Kindrid Foundation My name is Cassandra Sasse. My daughter Kindrid was born in 2005 with Hydrocephalus and Rhombencephalosynapsis. When Kindrid was diagnosed with RS we were told it was very rare and that they did not have any information or experts to refer us to. I started this site and foundation to offer support and information to other families and parents that have received the diagnosis of RS.
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