04 May 2026

Wishbone Day: Frequently Asked Questions

What is Wishbone Day?


Wishbone Day is the international day of awareness for Osteogenesis Imperfecta, also known as OI or brittle bones.

It is held each year on 6 May and is recognised around the world by individuals, families, communities, schools, health professionals and organisations who want to celebrate people with OI and increase understanding of what life with OI can look like.

At its heart, Wishbone Day is about people, voice, visibility and action.

It is not owned by one organisation. It is a global grassroots movement shaped by the people who take part.






When is Wishbone Day?


Wishbone Day is officially held on 6 May each year.

Some people and communities celebrate on the day itself. Others hold events, share stories, run activities or wear yellow during the week or month around 6 May. That is okay.

The date helps us connect globally, but participation can happen in whatever way works for your community.

Why yellow for Wishbone Day?

Yellow is the colour of Wishbone Day.


It was chosen because it is bright, bold and full of energy. It stands for visibility, optimism, celebration and connection. Wearing yellow, decorating with yellow, lighting buildings yellow or sharing yellow-themed images are simple ways people around the world show support for Wishbone Day.


Who can take part?

Everyone.


Wishbone Day is for people with OI, families, friends, schools, health professionals, community groups, disability services, hospitals, researchers, advocates and anyone who wants to help build understanding.


You do not need to be part of an organisation to take part.


You can participate as an individual, a family, a classroom, a workplace, a local group or a whole community.


How can I take part?

There are many ways to take part in Wishbone Day. You might:

  • Wear yellow
  • Share a story or photo
  • Talk about OI in your school, workplace or community
  • Host a yellow morning tea or gathering
  • Create artwork, posters or displays
  • Run an information session
  • Light up a building or landmark yellow
  • Share messages on social media using #WishboneDay
  • Support local OI advocates and families
  • Do something practical that improves inclusion, access or understanding


There is no one “right” way to take part. The best Wishbone Day actions are the ones that are meaningful, respectful and led by the people and communities involved.



Is Wishbone Day a fundraiser?

No. Wishbone Day was not created as a fundraiser.


Wishbone Day is an awareness and action movement. It exists to centre people with OI, challenge outdated ideas, and encourage communities to listen, learn and do something meaningful.


Some organisations may choose to fundraise as part of their own activities, but fundraising is not the purpose of Wishbone Day.



Is Wishbone Day run by an organisation?

No. Wishbone Day is a grassroots global movement.


It does not have paid staff, corporate sponsors or a formal central office. It has grown because individuals, families, advocates, communities and organisations around the world have chosen to take part.


This is part of what makes Wishbone Day powerful. It belongs to the people who show up, speak up and take action in their own communities.


Can organisations take part?

Yes. Organisations are welcome to take part.


The most important thing is to respect the purpose and spirit of Wishbone Day. That means centring people with OI, listening to lived experience, avoiding pity-based messaging, and using the recognised Wishbone Day colour and name.


Organisations should not use Wishbone Day simply as a fundraising opportunity or as a way to promote themselves. The focus should remain on people with OI and meaningful community action.


Why does Wishbone Day focus on awareness rather than fundraising?

Because awareness can change the way people think, speak and act.


For many people with OI, the biggest barriers are not only medical. They can also be social, physical, educational and attitudinal. Misunderstanding, overprotection, exclusion and low expectations all limit participation.


Wishbone Day asks people to look beyond bones and see whole lives: childhood, family, school, work, friendship, culture, creativity, leadership, independence and joy. Awareness matters when it leads to better understanding and better action.


What does “awareness into action” mean?

Awareness is only the beginning.


Awareness into action means asking: what can we actually do differently?


That might mean making a school more inclusive, improving access to a community event, listening to people with OI, challenging stereotypes, supporting families, changing policies, improving services, or making sure people with OI lead decisions that affect them.


Wishbone Day is not just about being seen. It is about being heard and respected.



Can schools take part?

Yes. 


Schools are a wonderful place to recognise Wishbone Day.


Students and teachers might wear yellow, create posters, read stories, learn about disability rights, or talk about how to make classrooms, playgrounds and communities more accessible.


School activities should be respectful and age-appropriate. They should focus on understanding and respect rather than fear or pity.


Can we hold a local Wishbone Day event?

Yes.


Local events are encouraged. They can be small or large, formal or informal. You might organise a picnic, morning tea, school activity, community display, yellow dress day, art project, information session or online gathering.


