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Everything you need for World Hemophilia Day 2024

World Hemophilia Day 2024 is coming soon! On April 17, 2024, the global bleeding disorders community will come together to celebrate World Hemophilia Day. The theme of the event this year is “Equitable access for all: recognizing all bleeding disorders”. The World Federation of Hemophilia (WFH) vision of Treatment for All is for a world where all people with inherited bleeding disorders have access to care, regardless of their type of bleeding disorder, gender, age, or where they live.

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The World Federation of Hemophilia (WFH) encourages everyone to engage with the community on April 17 and let your voice be heard! You can do this by posting your personal stories on our website, or on social media. Below you’ll find World Hemophilia Day resources you can use to get involved on April 17.

Please note that stories and posts shouldn’t contain references to (or show any images of) treatment product brand names.

About World Hemophilia Day

Since 1989, patient groups worldwide have annually marked World Hemophilia Day on April 17 to raise the awareness and understanding of hemophilia and other bleeding disorders. The date was chosen in honour of WFH founder Frank Schnabel, who was born on that day.

World Hemophilia Day aims to:

  • Promote the importance of taking coordinated and concerted actions to achieve the WFH vision of “Treatment for all”
  • Draw attention to the key issues and put hemophilia and bleeding disorders in the spotlight

 

2024 theme

April 17, 2024 is World Hemophilia Day. The theme of the event this year is “Equitable access for all: recognizing all bleeding disorders”. The WFH vision of Treatment for All is for a world where all people with inherited bleeding disorders have access to care, regardless of their type of bleeding disorder, gender, age, or where they live.

Use the following hashtags on social media to join the conversation

  • #WorldHemophiliaDay
  • #WHD2024
  • #LightItUpRed

Be part of “Light It Up Red” 

Every year, hundreds of landmarks “Light It Up Red” in a show of solidarity with the global bleeding disorders community. Here are some ways you can be part of this campaign:

  • Wear something red at home and share a selfie on social media
  • Challenge your coworkers or schoolmates to post a picture of themselves wearing red for the day—or post a picture collage of everyone in your organization wearing red!
  • Post pictures of landmarks you see lit up in red on social media and use hashtag #LightItUpRed
  • See the full list of landmarks lighting up red here
  • If you’re aware of a landmark that is lighting up red for World Hemophilia Day 2024 that is not on this list, please forward the official confirmation from the landmark to [email protected] to have it added

Spread the word

There are many ways you can spread the word in your community. Here are just a few:

  • Share the World Hemophilia Day website: worldhemophiliaday.org
  • Like, share and retweet WFH Hemophilia Day-related posts on social media
  • Share the World Hemophilia Day official poster (click on “Campaign Materials”)
  • Share our World Hemophilia Day resources on your website or through social media
  • Share the World Hemophilia Day Day story site—which is now accepting video submissions!

Examples of social media posts

Here are some social media posts you can use for your own campaigns:

  • #WorldHemophiliaDay is April 17! Learn more about this historic day at wfh.org/whd and download your own #WHD2024 poster!
  • #WorldHemophiliaDay is about celebrating the bleeding disorders community. Retweet/share if someone in your family is living with #hemophilia. #WHD2024
  • Mark your calendars! April 17th is #WorldHemophiliaDay. How will you be celebrating? I will be…
  • #WHD2024 is a day for everyone to learn more about #BleedingDisorders. Join the movement and learn more about #hemophilia on the WFH eLearning centre: org/education-and-elearning
  • This #WorldHemophiliaDay share YOUR story! Submit your story or video message to the #WHD2024 video series here: whdstories.wfh.org
  • We are now just a few weeks away from #WorldHemophiliaDay! This year, #WHD2024 will rally our community around the theme “Equitable access for all: recognizing all bleeding disorders”. We will focus on sharing our stories on how our community worked to engage our government. Share your story at whdstories.wfh.org
  • This #WorldHemophiliaDay share your story! The WFH has made a huge difference in the lives of children in India, bringing hope into their lives. Watch the video here: youtu.be/S96MOzW2CEA #hemophilia
  • How are you engaging our government? Share your story this #WHD2024! In Nepal, the WFH Humanitarian Aid Program has played a crucial role in helping the Nepal Hemophilia Society effectively advocate with multiple levels of government. Read the story: wfh.org/article/wfh-humanitarian-aid-program-supports-nepalese-nmo-advocacy
  • It’s here! Today is #WorldHemophiliaDay: a day dedicated to celebrating our community around the world! We’ve shared our story with the community, and you can too at wfh.org/whd

The WFH advocacy toolkit

There are many ways you can bring attention to hemophilia and other inherited bleeding disorders in your local and global community to raise awareness of the need for inclusion in national policy. This article covers many of them, but you can also get more information using the World Hemophilia Day Advocacy Toolkit. This handy guide will show you how to best use social media, how to organize an event, how to act locally—and more! Download it here (click on “Advocacy Toolkit”).

