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Get Ready to #ShowYourRare

2018 marks the 11th year that the international rare disease community celebrates Rare Disease Day.

On February 28, 2018 people living with or affected by a rare disease, patient organizations, politicians, carers, medical professionals, researchers and industry will come together in solidarity to raise awareness of rare diseases.


Rare Disease Day in Canada
Patient organisations in Canada have engaged in Rare Disease Day since its first year in 2008, arranging gala dinners and exchanges between researchers and patients, as well as regional events across Canada.

What Can You Do?
As a patient group, we encourage you to use the images in this email, as well as others from rarediseaseday.org, to promote the day and raise awareness. Consider using through your social media channels and sharing with your members to do the same, including the official hashtag #ShowYourRare.

You can also consider contacting local media to let them know about Rare Disease Day and offer to have your organization or one of your patients featured, to raise awareness. 

CORD and CIPO will be at Queen's Park in Toronto, meeting with elected officials and raising awareness.

After all, 1 in 12 Canadians is living with one of 7000 rare diseases. Though individually our patient groups may sometimes feel isolated, together we can make the collective voice of rare diseases heard!

the NRBDO is proud to support
 rareDIG Rare Disease Day 

McIntyre Medical Building, Martin Amphitheater
McGill University

February 28th, 2018

Reception 6:00-6:55PM. Talks begin at 7PM.

The NRBDO board was very excited when this new Medical Students' Society Rare Disease Interest Group (rareDIG) at McGill reached out to us. We are making plans to bring a representative from their group to our Spring Forum, but in the meantime we are a proud sponsor of their inaugural Rare Disease Day on February 28th, 2018! If you are in Montreal, please do check it out.

There is a reception followed by a series of talks given by individuals who have diverse perspectives on rare diseases. "The rareDIG Rare Disease Day 2018 event will challenge each of us to consider solutions to the inequities individuals with rare diseases experience and develop insight into the challenges they face. Learn about diseases that affect a handful of people and how policy, advocacy, and research can affect their lives."

Registration is open to everyone. Register here ($10 payable by eTransfer):

https://goo.gl/forms/JrZ3XWQyK0Vp6GXw1

Looking for more?
Rare Disease Day Social Media Toolkit, and Reproducible Posters!

Information packs, profile and cover photos, logos, posters, and even a website countdown are available for download at rarediseaseday.org.
Downloadable Communication Materials
Copyright © 2018 Network of Rare Blood Disorder Organizations, All rights reserved.


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