Events Archive - Li-Fraumeni Syndrome Association
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November 2020
The 3rd Annual LFSA Fall Gymnastics Invitational
The 3rd Annual LFSA Fall Gymnastics Invitational will be a fun-filled gymnastic competition and fundraiser to benefit our youth with Li-Fraumeni syndrome; a hereditary cancer predisposition syndrome. L1-L10 & Xcel Competitions Team Competition Special Drawing! November 14th & 15th, 2020 All American Gymnastic & Dance Academy 65 Post Office Park Wilbraham, MA 01095 (413) 596-0089 We are COVID-19 ready! All necessary steps will be taken to protect the health and safety of athletes, staff and spectators in accordance with…
Find out more »December 2020
Giving Tuesday 2020
There Are Many Ways You Can Support the LFSA this Holiday Season! The LFSA relies on your generosity and kindness to support our mission of a brighter future for those affected by LFS, and every little bit helps. You can do your part by making a donation, becoming a fundraiser, or designating LFS Association your charity through AmazonSmile. Your philanthropy is an investment in LFS research, educational and patient support programs. Make a Gift Give a gift, get a gift by making a…
Find out more »LFSA Annual Appeal
There Are Many Ways You Can Support the LFSA this Holiday Season! The LFSA relies on your generosity and kindness to support our mission of a brighter future for those affected by LFS, and every little bit helps. You can do your part by making a donation, becoming a fundraiser, or designating LFS Association your charity through AmazonSmile. Your philanthropy is an investment in LFS research, educational and patient support programs. Make a Gift Give a gift by making a donation to the…
Find out more »May 2021
May 3rd is LFS Awareness Day
Announcing International LFS Awareness Day! May 3 – 5/3 for p53 Join us in raising LFS awareness through the month of May! Click Here to Learn More!
Find out more »International Chapter Week
As part of International LFS Awareness Month, we are recognizing our LFSA International Chapters and the global LFS Community. Click Here to Learn More About International LFS Awareness Month!
Find out more »LFS Youth & Young Adult Week
During International LFS Awareness Month, are sharing new and exciting information about the LFSA Youth & Young Adult Program. Download the new LFS Youth & Young Adult Brochure to learn about the importance of empowering adolescents and young adults to drive key aspects of their healthcare and decision making. Click Here to Learn More About International LFS Awareness Month!
Find out more »LFS Research Week
Understand the importance of research. We'll announce LFSA's latest grant recipient and share information about the LFSA Grant Program. Click Here to Learn More About International LFS Awareness Month!
Find out more »June 2021
Youth Connect
Join us June 19th at 3pm EDT Youth Connect is a quarterly virtual event for teen and young adult participants ages 13 to 21 to be able to learn from and engage with an expert in the LFS field and make new friends with other LFS youth. For this first Youth Connect meeting, we will hear from Rowan Forbes-Shepherd, a postdoctoral researcher at the Peter MacCallum Cancer Centre in Victoria, Australia. Rowan will be speaking on his research and a…
Find out more »October 2021
Noelle’s Fight Club 2021
Noelle’s LFS Fight Club is taking a hike for its sixth annual fundraiser to benefit the Li-Fraumeni Syndrome Association. Noelle Johnson and her team are climbing to the top of Horsetooth Mountain, the most iconic rock in Fort Collins, CO. The six-mile hike features a 1,600-ft. elevation gain and a challenging scramble to the summit. We’re hiking for the Johnson family and others like them with Li-Fraumeni syndrome (LFS), a rare inherited genetic cancer disorder that greatly increases the risk…
Find out more »October 2022
6th International LFSA Symposium – REACH 22
The LFSA is looking forward to the gathering of providers, scientists, specialists, students, and families from around the world who are interested in and affected by LFS. REACH22, our 6th International Li-Fraumeni Syndrome Association Symposium, has been thoughtfully reformatted in response to the unprecedented challenge facing the LFS community and the world. REACH will be a hybrid live and virtual experience enabling scientists, doctors, geneticists and LFS families to make meaningful connections. We will welcome attendees joining in-person the afternoon…
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