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A Rollercoaster…

September 24, 2011

Recently we had an opportunity to take all of our kiddos to Hershey Park, a local amusement park, famous for the smell of chocolate in the air and roller coasters, lots of them.  Drew, Jack, and occasionally Megan and Sophie took advantage of as many of the rides as possible, Lucy and I rode the handicap accessible train over and over with the occasional carousel ride thrown in for variety.  Drew kept asking me if I wanted to trade places with him so that I could ride a roller coaster or two.  No thank you, our life is enough of a roller coaster ride for me .

Last weekend we participated in the DelVal 2nd Annual Energy for Life Walkathon…a high.  On Sunday we had issues with Lucy’s CVL (central line) which lets just say caused me to want to throw her pumps out the window…a low.  One Monday, one of the lumens on her line stopped working all together causing us to spend most of Monday at the hospital doing dye studies, consulting with surgery, tracking down Dr. R, and eventually landing in day med clot busting her line…another low.  On Tuesday morning Lucy started back with music.  She did better than I expected as did I…a high.  Therapy was a bit of struggle this week as it is becoming more and more obvious that our girl is just not able to tolerate as many of the activities that she once did…a low.  One Thursday morning I received a call from Lucy’s cardiologist that her holter monitor from last week came back showing ventricular tachycardia.  Lucy is going to need to wear an event monitor for the next month to get a better picture of what precisely is going on with her heart…major low.  We had a productive appointment with Dr. R Thursday afternoon…I guess you could call it a high.  He discussed some options for our girl that are not necessarily what a mama wants to think about…a low.  Last night Lucy woke with a fever, which landed us in the ED for most of the day…definite low!  We drew cultures and Dr. R gave her a round of antibiotics and sent us home, telling us that he would call if anything grew …a high cause we did not automatically get admitted.   Tonight we had dinner and movie night with our kids while Lucy slept…a high.  After dinner Dr. R sent me an e-mail that Lucy’s cultures are positive…a big time low.

We are currently on our way back to DuPont for the seventh time this week!   I would like to get off this ride please… I will update more when we know more.

Less than a week away…

September 15, 2011

The second annual Energy for Life Walkathon is this Saturday!  We want to thank all of you who have registered to walk, donated, or participated in a “For the Love of Lucy” fundraiser!  Your support, care, compassion, thoughts, prayers, love, friendships, loyalty, and dedication to helping a cause that is so near and dear to our hearts is quite simply…amazing!  We appreciate each and every one of you and want to thank you for all that you do, we could never do this alone!

That being said, if you have not yet registered or donated to our team “For the Love of Lucy” it’s not too late!  Click on the link in this post or over on our left side bar, and click on the yellow  join our team button or donate button and follow the directions on the website.   Help us to reach our goal of raising $10, 000 for mitochondrial research.  We are well on our way to doing this, but are not there yet.

The Energy for Life Walkathon is a pledge based walk, there is no fee to walk, you collect pledges or donations for walking.   It is the hope of the UMDF that by organizing the walk this way we will raise more money for mitochondrial disease as well as awareness as we explain to others why we are walking. 

If you ordered a For the Love of Lucy t-shirt, orders are in and can be picked up at our house or arranged to be delivered if I just happen to be in your neck of the woods within the next few day.  If you are one of our beloved supporters across the country who ordered a shirt, I will be contacting you via e-mail in the next few days to exchange addresses so that we can exchange goods.

Thanks as always for your love and support, thoughts and prayers…they mean so much!! 

Where I last left you…

September 7, 2011

Least you think we blew away during hurricane Irene, we did not.  We didn’t even loose power for more than a few minutes.  We weathered the storm with minimal damage, thankfully!  Lots of rain and heavy winds caused some flooding and streets to be covered in debris, as a result the first day of school had to be delayed by one day.  After some disappointment, we embraced the extra day of summer vacation and prepped for the first day of school Monday night.

