Top Tweets for #LFSAwarenessDay
It's #LFSAwarenessDay! Read this story about Elijah Johnson, who after he and his mother were diagnosed with Li-Fraumeni Syndrome, is now conducting research at the CU Cancer Center to help those with the disease ⬇️
https://t.co/U4TcdqtVHc
As today is #LFSAwarenessDay it's a pleasure to announce the first LiNCR/Oxford University conference. This is a science and health professionals conference bringing together the top experts on LFS across the UK.
https://t.co/rnQCRXPr2N
The #LiFraumeni #LFS Spectrum: Different Presentations of #TP53 Variants and Mosaics, a webinar for #LFSawarenessDay by #genetic counselors Jaclyn Schienda and Carly Grant. We are so grateful for this presentation for the Living LFS community! Watch: https://t.co/91Aji5Q6dv
We pledged $10k - we awarded $38k in #LFS Hardship Grants today, #LFSawarenessDay! With a #genetic #cancer syndrome like #LiFraumeni, a support community like Living LFS makes a huge difference. Thank you, from the bottom of our hearts, to ALL the donors that made this possible.
.@GP_TP53_Trust @LivingLFS #lifraumeni #cancer #lfsawareness #genetics #p53 #lfsawarenessday ❤️🐘#KaceySeddon
A member of Kacey’s family has set up a JustGiving page to help towards her funeral and memorial so that it’s a special day. We appreciate it’s a cost of living crisis so only donate if you can #donate on @justgiving Please also share and RT https://t.co/XCCil1Ud2p Thank you 🖤🤍
Happy #LiFraumeniSyndrome Awareness Day! Join us at 4pm PT/7pm ET for an educational presentation on the #LFS Spectrum: Different Presentations of #TP53 Variants and Mosaics. Register: https://t.co/4zQUd8S8oa
#lifraumeni #cancer #lfsawareness #genetics #p53 #lfsawarenessday
Happy #LiFraumeniSyndrome Awareness Day! Join us at 11am PT/2pm ET for our annual online gathering + LFS trivia! Register: https://t.co/xsydLINkzs
#lifraumeni #cancer #lifraumenisyndromeawareness #genetics #tp53 #lfsawarenessmonth #lifraumenisyndromeawarenessday #lfsawarenessday
And to celebrate #LFSAwarenessDay - here's our new directory of active projects for people with Li Fraumeni Syndrome:
https://t.co/VbG5q5pmoK
Today is #LFSAwarenessday - raising awareness of Li Fraumeni Syndrome - a rare cancer predisposition syndrome associated with a germline TP53 variant.
Find out more here:
https://t.co/YiwSa2GZzu
"The fundraising for #LivingLFS - #LiFraumeni Syndrome #LFS Hardship Grants for #LFSawarenessDay Monday March 20th is going AMAZING. I'm forecasting we're going to be able to fund ALL of the March applicants and maybe some for this coming October 🤩🤩🤩🤩🤩" -@missandilou
Join us & The George Pantziarka TP53 Trust for #LFSawarenessDay this coming Monday March 20! We have 2 online events that day - fun and educational ways to raise awareness and learn about Li-Fraumeni syndrome and genetic #cancer. More info + register at https://t.co/NtAVKWujpl
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
Order today (March 10) to get yours in time for #LFSawarenessDay March 20, and to fund hardship grants for families in need https://t.co/ryuVEjiBzc
Ten $1,000 LFS Hardship Grants, 31 grant applicants. Your purchase of #LFSAwarenessDay t-shirts can help us fund them all. https://t.co/PGRd58mlQA
Don't need a t-shirt? Buy and let us distribute them as free giveaways for the #LiFraumeni community in March! #LFSawarenessmonth
Ten $1,000 LFS Hardship Grants, 31 grant applicants. Your purchase of #LFSAwarenessDay t-shirts can help us fund them all. https://t.co/PGRd58mlQA
Don't need a t-shirt? Buy and let us distribute them as free giveaways for the #LiFraumeni community in March! #LFSawarenessmonth
March is Li-Fraumeni Syndrome Awareness Month! What's in store:
- Financial support for #Lifraumeni families in need
- Advocacy at #RareDisease Week on Capitol Hill with @EveryLifeOrg
- Education about #genetics and #cancer on #LFSAwarenessDay March 20
https://t.co/UiddTMqc5E
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
On #LFSAwarenessDay, we are excited to announce that George Pantziarka #TP53 Trust (@AnticancerOrgUK) and @The_MRC will support our research programme on somatic and #cancer evolution in #LiFraumeni Syndrome! Fantastic collab. with @R_Rahbari at @sangerinstitute. @emblebi
Today is #LFSAwarenessDay - and we have a very special announcement to make! Over £1 million of research funding from MRC to study Li Fraumeni Syndrome - details: https://t.co/jfrDpqbxvQ
Thank you @The_MRC, @sangerinstitute and @emblebi
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
Today is #LFSAwarenessDay - and we have a very special announcement to make! Over £1 million of research funding from MRC to study Li Fraumeni Syndrome - details: https://t.co/jfrDpqbxvQ
Thank you @The_MRC, @sangerinstitute and @emblebi
SUNDAY MARCH 20TH: LI-FRAUMENI SYNDROME AWARENESS DAY!! Zoom with us at 11 PDT, 2pm EDT for fun, LFS hardship grant updates, #LFSawarenessDay shirts, and to honor the birth anniversary of our founder Jennifer Mallory.
https://t.co/bMbK3FHxQv #lifraumeni #genetics #cancer #tp53
Every 100 #LFSawareness shirts we sell means another $1000 hardship grant we can award to a #LiFraumeni family in need on March 20th, #LFSAwarenessDay. Order yours now: https://t.co/xDwFR0B6XM
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