Showing posts with label #OIAwareness. Show all posts
Showing posts with label #OIAwareness. Show all posts

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.


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

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.

 

16 November 2017

Trents Aboriginal Art



I created this design last year to show our journey with our son and to help raise awareness of his medical condition Osteogensis Imperfect Type III Severe, and with the help from an amazing friend of ours Bree Sauer from Fresh Start Professional Healthcare who is also our son's Exercise Physiologist, RockTape Australia printed this art work on there RockTape. Proud was an understatement I can not describe how proud my family an I were to see this happen. To help Raise awearness of my son and my partners medical condition is somthing im very passionate about and so is our son's best friend Miss Nini. Please read her storie below. Goannas "Rocky" RockTape 🥊 🥊 Tahlia Earle has a massive passion for exercise including martial arts, footy, and boxing!! She is 9 years old and uses rocktape regularly for her knees. The artist of her favourite design "Goannas" is her best friend's dad, Trent Squires. She was so proud of the story behind the design she wanted to show everyone by having the design on her gloves. People ask her about it then she tells them the story of Marcellus who she loves so much! She really wants the awareness of Osteogenesis Imperfecta (OI) out there. 🦎🦎 Tahlia reckons having the rocktape on her wrist will give her strength to hit like a rock 🥊 **Osteogenesis Imperfecta (OI), commonly known as Brittle Bones, is a genetic disorder characterized by bones that break easily, often from little or no apparent cause. A person with OI may have just a few or as many as several hundred fractures in a lifetime. 💛 #gostrongerlonger #rocktapeaustralia #freshstartprofessionalhealthcare #goannas
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