RE: [pscmoms] Children & PSC

[Guest guest]

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Are there any organizations specific to children with psc?

Here are 5 web sites/articles/studies

to get you started. If you want

more, let me know.

This first one will be

really interesting to you. They

started their foundation, because their young son has PSC. Please note our group - PSC-Partners, is

a partner to & with, PSC Foundation. HTH

http://www.pscfoundation.org/

http://www.emedicine.com/ped/topic1895.htm

http://www.cincinnatichildrens.org/svc/alpha/l/liver/diseases/sclerosing.htm

http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve & db=PubMed & list_uids=12830004 & dopt=Abstract

http://www.medical-library.org/journals5a/primary_sclerosing_cholangitis2.htm

Barb in Texas - Together in the Fight, Whatever it Takes!

Son Ken (33) UC 91 - PSC 99 Listed 7/21/06 @ Baylor Dallas