Friday, March 04, 2011

Cousins, Trains and Transformers

Two weeks ago marked the first time I've been to the Portland Children's Museum. Jeanne and Daylon, at least once before. What a fun place! Each little venue was uniquely entertaining, the featured set being of Curious George. We didn't quite make it to the Curious George area but it goes on until June I believe. I don't think Daylon would mind it one bit if we went back a few more times. Especially if at the same time while taking in all the sights and sounds of the museum he can do so enjoying the time with his cousin Kaia. We had set up a play date for the cousins. It was such a treat to see the two of them have so much fun together. Pictures!

    
 
  


Daylon has recently starting building 'trains' using his toy cars and trucks. If that wasn't cute enough anytime we would ask Daylon about his trains or show him pictures of trains he would answer 'choo choo'. When we show him rabbits, 'bop bop bop'. How. Fun! Here is a picture of one of his trains.



A few of Daylon's train creations have included using GoBots I had brought out for him from storage. I grew up playing with GoBots, G.I. Joe, Star Wars of course, Transformers. It's been a blast digging through boxes finding and busting out 25+ year old hearty metal vintage toys I had as a young lad and handing them down for my son to play with. This photo link I posted a few days ago via Twitter shows the latest Transformer I handed to Daylon to enjoy playing with. A small coffee treat for whoever guesses correctly the name and year of the Transformer. I'm still figuring out the timing for when I want to bring out the ultimate Transformers keepsakes; original Megatron and JetFire. I still have all the accessories to go with them as well. Yeah, nerd. But Daylon will have jealous friends. And that's pretty important =).

Friday, February 18, 2011

Food Cart : PB&Js Grilled

As I mentioned in my previous post Portland is food cart crazy! We've tried a handful with oh so many more on our list to try. Last year Jeanne and Daylon found a gem of a cart up on 23rd, PB&Js Grilled. They were brand new. Jeanne immediately was interested and the three of us went back soon after and have been loyal regular customers ever since. Shane and Keena are the owners; super busy, super motivated, masters of their craft and creations and most of all super friendly, ready to have a good chat without ever losing their inviting smiles. We've enjoyed getting to know them and have admired their passion to provide such a tasty, unique yet original product (using fresh and organic ingredients made locally or made themselves).

Our first grilled sandwich was The Joy; smooth dark chocolate spread, sweet coconut filling and almond butter sandwiched between think pieces of challah bread lightly basted in butter then grilled to perfection. We've tried just about all their sandwiches (Spicy Thai! Betty!) and although all their treats are superb Jeanne finds herself enjoying their Pumpkin Pie creation (the perfect blend of their yummy pumpkin butter, Two Tarts caramel sauce, scrumptious pie crust and peanut butter again between butter basted challah bread all grilled together just right) most of the time where I always find myself craving that Joy. Daylon has nibbled on every one we've ordered and seems to be very indiscriminate. He loves them all. We know he would love having a whole sandwich to himself. One of these days when Jeanne and I aren't looking Shane and Keena just might hand him one. I don't think we'd mind. As long as Daylon shared.

This last weekend we met up with our good friends the Phipps' and they finally were able to experience PB&Js Grilled. We ordered our treats, enjoyed some hot beverages from Two Tarts (a local bakery/cookie/coffee cafe), shopped the toy store around the corner and enjoyed fellowship and pleasant conversation. Here is a photo of Shane and Keena working their magic :


Here be their menu and they are active on twitter @pbjsgrilledcom. I'm looking forward to when their newest idea/creation finally makes the menu : a Pecan Pie Sandwich!

Tuesday, February 15, 2011

2.0

I've neglected blogging. I blame Facebook. But I've said goodbye to that addictive networking horse and have been sober now for almost of month. Breathing the social site free air has been fresh and sweet.

So now what? Are there folks our there that still read my blog? Do I have an audience? Let me know. I thank those few that are indeed still here and dedicated. It is because of you that I feel reinvigorated and willing to pen my ramblings once again and share stories, pictures, thoughts, prayers.

