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Field's Disease; a chance to help and get better known?

nerve trembling

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#1 Logic

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Posted 15 January 2014 - 09:25 PM


I just watched a documentary on Discovery channel about Kirstie and Cathrine Fields.
Kirstie and Cathrine are twins with a degenerative nerve disease so rare that they are the only 2 people who have it and the disease is named after them.

The documentary was touching and got me thinking that there are a good nuber of talented people here that may be able to come up with a stack to help these young ladies.
As discovery Channel has already done a documentary on them any improvement in them might make for another documentary and some exposure for us..?

This is just a half backed idea atm and I don't really have the time to research the matter further myself.

So what do you think?

https://www.google.c...cathrine fields

#2 YOLF

  • Location:Delaware Delawhere, Delahere, Delathere!

Posted 15 January 2014 - 11:24 PM

It sounds like a good idea, though it appears, at least from wiki, that their condition is likely terminal. Still there is nothing wrong trying to help. I'll have to add them to my list of people who need cryonics.





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