7 Going on 70 20/20 Special Friday 10PM

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Rider_In_Ttown's avatar
Rider_In_Ttown
Posts: 246
Jul 28, 2011 2:08pm
The 20/20 special we did last year will re-air this Friday July 29th at 10PM. Last week this episode was nominated for an Emmy Award. The Emmy's are in September.

http://abcnews.go.com/2020
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vball10set
Posts: 24,795
Jul 28, 2011 2:11pm
Rider_In_Ttown;844602 wrote:The 20/20 special we did last year will re-air this Friday July 29th at 10PM. Last week this episode was nominated for an Emmy Award. The Emmy's are in September.

http://abcnews.go.com/2020

I'll watch it again--it sure was special...btw, how's Kaylee doing?
Fab4Runner's avatar
Fab4Runner
Posts: 6,196
Jul 28, 2011 2:18pm
Thanks for the heads up! And congrats again on the nomination...so cool!
Rider_In_Ttown's avatar
Rider_In_Ttown
Posts: 246
Jul 28, 2011 2:36pm
vball10set;844607 wrote:I'll watch it again--it sure was special...btw, how's Kaylee doing?

Kaylee is doing great, she just turned 8 last week. Really a lot of good things going on with research. I am hoping to be able to talk more about it soon (not allowed to due to FDA rules).


Tiger2003's avatar
Tiger2003
Posts: 15,421
Jul 28, 2011 3:23pm
Must have missed this the first go around. What's it about?
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vball10set
Posts: 24,795
Jul 28, 2011 3:26pm
Rider_In_Ttown;844635 wrote:Kaylee is doing great, she just turned 8 last week. Really a lot of good things going on with research. I am hoping to be able to talk more about it soon (not allowed to due to FDA rules).


that's awesome, rider--our prayers continue to be sent (and best of luck with the new research findings)
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vball10set
Posts: 24,795
Jul 28, 2011 3:31pm
Tiger2003;844719 wrote:Must have missed this the first go around. What's it about?

this is Rider-In-Ttown's daughter--it's a neat story about an amazing young girl and her family

http://abcnews.go.com/2020/barbara-walters-progeria-special-young-girls-living-progeria/story?id=11586041&page=2
As one of only eight girls in the U.S. who has progeria, it can be isolating .... amazingly, Kaylee Halko, 7, who has the same rare condition, lives an hour away in Monclova, Ohio. The two girls have become friends and because of progeria look strikingly similar. Kaylee is a confident, boisterous and fearless seven-year-old.

"[Kaylee] likes to say she's a star," her mother Marla Halko said.

The youngest of four children in the Halko brood, Kaylee -- at only three feet tall and weighing 24 pounds -- is noticeably different from her older brothers, but they have a close, loving relationship.
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Nate
Posts: 3,949
Jul 28, 2011 3:48pm
Kaylee will definitely put a smile on your face. I highly recommend that everyone watches/DVR's the re-air.
Midstate01's avatar
Midstate01
Posts: 14,766
Jul 28, 2011 4:13pm
Rider_In_Ttown;844635 wrote:Kaylee is doing great, she just turned 8 last week. Really a lot of good things going on with research. I am hoping to be able to talk more about it soon (not allowed to due to FDA rules).



You look extremely familiar....
Rider_In_Ttown's avatar
Rider_In_Ttown
Posts: 246
Jul 28, 2011 9:18pm
Midstate01;844794 wrote:You look extremely familiar....
Grew up in St. Marys. Went to Wright State for two years and then transferred to Toledo. Been in the Toledo areas ever since.
sonofsam's avatar
sonofsam
Posts: 2,052
Jul 28, 2011 10:09pm
Rider, Interesting to read about your daughter. I will keep up on the story and I wish you, your daughter and the rest of your family the best. She seems like a very personable and wonderful young girl. Very humbling story.
Iliketurtles's avatar
Iliketurtles
Posts: 8,191
Jul 29, 2011 11:33am
Will certainly watch this again. Glad to hear things are still going well for you guys! Hopefully you can continue to find more and more with the research.
power i's avatar
power i
Posts: 1,296
Jul 29, 2011 12:29pm
Lol at Kaylee and her peace sign. :D Glad to hear she's doing good and will def. watch it again.
O-Trap's avatar
O-Trap
Posts: 14,994
Jul 29, 2011 12:46pm
Kaylee with the backward peace sign. I dig! :cool:

What a personality that little girl has! I remember watching that and thinking that this was truly a very special person.

I will continue to pray for you and your family.
A
adog
Posts: 567
Jul 29, 2011 10:19pm
replay on right now..............................
THE4RINGZ's avatar
THE4RINGZ
Posts: 16,816
Jul 29, 2011 10:24pm
Awesome show. I hadn't seen it before tonight.

Amazing kids and families.
A
adog
Posts: 567
Jul 29, 2011 10:51pm
Yes it is
and yes they are...amazing kids....
THE4RINGZ's avatar
THE4RINGZ
Posts: 16,816
Jul 29, 2011 10:54pm
Is there a way we can donate money for research etc. in tribute to Kaylee?
thedynasty1998's avatar
thedynasty1998
Posts: 6,844
Jul 29, 2011 10:58pm
Just watched it with the wife. She was in tears with how inspiring your family is. Wish you all the best.
A
adog
Posts: 567
Jul 29, 2011 11:00pm
I by no means am endorsing this site as I just looked it up and do not know anything about it. Maybe Rider in Town can recommend a site or different research group than this one...

https://www.progeriaresearch.org/ways_to_donate.html
Rider_In_Ttown's avatar
Rider_In_Ttown
Posts: 246
Jul 30, 2011 12:56am
Thanks everyone. Kids come off pretty good on TV. They are just like any other kids though in real life, half the time I want to strangle them. 4rings - you can donate at www.progeriaresearch.org we are having a benefit in October. I will be in Wooster next Friday.
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vball10set
Posts: 24,795
Jul 30, 2011 7:51am
Rider_In_Ttown;846382 wrote:Thanks everyone. Kids come off pretty good on TV. They are just like any other kids though in real life, half the time I want to strangle them. 4rings - you can donate at www.progeriaresearch.org we are having a benefit in October. I will be in Wooster next Friday.

Good luck, Rider, and please keep us posted on the progress of the new research--God bless ;)
Really a lot of good things going on with research. I am hoping to be able to talk more about it soon (not allowed to due to FDA rules).