Become a member of the only national charity dedicated to supporting people affected by Osteogenesis Imperfecta
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Wheelchairs & Equipment
Find our how we can support you by providing funding towards essential equipment »
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What is Osteogenesis Imperfecta?
OI is a genetic bone disorder characterised by fragile bones that break easily. Find out more »
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Help us make a difference
Fundraising allows us to continue to support people affected by OI »
Supporting people affected by Osteogenesis Imperfecta
throughout the UK and Ireland
The Brittle Bone Society is the national charity that supports individuals and families affected by Osteogenesis Imperfecta (OI).
We’re here to help and support you and your loved ones.
See how we can help
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Get involved
Fundraise for us! Do something you love and turn it into a fundraiser for the BBS!
Latest News
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Research Consultation Report
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Job Vacancy: Communications Assistant
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The Wishbone Warriors on Eggheads
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OI Storytelling Competition – Winners Announced!
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European Reference Network – OI White Paper
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OI Storytelling Competition
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Increasing awareness at Healthcare Conferences
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Max Charms Thousands on BBC Radio 2
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Abbi Brown Guest Blog: University Top Tips
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Mia takes on Kilimanjaro
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Shani Dhanda Guest Blog: BBS Conference 2018
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Nicholas Oliver: a tribute
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History Bones: Liz’s Story
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Gem Turner Guest Blog: “What do you want to be when you’re older?”
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History Bones: David’s Story
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Margaret Grant MBE Honorary Degree
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Abbi Brown Guest Blog: BBS at Parliament
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History Bones: Elaine’s Story
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Shani Dhanda Guest Blog: Why it’s important to celebrate Wishbone Day
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Sam Renke Guest Blog: Don’t Take No For An Answer!
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Lizzie Williams: Sporting Success
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Abbi Brown Guest Blog: Getting into fitness
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Gem Turner Guest Blog: It’s Our Time To Shine
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Shani Dhanda Guest Blog: Lets talk about loneliness
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BBS Research Grant Winners
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Kids Club packs
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Call Out for History Bones Artifacts
@BrittleBoneUK
February 24th 2021 03:02:04
Many people with OI have Dentinogenesis. Please tell us your experiences of finding specialist dentists willing to… https://t.co/nYEIdTxJnq
@BrittleBoneUK
February 24th 2021 10:02:45
Please see the statement from the Brittle Bone Society Medical Advisory Board regarding which individuals with Oste… https://t.co/791FPB3tK4
@BrittleBoneUK
February 24th 2021 09:02:22
Please help support Rare Disease Day 2021 - add a BBS #Twibbon now! #RareDiseaseDay2021 https://t.co/XnFgnVZrk5
@BrittleBoneUK
February 23rd 2021 03:02:05
Rare Disease Day is the 28th Feb. Lets start raising awareness by joining the Rare Disease Community.
Please like… https://t.co/2fzRNE9B4c
@BrittleBoneUK
February 19th 2021 01:02:13
Thanks to everyone who used Amazon Smile, we have received £271.24 in the last 12 weeks! By visiting… https://t.co/pXsoCxSuW1
@BrittleBoneUK
February 19th 2021 10:02:18
Proud to be supporting the OI community in the UK for 52 years and look forward to celebrating Rare Disease Day!… https://t.co/nytW7ZSlzd
@BrittleBoneUK
February 16th 2021 10:02:28
It’s Pancake Day, and Ollie the OI Owl is excited to see all your pancake creations. Post below a photo of you baki… https://t.co/z2ND524GAD
@BrittleBoneUK
February 15th 2021 07:02:02
Do you have a child with OI in the Cool Bones age group? (aged 11-15) We are looking for parents to join our focus… https://t.co/r5W1vOWm07
@BrittleBoneUK
February 11th 2021 04:02:02
Do you have a child with OI in the Cool Bones age group? (aged 11-15) We are looking for parents to join our focus… https://t.co/M1f3XHl2Aq