The $3200 Garage Sale

You read that right.  $3,200.  The garage sale that we kept putting off due to sheer fear of the quantity of "stuff" ended up netting $3200 for the CHARGE Syndrome Foundation!  We ended up having the sale on July 8th and 9th.  Mike got the pleasure of coming home from his 7 day business trip to Columbia and enduring a two day garage sale!  I have to say though - we picked THE BEST weekend as the weather was gorgeous - certainly a million times better than the pressure cooker we are living in today!!

The sheer volume of sale items was insane.  I am incredibly grateful to all of our friends and family who donated their stuff, their time, and who even came by to shop.  A special thanks to my mom, Tammy, Gigi, Margaret (my mother in law), Amanda Marshall, Annie Cue, Cari Miller (and her mom!), Colleen Creedon, Gina Byers, Liza Parke, Lisa Michalak and many others who made the garage sale a HUGE success.  We raised just over $1000 and with Baxter (Mike's employer) matching the entire $1100 check we wrote and Aon Hewitt (my employer) matching up to $1,000 - our little garage sale made $3,200 for the Foundation.  Not bad.  As much as I cursed myself for coming up with this hair brained idea - it was indeed worth it.  In fact, our very special garage sale was made even more special as another CHARGE family from the area - the beautiful Crystal Masionis and her kids Eva (who also has CHARGE) and Bailey and her girlfriend Sarah and her little man Charlie.  It was the first time I had a chance to meet all of them in person and they drove quite a ways from Round Lake Beach to visit us.  Eva is 6 and she is an amazing little girl who in so many ways reminded me of Finley.  Our two princesses have many of the same mannerisms and watching Eva was almost like watching a grown up version of Finley.  Here are a couple of pictures of the ladies.  I especially like the second one because it looks like Eva is telling Finley a secret (and she probably was)!



Its been a busy month as we've had tons of doctor's visits hitting at once.  I feel like we are finally riding the down side of the wave though and I have admitted more than once in the last few weeks that I have definitely bitten off more than I can chew lately but I am vowing that after the CHARGE Conference next week, I will be laying low for a while!  That said, the week before last I took Finley to her appointment with Dr. Chin, the pediatric surgeon.  The visit was to address what course of action we'd take on her hiatal hernia.  Dr. Chin ordered a upper GI so that we can assess exactly how big the hernia is and then he will be consulting with Dr. Holinger (her ENT) and Dr. Bass (the GI doc) to get their opinions on how successful they think doing a Nissen Fundoplication would be for Finley.  Dr. Chin explained that normally they would not surgically correct a hiatal hernia for someone with no outward symptoms of reflux but since the reflux is exacerbating her airway issues, Finley may be a good candidate.  We will certainly not be rushing in to anything though.

Finley is getting around so well these days, the feeding pump, nor anything else seems to stop her.  When we brought her home on a continuous feed - we joked that if we had to eventually follow her around with the feeding pump we would if that meant that she was mobile and most days - that's exactly what we are doing!  The good news is that she is eating exceptionally well and able to be off her pump for most of the day now since she's tolerating bolus feeding so well.  She is making tremendous progress and we are just sitting back and watching in amazement!

Finley's PT brought this old school walker to see how she liked it.  She didn't know to move her feet but she sure loved standing in it!
On Thursday of next week (the 28th) Mike and I are heading to Orlando for the CHARGE Syndrome Conference.  Its a bi-annual conference and it will be our first and we are so excited (Okay - me definitely more so than Mike - he doesn't get as jazzed about these things as I do)!  I love seeing all of the posts and messages on Facebook from all of the other families that are going.  So many people that we've never had an opportunity to meet in person - not only families who have children with CHARGE - but many, many individuals that have CHARGE - young and old - it will truly be an experience like other!  The only trouble I foresee is that there are SO many incredible sessions scheduled - I worry that we won't possibly be able to get to all of the ones we want to.  This will however be the FIRST time Mike and I have ever been away from the kids overnight.  Yes, its true.  In nearly five years Mike and I have never had an adult only vacation or even sent the kiddos to the grandparents house for a sleepover.  So we are nervous.  Not that we are worried anything bad will happen, we are worried that Nate might be a basket case.  I hope its not a long 4 days for Gigi and the grandmas!

Gigi and her girl!

Nate trying to beat the heat!
No joking - he fell asleep like this on the stair after a long day at the garage sale!