Wishbone Day works best when local communities make it their own while staying connected to the shared global message.


Do we need permission to take part?

No. 


You do not need permission to wear yellow, share a message, host a local activity or recognise Wishbone Day.


WIshbone Day grows because people take initiative.


Please use the day respectfully, and help others understand why Wishbone Day matters.



Can I use the Wishbone Day name and logo?

Yes.


Permission is freely granted to use the Wishbone Day name, brand and Wishy logo for non-commercial awareness purposes.


This means individuals, families, schools, community groups and organisations may use Wishbone Day materials to promote Wishbone Day and raise awareness of Osteogenesis Imperfecta, provided the use is respectful and not for profit.


Use of the Wishbone Day name, brand and logo is permitted on the basis that:

  • it is used for Wishbone Day and OI awareness purposes only
  • it is not used for commercial or profit-making purposes
  • it is linked back to www.wishboneday.com
  • the hashtag #WishboneDay is used where appropriate
  • the meaning, purpose and spirit of Wishbone Day are respected

Who designed the Wishbone Day brand and logo?

The Wishbone Day brand and logo were designed by Dr Jo Ragen, who retains copyright. 


The Wishy logo is part of the Wishbone Day identity. The Wishbone Day brand and logo may be used only in ways that support awareness of Osteogenesis Imperfecta and the purpose of Wishbone Day.



Can organisations use the Wishbone Day logo?

Yes, organisations may use the Wishbone Day logo for non-commercial awareness purposes, provided the use respects the purpose of the day and links back to the wider movement at www.wishboneday.com.


Organisations should not present Wishbone Day as their own campaign, change the meaning of the day, use the logo to imply ownership, or use the brand primarily for fundraising or self-promotion.

Wishbone Day belongs to the global OI community. 


Can I use photos from the Wishbone Day website or social media?

No, not without permission from the photo owner.


All personal images of individuals, families or groups displayed on the Wishbone Day website or social media remain the property of the original photo owner.


Copying, downloading, distributing or reusing these images for any purpose is not permitted. This includes use in slideshows, YouTube videos, webpages, presentations, social media posts, promotional materials or other publications.


Please respect the privacy, dignity and ownership rights of the people represented in these images.


Can I share Wishbone Day social media posts?

Yes. Sharing Wishbone Day posts through normal social media sharing functions is encouraged.


Please do not copy, download, edit or republish personal images from Wishbone Day posts without permission. When sharing, please use #WishboneDay and link back to www.wishboneday.com where possible.


What hashtag should I use?

Use:


#WishboneDay


You can also use local or language-specific hashtags if they help your community connect. Using #WishboneDay helps link your post to the wider global movement.


Who owns Wishbone Day?

Wishbone Day belongs to the global OI community.


It began as a grassroots idea and has grown because people around the world continue to bring it to life. It is not the property of one organisation, one country or one person.


The strength of Wishbone Day comes from shared participation.







Why Yellow on Wishbone Day?

People often ask why yellow on Wishbone Day?

When we designed Wishbone Day, the colour yellow was chosen by our junior members of the OI community. They had decided that yellow best represented the colour of a wish and was by far the happiest colour in the pack. They also decided that wearing yellow would make it easier to find each other. 

Wishbone Day yellow shines with optimism and carries the promise of a positive future. Wishbone Day yellow is a symbol of that promise.

And we couldn't argue with that! 

What does Wishbone Day yellow mean to you?


18 March 2026

A quick update from Wishbone Day - March 2026

Wishbone day is now firmly part of the global OI commmunity. That has only been possible because of the people, places and moments that have shaped it over time. Thank you.  

As we look ahead, we're beginning a refresh of the website to better reflect what Wishbone Day has become, while staying true to the foundations that made it what it is today. 

You'll see changes roll out gradually as we simplify, clarify and celebrate the global movement it has grown into.  

At the same time, we're heading toward Wishbone Day 2026. 

Now is the perfect time to begin thinking about how you might take part this year, however that looks for you. Wishbone Day grows through what each of us brings to it. 

Show up. Take part. In your own way.   

If you share your moments, use #WishboneDay to help connect the global community.

The countdown to Wishbone Day has begun.


 



06 May 2024

Happy Wishbone Day!

Happy Wishbone Day everyone! 

