Top Tweets for #LivingLFS
Li-Fraumeni syndrome does not discriminate based on gender, race, age, or status. Neither do we. #pride #PrideMonth #lgbtqpride #lgbtqiaplus #lifraumeni #lifraumenisyndrome #LFSawareness #cancer #cancergenetics #LivingLFS #IAmLivingLFS #LFS
"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
A simple blood test has the power to save lives!
#lifraumeni #lifraumenisyndrome #livinglfs #lifraumenisyndromeawareness #p53 #tp53 #tp53gene #cancergenetics #geneticcancer #geneticmutation #rarediseases #cancerfighter #lifraumenisyndromeawarenessmonth #lfsawarenessmonth
March is Li-Fraumeni Syndrome #Awareness Month.
50% of patients with Li-Fraumeni will be diagnosed with cancer before age 50. @theearlydetective credits genetic testing with saving her life so she can now stay proactive for any potential future cancer diagnoses.
Genetic cancer SUCKS, but we still have fun!! We are celebrating March #LFSawarenessMonth and here's how you can get involved, from #LivingLFS board members Andi Last and Trishia Shelly-Stephens!
#LiFraumeni #LiFraumeniSyndrome #LFSawareness #cancer #genetics #TP53 #LFS
It's Day One of #LiFraumeniSyndromeAwareness Month, and Day Two at Rare Disease Week on Capitol Hill #RareDC2023! Lon and Nicole, thank you for representing #LivingLFS and the #LiFraumeni #genetic #cancer and #RareDisease communities! @EveryLifeOrg @RareAdvocates
@ambrosia_omG Cancer isn't a single disease. It's more than 100 diseases with various potential cures. Le sigh. So far to go...
#livinglfs
#LiFraumeni
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
May is #BrainTumorAwarenessMonth. People with #LiFraumeniSyndrome have an increased risk of developing #BrainCancer. Learn more: https://t.co/3mQz3604CD
#LFSawareness #LivingLFS #IAmLivingLFS #LiFraumeniSyndromeAwareness #LiFraumeni #LFSStrong #Glioblastoma #ChoroidPlexus
#LiFraumeniSyndrome in one handy image. Visit https://t.co/NtAVKWLmrl for more.
#LFSawareness #LivingLFS #IAmLivingLFS #LiFraumeniSyndromeAwareness #LiFraumeni #BreastCancer #LFSStrong #BrainCancer #sarcoma #P53 #TP53 #TP53gene #Cancer #CancerGenetics #GeneticCancer #genetics
Join us on clubhouse this Wednesday at noon ET as we continue to spread awareness for Li-Fraumeni syndrome!
#lifraumenisyndromeawarenessmonth #livinglfs #lifraumeni #lifraumenisyndrome #lfs
Join us tomorrow to chat about “🧬🐘 Why don’t elephants get cancer??” on @joinClubhouse at 12:00pm ET 👉🏻 https://t.co/itluWPx6vm @LivingLFS @hey_harps @AnjaliMalikMD @keishaydavis #CancerGeneticsClub #GCchat #LiFraumeniSyndrome #RareDisease #TP53 #Cancer #tuesdaymotivations
You made this happen. Thank you. LFS Awareness recap: https://t.co/jGex6PiDgS
#LFSawarenessMonth #LFSawareness #LFSawarenessDay #LiFraumeniSyndromeAwareness
#LiFraumeniSyndromeAwarenessMonth #LiFraumeni #LiFraumeniSyndrome #LivingLFS #IAmLivingLFS #P53 #TP53 #TP53gene #cancer
#LFSAwarenessDay is today, March 20!
I am #LivingLFS 💙
Wear blue today to support your friends and loved ones with LFS! 💙
@MDAndersonNews @lifraumeni
These beautiful ladies staying safe in their #LivingLFS face masks! Andrea (40), daughters Kierra (21) and Khloé (11) - 'We have #LFS💙🧬🐘🧬'
#LFSawarenessmonth #LFSawareness
#LFSawarenessDay #lifraumenisyndrome
#lifraumenisyndromeawarenessmonth #lifraumeni #IAmLivingLFS #TP53
Would you change anything for adult LFS patient screening? More or less screening?What are your thoughts? #lifraumeni #livingLFS #screening #oncology #lifraumenisyndrome #p53 #breastcancer #MRI #braincancer #sarcoma #melanoma #coloncancer #RareDisease #prophylacticmastectomy
Living LFS is thrilled to be offering a travel scholarship to this year’s rare disease week on Capitol Hill!
Link below to apply:
https://t.co/35Yj4zfkRG
#livinglfs #lifraumenisyndrome #lifraumeni #p53 #geneticcancer #geneticmutation #RareDisease #rarediseaseweekoncapitolhill
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