H A P P Y ST P A T T Y ' S D A Y

Still seizure free! :)

Taylor is working hard every day to rebuild his head control and motor skills.  We're very proud of his progress and we see great things for him in the future.  He can't wait to see all of you and show off his 5 new teeth.

Love you all and we promise to post a fun video soon.

Tay Makes a Big Splash at GiGi's Gala Fundraiser

Taylor's buddy - Jamal Anderson

Tonight was a special night.

We attended a fundraiser for GiGi's Playhouse.  There are currently 8 in the U.S. and in 2 months, our friend Adrienne Mulligan will be opening the 9th in Atlanta.  GiGi's Playhouses are Down syndrome awareness and educational centers that provide resources, specialized teaching, and support to individuals with Down syndrome, their families and the community...all for free.  (www.GiGisPlayhouse.org) 

Taylor looks forward to introducing you to GiGi's next time you visit.

:)

Time to Celebrate - Absolute Best News From Memphis !

We received the best news from our appointment in Memphis yesterday.  The doctors there are pretty amazing.  Taylor had his EEG at 8:30am.  By 10:30, the docs had studied the entire report and gave us the good news...Taylor's EEG was perfect! 

If he continues along this track, they believe he can start weening off the anti-seizure medicine in 6 months.  I'll let Taylor show you how happy he was to hear the news...
We took this video just as we exited off the interstate last night, just a few blocks from home.  The weather was perfect so we rolled Tay's window down so he could enjoy the breeze:

CLICK HERE TO SEE TAYLOR CELEBRATING

Tay is Happy As Can Be!

Taylor hasn't had a seizure since that single episode on Jan 30th.  He continues to learn new skills, many which involve his fine motor skills.

It's such a nice feeling, tucking Taylor into bed at night knowing that he had an incredible day.  Being able to watch the true little boy come out of his shell from this "seizure coma" he's been in for so long.  It sure takes a lot of stress out of our lives.  :)

We're headed back to Memphis tomorrow for his check-up on Monday.  We'll be sure to fill you in after we know more.  In the meantime, check out this video we recorded tonight:

CLICK HERE FOR VIDEO

2 Videos to Brighten Your Day

BUBBLES:

http://www.youtube.com/watch?v=DIj0-NGVpSY

MY NEW BIG BOY CHAIR

http://www.youtube.com/watch?v=2DkIC5-3_JA

Getting Stronger....!

Tay's immune system (and appetite) are continuing to build.  His eye focus and hand coordination are also on the rise.  He's falling back into a more normal sleep routine which mommy & daddy really appreciate!  He's only had 1 seizure in the past 16 days...yesterday :(

All in all, we feel Taylor is making incredible strides.  He's back fully engaged in his three 1 hour therapies a week.  My parents spent the last week with us in Atlanta, fully soaking up time with Taylor.  They are so good with him.  They have such sure, confident hands and really know how to comfort him (aka....SPOIL HIM!!!).  Lane and I took full advantage of the built-in babysitters!

A HUGE Thank You goes out to everyone that continues to follow this blog for Taylor.  He loves you all and can't wait to tell you himself one day soon.
:)

Again...I'll Let the Pictures & Videos Speak For Themselves

Taylor is really coming out of his shell.  I can't wait for you all to share in our joy of the new Tay:

You Will LOVE these videos:

CLICK HERE FOR VIDEO 1

CLICK HERE FOR VIDEO 2