This blog is dedicated to my amazing son Beau. In 2009 he was diagnosed with Partial Agenesis of the Corpus Callosum (P-ACC) as well as Epilepsy. I write this as a way to educate, inform and relate to other families that raise special needs children. To read more about Beau, see the very first blog; "Let's Talk About Beau".
Beau
Thursday, July 21, 2011
Upcoming NODCC Family Partnership Gathering
August will be here soon and I can't wait for our Midwest area to get together in Minneapolis for our NODCC regional gathering. I have organized this event in the hopes that families (affected by a disorder of the corpus callosum) from Iowa, Minnesota, Wisconsin and any other surrounding states might attend and find comfort in meeting others that "understand". I was certainly hoping that more might step forward and be able to attend, but as of right now there are only 3 others families besides ours that are coming. Some is always better than none, so I am grateful for those that are able to attend. It will be an awesome day with a great meal, great opportunities to talk and then fun at the indoor water park. We plan to follow it up the next day with a trip to the Como Park Zoo in Minneapolis. It will be a nice little vacation for our family from Iowa and we'll be able to make some new friends as a result. If anyone else is interested in attending, please contact me for details. The more the merrier!
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