Nate wearing my boots (note the foam sword tucked in to one)

Nate's bowling field trip - Daddy was a chaperone!

This picture did a good job capturing Nate's face of disgust when it was time to go home!

The sunflower that Nate planted at camp.

My beautiful tomato that I am waiting patiently to ripen!

The basil plant I nursed back to life.  Can't wait to combine this with the aforementioned tomato and some fresh mozzarella! (That is rosemary and a pathetic lavender plan in the background)
I hope you all are enjoying the summer and staying cool!

Untitled.

I have a lot of things swimming around in my head right now and among all of those things, a title for this post was no where in sight so this is as good as its going to get!


Lots of updates as it has again been forever since my last post.  We still haven't had that garage sale - UGH.  My garage and basement are swollen with the tremendously generous donations from our friends and family so THANK YOU!  We had to postpone it a couple of times because its been difficult to find the time to get everything ready.  But - at this point I have overwhelming motivation to get it done because we can't park on one side of the garage and so I think we are now shooting for the weekend after next...


Our team, Powered by Finley, participated in the 2011 Race for the Kids last weekend to benefit Children's Memorial Hospital.  We had a GREAT team which even included Finley's primary nurses from 5W and from the looks of the picture below - Finley was happy they could participate!  Thank you from the bottom of my heart to everyone who came out - it was a beautiful day!




We have been very busy with doctors appointments of late - them seem to ebb and flow like this - we will go a couple of months with a smattering here and there and then at all once, she comes due for a bunch of them and Mike and I find ourselves needing to divide and conquer.


Two weeks ago Monday, Finley saw the opthalmologist, Dr. Yoon, who was impressed with her glasses and the improvement of her nastagmus (sp?  Shaking of her left eye) but her left eye is still fairly lazy and Dr. Yoon wants us to come back in 3 months to check it again as he may want to do surgery if there is no improvement by then.  We definitely weren't  expecting this because we thought that the correction of her eye would be more cosmetic, in which case we would opt not to do it at this time - we will be having some additional discussions with Dr. Yoon on this front.

This was my view from the rocking chair of Finley chillin' in her crib.
We are frequently meeting with the cochlear implant audiologist.  Finley is trying out some loaner hearing aids that are more powerful that her previous ones and we've definitely seen some changes in how she is attending to different sounds.  This is obviously really good news but the wild card that remains is understanding how well she's hearing them - how loud and how clear things are.  Next we will be going for testing on her new left hearing aid and this will be particularly interesting because her left ear is the one that has the profound loss.  More to come on that...



Finley was having some trouble gaining weight for the last several months and so we took her in the week before last for a weight check.  I am happy to report that in the last 4 months she has gained almost 2 pounds and grown another inch!  This is largely attributed to the fact that girlfriend likes to eat (as evidenced below).  We have recently begun pureeing table food for her which means that she is eating a lot of what we eat now and she is really liking it.  She also LOVES chocolate chips cookies - which is what she was eating in the below pics - that is chocolate all over her face!  We finally got in her for another swallow study last week - it had been over a year since her last one - and she passed everything through honey thick liquids.  This is a great improvement for her and we think she actually would have done even better had we practiced some thinner liquids before her test but we were too nervous to give them to her.  Now we will work on syrup thick, nectar thick and and then regular thin liquids.  She is also doing really, really well with her bolus feeds and is up to 120 ml/hour (4 ounces) and then she's able to be off her pump for a few hours!  We are still finding though that the bolus alone doesn't seem to sustain her for the whole 3-4 hours off the pump and that we need to feed her in between to keep her blood sugar where it needs to be.  She has been able to spend most of the day off the pump though beginning in the morning and then going back on the in the evening.  She has become quite mobile in spite of the fact she isn't formally crawling yet but it doesn't matter to Finley - she either bunny hops (her modified version of the crawl), rolls or scoots on her back!  