We're super excited to see the varied Wishbone Day celebrations and contributions from around the world. Remember, if you want your Wishbone Day photos, stories or events to show up on our Wishbone Day community pages you must use the #WishboneDay hashtag on all of your social media platforms.

Help us find you! 

#WishboneDay



05 May 2024

What are the rights of a child with OI?

Have you seen CLAN’s Child- Friendly Rights Flyer that was launched on Wishbone Day?



In collaboration with the international OI community CLAN have developed and launched a child friendly human rights flyer. The flyer supports OI advocacy efforts and helps young people with OI and their families to understand their human rights as declared under the United Nations Convention on the Rights of the child.


The child friendly rights flyers are available in English, Indonesian and Korean languages and are available for download through CLAN's website. We extend our warmest thanks to the passionate partners involved with the flyer development and who are committed to engaging in collective advocacy efforts to highlight and protect the rights of #EVERYchild living with OI.



FOSTEO's Wishbone Day Celebration by Téa La




Wishbone Day is an annual awareness-raising day for the international Osteogenesis Imperfecta (OI) Community, and is celebrated every year on 6 May. Members of FOSTEO, the Indonesian OI community, travelled from as far away as East Java to attend a day of celebration in Jakarta, which was supported by CLAN (Caring & Living As Neighbours) and Yayasan Kesehatan Anak Global (YKAG).

This year 28 families gathered together on Saturday 21 May to strengthen the community’s bond in the spirit – and colour! – of WBD. The event was held at RS Pondok Indah Hospital in a spacious outdoor garden next to a community playground. Many passers-by could observe the sea of yellow-clothed people, yellow cupcakes, and yellow decorations. There was an education seminar for parents and a Q&A session with special guests Prof. Aman Pulungan and Dr. Dana Prihadi; fun painting class for children; and a sharing session led by six parents of children living with OI. The education seminar focused on valuable knowledge related to clinical aspects of OI, including holistic management, essential medicines, and tips for enjoying a happy and healthy life with OI. It was a great opportunity for families to learn more about OI, share their experiences and motivate one another.

Families left the event with smiles on their faces and an education booklet in hand. The booklet was developed by the team at YKAG and CLAN. Education resources help young people, families, and communities living with chronic health conditions optimise their self-management and quality of life, and achieve their fullest potential. Included in the education booklet was CLAN’s OI Child- Friendly Rights Flyer that was launched on WBD as part of collaborative celebrations with the international OI community. It is available in English, Indonesian and Korean languages on CLAN's website. The flyer supports OI advocacy efforts and helps children and young people understand their basic human rights as declared under the United Nations Convention on the Rights of the Child. We extend our warmest thanks to the passionate partners (seen below) involved with the flyer who are committed to engaging in collective advocacy efforts to highlight and protect the rights of #EVERYchild living with OI.

FOSTEO has grown in number and activities since their founding in 2012. They now have over 200 members living with OI across Indonesia. The community fosters a supportive and encouraging environment for new and old members alike, supporting them to come together and share their experiences. FOSTEO has a long history of enjoying expertly organised community events – many of which gained national TV coverage. However, financial burdens and the unprecedented COVID-19 pandemic had disrupted these annual activities for 5 years. CLAN and YKAG’s teams were so happy to see families once again gather in liveliness and reinvigorate the community’s spirit.

“Why is Wishbone Day Important? Because awareness makes a difference.”

This is the motto for WBD. The spirit of WBD is an opportunity to privilege the voices of OI communities across the globe and join with them in celebration of the achievements of all people living with OI. Awareness of OI in the wider community creates much-needed space to have these important discussions at a whole of society level and invite others to get involved in driving practical changes for people living with OI so we all enjoy our basic human rights of life to health, happiness, and well-being.

CLAN are incredibly honoured to have worked with FOSTEO and YKAG in preparation of this event. Téa La, an intern working with CLAN and a New Colombo Plan (NCP) Scholar from the Department of Foreign Affairs and Trade (DFAT), was on the ground in Indonesia in the weeks leading up to the event, helping with the logistics. Leading up to the event, Téa was mentored by Jo Ragen to create the OI Child-friendly Rights Flyer, and collaborated with local professionals to create an OI education booklet. At the WBD event, Téa communicated with families and learned about some of their daily challenges. She found that this has further motivated her to continue the amazing efforts with CLAN. Sincerest gratitude to Jo Ragen, Craig Munns, Peter Simm, Dr. Jin-Ho, Kate Armstrong, Catherine Cole, and Prof. Aman Pulungan for supporting Téa in her journey with the OI community so far.