Tuesday Morning everyone was up bright and early, and by everyone I mean Lucy too, in fact she was the first to wake at 4:45 am.  I noticed that her j-tube drainage was less than it was 24 hours prior, and also that her g-tube drainage had doubled in volume, my guess…her j-tube had migrated out again most likely causing her to be uncomfortable.  We were all  a little rusty when it came to the early morning routine, having Lucy awake made it even more challenging.  Scrambling around the kitchen, packing lunches, making breakfast, listening to Lucy cry because she wanted to smell everything we were making for the kids, packing backpacks, finding shoes that fit because flip flops are not appropriate footwear for school, brushing hair and teeth, and then lining them all up on the front porch for the infamous first day of school picture…I was tired and it was only 7:50am.  As the school bus pulled up in front of our house the kids ran off. I kissed them all and told them to “study hard”(memories from my childhood).   I yelled to Sophie to be good and to have a great first day of kindergarten, she turned around and shined me her “I’ve got it Mom smile” and then gave me a thumbs up.  Drew, Lucy and I waved to the kids from the front porch.  There was a kind of silence between us that morning, if spoken it would have expressed a sadness.  A sadness that our kids are growing up just as fast as everyone said they would,  but also a sadness that our baby may not grow up and live long enough to experience her first day of kindergarten.  These feelings manifested themselves in other ways and the stress of the morning came out in, lets just say,  not so nice ways as Drew and I said our good-byes that morning.  It was later in the day, when my mom called to ask how things were going, that I realized what Drew and I were “really” feeling and suddenly I started crying.  We try so hard to focus on the here and now, the positives in our life, and the blessings we have been giving…we love our life, even though it is full of challenges that are out of the ordinary…abnormal…down right difficult.  This can make feeling what we are “really” feeling difficult to express at times.

The kids all arrived home from school full of stories from their first days of school.  Sophie and Megan were thrilled about everything,  Jack had a look of fear on his face when describing his first day.  Jack has been blessed(although I think he would choose another word to describe it) with a very experienced, firm, authoritative type teacher.  I think he is going to learn a lot from her and she in turn will learn a lot from Jack.  As a mama it is always difficult to stand at the edge and watch your children learn to take flight as they realize the potential of their wing span…Jack is going to soar ,we know it, he just needs a little nudging! 

Wednesday morning went a little smoother even with Lucy awake.  She again woke early, before the kids, complaining of belly pain.  I called IR first thing Wednesday morning after e-mailing Dr. R on Tuesday, to see if they could get her in anytime after noon as I had to be home to get Sophie off of the bus before hand.  IR was booked solid all day and could not squeeze Lucy in until Thursday morning at nine.  Knowing that Lucy would most likely be awake at the crack of dawn, I agreed to the early morning time slot and felt more confident that if we could fix whatever problem she was having with her tube that she might just feel better and in turn sleep better.  Lucy’s tube was found to still be in position(yeah for Lucy!) but had an obstruction somewhere causing it to stop draining.  We went ahead and replaced her tube, which by the way only took ten minutes because  we could just thread the guide wire through her old tube and pull and replace it with a new one, once connected to drainage her j-tube  poured out over 200mls of bile…poor baby.  Lucy has been sleeping better since getting her new tubie,  I wish I had pushed harder to get it looked at sooner.

We are working at getting back into the routine of tip-toeing early in the morning so as not to wake the sleeping Lucy and getting dressed for school.  Packing lunches now times three at least two days a week as Sophie is enrolled in an extended day program on Tuesdays and Thursdays.  Daily homework and reading logs that need to be signed and returned the following school day.  Getting used to new daily schedules, therapy schedules, nursing schedules, after school activity schedules, and eating dinner before 7:00pm so that we can have everyone that needs to be on a school bus the next morning in their beds by 8:00pm(this one is proving to be a bit more challenging). 

It is an unusual balance of normal and abnormal that we are both blessed and challenged to live with.

Come on Irene…

August 28, 2011

Hurricane Irene is here!  It is raining horizontally, the winds are strong and making too much noise for some of our kiddos to fall asleep,  we are also under a severe thunderstorm warning, and apparently a tornado warning.  We are taking all of this seriously and are prepared.  We have filled our bathtubs with water just in case we lose power, and you know…have to flush our toilets, we have our flashlights charged, ice packs in the freezer so that we can put Lucy’s TPN and meds on ice if need be, and food in the pantry.  Many people have asked us about Lucy’s medical equipment.  All of her infusion pumps run on Duracell batteries, no matter what happens to our power she will continue to receive her TPN, meds, and fluids without interruption.  We also have enough o2  tanks to last us well into next week if need be.  We are safe and sound and obviously still have our power as I am typing this post.  Thanks for all of your thoughts and and concern.  It has been a crazy week,  first an earthquake and now a hurricane.   

T-Shirts…

August 25, 2011

Hurry and order your “For the Love of Lucy” team shirt today!  While your at it, register to walk with us on Saturday September 17th!  