A week ago (on Father's Day nonetheless) Finley was admitted for what we affectionately refer to as her 6 month "tune up".  This is the same testing she did in December where she had a bronchoscopy to look at the condition of her airway but this time she also had an endoscopy - and this was to see if the doctor could determine the cause of her reflux.  Her ENT, Dr. Holinger, shared that there was no change in her airway.  While it hadn't gotten worse, it also hadn't gotten better even in spite of the change in her medicine regimen.  This was a bit of a bummer because he said she still has chronic bronchitis - not like the kind that can be treated with antibiotics - chronic inflammation of the brocchioles due to irritation cause by the reflux of her stomach acid.  Her endoscopy on the other hand showed that she has a hiatal hernia which is likely the culprit causing the reflux and her GI doc, Dr. Bass, suggested that the best way to correct this would be Nissen Fundoplication (read: more surgey).  The Nissen is a procedure where they go in and sort of tie off the entrance of the stomach making it possible for things to go in but not come out.  While this seems straightforward enough, they don't always work - sometimes they tie them off too tight, sometimes not tight enough.  That said, we have an appt with the pediatric surgeon, Dr. Chin, on July 7th to discuss options.  Finley did great with her testing in spite of the sub par planning on the surgery coordinators and she was able to come home later on Monday as planned!  YEY!


Mr. Nate is growing by leaps and bounds and every single day he says or does something new and stops me in my tracks and makes me think about how fast he's growing up!  He is now in his second session of tennis and he's actually participating with the coach (and even hugging him on occasion!) and he started tee ball a couple of weeks ago and is doing AWESOME with that!  He's been my big helper in the yard this summer too as I have been working on getting some perennials planted around the yard.  When my peonies were getting ready to bloom - he was on peony watch for me and would check them EVERY day to see if they opened (see below).



Nate has been enjoying picking out his own clothes lately.  Here is his rendition of the "Green Lantern".  We're not quite there yet on the matching but he's getting there....

If there was one thing I could photograph every time it happens it would be this.  Finley loves to touch Mike's unshaven face and she takes his cheeks in both hands and pulls his face close to hers and then proceeds to go crazy and laugh!  Its the best thing in the world!

Nate with all of his soldier guys lined up on the window sill.





I had to share this final series of pictures because of Finley's hilarious obsession with the big orange ball.  This is an exercise ball that she uses for her therapies and when its sitting out, Finley will pursue this ball like its her job and frankly nothing with stand in her way - not even the fact that she is hooked up to her feeding pump!  Once she sets her sights on it, she gets to it however she needs to (per my previous comments above) and she mauls it.  She loves to lie there and put her feet all over it but most of all - she likes to lick it - if you look closely at the last picture - you can see her little tongue is out and she's ready to pounce!






The CHARGE Conference in Orlando is just about a month away now and Mike and I are all set to go - we are registered and our room and airfare is booked!  We are even going to stay and extra day so we can spend some time with Mike's Aunt Ruth and Uncle Fred - we are SO excited!  I just wanted to say a HUGE thank you to everyone who has donated items for the silent auction - I cannot possibly tell you how much I appreciate it!  I have been working with the folks at the Foundation to try to secure items for the auction and I was SO SUPER EXCITED that I ended up getting 2 round trip tickets from Southwest Airlines!!!  This came after I was receiving email after email of rejections and was frankly getting pretty discouraged.  That said if you or anyone you know might be interested/able to donate items for the auction - gift cards, merchandise, crafts, anything - please email me (Tracy_Yaiko@hotmail.com).  The silent auction at the conference is one of the primary sources of revenue for the Foundation (Charge it for CHARGE being the other).  So please - if you are able to help out that would be tremendous!  The conference is July 28th - 31st in Orlando so I would just need to receive the donation sometime before then.  THANKS!  

Have I lost you?

I am fairly certain there is probably not a soul reading this blog anymore as I realize that it has taken me forever to update it.  I am sorry but things have been a little out of control lately - work, life, you know...pretty much everything.  I've not had any time for well....anything really.  Exactly how long has it been?  Well - sometime between my last update on April 18th and today, Blogger completely reformatted their site - it took me about 5 minutes just to figure out how to do a post. The benefit of taking so long in between posts though is that this one will be a Picture Palooza!

As I mentioned, things have been busy.  Finley has been to the endocrinologist and unfortunately - she hasn't gained any weight in the last 8 months.  Her doctor reached out to the dietitian, whom I have not talked to directly yet, but she left me a message that seemed to indicate this didn't trouble her too much.  Meanwhile, we are working hard to try to fatten Finley up.  She is gobbling up her food like its her job and I went out and bought a Magic Bullet today so we could start semi-pureeing some regular foods (instead of baby foods) for her to eat so she can get a little variation and more calories.

