Deal or No Deal!!!

Emily65Roses

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>anonymous</b></i>

no one really cares</end quote></div>

Hmm... considering all the responses, I might have to argue with you. In fact, I think it proves you wrong flat out. So there. <img src="i/expressions/face-icon-small-tongue.gif" border="0">
 

rose4cale

New member
I think all of the contestants dance and over-react way too much. I didn't see her last night...could kick myself because I quit watching as soon as the gal before her stopped...bath time for kids....but I will tune in tomorrow for sure!!!!

I had people talk to me in awe that she had just had a double xplant. I hope she does well!!!!
 

anonymous

New member
i might start introducing myself like so; hi i'm janet i'm overweight and i have a huge nose, how do you do!!!!!!!!!!!!!!!!!!!!!<img src="i/expressions/face-icon-small-happy.gif" border="0"><img src="i/expressions/face-icon-small-smile.gif" border="0">sorry too much time on my hands
 

anonymous

New member
to: anon who posted
_______________________

no one really cares
________________________

YEAH- I GUESS NO ONE REALLY CARES YOU ARE ON HERE EITHER. SMARTA$S! I GUESS THERE IS ONE IN EVERY CROWD!
 

anonymous

New member
The show only chooses contestants who are perky and many of the contestants dance (if you watch the show you would know that). When she is dancing it shows that she can breathe......They look for animated people.

You guys are way to critical. Sounds like a little jealousy ringing....

It is great to read the uplifting posts who are happy for this young girl. I hope all of you who suffer with cf are as blessed as she is one day. She is providing great coverage for cff

Hope she wins the million. Did you ever think that it is possible that the CFF asked her to do the show on their behalf???



Kellie
 

anonymous

New member
I thought she was way too bouncy for having a lung transplant 2 years ago. She never even mentioned the hospital staff, doctors, or how much she owes in medical bills. After seeing my Dad go through a lung transplant 10 months ago, I felt like the whole thing was a scam. My Dad was still in rehab at 2 months post-op and he is still struggling with being on O2. My Dad had pulmonary fibrosis vs. CF. Could you guys fill me in on what life is like post-transplant for you all???
 

Mathews

New member
Remember, she was there to raise $$$ for the Cystic Fibrosis Foundation. I don't believe this is a SCAM. The CF Foundation reported this on their website. If it was a scam, this would not have been posted on their website.

I think it is great she was willing to share her story of CF with the viewing audience. I have met many adults that are hesitant to share their CF with folks for fear of not being accepted. My hat goes of to this lady for her courage.
 

Mathews

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>princessjdc</b></i>

How much did she wind up winning, I stopped watching it when she got offered the 50,000?</end quote></div>

I believe the amount was around $125,000.
 
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