Guest guest Posted May 27, 2008 Report Share Posted May 27, 2008 When I first discovered that my son had plagiocephaly, I was completely lost. I'm from France but I am currently living in Houston, TX. I had no idea what this was or where to find information about it, especially to read about it in English... Then I found your support group who helped me a lot & I am really thankful for that to all of you. Now I am trying to put together all the information under one page: my little one page " Remi " for future French parents who are like us, expat in the USA & lost. Sure it is written in French in case some expat cannot speak English yet, but I refer to this group & wanted you all to know that. With time, I will had more information & also about insurance (we are currently in the process of appeal... new discovery for us too to deal with medical insurance. ). Thank you so much for your support. http://www.webartvision.com/Plagio Karine. Quote Link to comment Share on other sites More sharing options...
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