There really is so much to tell since I last wrote. Too much really. Thinking it all over I can easily say that our Lord is Good, Gracious, Forgiving, and at work in our lives. We are healthy, we are joyful, we are active, and boy are we tired. Jeanne is more beautiful everyday and Daylon is growing up way too fast for our liking. Jeanne, I don't deserve, and Daylon, what a character. He runs and doesn't walk. He loves it when I toss him in the air and when I chase him. 'up', 'dada', 'ball' (which is Mom to him, heh heh), 'plea (se)'. And he sure does suck down his smoothies! Can it really be February 2011? Daylon coming up on 2 years old? Wow.

How about a few pictures to go along with my 'restarting' to blog?

Uncle Josh took this wonderful photo of me and Daylon playing on the
beach. It was over New Years where Jeanne and her siblings planned a
few days for us all to get away and spend time in wonderful fellowship,
eat glorious amounts of food and play plenty of board games.
Pacific City, Oregon, 2011.

The next photo is of Jeanne and Daylon reading at
Costco. He points to all the letters and numbers
he can and is doing super well recognizing them.
'O?' 'I?'. Cuuuute! Tigard, January 2011.

Portland is quickly becoming known for its food
cart craze. So many varieties, so many treats, so
many yummies. A few weeks ago the three of us
went to one called the Potato Champion. We
devoured our chili fries. And froze our rear-ends
off. PDX, January 2011.

I've abandoned Facebook, but I'm still somewhat active on Twitter. And you'll notice my tweets, twerps, twits, whatever, show up on the side of my blog over there. I make use of a photo tool called Instagram that I sometimes use to edit and post pictures that I then share via Twitter. Keep an eye out for those posts.

A few other things; Jeanne and I are hooked on Cake Boss and Fringe, I'm addicted to running, Daylon still loves wheels, trucks and cars, Jeanne grows more and more stunning every day (yeah, I mentioned it above but I'm trying to score some points here =) ), and Daylon loves the soft serve ice cream from Costco. He helps us out eating most of it.

Question: is BlogPress really a good tool to use for mobile?

Tuesday, July 21, 2009

Fantastic News!

This morning Daylon had a checkup appointment with his cardiologist. And it couldn't have some at a better time since we have been anxiously awaiting the results of Daylon's second Holter session from over two weeks ago.

Dr. LeGras' medical assistant first had Daylon weighed. She weighed him in at 11 pounds 13 ounces! Dr. LeGras than came in and after giving Daylon a quick checkup (everything sounded perfect) I immediately asked about his Holter results; no SVT episodes! We. Are. So. Excited! What does this mean though exactly? It means that the combination of Digoxin and Propanolol are working well together at their current dosage. Dr. LeGras instructed us to continue administering the medications at their current dosage for at least another three months until Daylon's next appointment. He'll have another Holter session done at that time as well.

There were two other brief points of discussion.

First, with Daylon gaining weight and getting bigger shouldn't the dosage of his medications be bumped up for body weight to medication ratios? Dr. LeGras seemed confident that the combination of the medications at their current dosage are working fine and he doesn't want to tinker with it. And as Daylon continues to grow, and because the current medications are working, his body each day is 'growing' out of possible reoccurring SVT episodes hopefully encouraging us to wean the meds away as we go. Jeanne and I have been and will continue to monitor Daylon's heart rate and if we suspect SVT's are reoccurring we can immediately call Dr. LeGras and he'll see Daylon, evaluate, and bump the med dosages up if need be. Dr. LeGras reminded us again that even though the second Holter session showed no SVT's in that 24 hour period Daylon's little heart could still at any moment go into SVT. The results showed that Daylon and his heart are heading in the right direction but it is still obvious and vital we continue the process of appointments, Holter sessions and medications.

Second, Daylon will be two months old tomorrow. We have a pediatricians appointment next week and a vaccination schedule will most likely be determined. Dr. LeGras said there are no interactions between the Digoxin/Propanolol heart meds and vaccinations and said so without any worries, concerns or hesitations.

What a wonderful day to start our Tuesday! Praise the Lord for His blessings and healing hands!

