PCD Foundation
PCD  Educational Events
 
Summer, 2007
 
July, 2007
Registration Forms
Please Join Us
 

The Primary Ciliary Dyskinesia (PCD) Foundation is pleased to invite you to two upcoming educational events: The fifth-annual PCD Foundation Family Education Weekend in Durham, North Carolina (August 10-12, 2007) and a full-day regional education meeting in Phoenix, Arizona (September 8, 2007).   
 

PCD clinical and research experts will be speaking at both events covering topics including PCD genetics, ciliary ultrastructure and function, diagnostic dilemmas in PCD, heterotaxy and congenital heart disease in PCD, nasal nitric oxide measurement in PCD, current best practices for treatment of PCD and much more.   Event details below. 
 

 
Sincerely,
 
Michele Manion
Fifth-Annual Family Education Weekend
 
Marriott Durham NC August 10-12, 2007, Durham, North Carolina


The relaxed setting of this weekend PCD retreat allows plenty of time for peer-to-peer support, as well as providing a safe environment to learn about PCD and ask questions of PCD medical professionals.  This annual educational meeting is the most eagerly anticipated event on the PCD calendar.

Who Should Attend?
Families, caregivers, patients, physicians and healthcare team members who are interested in learning more about PCD.
 


Event Details:
Marriott Research Triangle Park
4700 Guardian Drive
Durham, North Carolina 27703
Phone: 1-800-228-9290  (hotel Direct: 1-919-941-6200)
Conference room rate $89.00 + tax/night
Conference rooms available for booking now

Family registration fee $120/Individual registration fee: $90*
(Registration covers all sessions and most meals for the weekend)


Preliminary Program (speakers are confirmed--topics and order may change):

Session 1: Primary Ciliary Dyskinesia Defined:  Making the Diagnosis
 
  • PCD Research & Genetics, Michael Knowles, MD
  • Ciliary Ultrastructure & Function, John Carson, PhD
  • Nasal Nitric Oxide in PCD Diagnosis, TBD

       Group Lunch

Session 2: Treating the Clinical Consequences of PCD

  • ENT Issues in PCD, Amelia Drake, MD
  • Pulmonary Manifestations of PCD, Margaret Leigh, MD
  • End-stage Lung Disease and Transplant,
    Peadar Noone, MD
  • Heterotaxy and Congenital Heart Disease in PCD, Michael Knowles, MD
  • Integrative Medicine Approaches to Treament, Ann Auburn, DO

     
    In addition, the weekend program includes activities on Friday evening (reception), Saturday evening (dinner) and Sunday morning (patient panel discussion).
Phoenix PCD Education Meeting
Park Plaza Phx September 8, 2007

This meeting is the first in a new PCD Foundation regional education program aimed at reaching healthcare professionals and patients in discrete regions of North America.  The PCD community is small and geographically dispersed, making it difficult for patients and healthcare providers to access up-to-date information on PCD research and treatment.  The goal of this program is to bring the experts to the community and identify regional experts.  Regional education meetings will be shorter (one day), with a more data-intense program suitable for healthcare professionals.  However, patients and families are also very welcome and encouraged to attend.   As in all our educational programs, ample time will be provided for question and answer sessions.
 

Who Should Attend?
Physicians, healthcare team members, patients, families, caregivers and interested individuals.
 

Event Details:
Park Plaza Hotel
Family registration: $40/Individual registration: $25*
(Registration covers all sessions and Saturday lunch)

2641 West Union Hills Drive
Phoenix, Arizona 85027
(602) 978-2222
Conference room rate: $79.00 + tax/night
Conference rooms available for booking starting July 15, 2007

Preliminary Program (speakers are confirmed--topics and order may change):

Morning Session: Primary Ciliary Dyskinesia Defined: Making the Diagnosis

 
  • PCD research and genetics-Michael Knowles, MD
  • Ciliary ultrastructure-John Carson, PhD
  • The role of nasal nitric oxide in diagnosis-TBD
      Group Lunch
 

 Afternoon Session: Treating the Clinical Consequences of PCD

  • PCD in the southwest region-Paul Stillwell, MD
  • End-stage lung disease and transplant-Peadar Noone, MD
  • The GDMCC study-Scott Sagel, MD
  • New findings in PCD: What do they mean?-Michael Knowles, MD          
 
PCD Foundation
29252 N. 22nd Lane Phoenix, Arizona 85085
623-215-2032
www.pcdfoundation.org
info@pcdfoundation.org
 

For more information and preliminary programs, please visit the PCD Foundation website at www.pcdfoundation.org or call Michele Manion at the PCD Foundation 623-215-2032. 

 

*The PCD Foundation operates with a very limited budget.  However, it is our desire that everyone be able to attend educational events.  If the registration fee poses a financial hardship, please contact the PCD Foundation at 623-215-2032 or info@pcdfoundation.org to discuss registration fee options. 

 

 


PCD Foundation · 29252 N. 22nd Lane · Phoenix, AZ 85085 · (612)396-1179
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