The success of Wishbone Day 2023 in Indonesia was due to the combined efforts of the FOSTEO community, CLAN, YKAG, the Indonesian Pediatric Society, the team at Pondok Indah Hospital, Prof. Aman Pulungan, Dr. Dana Prihadi, Dr. Tiffanny Shabrina, Dr. Timothy Supit and all those who attended the event. The celebration came to fruition with the support and participation of everyone. Thank you!

This article by Téa La highlights the true passion of communities, professionals and partners seen at FOSTEO's Wishbone Day 2023 celebration, and the importance of collaborative efforts so that we #LeaveNoChildBehind.


23 April 2022

PEOPLE WITH OI - NOT PATIENTS: a message from Ingunn

Greetings from India

Greetings from the Indian OI organization

The Indian Osteogenesis Imperfecta Foundation has been a registered Trust since May 2018. The IOIF has been actively involved in raising awareness of OI and supporting the OI community in India since it was established, and is currently the most active OI organization in India. 

The IOIF has been added to the Wishbone Day OI around the world page to help people with OI and their allies to find OI support in India. For more information regarding the IOIF visit the website

Happy Wishbone Day!


Is your OI support foundation listed on the Wishbone Day website? (you can check here)

If your OI association or foundation is not listed, let us know so we can add you. Email us at info@wishboneday.com


13 April 2022

Wishbone Day: If fundraising is your motivation for taking part ... you've missed the point. A reminder

Wishbone Day is not a fundraising event. It is not a missed opportunity to raise money. If fundraising is your motivation for taking part, you've missed the point.

Every year in the lead up to Wishbone Day I am asked about why Wishbone Day is not a fundraising event. People often question it's design as a missed opportunity to raise money -- the typical purpose of awareness campaigns -- especially for those surrounding disability.

So let me explain.

People with OI, their families and friends created Wishbone Day. They wanted to be listened too. They wanted to be acknowledged and taken seriously. But most of all they wanted a community in which they were connected and that they belonged. Wishbone Day was created as a platform on which these voices could be heard and that communities could be built.

Fundraising was very deliberately left out of the Wishbone Day design and intention. Because if you couldn’t fundraise, Because if you couldn’t fundraise ... it could leave room for something more. When Wishbone Day was created it was an invitation to the world to join our OI community – to become one with us. It was an invitation to have conversations about who we are and what matters most, and to have people really listen and to understand. It was an invitation to play with us, to work with us, to eat with us, to accept and love us, and to celebrate with us! It was an invitation to create together a community in which we all truly belonged.

Wishbone Day was a new beginning. And in accepting the Wishbone Day invitation you choose to become one with us. On Wishbone Day we ask that you join with us as equals … not to cure us or to make us better … but to really be with us … to celebrate all that we are together, right here, right now. Enough. Just as we are.

Wishbone Day yellow shines with optimism and carries that promise of a positive future. It really is that simple. 


Happy Wishbone Day!
#WishboneDay


05 May 2021

#WishboneDay

Wishbone Day is fast approaching. Remember, if you want your Wishbone Day photos, stories or events to show up on our Wishbone Day community pages you must use the #WishboneDay hashtag on all of your social media platforms. Help us find you! #Wishboneday

Join Sammi Haney on Wishbone Day

 Join Sammi Haney, Netflix Raising Dion superstar on Wishbone Day. 

04 May 2021

Wishbone Day Everyday Open Platform: Hosted by Care4Bones.org

Danielle de Bakker and Dagmar Mekking will be hosting a Wishbone Day Everyday with Care4Bones open platform on May 6th. For the full program visit www.care4bones.org or pre-register at https://tinyurl.com/wishboneC4B




 

19 April 2021

Mask It Yellow - and be Covid safe on Wishbone Day

If you had told us last year that Covid would still be challenging our communities more than a year later, we would never have beleived you! But here we are ... another Wishbone Day and still no end to Covid. OI Ghana masked it yellow last year to keep covid-safe! We loved these Wishbone Day masks so much we hope that Mask it yellow continues this year. 

