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Hi, I don't post much here but I've been reading all of your posts for a long time. I post a little more at the official Cardinal site. I'm not accustomed to asking for help but I've really got no choice. I hope I'm not mis-using this board. Please visit my site. ( I've even used the Cards in the address ! ) Thanks alot , A Pennsylvania Cardinal Fan. www.geocities.com/zonacardinalfan/daniel.html
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Last edited by Cardiholic; March 29th, 2004 at 11:35 AM.
Reason: Forgot to add something
I think the guy who originally made that site called it "fark" because he use to say it instead of F***. I guess he thought that was funny? I don't know.
Anyhow, say a link to a story at somewebsite.com gets posted. Tons of people go there to check it out. Somewebsite.com can't handle the load and the server stops serving pages.
People on the forums there use fark as an adjective to describe the site as "farked". Or basically, "f**k'd".
A couple in Monroe County is desperately searching for answers. Doctors can't figure out why their baby is sick. It has the boy's parents in Saylorsburg taking some unusual measures.
According to doctors, Daniel Thalmann has a syndrome so rare there isn't even a name for it yet. The boy's parents have now put their story online for the world to see with hopes somebody can help.
Daniel is four and a half months old but he weighs what an average newborn weighs. His parents, Ann and Jim said he also has a fast heart beat, kidney problems and a feeding disorder. Years ago, they lost another baby boy at three days old who had similar symptoms.
Countless doctors are stumped. "They say it's a syndrome, but they don't know what that is. We have no idea what the prognosis is going to be," said Ann Thalmann.
"They've got geneticists all over the world trying to figure out what's wrong with Daniel. They say he's a mystery, can't figure him out," added Jim.
Soon after Daniel was born his web page was born. Funny, said Jim, because he's not all that computer savvy. It's the Thalmann's life; online pictures and stories, a list of people who've donated money for the baby's medical care. The Thalmanns hope somebody in the world sees it and may be able to shed a little light on what's wrong with Daniel.
"We just want to know what the future holds for him. We have no answers right now," said Jim.
If any of the baby's symptoms sound familiar, the Thalmann's would like to hear from you. They can be reached through their web site.
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