Where In The World 21. We are now completely legal!!!

UPDATE!!!!
I GOT THE JOB!!!! :cool1::cheer2::banana::dance3::woohoo::jumping1:party::dancer:

It's part time 27 hours a week (I think) same hourly rate as I make now. I will end up making less money because I will only work when there is school and won't work in the summer. But that's OK I won't have to be miserable where I am and I will enjoy having time off. HR is supposed to call me next week with more details.

Congrats Diane. That is great to hear.
 
So sad about the kids.



I'm using Flicker. It is easy to upload once I found the cloud with the up arrow in the upper right hand corner. And once I figured out that to share on here I had to open the individual picture. Then down in the bottom right click on the arrow pointing to the right. It will bring up a box. Copy the BBCode.

They now have an editing option which is fine. After all, it's free. But it does not resize. I can only resize on my Preview program on my computer. But, I would recommend Flickr.

I've been taking a painting class and this week's assignment was to paint a night scene so I painted this:

fullsizeoutput_1f8d by Denise Horner, on Flickr
Great job Denise. I love it.
 
Thinking want to drive one of them for my retirement job. What a fun time.

Been fight a cold/flu/bug for over a week now.

:rotfl2: I was JUST thinking about you when I was outside in the pool; was planning on sending you a text to see if you're still alive! :rotfl: Now I understand why we haven't heard from you in awhile. Summer cold/flu bug is AWFUL! A few people around here have the flu portion and it's taken them 7-10 days to feel better. Hope you're on the mend. Tell me again the dates of your Texas visit...now that we have a volleyball schedule we can start making some plans. :woohoo:

PERFECT retirement job for you...in addition to the Photopass Photographer. :thumbsup2 You know the Disney property "like the back of your hand"; shouldn't have any problem at all getting guests where they need to go! ::yes:: :tink:
 
Cute, cute, cute performance of Sleeping Beauty at the Unity Theater Summer Drama Camp. The Princess was one of the "fairies" and loved dressing up in those pretty, frilly "fairy dresses" :rotfl:; fun morning. Treated her to lunch and picked up a few groceries and couldn't wait to get home OUT OF THE HEAT! OMG...it's a scorcher out there today :sunny:...car thermometer said 99 when I drove in the garage! :beach:

0ff2339e-3e44-4ee4-85dd-68bc4c6c1725_zpsk6xz4pyz.jpg


Bingo Jeff...this is part of a Christmas display. It's not in Disney Springs or Boardwalk and not in a shop for sale. Nothing to do with Buzz Lightyear or transportation but could very loosely be associated with transportation. :tink:

Is it from the TTC?
 


Our entire little close knit community is grieving over the loss of this sweet little girl...

20374212_10211912729965461_4500792810500033106_n.jpg


Lilly was the daughter of one of DD's former employers and she has touched us all. I do not remember the name of it but Lilly (and her brother who passed away about 7 years ago) were victims of a very rare disorder; they were 2 of the 4 known victims in the world. After Lilly's brother passed away, and Lilly was showing signs of the same disease, her parents had genetic testing done. The findings were astonishing; either one of the parents could have had a healthy child with other people but together their "chemical makeup" resulted in this disorder. It took 9-12 months to discover this phenomenon because it is so rare. Their parents are amazing people; Lilly could not talk, walk, feed herself, etc. but they took her everywhere with them. She won the hearts of our entire community because the one thing she could do was smile. :lovestruc She had to have surgery last week when her seizures became more frequent and out of control but she never woke up. Her organs begin to fail and after 3 days of no improvement her family decided to turn the machines off. In the words of her Grandmother, "Lilly is now free and oh she has so much to learn but she and Stuart are finally able to play, love and talk to one another". Amazing family and our hearts go out to them. :sad1: :tink:


So sad.:grouphug:
 



::yes:: She's in a happier place but feel so bad for her family. We're all pretty devoted parents/grandparents but Lilly's family puts us all to shame. I never, in my life, have known parents that literally devoted their entire life to their ill children. Truly amazing. A few summers ago when we spent some days in Port Aransas for the Marlin Fishing Tournament, we had them over for dinner one evening...DGD and SIL were entered in the tournament with the Dad. They'd even take Lilly out on the boat with them when they went fishing. :lovestruc I babysat her a few times so her Mother could get a few hours "me" time when she was just a tiny baby but she'd never stay gone as long as she originally planned :goodvibes. She couldn't bear to be away from her. Remarkable family. :lovestruc :tink:
 
Thanks all. It really is the pits. When you think it is mid 90's with the heat index easily in 100's and one catches a cold. Crazy.

All training obviously has stopped. The event is Sunday October 29th. Didnt look yet to see when the expo is, bike check-in, packet pickup, any mandatory meetings/briefings are yet. Going to make it a 2 day drive each way. Hope not to sore when done. Have to celebrate at Food and Wine Festival on way back home.
 
Thanks all. It really is the pits. When you think it is mid 90's with the heat index easily in 100's and one catches a cold. Crazy.

All training obviously has stopped. The event is Sunday October 29th. Didnt look yet to see when the expo is, bike check-in, packet pickup, any mandatory meetings/briefings are yet. Going to make it a 2 day drive each way. Hope not to sore when done. Have to celebrate at Food and Wine Festival on way back home.