As a side note Daylon and his bum have been making for a wicked liquid bazooka as of late! In the past few days he has managed to project and shower us with poo during diaper changes. It has been glorious! What can we do but laugh, and laugh we did, till we were crying! We can see immediate relief on Daylon's face. And I'm sure he likes watching us laugh over seeing our arms drip with smelly yellowish orange goo. Proud parents =)!

Saturday, July 18, 2009

Big Smiles!

Daylon was so smiley all morning yesterday! I was able to capture a few on video. Enjoy!

Tuesday, July 14, 2009

Still waiting...

Almost three weeks ago, as part of his SVT monitoring and treatment, Daylon came home from his cardiologist with a Holter device. Holter devices capture EKG readings for a 24 hour period of time and in Daylon's case reveals how many SVT episodes he has in that period of time. This first Holter session revealed that he had had eight SVT episodes, not very encouraging at all. This meant that in addition to the Digoxin medication he was taking another medication, Propanolol, was prescribed.

After three days of taking the Propanolol four times a day another Holter session was done almost two weeks ago. The cardiologist was hoping that the additional medication would bring the number of episodes down, hopefully driving that number down to zero. Jeanne and I are little anxious, and worried to say the least, since we still haven't heard back about the results! We are praying Daylon and his little heart are indeed improving!

Here are links describing Digoxin and Propanolol. The short of it is is that Digoxin keeps the heart's electrical impulses at bay while the Propanolol is used for hypertension, for Daylon this means slowing his heart rate down just a little.

Photos!






Above photos were taken July 3rd. The last one is of Daylon and the Holter device. Poor guy!


Daylon meeting his Great-Grandpa Wood.

Sunday, June 21, 2009

Concealed Accessory Pathway...huh?

As you all know Daylon has been diagnosed with Supraventricular Tachycardia (SVT). This means that in addition to normal pediatric visits, Daylon's first 6 to 12 months (hopefully no longer than that) will also include appointments to a pediatric cardiologist. The first cardiologist appointment was this past Friday.

Before diving into the details of how Daylon's first appointment went I'm guessing most of you might still be wondering what SVT is exactly. Unfortunately there seems to be a lack of material on SVT, at least for non-medical persons. General materials on cardiology are plentiful but documentation on specific cardiac studies, such as bradycardiac and tachycardiac arrhythmia conditions, have been hard to find. Daylon's cardiologist provided us with some materials that describe basic cardiology and arrhythmias, and the following is a crude overview of those materials as best as I can decipher and understand it.

The heart as a pump
The heart has four chambers; two receiving chambers on top and two pumping chambers on the bottom. For the heart to function as a good pump, the top chambers (the atria) must squeeze first, filling the bottom chambers with blood. The bottom chambers (the ventricles) then squeeze, pumping blood from the right side to the lungs to get oxygen and from the left side, out the aorta to the body.

The normal electrical system
The normal pacemaker of the heart is on the right side in the top chamber. It controls the normal heart rate automatically (faster when you run or are excited, slower when you sleep or rest). An electrical wave passes from the pacemaker (also called the sinus node) through the top chambers of the heart, much like the ripples from a pebble thrown in a puddle. This electrical wave makes the top chambers squeeze.

The only way for the electrical signal to get to the bottom of the heart to make the ventricles squeeze is through the normal conduction system. This conduction system is like a cable the runs from the atria to the ventricles and is called the atrioventricular node (AV node). This AV node cable has a delay mechanism in the upper part that slows the electrical signal. When the signal reaches the middle of the heart, the electrical wave spreads rapidly to the bottom chambers making them squeeze. Once that happens, there is no way (normally) for the electrical signal to get back up to the top part of the heart.

The normal sequence of electrical events, therefore, allows the normal top-delay-bottom squeeze of the heart muscle for normal heart pump function.

Abnormal heart rhythms
Abnormal heart rhythms can be too slow or too fast. Slow rhythms are called bradycardias. Fast rhythms are called tachycardias. Daylon's condition is of the tachycardia type so I won't write anymore on bradycardias.

There are many types of tachycardias. Some are only located in the upper chambers of the heart (for example, atrial tachycardia, atrial flutter), some are located only in the bottom chambers (ventricular tachycardia or VT) and many involve both the top and bottom chambers (supraventricular tachycardia or SVT).