I have to have my order in to the printers by the end of the week so that we can have our shirts in time for the walk!!!!!!!

EFL Team Photo 2010 #4

Thanks to our amazing and talented friend Kimberly, our team has an awesome team logo that we just love!  Many people asked us if they can buy a shirt to support our team…why of course!

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Here are all the details:

  • Shirts come in both child and adult small, medium, large.  Adult shirts come in  XL and XXL as well.
  • Shirts come in pink, green, or black.  They all have the Energy For Life logo printed on the front, the UMDF logo printed on the sleeve, and our team logo printed on the back. 

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  • Shirts cost $10 for those of you who will be walking with us on the day of the walk Saturday, September 17th.  This price covers the cost of the shirt with the printing.

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  • If you want to buy a shirt to support our team we would be honored!  We are selling shirts for $15.00, with the extra $5.00 going towards life saving research.

Let’s do it… one step at a time we can make a difference!

Payments can be made to me via a check or cash.  Leave a comment if you need our mailing address. 

Here you have it, if you have any questions or concerns please feel free to leave me a comment with your e-mail and I will be sure to get back to you.

Just a reminder…

August 22, 2011

We look forward to seeing you at Grottos on Main Street in Newark, DE tomorrow between 4 and 9 pm!  Bring your friends, your family, anyone you know, and help us to raise awareness and funds “For the Love of Lucy”!

Grotto Pizza

*You will need to print this voucher and present it when you order!  Vouchers are valid for dine in and take out orders.  If you are unable to print this voucher, I will be sure to bring a few with me, we are just not allowed to pass vouchers out at the restaurant.

Mania…

August 17, 2011

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I am about to make the understatement of the year…I have a lot on my plate right now!  Sometimes it is just gratifying to write it out and sometimes it is not, let’s just see how I feel when I finish writing this post. 

The 2nd Annual Energy for Life Walk is VERY QUICKLY approaching!  I am not worried that we will not have an amazing walk team, but I am a bit worried that it will pull together at the very last minute, last minute stuff + our life = way too much stress.  Hint, hint, if you are planning to or are even thinking about joining our team “For the Love of Lucy” on September 17th we would be honored, please register!  Like last year, we are going to be selling our team shirts for those of you who are interested.  I am working on the details of just how best to go about doing this.  I will get back to you as soon as I know. 

You know that saying if you want something done ask a busy mom…In addition to getting our walk team together, I was asked if I could reach out to the other teams that are already registered for the walk and assist them with any questions or concerns they might have…really.  I am going to have to carve out some time to call eighteen team captains.  Hey, looking on the bright side, eighteen teams plus ours are going to be walking this year!

Lucy is acting manic…again.  She was awake most of the night yelling, “I-want-get-out-of- my-bed!”  I was so tempted to yell back to her, “I-don’t-want-get-out-of-my-bed”, but of course I didn’t.  Drew and I took turns dealing with all the requests and desires that our little one had up until the wee hours of the morn.  If we weren’t so tired ourselves, we probably would have laughed more than moaned about attending to the little Miss’s needs.  She finally crashed around 4 am, she looks exhausted, but for reasons beyond our comprehension just can not sleep.  Her autonomic body is “off”, her heart rates are swinging like crazy, she is acting crazy, she is very ataxic, her pulse ox numbers are up and down, she is flush and sweaty one minute and cold and clammy the next.  Too bad I couldn’t get all my phone calling done in the wee hours of the night…I had time.

In addition to not sleeping and taking on more than I should, I have the additional role of being a party planner this week.  We are gearing up to celebrate Sophie’s 6th birthday on Friday!  For Sophie this is the moment she waits for all year, this year she decided that a Hello Kitty themed birthday party was what she wanted with and emphasis on art….humm.  I am working on the details and will no doubt pull this off by Saturday for Soph, the day of her party.

Yes, times are a bit crazy around here.  Our main doc is back and we are scheduled to see him in clinic on Thursday, not a moment too soon.  Jack and Megs had their annual eye appointments this afternoon, which meant that I was out and about with the big kids so we spent some time gathering things for Sophie’s party. We are also in the midst of looking for buried treasure in the backyard to help us pay for a new handicap accessible vehicle that we are currently in the middle of negotiating.  At times I feel like my head is spinning, but know that I love to have all the things in my life that make my head spin :).