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“He is like a tree, planted by streams of water, which yields its fruit in season, and whose leaf does not wither.” --Psalms 1:3

Author: Daddy Created: 10/30/2006 6:06 PM
The cure4treebeard Blog page is your opportunity to walk with us, to be there as our family's story unfolds. Thank you in advance for joining us on the journey.

Day +478
By Daddy on 3/29/2008 7:19 PM
Home! JT was released from the hospital on Friday afternoon and both he and Jodi were here to greet me when I returned from my class late last night. It was great to see them.

JT is skinny but I was relieved to see him in high spirits. 

Jodi is following a nutritional plan for him, slowing increasing his feeds until he’s taking in more and more calories through the G-tube. His D and V episodes are sporadic – we hope that they’ll subside soon so that he can get back on track. In other news, he has recently swallowed a few dry Cheerios, which is huge for him. We do the “swallow dance” and he’s very proud of his progress. This is a journey of baby steps and we celebrate each one.

Jodi and the boys are over at camp tonight and I miss ‘em. I wrap up the gradua ...

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Day +475
By Daddy on 3/26/2008 5:37 PM
Jacob is back in the hospital. Let me fill in the gaps from the last time that I updated the blog…

It’s been a rough week and a half since I last wrote. Justy was sick for 3-4 days and bounced right back, jolly the whole time. JT started with the D and V and it hasn’t stopped. 

I took him to the hospital last week and our trip was a decent one. We had to stop 4 times during the drive down for D + V issues but the good news once we got there was that his liver numbers had improved to such an extent that Dr. Filipovich cancelled the consult with the liver doctors. Sweet.

Easter was low-key. The four of us celebrated Good Friday with a few holes of Frisbee Golf at Moraine State Park. The unexpected snow was a hit and we took advantage of it to make one last big snow fort in the yard. On ...

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Day +465
By Daddy on 3/16/2008 8:21 PM
What a week. 

Justice got sick first. The D and V had hit him pretty hard by Tuesday and Jodi did her best to keep the boys isolated from each other while takingcare of him. On Wednesday morning she met my sister halfway to my parents’ house and gave JT to her to in an effort to protect him from Justy’s illness. I signed up for a personal day, picked up JT in Ohio on Wednesday after school, and the two of us headed for Cincinnati.

So while Jodi took care of Justy in GC, JT and I logged a hospital day together. Access the port, three infusions. A nurse from GI came to look at how the site around the G-tube was healing. She gave us new instructions for cleaning and dressing – it takes a whole lot longer and the first two times we did it I had to hold JT down screaming and crying, not fun. Thankfully, tonight was much better.&n ...
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Day +459
By Daddy on 3/9/2008 6:49 PM
I taught a class this weekend while Jodi and the boys waited out the snowstorm an extra day at camp. The snow is still heavy on the pine trees behind our house – we’re enjoying the contrast of white on blue-green for one of the last times this year. Winter has been a good season.  Thanks to those of you who have sent encouragement in the face of discouraging news.

Jodi has the cold that I had last week and we ask for prayers that the boys will be protected and spared, especially given JT’s weakened immune system. 

Recently I read perhaps the best quote about life I’ve ever seen:

 “It began in mystery and it will end in mystery, but what a savage and beautiful country lies in between.” - Diane Ackerman   

That's perfect.

Day +454
By Daddy on 3/5/2008 7:09 PM
Jodi and JT spent last night at the Cincinnati Hannaford Suites and today at Cincinnati Children’s Hospital. His infusions went well and the meds are doing what they’re supposed to be doing – taking out whole sections of his immune system.

The good news is that both the CAT scan and the biopsies from last week look good, no problems. We’ll take it.

We thought we’d be on track for the light therapy treatment to begin this month but the hospital is on institutional time, which means “Hurry up and wait.” Not easy for someone like me who is constitutionally impatient.

The doctors told Jodi today that the areas of JT’s skin which have become pigmented and very hard will probably never soften, will be that way permanently. This was not my understanding of the situation; I thought there ...

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Day +449
By Daddy on 2/29/2008 8:18 PM
The other three members of my family rolled into Grove City this afternoon. Everybody’s home tonight. Pretty sweet. 

