Top Tweets for #WearBlueForLFS
We're happy to report that this year we will again be supporting our American cousins in @LivingLFS in celebrating March 20th as LFS Awareness Day.
Please share our LFS Awareness Page - and if you #WearBlueForLFS then please post a picture or two!
https://t.co/YiwSa2GZzu
Did you wear blue yesterday? It was the second #LFSAwarenessDay – a chance to raise awareness of the rare genetic #cancer condition called Li Fraumeni Syndrome. Discover why we support this:
https://t.co/pdZ0mEh9v3
#anticancerfund #WearBlueForLFS
Congratulations to @isidrolauscher and colleagues for your @The_MRC grant to study LFS 👏
You’re all looking fantastic here for #wearblueforLFS 👕 @embl
👕 Today is Li Fraumeni Syndrome Day, and @R_Rahbari's team has been wearing blue this week to raise awareness of this little-known cancer syndrome
Researchers at Sanger and @emblebi have been awarded a @The_MRC grant to study LFS
#WearBlueForLFS #TP53
https://t.co/TXcsv0zpaf
👕 Today is Li Fraumeni Syndrome Day, and @R_Rahbari's team has been wearing blue this week to raise awareness of this little-known cancer syndrome
Researchers at Sanger and @emblebi have been awarded a @The_MRC grant to study LFS
#WearBlueForLFS #TP53
https://t.co/TXcsv0zpaf
It's LFS Awareness Day and to show our support we wore blue in the office on Friday.
Find out more about LFS Awareness Day and the work done by The George Pantziarka TP53 Trust: https://t.co/1gv5O3lypQ
#WearBlueForLFS #LFSawarenessday #lifraumenisyndrome #TP53
Sunday March 20 is #LiFraumeni Syndrome Awareness Day! Join us on Zoom at 11 Pacific/2 Eastern for exciting #LFS Hardship Grant updates, show off #WearBlueForLFS gear, + honor #LivingLFS founder Jen Mallory 💙 Email [email protected] for Zoom link! #LFSawareness #cancer #tp53
#WearBlueForLFS all March long for #LFSawarenessMonth! Thank you Amanda for supporting those with #LiFraumeni syndrome, caused by a genetic mutation that increases the risk of developing #cancer #tp53 #genetics #p53 #IAmLivingLFS
Today is #LFSawarenessDay! #WearBlueforLFS to support our amazing families with #LiFraumeniSyndrome! Loving that it falls on the first day of Spring/ Persian New Year, #Nowruz A symbolic time to heal, for rebirth and to LIVE! Let’s celebrate those living w/LFS! #TP53
Today, March 20, is Li-Fraumeni Syndrome Awareness Day!
https://t.co/a3h1vdtjmQ
Wear blue and use these hashtags to show your support:
#LiFraumeniSyndromeAwarenessDay
#LFSawarenessDay
#LiFraumeniSyndrome
#LiFraumeni
#LFSawareness
#LFSawarenessMonth
#WearBlueForLFS
#IAmLivingLFS
Today, March 20, is Li-Fraumeni Syndrome Awareness Day!
https://t.co/a3h1vdtjmQ
Wear blue and use these hashtags to show your support:
#LiFraumeniSyndromeAwarenessDay
#LFSawarenessDay
#LiFraumeniSyndrome
#LiFraumeni
#LFSawareness
#LFSawarenessMonth
#WearBlueForLFS
#IAmLivingLFS
Tomorrow is #LFSAwarenessDay
LFS stands for #LiFraumeniSyndrome. A genetic condition caused by a mutation in a gene called TP53 - the most important tumour suppressor gene in the body.
Tomorrow, help raise awareness and #WearBlueForLFS
https://t.co/yS2mXqJZNo
#WearBlueForLFS on March 20th and help raise awareness of #LiFraumeniSyndrome
https://t.co/P2yiGZ8F0x
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