So Sorry! We are so disappointed that we cannot celebrate this year’s Rare Disease Day with a scrumptious breakfast and all the accompanying fanfare at Queen’s Park. Despite the very best efforts of all of CORD’s friends, we have not been to secure the venue at Queen’s Park for breakfast.
CORD will be present on February 28th at Queen’s Park for Question Period starting at 10:30 AM. We would be so grateful if you would join us to present a show of force of the Rare Disease community.
We will provide details in the coming week but ask that you email us at firstname.lastname@example.org to indicate whether you can join us for Question Period.
Thank you for your commitment.
President & CEO
Canadian Organization for Rare Disorders
151 Bloor Street West, Suite 600
Toronto, Ontario M5S 1S4
T: 416-969-7464 / 1-877-302-7273
We need your support! Sign the petition for Funding of Spinraza for all Canadian patients affected by Spinal Muscular Atrophy (SMA) Cure SMA Canada, CORD, the Canadian SMA families and our supporters appeal to our provincial health ministers to provide all patients access to the only treatment available for this life threatening disease.
March 21, 2018
Delta Hotels Ottawa City Centre: 101 Lyon Street North, Ottawa
6th Annual Rare Disease Day Awards Gala Join us on Wednesday evening, March 21st, when CORD will host its annual Rare Disease Day Awards Gala. We will recognize those individuals and organizations that have made extraordinary contributions to the Canadian rare disease community over this past year. Cocktail reception at 6:00 pm followed by dinner at 7:00 pm Business or Smart Cocktail Attire Gala Ticket: $195 Patient Gala Ticket: $125 Table of 8: $1500