Hey, by the way, everyone--have you all checked out the Moebius Syndrome Foundation's new and improved website lately????
If you haven't, be sure and do so. So much of the credit for the improvement goes to the MSF's new executive director, Kim Cunningham, and those she worked with to improve it (and of course Natalie Abbott has been our webmaster for a long time, and she played a huge role as well).
But check it out. If you are a parent with a newborn with Moebius, there is a lot of stuff there for you.
If you are a professional in the health care field and need more information about Moebius, the site is also for you.
If you are a Moebius adult or young adult, and want to connect with others and learn more about living with Moebius, there is plenty there for you.
And there's lots more. There is information; there are ways to connect with others; and the MSF wants to hear from you and to connect with you. See all the ways you can do on moebiussyndrome.org.
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