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.
Wednesday, February 27, 2008
Appetite returns with a vengance
Saturday, February 23, 2008
Near Miss
I prayed. I cried. I tried not to hear his screaming and whimpering. My feet were searing hot with panic. I was exhausted, but only experiencing a fraction of the discomfort of this poor little baby.
I was so out of my mind in the week working up to this night, as Bo had not been able to keep anything down, and was gagging and retching each night. I threatened to get rid of Murray cat, that's how insane I was getting.
We found an arrowhead shaped stone in his morning diaper. I thought that would be the end of his discomfort, but he spiked a fever, who knows why, and it was off to emergency.
It is no secret that parents of special needs kids suffer a much higher rate of: divorce, depression, and substance abuse. All I wanted upon our return home was a stiff drink. Especially since the ultrasound showed at least one more stone he will have to pass. February has been pretty rough for Bo. Jose and I have had our share of sleepless nights, but it is not hard to remind myself that he is the one in pain. I'm just relieved we haven't had to stay at the hospital and expose him to all the MRSA, flu and infectious diseases floating around this time of year.
He slept 13 hours straight last night, had a 2.5 hour morning nap, and is currently 1.5 hours into an afternoon nap. Hopefully all this sleep will help him recover from a thoroughly exhausting week. And while I am grateful to avoid being in-patient so far for the month of February, passing two stones in one month is hardly what I consider a break.
Thursday, February 21, 2008
Lunar Eclipse Madness
Monday, February 18, 2008
Debunking the Parenting Myth: not really reading it
Saturday, February 16, 2008
The Crucible, the lesser
Wednesday, February 13, 2008
A Day in the Life of Bo's Care: not for the faint of heart
Above, a new dressing on the catheter that goes through his subclavian vein into the jugular that feeds right into the heart. Bo's Omegaven and TPN (all his nutritional needs) get pumped into his body through this "line" into his heart, and to all the cells in his body.
Below is a description of all the stuff we do for Bo on any given day. In the medical/insurance world, this is called a "24-hour plan of care," and must be incredibly detailed. Also, this list is to try and convince the audience (insurance) that we need more nursing care in the home.
And while this list seems daunting, the reality is that the biggest problem we are having is keeping him from getting bored during the day. The weather is too cold and snowy for our daily walkies anymore. So he ends up getting toted around a lot. He probably has a few more diapers than his peers, and they're probably bigger diapers, and you have to sling his TPN backpack over one shoulder for the morning, but taking care of him during the day is probably not that different from any other baby in most other ways. And he sleeps through the night, so after, say 7pm, it's all grown-up time.
- 6:15-7:15pm aseptic connections for tubing set-up (this is also done if his line ends up on a pool of excrement in the morning, requiring stopping the pumps and re-spiking the bags with new aseptically connected lines as an infection prevention measure)
- 7-7:05am aseptically flush lipid (Omegaven) line with saline
- 3-3:05pm aseptically flush and heparin lock Broviac (CVL)
- hourly (24hrs) monitor input and output for dehydration (typically 4-7 watery and explosive defecations, 6-7 urine output)
- every 4-5hrs (24hrs) monitor temperature 3-4x for elevated temperature as an indication of infection
- 24hrs monitoring and adjusting lines for security and to prevent CVL breakage/removal
- 24hrs monitoring skin pallor for jaundice as indication of return of cholestasis
- 24hrs administer IV antibiotics and fluids as needed
- weekly measure weight, length and head circumference to ensure proper nutrition compounded in TPN
- several hours a day, daily maintain sterile technique, and a clean environment conducive to aseptic line construction
- 6:30-7am clean bedding from fecal matter to prevent line infection
- weekly/as needed perform cap changes with sterile technique
- weekly/as needed perform CVL site dressing changes using sterile technique; this can be done more frequently if the dressing detaches itself from the child before the week is up, if it becomes soiled with vomit or other moisture, or if the catheter loop has been pulled out.
