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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.

Another ER Visit
By Daddy on 1/25/2009 7:59 PM

Hi Everyone- Just a quick update...Jacob got another fever Friday night.  This seemed a little different as he was acting a bit more sick than the other times, moaning and throwing up.  Brian took him into the ER and they drew the CBC, blood culture and started the anitbiotics.  His white blood cell count and ANC came back pretty high, which can suggest infection.  The docs at Grove City and Cincy talked and it was decided to admit Jacob for 48 hours of observation and anitbiotics.  He had a low grade fever all night and finally returned to normal Saturday morning.  JT was back to his old self all day and felt fine the rest of the stay.  Brian and I traded on and off all weekend, one staying at the hospital and the other staying with Justy.  We were all a little bummed as we were looking forward to spending the weekend together as a family.  The good news is that our pediatrician in Grove City allowed us to be d ...

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Cincinnati Trip
By Daddy on 1/22/2009 2:53 PM

Jacob and I drove to Cincinnati yesterday for his photo treatments and infusions.  We arrived around 12:30pm, but were not able to start the photopheresis treatment until 5:45pm.  When we first get to the hospital Jacob gets his port accessed and then they draw a CBC to check his hematocrit level (the number of baby red blood cells).  This takes about an hour or so.  As has been happening the last several trips to Cincy, his level did not come back high enough, so he had to get a blood transf ...

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Happy New Year!
By Daddy on 1/14/2009 2:43 PM

 

 

Mommy here...I know I’m in the doghouse with many of you.  The truth is I did write a lengthy update last week at the hospital and then lost it trying to post it.  I am sorry that you all have not known what has been going on with Jacob.  We really are thankful for your continued love, support and prayers.  I fell off the blog wagon before the holidays and just had a really hard time getting back to it (I don’t know why, I just did. – sorry everyone.)

& ...

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St. Nicholas Day, 2008
By Daddy on 12/7/2008 2:52 PM

Yesterday was bittersweet. 

In the morning, we attended the funeral for Jodi's grandmother.  She was 95.  At the service, Uncle Ray spoke of her legacy, of her family.  The room was full of the expressions of her love, in all ages, shapes and sizes.

Back in Pennsylvania, JT didn't understand when we told him that we'd be gone for much of the day, that our St. Nicholas Day party had to be cancelled.  We were all disappointed and sad on several levels.

But we hadn't counted on grace.  When we called home between the funeral and luncheon, JT was beside himself with excitement, shouting into the phone that he'd received a balloon bouquet in the mail, a huge cluster of helium balloons with a candy basket for ballast.  (Thank you to the Fritz family - you can't imagine how your kindness saved the day.  Really.)  &l ...

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Two Year Anniversary
By Daddy on 12/6/2008 7:55 PM

Hi Everyone.  Too much time has passed since our last blog entry - sorry about that!  I was just reading what the last update I posted said and feeling very thankful for where we are today.  For starters, today marks the 2nd year anniversary of Jacob's transplant.  To be completely honest, we were hoping to be in a little different place than we are, but having said that, we're thrilled that Jacob is thriving and still fighting the good, brave fight!  We are so grateful to our donor who so selflessly sacrificed to give our child life.  I'm also so happy to share that this was the first week since May that we did NOT have to travel to Cincinnati.  I didn't really want to write it until it actually happened and it did!  Jacob's skin continues to soften and Dr. Filipovich felt it was ok to move to Photopheresis treatments 2 days a week, every other week.  What a wonderful change this is for our entire family on so many leve ...

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Justy's trip to Cincy
By Daddy on 11/15/2008 11:35 AM

Well...we survived!  There were definitely a few bumps, but overall a good trip.  The first hiccup was that the childlife center (playroom) was closed both days we were at the hospital for special cleaning.  In all the time we've been at the hospital we never knew they did that.  Jacob and I had been telling Justy all about how much fun it is and how they bring you toys to the room and then when you're done playing with those they bring you more.  Thankfully our wonderful childlife specialist, Amy, had pulled a few toys aside for us and we managed just fine.

Second hiccup was that at 7:00pm on our first day at the hospital Jacob accidentally pulled his line out.  Now in the back of my mind I thought that perhaps this might happen, I just thought that it would be Justy that did it.  Jacob was getting his second infusion when it happened and it wasn't quite finished yet so they had to re-access his port ...

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Staying Healthy
By Daddy on 11/11/2008 10:11 AM

Hi Everyone.  Sorry for the lapse in time since the last blog.  I've been enjoying the time at home with Brian and the boys and have gotten caught up in day to day living - yeah! 

Jacob has been good since the last hospitalization.  He still has a little residual cough that the doctors told us could last for some time.  Brian did catch a mild version of the virus too, but is doing ok now.  We've been having lots of fun taking in the last of the Fall beauty with lots of hikes and caches.  It's strange not taking the boys to preschool.  They miss it.  Just the other day we were in the car and Jacob said, "Mommy, I wish I could go to preschool.  I miss going there."  And then Justy pipes in, "Me too.  Are we still taking a break from that Mommy?"  Ugh. The preschool class has been wonderful though, sending e-mails and pictur ...

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Home sweet home
By Daddy on 10/25/2008 11:25 AM

This morning we all woke up in the same house.  Very sweet.

Jodi and JT limped home Wednesday night and Jodi was in bad shape.  After some real sleep at home and some homemade food (thank you to those who have fed us recently!) she seems to be getting back onto her feet.  JT still has a nasty cough, esp. at night, and we nearly had a temperature situation this morning, but we're hoping to spend the weekend together for once.  We all need it.

Pre-school will have to wait until a later time.  We're disappointed because both boys were learning so much and enjoying the company of other kids but our doctor agreed wholeheartedly - it's simply too much risk at this point.  Spending so much time in the hospital is regress, not progress.  Hopefully we can try again in the spring after the cold/flu season; by that time, perhaps JT will be off the huge doses of ster ...

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Daddy in for the weekend
By Daddy on 10/18/2008 5:31 PM

Brian here in Cincinnati.  Here's the scoop:

JT is a whole lot better than when I left here last Monday.  He's breathing okay and he's been fever-free for 48 hours so the doctor discontinued antibiotics this morning.  The allergic reaction he experienced yesterday (presumably from the IVIG infusion) has abated.   His white blood cell count jumped way up after the GCF infusion.  He's tolerating his feeds well but still experiencing D when he sits down on the toilet.  The next time he goes they want a culture.  His coughing fits are troubling and they're violent when he's in the midst of one.  The doctor told me today that the cough would linger after the other symptoms have subsided. 

Jodi has been feeling terrible.  She headed off to the Hannaford Suites last night after I arrived and I hoped that she would feel much better after a night ...

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Better Morning
By Daddy on 10/17/2008 10:11 AM

For the first time in several days JT woke me up by saying, "Good morning mommy."  He had gotten unhooked from the IV pole for the first time since he arrived and had come to sleep next to me on the pull out couch.  He hopped out of bed and acted a little crazy and was seeming his old self.  But a half hour later he started really complaining that his throat hurt him.  I gave him some tylenol and benedryl and he's a little more comfortable now.  He still has coughing fits about every half hour, which can't help his throat.

We just finished rounds with the team and the plan at this point is for a Sunday discharge.  Clinically Jacob's doing better, but his white blood count dropped to 1.0 this morning.  They are going to give him a drug to help stimulate his WBC count today.  His blood cultures remain negative so that is good.  He's tolerating his feeds as well.  Brian is comi ...

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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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