🧬 95% of rare diseases have no treatment. This Rare Disease Day, we’re working to change that by accelerating breakthroughs—40 new treatments by 2034—through world-class research & drug development.
Learn more: tinyurl.com/2ab5zecf
#RareDiseaseDay #CareForRare www.youtube.com/watch?v=sKEf...
Learn more: tinyurl.com/2ab5zecf
#RareDiseaseDay #CareForRare www.youtube.com/watch?v=sKEf...
Transforming Rare Disease Treatment | The Oxford-Harrington Rare Disease Centre
YouTube video by Oxford-Harrington Rare Disease Centre
www.youtube.com
February 27, 2025 at 1:28 PM
🧬 95% of rare diseases have no treatment. This Rare Disease Day, we’re working to change that by accelerating breakthroughs—40 new treatments by 2034—through world-class research & drug development.
Learn more: tinyurl.com/2ab5zecf
#RareDiseaseDay #CareForRare www.youtube.com/watch?v=sKEf...
Learn more: tinyurl.com/2ab5zecf
#RareDiseaseDay #CareForRare www.youtube.com/watch?v=sKEf...
Did you know 1 in 17 people will be affected by a rare condition at some point in their lives?
Take a look around you and have a think about how many people that really is! Help us spread the word so changemakers know why they should #CareForRare.
#RareDiseaseDay #Rarequity
Take a look around you and have a think about how many people that really is! Help us spread the word so changemakers know why they should #CareForRare.
#RareDiseaseDay #Rarequity
February 7, 2026 at 11:00 AM
Did you know 1 in 17 people will be affected by a rare condition at some point in their lives?
Take a look around you and have a think about how many people that really is! Help us spread the word so changemakers know why they should #CareForRare.
#RareDiseaseDay #Rarequity
Take a look around you and have a think about how many people that really is! Help us spread the word so changemakers know why they should #CareForRare.
#RareDiseaseDay #Rarequity
February is #RareDisease awareness month.
#CAFSociety #CassieAndFriends support children, teens, young adults, and their families - living with rare rheumatic diseases - across Canada. 🇨🇦
#CareForRare
cassieandfriends.ca
#CAFSociety #CassieAndFriends support children, teens, young adults, and their families - living with rare rheumatic diseases - across Canada. 🇨🇦
#CareForRare
cassieandfriends.ca
February 9, 2025 at 7:25 PM
February is #RareDisease awareness month.
#CAFSociety #CassieAndFriends support children, teens, young adults, and their families - living with rare rheumatic diseases - across Canada. 🇨🇦
#CareForRare
cassieandfriends.ca
#CAFSociety #CassieAndFriends support children, teens, young adults, and their families - living with rare rheumatic diseases - across Canada. 🇨🇦
#CareForRare
cassieandfriends.ca
Today is the day to #ShowYourStripes! So raise awareness & show your support by taking part in
@medicsforrare.bsky.social campaign 🦓
🧦 Post a snap of your stripey socks with the hashtags #ShowYourStripes for #RareDiseaseDay & share your story. Wear your stripes to #CareForRare! (7/9)
@medicsforrare.bsky.social campaign 🦓
🧦 Post a snap of your stripey socks with the hashtags #ShowYourStripes for #RareDiseaseDay & share your story. Wear your stripes to #CareForRare! (7/9)
February 28, 2025 at 9:54 AM
Today is the day to #ShowYourStripes! So raise awareness & show your support by taking part in
@medicsforrare.bsky.social campaign 🦓
🧦 Post a snap of your stripey socks with the hashtags #ShowYourStripes for #RareDiseaseDay & share your story. Wear your stripes to #CareForRare! (7/9)
@medicsforrare.bsky.social campaign 🦓
🧦 Post a snap of your stripey socks with the hashtags #ShowYourStripes for #RareDiseaseDay & share your story. Wear your stripes to #CareForRare! (7/9)
Whatever it is, find your dazzle (group of zebras 🦓 the mascot of rare disease) and know you are NEVER alone!
#RareDiseaseWeek #OntheHill #TelomereBiologyDisorders #TeamTelomere #RareDiseaseDay #CareforRare #TBDResearch
#RareDiseaseWeek #OntheHill #TelomereBiologyDisorders #TeamTelomere #RareDiseaseDay #CareforRare #TBDResearch
February 25, 2025 at 8:32 PM
Whatever it is, find your dazzle (group of zebras 🦓 the mascot of rare disease) and know you are NEVER alone!
#RareDiseaseWeek #OntheHill #TelomereBiologyDisorders #TeamTelomere #RareDiseaseDay #CareforRare #TBDResearch
#RareDiseaseWeek #OntheHill #TelomereBiologyDisorders #TeamTelomere #RareDiseaseDay #CareforRare #TBDResearch
Show us your #1 for GM1 Awareness Day 💙
Share a photo, spread the word, and help fund hope for families affected by GM1 Gangliosidosis. Donate today: curegm1.org/donate
#curegm1 #gm1day #makeadifference #careforrare
Share a photo, spread the word, and help fund hope for families affected by GM1 Gangliosidosis. Donate today: curegm1.org/donate
#curegm1 #gm1day #makeadifference #careforrare
May 23, 2026 at 4:31 PM
Show us your #1 for GM1 Awareness Day 💙
Share a photo, spread the word, and help fund hope for families affected by GM1 Gangliosidosis. Donate today: curegm1.org/donate
#curegm1 #gm1day #makeadifference #careforrare
Share a photo, spread the word, and help fund hope for families affected by GM1 Gangliosidosis. Donate today: curegm1.org/donate
#curegm1 #gm1day #makeadifference #careforrare
DYK 70% of genetic rare diseases start in childhood? For many, chronic pain is a daily struggle. This #RareDiseaseDay, we’re raising awareness and advocating for better pain management.🌟Keep reading for helpful resources! ⬇️
#CareForRare #ItDoesntHaveToHurt
#CareForRare #ItDoesntHaveToHurt
February 28, 2025 at 2:28 PM
DYK 70% of genetic rare diseases start in childhood? For many, chronic pain is a daily struggle. This #RareDiseaseDay, we’re raising awareness and advocating for better pain management.🌟Keep reading for helpful resources! ⬇️
#CareForRare #ItDoesntHaveToHurt
#CareForRare #ItDoesntHaveToHurt
