thelamfoundation.org The LAM Foundation | A Breath of Hope

thelamfoundation.org
Title: The LAM Foundation | A Breath of Hope
Keywords: ,DotNetNuke,DNN
Description: The LAM Foundation urgently seeks safe and effective treatments, and ultimately a cure, for lymphangioleiomyomatosis (LAM) through advocacy and the funding of promising research.
thelamfoundation.org is ranked 1423923 in the world (amongst the 40 million domains). A low-numbered rank means that this website gets lots of visitors. This site is relatively popular among users in the united states. It gets 50% of its traffic from the united states .This site is estimated to be worth $6,589. This site has a low Pagerank(0/10). It has 1 backlinks. thelamfoundation.org has 43% seo score.

thelamfoundation.org Information

Website / Domain: thelamfoundation.org
Website IP Address: 198.55.245.101
Domain DNS Server: ns40.domaincontrol.com,ns39.domaincontrol.com

thelamfoundation.org Rank

Alexa Rank: 1423923
Google Page Rank: 0/10 (Google Pagerank Has Been Closed)

thelamfoundation.org Traffic & Earnings

Purchase/Sale Value: $6,589
Daily Revenue: $18
Monthly Revenue $541
Yearly Revenue: $6,589
Daily Unique Visitors 1,661
Monthly Unique Visitors: 49,830
Yearly Unique Visitors: 606,265

thelamfoundation.org WebSite Httpheader

StatusCode 200
Cache-Control private
Content-Type text/html; charset=utf-8
Server Microsoft-IIS/8.5
Date Wed, 27 Jul 2016 21:54:12 GMT