You'll deserve a celebration party:after it's all done, that's for sure! party: We'll have the final District Volleyball game on Monday, Oct. 24th so we'll have the 25th-27th free. The football game on Friday night will be in Tarkington ... almost 1 1/2 hours east of us so we'll skip that trip! Volleyball playoffs begin Monday, the 30th or Tuesday, the 31st and those games will be "road trip" games, probably to our south. Let us know your schedule when you get it and we'll see what we can do about meeting you somewhere in the 100 mile radius of Bellville and Austin. :rotfl: Hard to understand HOW one catches a "summer cold" but those sucker zap you to the core! Take it easy... :tink:
 
Our entire little close knit community is grieving over the loss of this sweet little girl...

20374212_10211912729965461_4500792810500033106_n.jpg


Lilly was the daughter of one of DD's former employers and she has touched us all. I do not remember the name of it but Lilly (and her brother who passed away about 7 years ago) were victims of a very rare disorder; they were 2 of the 4 known victims in the world. After Lilly's brother passed away, and Lilly was showing signs of the same disease, her parents had genetic testing done. The findings were astonishing; either one of the parents could have had a healthy child with other people but together their "chemical makeup" resulted in this disorder. It took 9-12 months to discover this phenomenon because it is so rare. Their parents are amazing people; Lilly could not talk, walk, feed herself, etc. but they took her everywhere with them. She won the hearts of our entire community because the one thing she could do was smile. :lovestruc She had to have surgery last week when her seizures became more frequent and out of control but she never woke up. Her organs begin to fail and after 3 days of no improvement her family decided to turn the machines off. In the words of her Grandmother, "Lilly is now free and oh she has so much to learn but she and Stuart are finally able to play, love and talk to one another". Amazing family and our hearts go out to them. :sad1: :tink:

That's so sad I feel for their family
 
Thanks all. It really is the pits. When you think it is mid 90's with the heat index easily in 100's and one catches a cold. Crazy.

All training obviously has stopped. The event is Sunday October 29th. Didnt look yet to see when the expo is, bike check-in, packet pickup, any mandatory meetings/briefings are yet. Going to make it a 2 day drive each way. Hope not to sore when done. Have to celebrate at Food and Wine Festival on way back home.

It's all that AC down there lol
 
That's so sad I feel for their family

Having a young child, it really "hits home" for you, doesn't it? The thought of loosing one child is bad but loosing two is just unbearable. They have a lot of community support but know their pain is great. SO glad they adopted a little girl a few years ago. Not that she'll ever replace Stuart and Lilly but she's a blessing for them at this sad time. :lovestruc :tink:
 
CrAzY :crazy: but Redstorm got her LETTERMAN'S JACKET today! That's exactly what she needs...a wool and leather jacket in TEXAS in JULY! :lmao: But...I'll bet the girls wear them the first day of school! :lmao: (It's "all those AC's down here":rotfl2: and the high school has had a new AC unit installed this summer! :rotfl:) Doesn't matter how hot it is...she's pretty proud and she deserves to be! :worship: A lot of long hours and hard work went into earning this sucker! :goodvibes And Diane...NO "RICKY BOBBY" ON THE BACK :lmao:...she actually had them put her "real" name! :rotfl2:

P1210402_zpskv0brl6l.jpg
:tink:
 
...and our little Sleeping Beauty fairy and her BFF at Drama Camp:

P1210392_zpsuxgfjkii.jpg


...along with a nice surprise when I discovered her picture from Miracle on 34th Street on the "Wall of Honor" in the Unity Theater:yay::

P1210388_zpsjhkfvbkw.jpg
:tink:
 
Our entire little close knit community is grieving over the loss of this sweet little girl...

20374212_10211912729965461_4500792810500033106_n.jpg


Lilly was the daughter of one of DD's former employers and she has touched us all. I do not remember the name of it but Lilly (and her brother who passed away about 7 years ago) were victims of a very rare disorder; they were 2 of the 4 known victims in the world. After Lilly's brother passed away, and Lilly was showing signs of the same disease, her parents had genetic testing done. The findings were astonishing; either one of the parents could have had a healthy child with other people but together their "chemical makeup" resulted in this disorder. It took 9-12 months to discover this phenomenon because it is so rare. Their parents are amazing people; Lilly could not talk, walk, feed herself, etc. but they took her everywhere with them. She won the hearts of our entire community because the one thing she could do was smile. :lovestruc She had to have surgery last week when her seizures became more frequent and out of control but she never woke up. Her organs begin to fail and after 3 days of no improvement her family decided to turn the machines off. In the words of her Grandmother, "Lilly is now free and oh she has so much to learn but she and Stuart are finally able to play, love and talk to one another". Amazing family and our hearts go out to them. :sad1: :tink:


This really hit close to home. I feel for the parents as I too lost my son in 2014 to a rare seizure disorder. We also had to make the hardest decision a parent will ever have to make in taking your child off life support. Luckily we were at an amazing children's hospital and had the total support of all the staff. It was heartbreaking to lose one child, I could not imagine losing both. My thoughts and prayers are with the family.
 

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