Show us your Wishbone Day masks. #BeCovidSafe #WIshboneDay #BecauseAwarenessMakesADifference

Say Cheese! A Wishbone Day Photography Challenge




#IOIF #IndianOIFoundation #WishboneDay #AwarenessMakesADifference

09 October 2020

Through my eyes: In conversation with Dr Evianne Grosvenor and Melinda Montgomery

Join this free interactive webinar on identity, inclusion and self-portraiture. 

REGISTER FOR FREE

Through My Eyesis a collaborative, arts-based knowledge translation research project initiated at the Black Dog Institute and UNSW Sydney. Through participant-led photographic enquiry, the project seeks to reveal fresh perspectives on disability to challenge pervasive, limiting negative attitudes and assumptions.

In this interactive webinar, Evi and Mel present a series of self-portraits included in the resulting exhibition. They will discuss how each work was constructed, the influence of feminist themes and how the images call for greater inclusion. This talk provides an opportunity to understand how seeing and thinking more about diversity in bodies and abilities can benefit all women. 

The webinar will have live captions. An interactive chat room will also offer a platform to connect to others through shared experiences.

Dr Evianne Grosvenor is a photographer and manages formal complaints at Macquarie University. She holds a PhD in Psychology, focusing on child sexual abuse and children’s memories of traumatic events.

Melinda Montgomery is a photographic artist from Wollongong who has been behind the lens for over 20 years. She credits her unique style to adapting to the restrictions of the world around her and her wheelchair and encourages others to view the world through her perspective.


Event and registration details:

Wed 28th Oct 2020, 1:00 pm - 2:00 pm AEDT



27 May 2018

Ketut Budiarsa is most certainly not ordinary, at all.



Ketut Budiarsa is most certainly not ordinary, at all. Ketut is one of three brothers living with OI in Bali. He is a proud Balinese man. Let us share with you his story of life with OI in Bali, his work as a human rights activist and public speaker, and his use of art to tell stories. Visit his website at http://ketutbudiarsa.weebly.com




07 May 2018

Have you joined our Wishbone Day tribe?

Be part of the big Wishbone Day picture!! -- share with us your Wishbone Day photos, videos or posts by tagging our social media pages @Wishbone Day or #WishboneDay on facebook, Instagram or twitter!  We can't see your posts unless you share them with us! 

Facebook @WishboneDay
Instagram @WishboneDay or #WishboneDay
Twitter @WishboneDay or #WishboneDay

Send us your photos! Join our tribe.
Once we were one. Now we are many!


This week we welcome new Wishbone Day friends in China!
Wishbone Day China.  Image Credit: Wen Liu

Wishbone Day Art by ArtArtzy



06 February 2018

You are beautiful!

By Stacy Mason

At the end of last year I was chosen to be a model for a photo exhibit called Embrace Your Body. This exhibit featured glamorous pictures of many beautiful women with all different body types beyond the stereotypical "magazine model." I was the only woman chosen who uses a wheelchair.

I decided to do the exhibit for my myself and for my daughter. We both have Type 5 OI. As most of you know, having OI usually means having deformities and not looking "normal." I have struggled with accepting parts of my body for a long time. My right leg is my most hated. I broke it so many times in late elementary school/beginning of middle school. It was in a cast so many times it's significantly shorter then the other. I was/am a chronic leg crosser which with soft bones meant that leg eventually curved around the other leg which is why it has a significant curve to it. Its the main reason you will rarely find me wearing anything that shows my legs. I know my spine is very curved and as a result I have a noticeable "hunch back" and I know my arms are not straight in the slightest either, but for some reason its my legs that I want to hide.

My daughter will be 5 soon, and she already has some unique characters about her body. Its my job to show her she is beautiful no matter what, but how can I do that when I struggle with it myself? So, I went way outside my comfort zone and did this.

 

I felt beautiful (but nervous!!!) and these photos are gorgeous, if I do say so myself! I hope my confidence to share my body and embrace it will encourage others in this community who may be struggling to love themselves too. You are beautiful and you are worth it!

(Click to follow Stacy on Facebook)

17 January 2018

Mummy on Wheels

On Saturday we shared Unbreakable: a film by Rebecca Kirwan, which is a short documentary about Jodie, and her husband Todd. If you missed it you can catch up here.  The documentary ends with the question, what next for Jodie and Todd?

Today we congratulate Jodie and Todd on the safe arrival of Ethan, their first baby boy.

Mum, bub and Daddy are all doing well.

You can follow Jodie's story from her Facebook page Mummy on Wheels.