JourneyWithTheCrosiers

Sunday, June 20, 2010

37 Weeks...12 more days!





Posted by JourneyWithTheCrosiers at 5:20 PM
Email ThisBlogThis!Share to XShare to FacebookShare to Pinterest

1 comment:

The Harrell Family said...

Cute Pics! You guys look SO happy! Paisley is so so cute!!

June 21, 2010 at 10:36 PM

Post a Comment

Newer Post Older Post Home
Subscribe to: Post Comments (Atom)

Birthday Tickers from WiddlyTinks.com

Birthday Tickers from WiddlyTinks.com
Wordle: Crosier

Visitors To Our Blog

hit counter

Followers

Blogs We Write

  • ►  2011 (44)
    • ►  November (1)
    • ►  September (1)
    • ►  August (3)
    • ►  July (5)
    • ►  June (4)
    • ►  May (4)
    • ►  April (5)
    • ►  March (4)
    • ►  February (8)
    • ►  January (9)
  • ▼  2010 (114)
    • ►  December (12)
    • ►  November (5)
    • ►  October (5)
    • ►  September (9)
    • ►  August (17)
    • ►  July (26)
    • ▼  June (17)
      • I am...
      • 2 Days Earlier!
      • 37 Weeks...12 more days!
      • Dada's Day
      • Neurosurgeon Update
      • Pool Girl!
      • Couldn't Be Happier
      • New "Beckett Arrival Date"
      • Oh, the imagination of a 2 1/2 year old!
      • The NAME Announcement
      • Little Mommy
      • My Little "Fwimmin" Girl
      • Autumn, Christian, and Kylie
      • Wigglin' Piggies
      • New bedding
      • My Big Helper!
      • Whatever Eli does!
    • ►  May (11)
    • ►  April (4)
    • ►  March (8)

Blogs of Friends

  • The Elders
    Laynie
  • Star and Erin
    Creative Photography Newborn Photoshoot
  • The Farming McAfee's
    6th annual blogger playdate
  • Paws & Puzzles
    Seoyandira Penyedia Jasa SEO Terpercaya
  • Just For the Record
    Kate is 8
  • Steece's Pieces
    Kellogg's Cereal in a Cup- a Busy Mom's Dream!
  • The Utley Crew
  • The Davis Family
    DSC_0316e
  • A Day in the Life of the Davidsons
    Happy Easter!
  • The Jolley Chronicles
    An Upcoming Change
  • Rollin' with the Rooneys
    My blog up and running
  • Quintsofkentuckiana's Blog
    Pics!
  • Brooke, Ryan, and Kira
    Emotional Mess
  • The Pitmans
    One word..........
  • The Sanders Family
    Been A While
  • The Utz Family
    New Pic In The Living Room!
  • The Ott Family
    The Perfect Day!
  • The Nickrand Family
  • The Harrell Family
  • Daniel, Alicia, Sam, and Jake
  • Derek ~ Khirstin ~ Braeden ~ Winston

Amazing SB Friends and Families

  • The Great Umbrella Heist
    Everyone loves a meal plan.
  • Beyond Measure
    Benjamin's 11th Birthday Party: Fortnite meets Ninja!
  • HennHouse
    Surgery #1 (and recovery)
  • Texas Triggs
    New Trailer for the Wheelchair
  • Tuttle Tots
    You never know what the future holds
  • Ridding Family
    More Walking
  • The Kowalski Krew
    The Remaking of Life
  • Controlled Chaos!
    Brain trumps cord .... latest recooperation update on Shea
  • Immeasurably More
    Photo A Day...August 2015
  • Choo Choos and TuTus
    2015
  • Amanda Kern
    Why my child doesn’t suffer from spina bifida
  • Our Lemonade Stand
    Unanswered Questions
  • Our Redirected Flight
    Why now and why New York
  • Trinity Sue Arthur
    Judi online slot
  • Heaven Sent
    Out Loud
  • Having a "Hull" lot of FUN
    Ella's First Tween Jewelry Booth at the Summer Penelope Lane Boutique THIS Saturday
  • Prayers for baby Rachel
    Skater Girl Fun
  • The Little King
    Countdown to Number Six
  • Our Little Miracle
    4 years. 4 weeks : An adoption story
  • Pieces of a Life Well Lived
    Success Maybe
  • Our Special Blessings
    Three.
  • Andrew's Journey
    Happy Endings
  • Spina Bifida Kids
    SPINA BIFIDA ASSOCIATION OF KENTUCKY NEW DESIGN SB SHIRTS
  • Annabelle Grace Flower Summers
    Facebook killed my blog!
  • Our double blessings
    A look back, the boys journey.
  • Braelyn and Gwendolyn
    Smile BIG
  • Journey of a Lifetime
  • Running With Triplets
    I run because some cannot.
  • Love Like Rain
    Perks of an SB kid!
  • Avery's Odyssey
    Avery is trying to stand
  • Our little Gibblet
    Roller skating party
  • Potters a plenty!
    A life of fortune.
  • The Mathews Children
    A "Whole" New Therapy
  • Baby Boy Bush
    update time!
  • Dancing in the Rain
    No, I have not fallen off the face of the Earth
  • A Gaggle of Giggles with the Gowers
    Video with the Girls
  • Whitney's Family's Blog
    From Four to Five times Two
  • Growing from the Obstacles...
  • Baby Keicher
  • My Many Blessings
  • our family
  • Krousehouse
  • Lance, Nicole, and Jacob
  • The Thompson Family

Facebook Badge

Meghan Faith Crosier

Create Your Badge

Rodney and Meghan

Rodney and I started dating in November 2000, when we were juniors in high school. We were married June 17, 2006.

