I found out about the Acoustic Neuroma Association and requested an information packet from them. Looks like there is a D.C. support group meeting later this month. I also started reading the ANA discussion forums and am finding it very helpful to hear from people who have been through this. I'm learning a lot but I'm too nervous to actually post yet.
http://www.anausa.org/
(In the interest of full disclosure, this post was actually written on 1/29/09.)
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