Rare Disease Day in 2023

Rare Disease Day Quick Facts - GB 2023

ℹ HashtagsCompiled on 1 March 2023 at 05:05	#RareDiseaseDay, #RareDiseaseDay2023
Related Hashtags	#RareDisease, #Rarediseases
2023 Date	28 February 2023
2024 Date	29 February 2024

2023 Holidays & Dates

Rare Disease Day in

Tuesday, 28 Feb

Days to go:

Top X Posts (formerly Tweets) for Rare Disease Day -
in 2023

Updated 1 March 2023 at 05:05

Today is Rare Disease Day and it’s a day to raise awareness for the 300 Million people in the world with over 6000 rare diseases. If you or a loved one have a rare disease write it in the comments and make it seen. #RareDisease #RareDiseaseDay #RareDiseaseDay2023 https://t.co/mGY8aK4RhB
— All On The Board (@allontheboard) February 28, 2023

Today is Rare Disease Day. Three hundred million people globally live with a rare disease, including those with rare or unclassified bleeding disorders. People affected by rare or unclassified bleeding disorders can often feel like some of the most isolated in our community. https://t.co/j4Jy6gGv5Y
— Haemophilia Society (@HaemoSocUK) February 28, 2023

Today is Rare Disease Day TTP is called a Rare disease, so Rare that even some medical professionals do not know about TTP Lack of awareness of Rare diseases equals a lack of prompt diagnosis and appropriate treatment. This is why awareness of rare diseases like TTP is key https://t.co/bbbwIGH8at
— AOFAC Foundation (@aofac) February 28, 2023

Today is Rare Disease Day! PSC is a rare disease. Watch to find out more. #RareDiseaseDay #RareDiseaseDay2023 https://t.co/tbROblPPaX
— PSC Support (@PSCSupportUK) February 28, 2023

Today is Rare Disease Day. Ezra & I will carry on doing what we can to help raise awareness. Today we are off to London to see Drs about Ed & his friends. This appointment has been a wait of 3 years & 14 days.Let’s see if it’s worth it #RareDiseaseDay #EhlersDanlosSyndrome https://t.co/X9X5HOG6Vn
— Darren (@Ezra_Who_) February 28, 2023

Today is Rare Disease Day! 300 million people worldwide live with a rare disease and have to deal with limited knowledge/treatments about their condition. Today is a great day to support anyone living with a rare disease and show them that we care. https://t.co/w9In6jad5W
— Liz Twist MP (@LizTwistMP) February 28, 2023

LDA Research supports Rare Disease Day, working to bridge the gap between patients and health care professionals by carrying out international medical market research. Today we launch our Rare Disease Network, uniting people across the globe affected by a rare disease diagnosis. https://t.co/h2cAnJLC7b
— LDA Research (@LDAResearch) February 28, 2023

I'm so proud to share my birthday today with Rare Disease Day!! https://t.co/BBZ8UZmu2G
— Truth About Life With PKU (@danellmer) February 28, 2023

Today is Rare Disease Day, a day to raise awareness for the 1 in 17 individuals who live with a rare condition. Please share your rare loved one ♥ I'll go first, here's my son Joe who has Duchenne muscular dystrophy https://t.co/Wrp9kpuW81
— Susanne Driffield (@s_driffield) February 28, 2023

Such an important day for the rare disease community 📣 I have an ultra-rare disease known as Occipital Horn Syndrome. #RareDiseaseDay #RareDiseaseDay2023 https://t.co/hmi44nmSQ7
— David Rose (@davidrose88) February 28, 2023