Remember in a normal electrical system that the only way for the impulse to get from the top to the bottom of the heart is through the AV node. Sometimes, even if the heart is structurally normal (normal valves and chambers), there is a "short circuit" in the system. If you consider the AV node the normal electrical connection in the heart, these short circuits may be called "accessory" (extra) connections. They are tiny strands of muscle, smaller than a piece of hair, that bridge the areas where the atria meet the ventricles. This allows an electrical impulse to get from the top to the bottom through a route other than the AV node and can also conduct from bottom to top, allowing impulses to get back up to the top from the ventricles after a normal heart beat.

There are two main problems that accessory connections permit. The first involves conduction from top to bottom. If an abnormal atrial rhythm call atrial fibrillation occurs, the top of the heart beats very fast and irregularly (quivers like jello), the accessory connection can allow rapid conduction to the ventricles causing ventricular fibrillation. This is very rare, but very dangerous and life-threatening. Daylon does NOT have this sub-type of SVT. The second problem is with conduction form bottom to top. Normal conduction does not allow this to happen. Sometimes, the accessory connection does and the electrical signal "re-enters" the top chamber of the heart. Once that happens, the normal conductor doesn't care where the impulse comes from and it conducts again to the bottom chambers. A tachycardia "circuit" can be set-up, with a fast rhythm going top-bottom-top-bottom-top...until somthing makes it stop (vagal maneuvers or drugs such as Digoxin). This second sub-type of SVT is indeed what Daylon is most likely having episodes of.


Phew. Now, Daylon's appointment. He had both an electrocardiogram (EKG) and an echocardiogram (ultrasound). The EKG quickly told the cardiologist that Daylon does NOT have the Wolff-Parkinson-White (WPW) syndrome SVT. WPW is an SVT where if an abnormal conduction pathway runs between the atria and the ventricles, much like an accessory pathway, the electrical signal arrives at the ventricles sooner than normal. The cardiologist was quick to note that this SVT is not good at all so it was a relief to hear that Daylon's SVT is of the above mentioned non-life threatening accessory pathway SVT. The ultrasound indicated that Daylon does indeed have a murmur as well but it is benign. Another interesting bit that the ultrasound revealed is that Daylon's heart has a tiny, tiny hole called a patent foramen ovale. This too is benign and can actually be found in 25% of adults apparently. The ovale hole is a mechanism that helps the unborn baby and his or her heart pump normally while in the placenta. During the strenuous laboring and birthing process this hole seems to close up, but in plenty of cases this hole persists after birth and closes as the baby ages and grows. The cardiologist also noted that Daylon most likely had a brief SVT episode while being examined under the ultrasound.

A nurse weighed Daylon after the ultrasound. He is at 8 pounds 11 ounces, having gained almost a full pound in one week! Because of his growth and increased body weight Daylon's dosage of Digoxin has increased. After six months of Digoxin and with Daylon's continued body development the goal is to hopefully have the number of SVT episodes or occurrences as close to 0 as possible, if not 0. The other goal is that the condition will have been outgrown or in the process there of and that we can start weaning him off Digoxin medication. Note that the Digoxin medication (derived from the foxglove plant) keeps the heart in normal rhythm as much as possible and tries to keep the heart from using, in Daylon's case, the accessory pathway that causes the heart to race. Simply put, Digoxin keeps the number of SVT episodes to a minimum in hopes that as Daylon grows his heart will out-grow the SVT.

And finally tomorrow we are scheduled to take Daylon in to get fitted for a Holter device. This device provides for a continuous 24 hour period EKG reading. Though the cardiologist is almost positive Daylon has the accessory pathway SVT sub-type, the 24 hour reading will give the doctor a very accurate assessment of the SVT condition and will also indicate how well the current dosage of Digoxin is working. In one month we are scheduled for another visit to review the progress of Daylon's SVT and to review his body weight and dosage of Digoxin.

Friday, June 19, 2009

3 Weeks Old

Daylon is 3 weeks old! He. Is. Beautiful. And healthy. And hungry. And fills his diapers well. And cuddly. And smiley. Jeanne and I are totally in love with him!