thelamfoundation.org Keywords accounting

Keyword Count Percentage
DotNetNuke 0 0.00%
DNN 0 0.00%

thelamfoundation.org Traffic Sources Chart

thelamfoundation.org Similar Website

Domain Site Title

thelamfoundation.org Alexa Rank History Chart

thelamfoundation.org aleax

thelamfoundation.org Html To Plain Text

The LAM Foundation | A Breath of Hope Search Register Login Donate About Us | Donate Newly Diagnosed Learning About LAM About LAM Diagnosing LAM Symptoms of LAM Living With LAM Living with LAM Patient Resources New Patient Checklist More Resources LAMposium Join Us Voices of LAM US LAM Clinics International LAM Clinics LAM Liaison Patient Network LAM Patients, Family & Friends Support LAM Liaison Patient Network Patient Resources Friend and Family Assistance Worldwide LAM Patient Coalition (WLPC) In Memory Education Educational Webinars LAMposium Upcoming Educational Events Resources US LAM Clinics International LAM Clinics LAM Handbook Supplemental Oxygen Guide LAM as Cancer Tissue Donation Current Trials and Studies LAM Articles Publications Currents Journeys News Healthcare Providers Diagnosis & Treatment What is LAM? Diagnosing LAM Clinical Representation and Course of LAM Patient Care LAM Management ER Medicine Quick Facts US LAM Clinics ERS Standards International LAM Clinics Education Educational Materials for Patients Educational Events LAM Scientific Slides Current LAM Scientific Articles News Publication Archives Research Current Trials & Studies Tissue Donation Scientific Meetings & Conferences Scientific Advisory Board Investigators Grants LAM Grant Programs Overview Grant Opportunities Research Portfolio Scientific Plan Other Programs LAM Biomarker Innovation Summit Grants UPENN Orphan Disease Program Grants Current Trials & Studies Resources Scientific Advisory Board Current LAM Scientific Articles Publication Archives Scientific Meetings & Conferences Take Action Help Raise Funds Donate Now Fundraising Ideas Other Ways to Give Get Involved Participate in Research LAM Liaison Patient Network Contribute Your Experience Calendar of Events Speak Up LAM Merchandise Other Advocacy News For the Media The LAM Foundation About Us About Us Our History Board & Staff Partnerships Financial Statements Publications Privacy Policy Events Conference Overview Information Patients Family Friends Professionals Travel Grants Sponsors Partners Registration FAQ Menu Newly Diagnosed Learning About LAM About LAM Diagnosing LAM Symptoms of LAM Living With LAM Living with LAM Patient Resources New Patient Checklist More Resources LAMposium Join Us Voices of LAM US LAM Clinics International LAM Clinics LAM Liaison Patient Network LAM Patients, Family & Friends Support LAM Liaison Patient Network Patient Resources Friend and Family Assistance Worldwide LAM Patient Coalition (WLPC) In Memory Education Educational Webinars LAMposium Upcoming Educational Events Resources US LAM Clinics International LAM Clinics LAM Handbook Supplemental Oxygen Guide LAM as Cancer Tissue Donation Current Trials and Studies LAM Articles Publications Currents Journeys News Healthcare Providers Diagnosis & Treatment What is LAM? Diagnosing LAM Clinical Representation and Course of LAM Patient Care LAM Management ER Medicine Quick Facts US LAM Clinics ERS Standards International LAM Clinics Education Educational Materials for Patients Educational Events LAM Scientific Slides Current LAM Scientific Articles News Publication Archives Research Current Trials & Studies Tissue Donation Scientific Meetings & Conferences Scientific Advisory Board Investigators Grants LAM Grant Programs Overview Grant Opportunities Research Portfolio Scientific Plan Other Programs LAM Biomarker Innovation Summit Grants UPENN Orphan Disease Program Grants Current Trials & Studies Resources Scientific Advisory Board Current LAM Scientific Articles Publication Archives Scientific Meetings & Conferences Take Action Help Raise Funds Donate Now Fundraising Ideas Other Ways to Give Get Involved Participate in Research LAM Liaison Patient Network Contribute Your Experience Calendar of Events Speak Up LAM Merchandise Other Advocacy News For the Media The LAM Foundation About Us About Us Our History Board & Staff Partnerships Financial Statements Publications Privacy Policy Events Conference Overview Information Patients Family Friends Professionals Travel Grants Sponsors Partners Registration FAQ Search DonateTo Help Find a Cure LearnWhat is LAM? EngageRegister to Join the LAM Community About The LAM Foundation The LAM Foundation urgently seeks safe and effective treatments, and ultimately a cure, for lymphangioleiomyomatosis (LAM) through advocacy and the funding of promising research. We are dedicated to serving the scientific, medical and patient communities by offering information, resources and a worldwide network of hope and support. Watch The Video LAMposium 2016 Save the Date for LAMposium 2016 – September 22 – 25, 2016 in Cincinnati, OH. LAMposium 2016 RLDC · 2016 Save the Date for the Rare Lung Disease Conference 2016 – September 22 – 25, 2016 in Cincinnati, OH. RLDC · 2016 · Cincinnati US LAM Clinics Find a LAM expert at one of our 31 LAM clinics located across the United States. US LAM Clinics International LAM Clinics LAM clinics are located around the world to support as many women with LAM as possible. International LAM Clinics LAM Research Check out The LAM Foundation’s research portfolio to learn about the exciting work our scientists have done. LAM Research Fundraising Ideas Need an idea for a fundraiser for The LAM Foundation? See what others in the LAM community have done and learn how you can do it, too! Fundraising Ideas Events Calendar Find out what’s happening in the LAM community. Events Calendar Participate in Research Find out more about current trials and studies and how you can partipate. Participate in Research Donate Now Help us find a cure for LAM and provide critical support and HOPE for all women with LAM. Donate Now LAM Liaison Patient Network Find out more about The LAM Liaison Patient Network and how we support all women with LAM. LAM Liaison Patient Network Tissue Donation You can help LAM Foundation scientists become more knowledgeable about LAM by donating your tissue for LAM-related studies. Tissue Donation What is LAM? Learn about this rare lung disease. What is LAM? Latest News Add Your Personal Touch to this Year’s LAM Quilts Read More Read More ATTENTION LAM ADVOCATES: We need your help! Read More Read More The LAM Foundation Attends the American Thoracic Society Conference Read More Read More Highlights from the Million Dollar Bike Ride Read More Read More Register Now Register with The LAM Foundation today to stay up to date on everything that is happening in the LAM community, including the latest in scientific research and finding out how to participate in community and educational events. Connect The LAM Foundation 4520 Cooper Road Suite 300 Cincinnati, OH 45242 Contact Phone: (513) 777-6889 Toll-Free: (877) CURE-LAM (877) 287-3526 Email: info@thelamfoundation.org Quick Links LAMposium Donate Now News Events Calendar Publications ? 2016 LAM Foundation | Disclaimer| Privacy| The LAM Foundation is a nonprofit, tax-exempt charitable organization under Section 501(c)(3) of the Internal Revenue Code.

thelamfoundation.org Whois

Domain Name: THELAMFOUNDATION.ORG