
Living LFS
Supporting patients with Li-Fraumeni syndrome, an inherited #cancer predisposition. #LFS #LiFraumeni #LiFraumeniSyndrome #TP53 #P53 #GeneticCancer #genetics Encouraging, empowering, & educating those living with Li-Fraumeni Syndrome (LFS) and genetic cancer. At Living LFS, we encourage, empower, and educate those living with Li-Fraumeni syndrome by connecting them with care, resources, and others who are Living LFS.

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Home | Living LFS: Li-Fraumeni Syndrome What is LiFraumeni Syndrome LFS. Our Work Events MRI PETCT Scan Toronto Protocol Shop LFS AwarenessMonth Day In Memoriam What is LiFraumeni Syndrome LFS. Our Work Events PETCT Scan MRI Toronto Protocol Shop LFS AwarenessMonth Day In Memoriam What is LiFraumeni Syndrome LFS. Our Work Events PETCT Scan MRI Toronto Protocol Shop LFS AwarenessMonth Day In Memoriam LiFraumeni Syndrome LFS LiFraumeni Syndrome LFS is linked to a mutation in the TP53 tumor suppressor gene.
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Specifically Named Diseases Category
Organisations with similar rank to Living LFS in category Specifically Named Diseases

127. The Corneal Dystrophy Foundation
http://www.

128. SCLERODERMA FOUNDATION TRI-STATE INC CHAPTER
National Scleroderma Foundation Tri-State Chapter.

Encouraging, empowering, & educating those living with Li-Fraumeni Syndrome (LFS) and genetic cancer.

Outpatient Treatment Center for Substance Use Disorders.
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Organisations from Living LFS

Encouraging, empowering, & educating those living with Li-Fraumeni Syndrome (LFS) and genetic cancer.

2. North American Craft-Maltsters Guild Inc
The Craft Maltsters Guild was founded to educate about the tradition of craft malting, provide educat.

3. Soroptimist International of Cumberland County NJ, Inc.
Business Meeting: 2nd Wednesday @ 7:00 pm.
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Similar organisations to Living LFS based on mission, location, activites.

Tourette Association of America Inc
Established over 50 years ago, the TAA is the only national organization that serves the Tourette Syndrome & Tic Disorder community through awareness, research, and support.

The LSA is an international organization dedicated to helping children with Lowe syndrome and their.

Raising awareness and funding for Wolfram Syndrome research, an ultra rare disease.
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Organisations in the world similar to Living LFS.

VHL,HLRCC and BHD are genetic forms of cancer.

Information, updates and advice about Kleefstra Syndrome, hosted by Kleefstra Syndrome UK.

Cancer52 - the common voice for rare & less common cancers.

THE GEORGE PANTZIARKA TP53 TRUST (uk)
We are the George Pantziarka TP53 Trust - the UK advocacy group for Li Fraumeni Syndrome.
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Raising awareness and funding for Wolfram Syndrome research, an ultra rare disease.

Encouraging, empowering, & educating those living with Li-Fraumeni Syndrome (LFS) and genetic cancer.
Similar social media (3564)
Organisations with similar social media impact to Living LFS

96334. South Shore Peer Recovery Inc
South Shore Peer Recovery is creating a safe space in the heart of the community.

96335. Safe Haven Medical Outreach Program Inc
Safe Haven Medical Outreach supports children with disabilities & complex medical needs in Cambodia.

Encouraging, empowering, & educating those living with Li-Fraumeni Syndrome (LFS) and genetic cancer.

96337. Tax Education Support Organization
We seek a better future for Iowans through research and policy solutions.

The Pear Fair is a celebration of the annual Bartlett Pear Harvest in the Sacramento River Delta region of California - βAlways the Last Sunday in Julyβ.
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Exciting breakthrough from Chiba University! π A novel molecule has been identified as a key player in kidney injury and repair, offering hope for those battling chronic kidney disease. Together, we can support advancements in health that make a real difference! π #KidneyHealth #PositiveNews
Novel molecule found to be a key player in kidney injury and repair
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