Blink of an Eye: Busy, busy, busy

Tuesday, June 15, 2010

Busy, busy, busy

Ok, Ok, Ok...I know it's been eons {or at least a week} since I've blogged. We've been just a tad bit busy here. I finished my last week of school {I am officially a SAHM for 9 weeks}, Noah was discharged from his special needs pre-school, Uncle Drew, Auntie Nessa and Cuz Jonah flew out from Iowa, we all traveled to Paso Robles for a be-au-ti-ful wedding in the wine country, Uncle Adam, Auntie Mel, Cuz Hunter and Cuz Brooklyn drove down from Susanville, family time was spent together, we celebrated Cuz Jonah's first birthday, and today Noah had a doctor's appointment, his first toddler group through CitiKids, and we are meeting with an OT {occupational therapist} at Children's Hospital for an initial evaluation. WOW! I promise to post plenty of pictures soon...as soon as I can recover just slightly.

Oh, and Yippee Skippy, Kc was offered a new, full-time job {he's been part time since January}. The Lord has been so faithful and we are excited about this new chapter in Kc's career. More details to follow.

3 comments:

Shelly CunninghamJune 15, 2010 at 7:57 PM
Congratulations on the full time job offer! I am wishing the same for my hubby... send those "good job" vibes this way when you're done with 'em! :)
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DebbieJune 16, 2010 at 6:06 PM
F-U-L-L-T-I-M-E, What's that spell? Full-time, full-time! Yaaaay, full-time!! Hip, hip, hooray for the job coming your way! Congrats, Kc!!

From one SAHM to another: Enjoy, Rebecca!
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AnonymousJune 17, 2010 at 7:56 AM
Wow I need a nap after reading this! So happy for you guys and so glad we get to see Gods love, faithfulness and awesomeness play out through your lives. Katy Mc
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The Story

Our son, Noah Stone Jackson, was born with a very rare genetic disorder called Fraser syndrome. Among his many challenges are one “hidden eye”, a narrow trachea (which required him to have a tracheotomy), an imperforate anus (which required a colostomy), difficulty swallowing (which required a G-Tube for feedings), the fusing of his vocal chords (which means he may never speak), and club feet (which are being corrected with braces). Our family is on an amazing journey together. We are learning to walk along this path that God has planned for us, trusting in His infinite love and wisdom. We are taking each day (or each moment) as it comes and relying on each other, our friends and family, and our God for strength. We have a long road ahead of us filled with several more surgeries, lots of recovery, countless hours of therapy, and many trips to specialists around the state. Every day brings us challenges but they pale in comparison to the smiles and cuddles from our little man. Noah is our son, a true gift from God, and we cannot wait to see where this adventure leads.