Tuesday, June 02, 2015

Sweet Summertime


     Summer has officially arrived and so has the heat!!!  I love this time of the year-- even with the awful heat.  Nothing beats summer produce-- fresh fruits, veggies, salads, YUM!  And I love watching my sweet babies play outside to their heart's content.  Playing outside when it's cold is not much fun but when its hot outside, you can just turn some sprinklers on!  We have a packed summer planned full of swimming, playing, the beach, etc.  Matt just got over a bout of the tummy bug but I'm still praying this summer is filled with less illness, less doctor visits, and more fun times.  We will see-- we will be praying for a fun, safe, and healthy summer for everyone!


Outdoor Pic'Nickin!

Having fun on Chad's bouncy house

Sprinkler Time!

His face says it all

Loving it!



Future golfer?

Sweet Face

Just like Daddy

Love those freckles!

And I love her little crossbite...

Silly Kiddos

Sweetness.

Ice Cream Cones with Miss Erica!

The look I received after haircut in which the lady received a 90% tip and one person walked out right after they walked in...  

Miss Erica captured this sweet scrunchie face!

Ready for shopping day with the girls!

LAKE DAY!

First jet ski ride of the summer
This is Matt's idea of a day at the lake- swinging in the porch shade!

Seriously growing up way too fast.

Clemson hat time!

Mowing the grass.

Sleeping with my blanket that I had when I was a baby...

Too cool for words.

ALL boy.  Seriously.  100%.

CHEEEESEEEE!

Monday, June 01, 2015

Cole and Caroline

     Cole and Caroline made their arrival into this world 9 weeks early on May 4th!  Cole was 2lbs 15oz and Caroline was 3lbs 3oz.  They were born a mere 35 seconds apart at 11:19am-- that is SUPER rare for twins to be born at almost the same time!  Melissa did great and has thankfully had an easy recovery.  I was able to visit the babies in the NICU when they were a week old and take a ton of pictures which I will share below.  They have hit few, if any, bumps in the road during their NICU stay and are hopefully coming home next week!  Now the real fun begins...  ;)  I am so thankful that they are here and have done so well.  Continued prayers please for their first year of life as they continue to grow stronger, get bigger, and give their mom and dad more grey hairs than they can imagine!











Saturday, May 30, 2015

Hives from Hades

**This post contains pictures of Matt's Erythema Multiforme rash.  It looks terrible so I felt it deserved a warning!
   
     Matt's immune system remains subpar even though he is doing better than he had been!  Having him at home with our babysitter has made a huge difference but he is undoubtedly going to get cold viruses every now and then.  After having one that we couldn't get to go away, we ended up taking him to the doctor for some issues with his stools, runny nose, cough, etc.  She did a stool culture and then put him on some antibiotics: cefprozil.  He has had hives in the past from augmentin but thankfully not from anything else.  Well, the upper respiratory infection went away, but on day 9 out of 10 of the antibiotics, I noticed he had hives.  I racked my brain thinking what could be the cause of them- he is already on 2 different daily antihistamines!  I didn't think it would be the antibiotic since he had been on it for almost 10 days.  The hives were small and didn't seem to be bothering him at all so I didn't think anything of it.  I gave him some benadryl that night and continued his antibiotic.  The next day, the hives were still there- just more of them.  At this point, I thought it had to be the antibiotic because nothing else had changed, he hadn't eaten anything new, used any new detergents or lotions, etc.  I gave him some more benadryl and figured they would go away completely on their own in a day or two.  I was wrong.  Matt had something called erythema multiforme (EM).  A classic sign of this is a hive that doesn't move around.  For instance, all of his spots stayed in place instead of fading and changing locations.  And not only did they stay in place but they spread and continued to get worse over time.  I took him to the doctor Tuesday morning who suspected he had EM and told me to keep an eye on him.  He gave us a prescription antihistamine to help Matt sleep since that had been impossible the night before.  It just so happened that we had a visit scheduled with his allergy/immunology doctor this week!  What perfect timing since had we not had that visit already scheduled, I may have taken him to the ER on Wednesday with the way his skin looked.  She said he definitely does not need to take cephalosporins ever again.  Lesson learned: antibiotics can cause allergic reactions at any point in the treatment.  Thankfully Matt did not experience any other symptoms that can accompany EM including fever and joint pain.  I was actually very fortunate in that if you didn't know he had hives under his shirt and hair, you probably couldn't tell by the way he acted because they only really bothered him at night.
     As a side note, Matt has also been diagnosed as Failure to Thrive.  This means he isn't growing like he should be for a child his age.  Since last year, he has dropped 3 growth curve percentiles and his weight isn't budging.  I am not sure of what the plan is from this point forward.  The immunologist did some labwork on him and we will see what speech therapy says next week.  We may end up with a consult from a GI doctor when it's all said and done.  I am very proud of him and how much he has been eating lately, but it doesn't seem to be doing the trick.  Prayers please for my stubborn mystery child.  I love him to pieces!


Sunday night- Just a few spots!

Monday morning

Monday morning

Monday night

Monday night

Tuesday night- Thankfully had taken him to the doctor that morning.  You can see the how the areas stay in one place and only get worse in the next progression of pictures.

Wednesday morning :(
Wednesday night.  Thankfully had an appointment schedule with Dr. Wray in the morning or I would have been tempted to take him to the ER.

Wednesday night

Thursday morning.  First sign of improvement thank goodness!!  This meant no steroids needed and it was on its way out of his system!
Such a trooper at the doctor!  And Emily's iPad doesn't hurt to have either ;)



Wednesday, May 27, 2015

Dancing Princess


     Emily is extremely shy but give her a giant stage and a room full of people and that little girl will dance her heart away.  If you ask her to do it at home, nope-- she prefers a crowd!  She had a GREAT year this past year at Carolina Dance.  Next year she will be doing Tap and Jazz!  She said she wants to dance to something with a beat to it... I love her and I love watching her dance!  Can't wait for next year!

Dance Friends

Sweet girls- second year together dancing!

Lashes for miles and miles!  This was for rehearsal and pictures!

Proud girl with her flowers and candy!
She did SO good!


Tired Dancing Legs