lfsassociation.orgLi-Fraumeni Syndrome Association | Providing Information, Advocacy, and Support for Families with L...

lfsassociation.org Profile


Title:Li-Fraumeni Syndrome Association | Providing Information, Advocacy, and Support for Families with L...

Description:LFS Association provides a wide range of information, advocacy, and support services for individuals and families with Li-Fraumeni Syndrome.

Keywords:Li-Fraumeni,Li Fraumeni,Li-Fraumeni Syndrome,Li Fraumeni Syndrome,LFS,LFSA,Li-Fraumeni Syndrome Association,Li Fraumeni Syndrome Association,familial cancer syndrome,gene mutations,tumor suppressor,p...

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lfsassociation.org Information

Website / Domain: lfsassociation.org
Website IP Address:
Domain DNS Server: dns2.stabletransit.com,dns1.stabletransit.com

lfsassociation.org Rank

Alexa Rank: 2344487
existsite Rank: 3
Google Page Rank: 0/10 (Google Pagerank Has Been Closed)

lfsassociation.org Traffic & Earnings

Purchase/Sale Value: $6,169
Daily Revenue: $16
Monthly Revenue: $507
Yearly Revenue: $6,169
Daily Unique Visitors: 1,555
Monthly Unique Visitors: 46,650
Yearly Unique Visitors: 567,575

lfsassociation.org Keywords accounting

Keyword Count Percentage
Li-Fraumeni 8 2.47%
Li Fraumeni 0 0.00%
Li-Fraumeni Syndrome 8 4.58%
Li Fraumeni Syndrome 0 0.00%
LFS 36 3.04%
LFSA 6 0.66%
Li-Fraumeni Syndrome Association 3 2.70%
Li Fraumeni Syndrome Association 0 0.00%
familial cancer syndrome 0 0.00%
gene mutations 0 0.00%
tumor suppressor 0 0.00%
p... 0 0.00%

lfsassociation.org WebSite Httpheader

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Cache-Control no-store, no-cache, must-revalidate, post-check=0, pre-check=0
Content-Type text/html; charset=UTF-8
Server Sucuri/Cloudproxy
Date Sun, 25 Feb 2018 03:11:18 GMT

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lfsassociation.org Html To Plain Text

Li-Fraumeni Syndrome Association | Providing Information, Advocacy, and Support for Families with Li-Fraumeni Syndrome | #LFSstrong ?Select Language:TranslationEnglishAfrikaansShqip??????????????az?rbaycan diliEuskaraБеларуская?????bosanski jezikБългарскиCatalàBinisaya中文(简体)中文(漢字)Hrvatski?e?tinaDanskNederlandsEsperantoEesti keelSuomiFran?aisGalego???????DeutschΕλληνικ????????Kreyòl ayisyenHarshen HausaHmoobHmoob Daw???????????; ?????MagyaríslenskaAs?s? IgboBahasa IndonesiaGaeilgeItaliano日本語basa Jawa????????????????????????LatīnaLatvie?u valodaLietuvi? kalbaмакедонски ?азикBahasa MelayuMaltiTe Reo Māori?????Монгол??????Norsk?????PolskiPortuguês??????Roman?РусскийCрпски ?езикSloven?inaSloven??inaAf-SoomaaliEspa?olKiswahiliSvenskaTagalog??????????????????Türk?eУкра?нська????Ti?ng Vi?tCymraeg??????èdè YorùbáisiZulu Donate Home What is LFS? What is LFS? What causes LFS? Who has LFS? Who should be tested for LFS? Is there screening or prevention for LFS cancers? Is there treatment for LFS? What are the reproductive issues? Founding Founding Fathers Dr. Frederick Pei Li Obituary Mission Statement Vision Statement LFSA Board Medical Advisory Board 2016 Impact Report Salute! Gala Medical Resources Resources Research News Treatment Facilities (search) Reference Clinical Trials, Patient Studies, and Surveillance Programs Patient Support Patient Support Information LFS Events and Activities TitanTough21 Foundation Launch Event Cancers Genetic Testing Screening Immunology, Oncolysis, and Targeting Genes Nutrition Exercise Lifestyles, Research, and Survivors Financial Concerns Online Publications Webinars Nutrition and Cancer with Dr. Walter Willett 2nd Annual “Living with LFS” Webinar Conference Living with LFS Webinar LFS Talk with Dr. Judy E. Garber LFS and Chemo Prevention LFS – Recent Findings and Future Directions Conferences 1st Annual Li-Fraumeni Syndrome Conference 2nd Annual “Living with LFS” Webinar Conference The 2016 International LFS Conference & The 3rd Annual LiFE Consortium and LFS Association Conference Forum Contact Check back soon for highlights from The 2016 International LFS Conference & The 3rd Annual LiFE Consortium and LFS Association Conference!!!!!! Click here to view the LFSA 2016 Impact Report! What is LFS? Li-Fraumeni Syndrome is a rare inherited disorder that greatly increases one’s risk of developing cancer during their lifetime... What is LFS? LFS Association We are families, like you who have been devastated by the effects of Li-Fraumeni Syndrome, a hereditary cancer predisposition syndrome. Our hopes are to educate, raise awareness and find better screening programs and treatments for LFS. Read more... Medical Resources We've compiled a list of doctors available to answer your questions, LFS support and treatment. They specialize in many different areas, which have been listed with their information. Read more... LFS News Personal Appeal for Notes of Appreciation for LFS Founding Fathers. Click to View PDF... Community Events 2017 Annual Mo Songs for Kerry Come out and help support the Li-Fraumeni Syndrome community at this all day event. Read more... LFS Webinars Check out our library to watch past LFS webinars, and to find out about upcoming webinars! Learn more... LFS Awareness Brochure Myriad Genetics is proud to partner with LFSA to launch the global LFS Education and Awareness Campaign! Read more... ? 2017 Li-Fraumeni Syndrome Association | P.O. Box 6458 | Holliston, MA 01746 USA | 855-239-LFSA (5372) | info@lfsassociation.org | Terms of Use Li-Fraumeni Syndrome Association (LFSA) is a 501(c)(3) charitable organization. Website Donated by: Sabre Digital Creative

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