CODErouge

CODErouge The coderouge program aims to increase diagnosis and access to care for women and girls with inherited bleeding disorders.

On RARE DISEASE DAY, it is important to remember that equity in access to care is, more than ever, at the heart of the C...
02/28/2026

On RARE DISEASE DAY, it is important to remember that equity in access to care is, more than ever, at the heart of the Canadian Hemophilia Society's mission.

Numbers count. When RARE doesn’t seem that rare after all …
02/28/2026

Numbers count. When RARE doesn’t seem that rare after all …

Today is RARE DISEASE DAY!With over 300 million people globally living with a rare disease, we join hands across borders...
02/28/2026

Today is RARE DISEASE DAY!
With over 300 million people globally living with a rare disease, we join hands across borders and amidst the 6,000+ rare diseases to advocate for equitable access to diagnosis, treatment, care, and social opportunities.

A new CHS podcast series has been launched: NOVEL THERAPIES FOR BLEEDING DISORDERS2 topics, 4 podcasts, each topic being...
02/20/2026

A new CHS podcast series has been launched: NOVEL THERAPIES FOR BLEEDING DISORDERS
2 topics, 4 podcasts, each topic being covered in English and in French.
Video and audio formats, available on YouTube, Amazon Music, Apple Podcasts, and Spotify.
Go to www.hemophilia.ca/novel-therapies.

This year marks an important milestone for the Canadian bleeding disorder community as we introduce a new national organ...
02/13/2026

This year marks an important milestone for the Canadian bleeding disorder community as we introduce a new national organizational name that reflects who we are today and who we are becoming.
CLICK on the link to read all about it:
chscontact.ca/introducing-our-new-name

Check the current recruitment notices to see if you could participate in any of these studies.bit.ly/Research-Notice
02/06/2026

Check the current recruitment notices to see if you could participate in any of these studies.
bit.ly/Research-Notice

Go to CHS CONTACT to read all about it.bit.ly/CHS-CONTACT-Beyond9-article
02/05/2026

Go to CHS CONTACT to read all about it.
bit.ly/CHS-CONTACT-Beyond9-article

Two new podcasts discussing hemophilia gene therapy have been released! Available in video and audio formats.EPISODE 12 ...
02/04/2026

Two new podcasts discussing hemophilia gene therapy have been released! Available in video and audio formats.

EPISODE 12 – Overview of gene therapy approaches
bit.ly/gene-therapy-podcast-Episode12

EPISODE 13 – If gene therapy for hemophilia B were available tomorrow, would you want to receive it?
bit.ly/gene-therapy-podcast-Episode13

Help develop a quality-of-life tool for people with VWD around the world by sharing your experiences living with VWD.You...
02/03/2026

Help develop a quality-of-life tool for people with VWD around the world by sharing your experiences living with VWD.
Your voice can help shape future care, treatment, and research for the global VWD community.
Check your eligibility to participate at: www.surveymonkey.com/r/SXZTPGC

You would like to have a significant impact in the Canadian bleeding disorder community? Here's your chance, the CHS Boa...
02/02/2026

You would like to have a significant impact in the Canadian bleeding disorder community? Here's your chance, the CHS Board of Directors is recruiting.
Go to bit.ly/CHS-BoD-recruits-2026 for all the details and to submit your candidacy.
Deadline to apply is MARCH 16, 2026.

Address

301-666 Sherbrooke Street West
Montreal, QC
H3A1E7

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 4:30pm

Telephone

+18006682686

Website

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