Living LFS

Supporting patients with Li-Fraumeni syndrome, an inherited #cancer predisposition.

#LFS #LiFraumeni #LiFraumeniSyndrome #TP53 #P53 #GeneticCancer #genetics

[Living LFS @LivingLFS]

March is Li-Fraumeni Syndrome Awareness Month! Visit https://t.co/NtAVKWujpl to learn about our rare #genetic mutation and to help those who are extra likely to develop a wide range of cancers because of it. Thank you for sharing, and thank you for supporting! #Cancer #lifraumeni

[CGA-IGC @CGAIGC]

1/ Welcome to the February 2024 #CGAJS Tweetorial on the Cancer Risks Associated w/ Li-Fraumeni Syndrome by CGA-IGC communications committee member @asafmaoz

➡️The full article from @JCOPO_ASCO can be found at 👉🔗https://t.co/8frvVSyEw3
🧵
@QIMRB_Institute
#HereditaryGICancer

[Patrick R. Benusiglio @PBenusiglio]

#LiFraumeni. Cumulative cancer risks in #TP53 PV carriers, based on 146 families. For example:
-#Breastcancer, females: 7% -> age 30 yrs, 71% lifetime
-Any cancer, females: 98% lifetime
- 🫁#Lungcancer, males: 9% -> age 60
- 🧠#Glioma, males: 15% lifetime
https://t.co/z45l0dDnXG

[Living LFS @LivingLFS]

LFS Awareness Day - March 20, 2024 - is fast approaching. It's time to order your gear in time to spread awareness and raise much needed funds for our Hardship Grant Program. A minimum of $10 from every item sold goes towards helping families with LFS. https://t.co/wxV0CNRkvO

[Living LFS @LivingLFS]

There is still time to donate $100 or more to receive a free t-shirt, mug, or tote as thanks for your support of families devastated by cancer. Sharing and spreading the word is equally important and equally appreciated. 💙💚💙
https://t.co/HnkmCQuEHP
#GivingTuesday

[Living LFS @LivingLFS]

As of this writing,
Living LFS has received $8 more in #GivingTuesday donations today than on Giving Tuesday 2022. I call that a success! We would be grateful an even bigger difference.

[Living LFS @LivingLFS]

Donate $100 or more to Living LFS today and get free swag! It's our thanks to you on this #GivingTuesday for supporting those with #LiFraumeni syndrome and inherited #cancer. Donate: https://t.co/5nSTxxEFkb

[Living LFS @LivingLFS]

Thank you from the entire #LiFraumeni syndrome community for donating to Living LFS and supporting those with #geneticcancer this #GivingTuesday!

Donate: https://t.co/5nSTxxFd9J

@SnarkyCancer's Living LFS’s collection: https://t.co/lmfYKEXdt9

#Cancer #nonprofit

[Living LFS @LivingLFS]

Donate $100+ to Living LFS today, choose one piece of merchandise from @SnarkyCancer's Living LFS collection FREE. It's our way of saying "Thank You" on #GivingTuesday. Donate: https://t.co/5nSTxxFd9J

See the full collection: https://t.co/lmfYKEXdt9

#lifraumeni #cancer #p53

[Living LFS @LivingLFS]

Help us continue supporting those with #LFS. Every donation, large or small, makes a difference. Sharing this message helps as well! We are grateful for your support. Donate here: https://t.co/5nSTxxFd9J
#GivingTuesday
#cancer #lifraumeni

[Living LFS @LivingLFS]

Happy Thanksgiving from all of us at Living LFS! We are thankful for YOU! #lifraumeni #lifraumenisyndrome #cancer #genetics

[Living LFS @LivingLFS]

WOO HOO! Today we're awarding nine $1,000 LFS Hardship Grants to people with #LiFraumeni syndrome and #cancer, with the help of our partners at @snarkycancer!

You can help fund future grants!
Donate: https://t.co/owKcgR6pOB
Merch: https://t.co/A57Tuycgvy

[Living LFS @LivingLFS]

Email us for the registration link to the next one, Thursday Sep 14, 2023, 5pm Pacific, 8pm Eastern https://t.co/gFnq3qPtUg

[Living LFS @LivingLFS]

@GP_TP53_Trust Thank you for this!

[Living LFS @LivingLFS]

Calling all researchers and clinicians working on #lifraumenisyndrome #lifraumeni #tp53 #tp53gene #p53 #geneticcancer #inheritedcancer #hereditarycancer #CancerResearch #cancer #genechat

[The George Pantziarka TP53 Trust @GP_TP53_Trust]

Scientific networks are key to making progress - especially in medicine. So we're very happy that we are working to create LiNCR - LI Fraumeni Network for Clinicians and Researchers

https://t.co/ppQMEOOhOj

[The George Pantziarka TP53 Trust @GP_TP53_Trust]

Scientific networks are key to making progress - especially in medicine. So we're very happy that we are working to create LiNCR - LI Fraumeni Network for Clinicians and Researchers

https://t.co/ppQMEOOhOj

[Valli Subasri @vallisubasri]

My amazing lab mates presenting their work on #lifraumenisyndrome today at GFCC Cancer Research Day 🤩✨ @SickKidsCancer @cgiovino

[Inherited Cancer Registry (ICARE) @inheritedcancer]

Check out yesterday's #ICARE #Genetics Case Conference, during which Bita Nehoray, MS, CGC (@BeetsWhoTweets) from the City of Hope presents on #CHIP and variant interpretation in #LiFraumeni #Syndrome 👇
https://t.co/T5oBjn89Ud

#InheritedCancer #TP53 #CancerPrevention