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LFS Association

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So far LFS Association has created 20 blog entries.

Krystal

I was diagnosed with Li-Fraumeni syndrome in my late twenties and the diagnosis shocked me. First of all, I’d never heard of it and secondly, although I knew there had been a lot of family members affected by cancer I never thought I’d be one of them. I met with my genetics counselor before finding

By |2024-07-11T15:16:54-04:00April 27th, 2023|LFS Family Stories|Comments Off on Krystal

Debora

Debora Scardino Mancebo, 34 years old, from São Paulo, Brazil. She had breast cancer at 30 years old. Cancer has always been something I had to deal with in my family, because my dad, aunt and grandfather has passed away of cancer. So I already knew that, someday day, I could have it too. I

By |2024-07-11T15:16:54-04:00April 27th, 2023|LFS Family Stories|Comments Off on Debora

Olivia

Olívia Naves, 22 years old, she never had cancer, from São Paulo, Brazil Hello! My name is Olívia Naves and I’m 22 years old. Having Li-Fraumeni has changed completely the way I deal with my health. In the beginning it’s hard not to drown with the anxiety about the fact you’re more vulnerable to cancer.

By |2024-07-11T15:16:54-04:00April 27th, 2023|LFS Family Stories|Comments Off on Olivia

Ana

Ana Caroline, 37 years old, from Belo Horizonte, Brazil. Never had cancer. When I was diagnosed with Li-Fraumeni, I was impacted in many ways because I already had a feeling that I would have it since my family has many cases of cancer. I felt the fear of having cancer, apprehension with the test results

By |2024-07-11T15:16:55-04:00April 26th, 2023|LFS Family Stories|Comments Off on Ana

Lakita

Lakita was born healthy with no medical issues in 2006 and loved dancing and art. At the age of 10 In the year (2017) she was diagnosed with cancer of the bones (Osteosarcoma) related to LFS. She went through tough cancer treatment and surgery and after one year she was done with treatment. In January

By |2024-07-11T15:16:55-04:00April 26th, 2023|LFS Family Stories|Comments Off on Lakita

Hot off the press!!! Genotype–phenotype associations within the Li-Fraumeni spectrum: a report from the German Registry.

In 2017, not only did Dr. Christian Kratz launch our international chapter, LFSA – Germany, but he also founded the German Cancer Predisposition Syndrome Registry based at Hannover Medical School, Hannover, Germany. The registry collects information on genotypes, personal medical details, family histories, and surveillance, as well as a range of biospecimens.  In today’s

By |2024-07-11T15:16:55-04:00August 16th, 2022|LFS News|0 Comments

New publication! Cancer surveillance for patients with LFS in Brazil

Dr. Maria Isabel Achatz led a recent publication on the cost-effectiveness of Cancer surveillance for patients with LFS in Brazil using the Toronto Protocol screening guidelines. Brazil has a higher prevalence of LFS compared to other countries, due to a founder mutation in the TP53 gene.

By |2024-07-11T15:16:55-04:00May 11th, 2022|LFS News|0 Comments

NCI: Making Strides Toward Precision Medicine for Individuals with Li-Fraumeni Syndrome

Read about the advancements in LFS research that our team at the Division of Cancer Epidemiology and Genetics, Clinical Genetics Branch, have accomplished in their March 2022 news update.

By |2024-07-11T15:16:55-04:00March 8th, 2022|LFS News|0 Comments

Li-Fraumeni Syndrome Association Lauds Advancements in Classifying Hereditary Cancer Risks

HOLLISTON, MA -- The Li-Fraumeni Syndrome Association (LFSA), dedicated to furthering research and worldwide awareness of the inherited cancer predisposition disorder, celebrates new findings published in the renowned JAMA Oncology journal with implications to better predict cancer risk. First presented at LFSA's 5th International Symposium last year, the concept of analyzing tumor patterns and

By |2024-07-11T15:16:55-04:00October 28th, 2021|LFS News, Press Release|0 Comments
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