- 5-5:45pm bathe infant with CVL
- every 4-5hrs (24hrs) monitor skin integrity and CVL entry site for discharge, discoloration and patency monitor skin integrity of diaper area for dermatitis (he is at high risk for this due to excessive, watery, and explosive diarrhea)
- 24hrs constant vigilence 24-hour supervision for 20-hr TPN cycle and 12-hr lipid cycle; monitor line integrity
- 7:15-8:30am, 10:30am-1pm, 3-5pm developmental play to achieve age-appropriate milestones: OT/PT/speech therapy
- 7:05-7:30am, 12:30-1pm, 6-6:30pm express milk into bottles, label and freeze milk, wash and sterilize pump parts
- 7:30-7:45am, 1-1:15pm, 6:30-6:45pm- nurse for comfort and to maintain oral-motor development
- 5:45-6:15pm monitor and manage medical supplies: stocking, receiving and re-ordering1-5hrs, daily, depending on whether Bo is in-patient, and other variables medical communication management: pediatrician, GI specialist, visiting nurse, EarlyOn, Great Start, home infusion company pharmacist, primary insurance case manager, secondary insurance case manager, hospital staff (as needed)
- 24hrs constant vigilence monitor pumps and adjust as needed with alarm
The only meds Bo is currently on are his TPN and Omegaven. When he has a line infection, the antibiotic and dosage is determined by the microbiology results. For instance, his last (and only, knock wood) line infection required a Vancomycin dose of 50cc @ 1cc/hr. This was administered Q6 for 10 days. The schedule was grueling and was like so:
- 5am- take antibiotic out of refrigerator to achieve room temperature by time of administration
- 5:30-6am- aseptically assemble tubing and additional pump for antibiotic administration
- 6-7am- aseptically flush 3rd lumen of triple splitter, clamp the Omegaven line and stop its pump (as its compatability with anything has not been studied), administer antibiotic
- 7-7:10am- stop the antibiotic pump, flush that third lumen again, re-start Omegaven pump
- rinse, lather, repeat 11am-1:10pm, 5:30-7:10pm, and 11pm-1:10am... for 10 days.
It should be noted that monitoring diaper area during this course, and for the week following must be incredibly diligent, as the natural microflora of the skin is also disrupted and often results in yeast blooms in that area when the normal bacteria are destroyed. Break-down of skin, red bumps, rash, raised plaques, etc. Often we will use prescription diaper cream with miconozole prophylactically during and for 5 days after antibiotic treatment to prevent diaper rash from occuring. This must be administered at each diaper change (7-10x/daily). Then, when he had pink eye, the procedure require eye drops administered 4x/day for 7 days:7-7:10am- dose both eyes with 2 drops each, and again at 11am, 3pm, and 7pm.
Additionally, because of his excessive, watery and explosive diahrrea, in the mornings, after we clean his bed, change his clothes and give him a new diaper, we have to monitor his penis for engorgement with puss and discharge, which may be a precursor to a urinary tract infection. This requires pulling back the foreskin, inspecting for redness or discharge, squeezing the penis and inspecting for discharge, and monitoring for swelling or redness in the penis. This last step is performed at every diaper change.
Monday, February 11, 2008
Bo Takes Chicago
Bo models his SuperHero Frubi's in anticipation of sunnier days.
Our first non-medical trip was a great success. Bo was an inspiring addition to the Oley Foundation's regional conference, he crashed the APSPEN professional conference, and attended a GSB alumni brunch! He did have a virus that made him gag and retch with nausea (and his mommie very anxious) at night, and we drove home in a white-out, but we got home in time to hook him up, and we even got to squeeze in a visit with his favorite docs from Boston, Drs Gura and Puder! They agree with Nurse Kathy that Doc Cloney is doing a fine job with his weight; not too skinny, not bloated with TPN. And he even said Puder! Well, it came out as, "puh-puh-puh." But he has the right idea.
Once again, Tio Ren and Auntie Jennie provided invaluable help getting us both settled in and packed up, as well as general Bo-duty.
Medical update: He weighed in this morning at 14.78lbs, and his labs have been reduced from weekly to biweekly! I have mixed feelings about this, as we love being able to consult with our rockin' visiting nurse weekly, but the reduction of draws means a reduction of opportunity for his line to get contaminated, and it also means that his GI thinks he's stable enough to not need to see weekly lab data.