LFS Association

@LFSAssociation

We are families, like you, who have been devastated by the effects of Li-Fraumeni syndrome, a hereditary cancer predisposition syndrome.

Holliston, MA 01746 lfsassociation.org Joined May 2013

436 Following 699 Followers 2.1K Posts

Latest posts 5

LFS Association @LFSAssociation Oct 29

TODAY! 3 PM EST, sign up at bit.ly/4eZrp1f

us02web.zoom.us Welcome! You are invited to join a webinar: Designing Family RISE – Special seminar for LFS youth... Risk Information and Screening Education for Children with Cancer Risk and their Families Join us for the special seminar to design an intervention for children with cancer risk and their families....

LFS Association @LFSAssociation Oct 27

Families managing Li-Fraumeni syndrome, please join us for two webinars this week to provide input, help shape new educational programs and connect with valuable expertise.

Researchers at @DanaFarber and @BostonChildrens want to hear about your experiences to develop resources that better meet the needs of children with cancer risk and their families.

Please visit lfsassociation.org to sign up separately:
October 29 at 3:00 PM EST - designed for LFS youth aged 12+
October 30 at 10:00 AM EST - intended for parents in LFS families

This is an opportunity to hear from and connect directly with two incredible leaders working on behalf of the LFS community, our sincere thanks to Jennifer Mack, MD, MPH, and Junne Kamihara, MD, PhD.

#lifraumeni #lifraumenisyndrome

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LFS Association @LFSAssociation Oct 27

Families managing Li-Fraumeni syndrome, please join us for two webinars this week to provide input, help shape new educational programs and connect with valuable expertise.

Researchers at @DanaFarber and @BostonChildrens want to hear about your experiences to develop resources that better meet the needs of children with cancer risk and their families.

Please visit lfsassociation.org to sign up separately:
October 29 at 3:00 PM EST - designed for LFS youth aged 12+
October 30 at 10:00 AM EST - intended for parents in LFS families

This is an opportunity to hear from and connect directly with two incredible leaders working on behalf of the LFS community, our sincere thanks to Jennifer Mack, MD, MPH, and Junne Kamihara, MD, PhD.

#lifraumeni #lifraumenisyndrome

LFS Association @LFSAssociation Oct 7

We are proud to be a Supporting Sponsor of the 3rd Annual Oncology Venture, Innovation & Partnering Summit, taking place Oct. 19-20 in Cambridge, MA.

Join oncology entrepreneurs, investors, biopharma leaders and other industry experts for two days of discussion on funding, emerging therapeutics, partnering and commercialization.

Explore the agenda and register at bit.ly/4dopNNX

Members of the LFSA community, save 25% with code LFSA25 (valid for new registrations only). We hope to see you there!

#OncologyVIP #Oncology #CancerResearch

LFS Association @LFSAssociation Oct 3

REACH26 day two is starting off with updates from our international community. Virtual access is still open to follow live, sessions are being updated to the app within 24-48 hours: bit.ly/4vL6sNd

LFS Association @LFSAssociation Oct 3

Yesterday at @UTMDAnderson we closed out #REACH26 with poster sessions and a meaningful presentation of the LFSA Guardian Angel Award to the very deserving Arnie Levine. A true champion of LFSA and the Li-Fraumeni syndrome community, Arnie has contributed immeasurably through the years.