We've also been to the audiologist and she took new ear molds for Finley's hearing aids.  She also moved her high power left aid to the right ear and gave us another high power loaner for the left ear.  We've not been able to try it yet though because she accidentally broke Finley's hearing aid mold on the left and so we will get the new ones tomorrow.  She also finally tested well in the testing booth and the results were exactly consistent with her ABR that she had in December (which is good).  Tomorrow she will see the audiologist again to get her new molds and be tested in the booth again - this time with her hearing aids in - and she will also have some bone conduction testing done.  And by the way - we LOVE our new audiologist Megan.  There is such a difference between Megan (from Children's) and the one we were seeing at Lutheran General.  Although we liked the last one - Megan is just completely of a different caliber.  YEY!


Finley rocking a pony tail.  Which didn't last long once she laid down on it and pulled it all out.

Finley and her boyfriend Tad.  She will do anything for that chubby green frog.

"Hey Ms. Marla - I can see this book now!"

We had a great Easter at my mom's house.  The day before, Nate and I enjoyed coloring Easter eggs.  I made a point of trying to take a bunch of pictures there because frankly I just forget most of the time.  I got lots this time!

Nate's Easter masterpieces

Uncle Javy and Viola

Silly Lily

Auntie Tammy and our Princess

Can't see.  Sun. In. Our. Eyes.

Trying to get a picture of me and all of the girls was nothing short of comical as you can see.

Well - at least we are all in the picture

Momma and her sweethearts

One of the best pictures ever.

This was a picture my brother in law Jim took imitating my mom's picture taking ability

Much better!

I am a sucker for babies who sleep with their butts in the air.

Long day at Grammy's.  This is what the back seat looked like on the way home.  But the peace didn't last....

When we got home, I turned on to a circus clown and tried my hand at making balloon animals.  Balloon kit courtesy of Auntie Tammy.

In case you were wondering what granulation tissue looks like - here it is.  This is actually a picture I took and emailed to the g-tube nurse at Children's and she confirmed my diagnosis and called in a prescription and saved me a trip to the city!  Thanks Teri!

Nate getting ready to chop down the light pole in the backyard.


This is one of my most favorite pictures ever.  I didn't take it - Mike did. I picked up my camera one day and was looking through my pictures and I found this one.  Love it!

Nate cuddling with his sissy.

Hilarious picture of Finley sleeping.  She looks like she's posing.
Let's see.  Other things that have happened since I last posted...I have postponed my garage sale because I started getting anxiety about being ready by the end of the month.  It was impossible.  So right now, we are targeting the second weekend in June.  Thank you to everyone who has donated things for the garage sale: Mom, Tammy, Cari, Amanda and Gigi and to all of those who have stuff coming!  Anyone out there who is going to be doing some spring cleaning let me know if you are interested in donating!

I am also currently working on collecting items for the silent auction that will be held at the CHARGE Conference at the end of July.  I have been sending letters, emails, proposals, you name it.  Its absolutely crazy to me how restrictive some organizations are in terms of only donating to specific charities, need 6 months lead time, etc.  Nuts.  Anyway, I hope some good donations come out of this.  If any of you reading this would be willing to make a donation - please email me (Tracy_Yaiko@hotmail.com) and I will send you more details.  Also, if you know someone that might be able to donate - by all means ask if they are willing to contribute.  Some of the things that people can donate - season ticket holders can donate a pair of tickets for a game, un-used airline miles, gift cards, etc.  Other things to consider - themed baskets, etc.  Again, if you or someone you know is able to contribute - please let me know!

TTFN.

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Finley's Medical History

Born on 8/8/2009 - Finley is taken to Children's Memorial Hospital via the transport team 12 hours after she is born.  She is having trouble breathing and is turning blue.  She is immediately admitted to the NICU.

8/9/2009 - Finley is diagnosed with Tetralogy of Fallot, a congenital heart defect and laryngomalacia, a condition that causes her to aspirate whatever she swallows in to her lungs.

8/21/2009 - Finley has open heart surgery to place a Blalock Taussig shunt to help facilitate proper blood flow.  When she is older, she will require a full repair of her heart.

9/10/2009 - Finley is released from the NICU.  Because of her laryngomalacia and reflux, she is fed 100% through a nasal gastric tube.

9/14/2009 - Finley is re-admitted to the hospital for an infection in her surgical wound.  Finley's genetic test comes back - she is diagnosed with CHARGE Syndrome.

9/15/2009 - During a CT scan to assess the infection, the doctors notice something strange on her CT.  It appears Finley has a malrotated bowel and will require surgery.