 

Send a letter to a government official

One way to help make a difference this World Hemophilia Day is to contact government officials and policymakers with a letter. A small personal note from someone from the community can often be the first step on a journey that can lead to major change. The WFH has a template letter that you can adapt to your needs. The letter covers everything you need to know, including:

  • Opening the letter with an official address
  • Explaining the purpose of your letter
  • Explaining your concern related to inherited bleeding disorders
  • Using personal or relevant stories and examples
  • Acknowledging any past support
  • Describing what action you hope the official will take
  • Proposing how you or your organization can help


You can download the letter template here (click on “Advocacy Toolkit”) which you can use at a starting point.

Download everything you need to populate your feed with World Hemophilia Day content and stories! The following shareable images and content are available here in English, French and Spanish:

  • Poster
  • Website banner
  • Email signature graphic
  • “How to get involved” one-pager
  • “Light it up Red” sample letter
  • Advocacy toolkit detailing more ways to get involved
  • Instagram graphic templates
  • Social media cover photos and graphics
  • Zoom background
  • And more!


Access these free downloads here.

Let us know what you are planning!

We want to support you and help you amplify your efforts! Let us know about what you’ve done—or what you’re planning on doing—on April 17. Stories, pictures, or social media posts are all welcome. Please note that stories and posts shouldn’t contain references to (or show any images of) treatment product brand names. Feel free to share your events with the WFH Marketing & Communications department at [email protected].

The WFH would like to thank our 2024 World Hemophilia Day sponsors for their continued support: Bayer, BioMarin Pharmaceutical Inc., Biotest, CSL Behring, F. Hoffman-La Roche Ltd., GC Pharma, Grifols, Kedrion, LFB S.A, Novo Nordisk, Octapharma, Pfizer, Sanofi, Sobi, Spark Therapeutics, and Takeda.

We’ve accomplished a lot this year, we need your help to continue strong.

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Disclaimer

The information on the WFH website is provided for general information purposes only. The WFH does not engage in the practice of medicine and under no circumstances recommends particular treatment for specific individuals. For diagnosis or consultation on a specific medical problem, the WFH recommends that you contact your physician or local treatment centre. Before administering any products, the WFH urges patients to check dosages with a physician or hemophilia centre staff, and to consult the pharmaceutical company’s printed instructions.

While every effort has been made to ensure the accuracy of the information on this site, the WFH does not guarantee the information is accurate, and is not responsible in any way whatsoever for damages arising out of the use of this website or any of the information contained herein.

Messages posted to WFH discussion forums, Facebook, Twitter, and other social media platforms do not represent the opinions of the World Federation of Hemophilia, its staff, or Board of Directors. The author of a message is solely responsibility for its content. Information posted on WFH social networks and platforms should never be a substitute for individualized professional medical advice, even when the author has medical qualifications or is considered an authority. Information posted to a discussion group should not be used to diagnose or treat a specific health problem without consulting a qualified healthcare professional. The WFH recommends that you contact your physician or local treatment centre if you have any individual questions or concerns.

References and links to other websites or references to other organizations, products, services, or publications do not constitute endorsement or approval by the WFH. The WFH is not responsible and assumes no liability for the content of any linked websites.

Fraud Alert

Unauthorized solicitations – Warning

The WFH has been made aware of various correspondences—circulated via e-mail and telephone—coming from individuals impersonating WFH staff or falsely stating that they are associated with the WFH. These correspondences, which may seek to obtain money using the name of someone affiliated with the WFH, are fraudulent and come from outside of our organization.

If you receive a suspicious solicitation, exercise extreme caution. In the case of an email, look at the email address to see if it looks suspicious (for example, all WFH emails come from @wfh.org).

We are asking you to remain vigilant, and if you have any doubts about the correspondence, please forward the email to the WFH at [email protected] or call +1 514-875-7944.