecisiveness of ThisMoment
I keep waiting for things to be settled. For things to be known before I send another post of electrical impulses into the universe forever. A Morse code of pixels and punctuation.
School starts in a few short weeks and we still don't know where Bo is going to school for sure. But really, do we know anything about tomorrow for sure? I want guarantees. I want to be pandered to. I want someone to sooth my anxiety and fear. I'm certain the superintendant is not really qualified for that.
School starts in a few short weeks and we still don't know where Bo is going to school for sure. But really, do we know anything about tomorrow for sure? I want guarantees. I want to be pandered to. I want someone to sooth my anxiety and fear. I'm certain the superintendant is not really qualified for that.
Wednesday, August 8, 2012
Happy Trails, Laura the Elephant
Turns out that Laura retired, so I didn't have to face the question of whether or not to ride the elephant. Bo enjoyed all the carnival games, and Ahn enjoyed all the sno-cones. The company carnival was a blast and they will be sure to enjoy it even more next year.
Wednesday, August 1, 2012
My Peace, I Give to You... or at least, my toes
There's a part where the priest quotes, "my peace, I give to you." I am rocking A and singing lullabies when I look down at her leg draped across me, and her toes, parallel to mine. And I realize that my joy at seeing this resonance in the smallest feature between us, our toes, is not about seeing myself in her (since we really look nothing alike).
It is the comfort of knowing that she can see me in herself. For as long as she has those toes, she will have a part of me. She may never feel the same way about Jesus as I do. She may never know how I feel about my toes (grudgingly appreciative, they are not cute, but are so so important for balance!). She will probably think my ideas on politics and literature a drippy. But she can look down and know KNOW that there is a very literal part of me that she will carry with her until she too returns to dust.
Of all that is seen and unseen (toes, and DNA, in this case).
My toes, I give to you.
It is the comfort of knowing that she can see me in herself. For as long as she has those toes, she will have a part of me. She may never feel the same way about Jesus as I do. She may never know how I feel about my toes (grudgingly appreciative, they are not cute, but are so so important for balance!). She will probably think my ideas on politics and literature a drippy. But she can look down and know KNOW that there is a very literal part of me that she will carry with her until she too returns to dust.
Of all that is seen and unseen (toes, and DNA, in this case).
My toes, I give to you.
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