Tomorrow (or this morning rather) we head to the cardiologist to get a current status on Daylon's supraventricular tachycardia condition. Not quite sure what sub-type of SVT Daylon has, certainly a question I'll try and remember to ask the specialist. We are praying that we'll find that his body is 'working' or 'healing' itself out and that we can start to wean him of his Digoxin medication. Later on in the day I'll post an update on how the appointment went.

In the meantime, photos, lots of them!!!


That boppy sure is comfy!


Aunt Joanne.


Uncle Andy.


Cousins Daylon and Jude.


Cousin Jude.


Daylon's first bath.






Jeanne, Daylon, and Cousin Kaia.


Cousin Kaia.


Cousin Kaia and Uncle Woody.


Aunt Brinda.


Proud Grandparents.


Grandparents and Grandchildren. I love this shot!






Hi there bright eyes!




3 weeks old!

Tuesday, June 02, 2009

Daylon's Homecoming!

At 11am this morning our Daylon was discharged from St. Vincents NICU! Beyond words how wonderful it feels to be home with our son. All I can do is sing Praises to the Lord! Photo time!


May 29. Snuggle time with Grandma Forbes.


June 1. Proud, beautiful mom!


June 1. Meeting Grandma and Grandpa! Grandpa gave him his first noogie! And Grandma started him out right with a jersey t-shirt of Griffey Jr.!


June 2. Finally get to go home!


June 2. Simply....perfect!


June 2. Giddy-up! I want to go home =)!


June 2. Proud parents just arriving back home.


June 2. Post feeding comatose =).


June 2. Sweet, sweet boy. In love.

Friday, May 29, 2009

Baby Daylon

On May 27, 2009 at about 6:15pm our son Daylon Emery Wood was born. Our beautiful boy is here!

Over the past 8 and half months we had the perfect pregnancy. We prayed and prepared for an all natural process and birth through and through. But on his birthday and during a regular weekly midwivery visit we were very suprised to find that Daylon's heart rate was at a scary 200-220. Our wonderful midwife hustled us over to the hospital here at St. Vincents and after evaluating his heart rate some more and taking a look at his heart via an ultrasound it was determined we needed to have an emergency c-section performed.

Jeanne. Was. Awesome. I love her so, so much. What a rock. But our little man was giving us more of a scare when his heart starting racing at around 240-250 right after his birth. I followed him into NICU where immediately he was put on monitors and IVs. Broke my heart and I had plenty of tears. Even more tears came when a few hours later and with plenty of medications in him for the determined condition I mention below his heart rate was dropping which was good but he was struggling to breathe. He finally normalized around 7am on the 28th.

It was determined that he has Supraventricular Tachycardia (SVT), not life threatening, but certainly scary when dealing with the heart. Basically his heart and the electrical methods that fire his heart into pumping are doing so off rhythm and when natural Valsalva maneuvers don't succeed, medications are needed to get the heart calm. His body could decide to completely normalize and have no need for meds in a day, a week, but most likely it'll be a few months before he'll outgrow the condition.

We named our son Daylon Emery after Daylon Emery Harrington who passed away over the Memorial Day weekend. Our deepest condolences, love, and prayer to his family. From the bottom of our hearts we so, so, so much appreciate the Harringtons' blessings to name our son after their son. What an honor and privilege.

Praises to the Lord for giving us such a beautiful, perfect, healthy baby boy. And all our love, prayers, and thanksgiving to all our family and friends for their love and prayers! We sure can't wait for you all to meet him.











Update: Monday June, 1. Jeanne was discharged yesterday and was sent home with some nice pain killers and well wishes from the wonderful doctors and nurses. We have continued to go back to the NICU almost every 3 hours to feed and change Daylon, and of course hold and snuggle with him. Tomorrow is a big day! He is coming home! We picked up his Digoxin medication for his heart, learned exactly how to administer it and listen to his heart with a home stethoscope, and Jeanne and I feel well prepared for having him home given he has been on a pretty consistent diaper/feeding schedule in the ICU. All is ready for him. Lord, we ask for your wisdom and for your love.

With all our hearts we love and thank our Lord, family, and friends!