Guest guest Posted September 10, 2003 Report Share Posted September 10, 2003 In a message dated 9/9/2003 8:33:36 AM Central Daylight Time, MAILER-DAEMON@... writes: > > Dear All: > > Following is a repeat of info about a conference in San Diego for BPs and > clinicians in November. For more info see the URL below. I am speaking to > clinicians on Wed. November 12. > > > >> >> Hi Randi, >> >> If you get a chance, could you post this to your groups? >> >> Thanks, >> >> >> >> This is a reminder there are only a few days left for early registration >> for the BPD Recovery retreat and/or conference. People register for either the >> retreat or conference by September 15 will receive $50 off tuition, a free >> commemorative video and you will also be entered in a drawing to receive >> books by all five authors! If you are able to send payment before this date, >> you can still have until October 10 to turn in your completed application >> package. However, I would prefer that applications are also submitted as soon as >> possible. >> The cost for the conference is only $275 until September 15. The cost for >> the retreat is only $400 before September 15. For people receiving SSI, the >> cost is only $150. At the moment, spaces are still available for those on >> SSI, but they available only on a limited basis and they are going fast! The >> price has been reduced quite a bit since initial launch of the event >> information, and these special discounts are only for a limited time. >> >> For more information, please see: >> <A HREF= " http://www.laurapaxton.com/conference.html " >http://www.laurapaxton.com/con\ ference.html</A> >> or >> <A HREF= " http://www.laurapaxton.com/retreat.html " >http://www.laurapaxton.com/retrea\ t.html</A> >> >> We hope to see you there! >> > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 11, 2010 Report Share Posted February 11, 2010 Yes! You are welcome at the convention if your child has PMG and Macrocephaly. Your child does not have to have microcephaly to attend. The children do not have to have more than one of these diagnosis'. The two below links from the FCM site have more info. http://www.childrenwithmicro.org/aboutus.html http://www.childrenwithmicro.org/causes.html The dates for the Convention are Thursday, June 17th to Sunday, June 20th. It will be held in sdale, AZ. Here is the link for more information, http://www.childrenwithmicro.org/wearenotalone.html Take care, Jepson FCM Rep for Michigan > > > > > > I am just wondering if there is any information on a conference for PMG anywhere > > > > > > Thanks > > > Krista Ortyl(Jazmyn's mom) > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 11, 2010 Report Share Posted February 11, 2010 I was just curious how the location for future conventions is chosen and would there ever be a thought for it on the east coast? Would love to attend but wish it was closer to Boston. -- Sent from my Palm Pre sjepson wrote: Â Yes! You are welcome at the convention if your child has PMG and Macrocephaly. Your child does not have to have microcephaly to attend. The children do not have to have more than one of these diagnosis'. The two below links from the FCM site have more info. http://www.childrenwithmicro.org/aboutus.html http://www.childrenwithmicro.org/causes.html The dates for the Convention are Thursday, June 17th to Sunday, June 20th. It will be held in sdale, AZ. Here is the link for more information, http://www.childrenwithmicro.org/wearenotalone.html Take care, Jepson FCM Rep for Michigan > > > > > > I am just wondering if there is any information on a conference for PMG anywhere > > > > > > Thanks > > > Krista Ortyl(Jazmyn's mom) > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 12, 2010 Report Share Posted February 12, 2010 Hi , There have been many requests for the FCM Convention to be held on the east coast, and in many other places too. Last year we experimented and had the Convention in California. While the Convention there was amazing, with the organization growing drastically, at this time it is too hard for Jenni, the Founder of FCM, to plan it anywhere else but close to where she lives in Arizona. As the years go on I am sure we will again explore holding the Convention elsewhere and my guess would be that we will look east, but that is at least a few years into the future. Keep in touch, check the website for updates and information and I hope to see you at a Convention soon. www.childrenwithmicro.org Take care, Jepson FCM Michigan State Rep > > > > > > > > > > I am just wondering if there is any information on a conference for PMG anywhere > > > > > > > > > > Thanks > > > > > Krista Ortyl(Jazmyn's mom) > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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