BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//PCD Foundation - ECPv6.15.11//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-ORIGINAL-URL:https://www.pcdfoundation.org
X-WR-CALDESC:Events for PCD Foundation
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:UTC
BEGIN:STANDARD
TZOFFSETFROM:+0000
TZOFFSETTO:+0000
TZNAME:UTC
DTSTART:20250101T000000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=UTC:20261001T000000
DTEND;TZID=UTC:20261031T235959
DTSTAMP:20261023T211927
CREATED:20250925T180836Z
LAST-MODIFIED:20260630T151804Z
UID:787-1790812800-1793491199@www.pcdfoundation.org
SUMMARY:October is PCD Awareness Month
DESCRIPTION:Each year in October we come together for PCD Awareness Month – a dedicated time for PCD families\, advocates and supporters of the PCD Foundation to raise awareness and funds for primary ciliary dyskinesia (PCD). What started as a one-day national walk for the PCD Foundation in the early 2000’s\, has grown into an international awareness month for PCD. \n\n\n\nIt is a time for all of us to share in the efforts of the PCD Foundation\, fellow PCD patient organizations across the world\, and the PCD medical and research community – all working to improve diagnosis\, access to comprehensive care\, treatment\, research and ultimately a cure. \n\n\n\n\nLearn More
URL:https://www.pcdfoundation.org/event/pcd-awareness-month/
ATTACH;FMTTYPE=image/png:https://www.pcdfoundation.org/wp-content/uploads/2025/09/Rebecca-2-Cropped-1-246x300-1.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20261007T110000
DTEND;TZID=UTC:20261007T120000
DTSTAMP:20261023T211927
CREATED:20260929T143403Z
LAST-MODIFIED:20261002T210021Z
UID:1447-1791370800-1791374400@www.pcdfoundation.org
SUMMARY:The Power of Patients: PCDF Registries - Webinar
DESCRIPTION:Every person with PCD has a role to play in shaping the future of PCD research. \n\n\n\nThe PCD Foundation’s Registries give patients an opportunity to get involved\, make their voices heard\, and help researchers better understand PCD. That participation can help advance research\, inform clinical trials\, and move us toward better treatments. \n\n\n\nJoin us on October 7th at 11:00 am CT / 12:00 pm ET as Dr. Michael O’Connor (Associate Professor of Pediatrics at Vanderbilt University and Medical Director for the PCDF Registry) and Michele Manion (President and Executive Director at PCDF) will provide an overview of our PCDF Connect and Research Registries and the benefits of tracking patients with PCD. Sigrid Almeida (Research Coordinator at Connecticut Children’s) will walk through considerations and approaches to getting enrolled. \n\n\n\nRegister here: https://us02web.zoom.us/webinar/register/WN_BPcK5ZKGR_2QLMrehZNZaA#/registration \n\n\n\nLearn more about the PCDF Registries here ahead of the webinar: \n\n\n\n\nPCDF Connect Registry: https://www.pcdfoundation.org/pcdfconnect/\n\n\n\nResearch Registry: https://www.pcdfoundation.org/registry/
URL:https://www.pcdfoundation.org/event/the-power-of-patients-pcdf-registries-webinar/
ATTACH;FMTTYPE=image/png:https://www.pcdfoundation.org/wp-content/uploads/2026/09/PCDF-Registries-Graphic.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20261016T183000
DTEND;TZID=UTC:20261016T223000
DTSTAMP:20261023T211927
CREATED:20260423T181205Z
LAST-MODIFIED:20261007T180432Z
UID:937-1792175400-1792189800@www.pcdfoundation.org
SUMMARY:An Evening to Ignite Hope
DESCRIPTION:We look forward to seeing you at An Evening to Ignite Hope! \n\n\n\nPCD Foundation: An Evening to Ignite HopeFriday\, October 16\, 2026Pepper Family Wildlife Center at Lincoln Park ZooChicago\, Illinois 60614 \n\n\n\nIgnite Hope Now!
URL:https://www.pcdfoundation.org/event/an-evening-to-ignite-hope/
ATTACH;FMTTYPE=image/png:https://www.pcdfoundation.org/wp-content/uploads/2026/04/An-Evening-to-Ignite-Hope.png
END:VEVENT
END:VCALENDAR