JT tells me, “my new belly friend is tender” and he is taking it easy. I was a little surprised how big the tube is that comes right out of his stomach. The doctor told Jodi that it looks to be healing even better than she would have expected. JT seems very protective of it and that’s probably a good thing. 

He looks different. It’s great to see him without that NG tube taped to his face. At the same time, the steroids are making his face swell up again and it’s always hard to see him not quite looking like himself. 

His skin remains troubling, the GVHD still very much present. However, the initial read on yesterday&rsq ...

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Day +447
By Daddy on 2/27/2008 8:49 PM
Just spoke with Jodi: they’re still in the hospital. JT’s scope went well. The doctors don’t celebrate until the biopsies come back negative but everything was visually clear and healthy in his esophagus and stomach and that’s celebratory news to us. The surgeon was able to place the G-tube so JT has gone from having a “nose friend” to having a new “belly friend.” They just started running feeds through it today and Jodi is going to try a bolus feed tonight before he goes to sleep. He was on morphine yesterday and complained of pain this morning but as the day wore on he seemed to get more and more comfortable.

New news: Dr. Filipovich ordered a full-body CAT scan for tomorrow; that’s why they’re still in Cincinnati. JT’s IGM levels are hyper-elevated and the doctors don’t ha ...

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Day +444
By Daddy on 2/24/2008 9:13 PM
Thanks for your prayers. Our weekend together was awesome. We ate pizza, went sled riding, launched indoor balloons, jumped on the bed, hiked at Jennings, made a snow tunnel in a huge drift; it was wonderful. The boys are so good with each other and we enjoyed their company very much. It’s hard to imagine life or parenting getting much better than it was over the last two days.

Tomorrow Jodi will drop Justy at my parents’ house in Ohio and she and JT will head south to Cincinnati again. His scope and subsequent G-tube surgery is scheduled for Tuesday morning. The way I understand it, they’ll go down his esophagus and take a good look around first, taking a bunch of biopsies while they’re at it. If things look reasonably clear, the surgeon will insert the G-tube so that it comes right out through the wall of his stomach.

They wi ...
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Day +441
By Daddy on 2/21/2008 8:11 PM
Thanks to all of you who have signed the guestbook and sent emails and let us know in other ways that you’re thinking of us. As Jacob always says, we’re “getting through it.”

It’s been a week of mixed news. Good news first: the doctors currently believe that the blood culture indicating an infection was a “false positive.” The type of bacteria that grew out commonly exists on the surface of skin and the new hypothesis is that the original sample was contaminated at some point. All cultures taken in Cincinnati have been negative for bacteria. This is an answer to prayer and after several days of IV antibiotics, they actually discharged JT late this afternoon for a three-day weekend. He and Jodi will arrive home late tonight and our family will be together over the weekend before he heads back on Monday for scopes, surgery, and more in ...

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Day +438
By Daddy on 2/18/2008 7:30 PM
Thank God for Jodi’s intuition that the earlier Dr. Filipovich could see JT this week, the better. When I spoke with her over lunch, she and JT were heading through Columbus and she was feeling a strong sense of peace about making the long trip. Then JT’s nurse coordinator got in touch with troubling news: his blood culture last week has grown out a bacterial infection. The coordinator kindly wanted to give Jodi an opportunity to process what this means during the remaining drive time before she got hit with it upon arrival. It means a minimum week-long stay on the BMT inpatient floor, heavy-hitting IV antibiotics, etc.

Dr. Filipovich’s working hypothesis is that his port (central line) is infected. At this point in the evening he’s already received antibiotic infusions and they pulled a bunch of blood for testing:  the next three days will give us a much better ...

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Raise money for the National Foundation for Ectodermal Dysplasias simply by clicking your mouseGoodSearch.com (powered by yahoo.com) is donating money to charities for use of their search engine.  To use it, install the GoodSearch toolbar to the top of your browser screen and then type in the charity (National Foundation for Ectodermal Dysplasias) and then search as you would on Google.com or Yahoo.com.  The NFED gets a monetary donation for every search!  The more folks that know about this, the greater the donation to NFED, and hence the more money there is to fund research on Jacob's condition and others like his.  Thank you!

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