I am a third grade teacher at North Harrison Elementary School in Ramsey, Indiana. I am currently in school earning my Master's degree.

Rodney is a truss designer at Classic Truss in Clarksville, Indiana. He also designs plans for entire houses.

Paisley Faith

Paisley is three years old. I can hardly believe she is growing up so fast! She rarely stops talking until she is fast asleep. Paisley loves to sing and does so pretty much all. day. long! She is quite a spit fire of a little girl, but is also the sweetest child in the world. She has a memory that is even better than mine! Love that silly girl!

Beckett Josiah

Beckett is so sweet and loves to have all the attention. He laughs and smiles all. the. time! Beckett hates tummy time, but loves to sit and play. Beckett loves his big sister and lights up when she plays with him. After a rough start with 20 days in the NICU and 2 surgeries, Beckett is doing awesome!

Beckett's Beginning

6/30/10: Born at 1:20 pm, 8 pounds 7 ounces, 20 inches long
7/1/10: Myelomeningocele repair surgery and insertion of EVD (exterior ventricular drain) to temporarily drain fluid from the brain. 2:45 pm-6:45 pm. Off the ventilator in recovery room. We saw him around 7:30.
7/2/10: Lots of waiting and staring at our beautiful boy! Finally ready to eat for the first time around 5:00 pm after the anesthesia wore off. What a relief!
7/3/10: Beckett was in a lot of pain as the anesthesia was completely gone by this point. Pain meds/Tylenol today!
7/4/10: Bandages from back incision removed.
7/9/10: Removal of EVD and shunt placement. 1:15 pm-5:30.
7/15/10: "Flip Day!" Beckett was given the okay to be on his back today, which means...we finally got to hold him! Lots of snuggling! :)
7/19/10: VCUG-normal. :) Hip Ultrasound-normal. :) Renal Ultrasound-normal. :) Circumcised.
7/20/10: HOME!!! After 20 days in the NICU. Discharge weight: 8 pounds 6.7 ounces.
7/23/10: First visit to see Dr. Nassim. Weight: 8 pounds 6.7 ounces.
7/29/10: Suture removal and wound check with Joy at Dr. Moriarty's office. No problems.
Weight check/One month check-up with Dr. McMonigle. 8 pounds 12 ounces (30th %). 21 1/4 inches long (75th %). Head circumference 37 cm (50th %). All looks great! :)
8/9/10: No more weight checks needed for this big guy... 9 pounds 7 ounces!!!!
8/11/10: First Steps Case Conference...Beckett will receive PT once a week for one hour. There is no real concern with his development at this point, but he qualifies for services, so he might as well get them!
9/1/10: Head CT...all normal. A little fluid. Back Dec. 15 for an MRI.
12/15/10: MRI. Fluid in the ventricles similar to the day the shunt was placed on July 9. Shunt revision on Friday. :(
12/17/10: New shunt placed by Dr. Moriarty. New location...behind the right ear instead of the frontal location! :) In Kosair Children's Hospital until 12/19/10.

My Family from WiddlyTinks.com

Medical Terms I Frequently Use

Spina Bifida (SB): is a developmental birth defect caused by the incomplete closure of the embryonic neural tube. Spina bifida malformations fall into four categories: spina bifida occulta, spina bifida cystica (myelomeningocele), meningocele and lipomeningocele. The most common location of the malformations is the lumbar and sacral areas.
**Beckett's defect was at S2 and was removed on July 1, 2010**

Hydrocephalus: also known as Water on the Brain, is a medical condition. Children with spina bifida often have hydrocephalus, which consists of excessive accumulation of cerebrospinal fluid in the ventricles of the brain.

Shunt: Shunts have been used to treat hydrocephalus for more than 50 years. The devices allow excess cerebrospinal fluid to drain to another area of the body.
**Beckett's shunt was placed on 7/9/10.**

Meningocele: The least common form of spina bifida is a posterior meningocele (or meningeal cyst). In a posterior meningocele, the vertebrae develop normally, however the meninges are forced into the gaps between the vertebrae. As the nervous system remains undamaged, individuals with meningocele are unlikely to suffer long-term health problems.

Myelomeingocele: the most serious and common form, the unfused portion of the spinal column allows the spinal cord to protrude through an opening. The meningeal membranes that cover the spinal cord form a sac enclosing the spinal elements. The protruded portion of the spinal cord and the nerves which originate at that level of the cord are damaged or not properly developed. As a result, there is usually some degree of paralysis and loss of sensation below the level of the spinal cord defect. Thus, the higher the level of the defect the more severe the associated nerve dysfunction and resultant paralysis.
**Beckett's defect was classified as myelo, however it appears at this time, that he has very little if any, nerve damage.**

Chiari Malformation (he does NOT have this): Many individuals with spina bifida will have an associated abnormality of the cerebellum, called the Arnold Chiari II malformation. In affected individuals the back portion of the brain is displaced from the back of the skull down into the upper neck. In approximately 90 percent of the people with myelomeningocele, hydrocephalus will also occur because the displaced cerebellum interferes with the normal flow of cerebrospinal fluid.

Perinatologist: Dr. Marcello Pietrantoni

Neurosurgeon: Dr. Thomas Moriarty / Dr. Charles Stevenson

Plastic Surgeon: Dr. Mark Chariker

Pediatrician: Dr. Cynthia Nassim
Travel theme. Powered by Blogger.