9/23/2009 - Finley is examined by the opthalmologist and she is found to have colobomas, a condition common with CHARGE Syndrome, in both eyes.  The degree of her visual impairment is unknown.

9/30/2009 - Finley has the Ladd's Procedure to correct the malrotation and also has a g-tube placed.  

10/7/2009 - Finley has a sedated ABR to check her hearing.  She has a mild hearing loss in her right ear and a moderate to severe loss in her left.  Her loss can be at least partially corrected with hearing aids.

10/8/2009 - Finley is supposed to be released from the hospital today but she has been having low blood sugars.  The endocrinology is called in to evaluate her.

10/29/2009 - Finley is finally released from the hospital with a unconfirmed diagnosis of hyperinsulinism.  Actual diagnosis requires fasting blood tests - because of her heart condition, it is not safe for her to fast.  She needs to have her blood sugar tested every three hours and we are taught how to administer an emergency glucagon injection in case her blood sugar gets to low.

11/1/2009 - Finley requires emergency injection because she cannot sustain her blood sugar.  She is taken to the local ER and transported via the transport team to Childrens Memorial.

11/10/2009 - Finley is discharged from the hospital on a 24 hour continuous feed.  We add polycose to her milk to help her keep her blood sugar at an acceptable level.

11/22/2009 - Finley is taken to the local emergency room with a bad cold - she is having trouble breathing and her oxygen saturations are low.   She is transported via the transport team up to Children's Memorial.

11/25/2009 - Finley is released from the hospital - just in time for Thanksgiving.

12/8/2009 - Finley is taken to the local emergency room for observation - she has a bad cold.

12/21/2009 - Nate is chasing the dog and the dog runs in to Finley's IV pole, knocks it down and pulls out her g-tube.  She is taken to the ER at Childrens to have it put back in.

2/10/2010 - Finley is admitted through the ER at Childrens - she has a bad cold again.  Oxygen saturations are low and breathing is labored.

2/13/2010 - Finley is released from the hospital.

4/17/2010 - Finley is taken to the ER at Childrens - she has pus draining from her belly button.  They suspect a urachal cyst - they send us home with orders to return on  Tuesday (during our scheduled visit) for an abdominal ultrasound.

4/20/2010 - Finley is admitted to Childrens for an overnight stay.  She will have a swallow study and abdominal ultrasound on Tuesday and a CT and sedated echocardiogram on Wednesday which will require anesthesia.

4/21/2010 - The anesthesiologists have trouble intubating Finley, so they call in her ENT to have a look at her.  He observes that her airway is 75% closed off - partially due to scar tissue from previous intubation and partially due to an infection.  The diagnosis is subglottic stenosis and may require her to have surgery on her airway.  She is immediately admitted to the PICU and put on a 24/7 breathing treatment and antibiotics and steroids to help reduce the inflammation.

4/26/2010 - Finley is well enough to be taken off of all oxygen.  Immunology and Infectious Disease are called in to examine Finley because the culture of her throat are growing staph and strep.  Infectious Disease is trying to figure out what could have caused her infection.  Immunology labs will be drawn to determine if Finley has an immune problem which sometime occurs with children with CHARGE.  This is the second significant infection she has had since she was born.

4/27/2010 - The lab calls to say that they mis-read Finley's airway culture.  It's not growing staph - its only growing strep.

4/28/2010 - Immunology labs are back and don't show anything significant.  Finley's lymphocyte counts are low but that isn't unusual for a child who is fighting an infection.  The doctor wants to re-examine her before her first birthday.  In the meantime she cannot have any live vaccines.

4/29/2010 - Finley is discharged from the hospital.  The ENT will do a bronchoscopy before her heart repair surgery to determine next steps on her airway issue.

5/11/2010 - Finley has open heart surgery to repair her heart.

5/17/2010 - Finley begins to show signs of infection which is later identified as a urinary tract infection.

5/25/2010 - Finley is discharged from the hospital.

5/30/2010 - Finley goes to the ER at Childrens because of fussiness, sweating, heavy breathing.  And echo later identifies that the pressure gradient around Finley's pulmonary valve is an astounding 90%.

6/1/2010 - Finley is admitted to Childrens to try a medication called Propranolol to help ease the pressure in her heart.

6/2/2010 - The Propranolol brings the pressure in Finley's heart down from 90% to 50%.  Finley has a positive test for C. difficile which will require antibiotic treatment.

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