Those living with the K word have no easy road. Countless hurdles lay ahead and behind, and they are forever striving to help one another out and make the journey a little bit easier on those that go behind.
There are many ways for families affected by kernicterus to connect to our group. The best and most accessible of these is on facebook. Our private support group there is called:
Are you newly diagnosed or suspecting kernicterus?
This is the post for you: “Newly Diagnosed”
If you aren’t on facebook, you can post questions and read older posts on our yahoo group:
Other Resources and Links:
Teen FB Hangout