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FOP Science Made Simple 

Int'l Fibrodysplasia Ossificans Progressiva Assoc
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💚 FOP (Fibrodysplasia Ossificans Progressiva) is an ultra-rare disease that turns muscle into bone, obstructing movement and hindering lives: ifopa.org/what...
🌎 The International FOP Association (IFOPA) is here to help find a cure through funding research, raising awareness, and supporting the community: ifopa.org/abou...
👋🏽 CONNECT:
IFOPA
/ cure_fop
/ ifopa
/ international-fop-asso...
📬 Sign up for the newsletter and stay on top of the community and the path towards a cure: ifopa.org/connect
👨‍👩‍👧‍👦 Register for the next Family Gathering: ifopa.org/fami.... Relive sessions from past Gatherings: ifopa.org/fami...
🛠️ Check out the Ability Toolbox Guidebook featuring tools and home adaptations for independent living: guidebook.ifop...
📆 Get involved with our family services, fundraising and awareness events: ifopa.org/cale...
📗 Learn the scientific terminology surrounding FOP in the IFOPA Glossary: ifopa.org/glos...
❤️ DONATE and join us to fight FOP and support families in their journey: ifopa.org/donate
🙋🏽 FOP Frequently Asked Questions: ifopa.org/fop_faq
#cureFOP #RareDisease #disability #RAREParenting #caregiver

Опубликовано:

 

11 сен 2024

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Комментарии : 9   
@ahmadbakro6062
@ahmadbakro6062 9 месяцев назад
Hello. Can you help me? A 5-year-old child with FOP syndrome. He lives in Syria. Can anyone help?
@Tissues9738
@Tissues9738 8 месяцев назад
There is no cure or vaccine so sadly I can't really do anything about it.
@sorena5542
@sorena5542 5 месяцев назад
Nature can be sometimes cruel and unfair 😢 Can't imagine living my life unable to escape my fate.
@MarcoFiemme
@MarcoFiemme 4 месяца назад
Is he doing okay?
@wolfiethetimberwolf1363
@wolfiethetimberwolf1363 4 месяца назад
How much pain is he in?
@cupricwheat
@cupricwheat 4 месяца назад
We can't do nothing about FOP, it has no vaccine nor a cure, so he has to deal with it, it's sound cruel, but that's natures barbaric and brutal side.
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