EveryLife Foundation for Rare Diseases

The EveryLife Foundation for Rare Diseases is dedicated to accelerating biotech innovation for rare disease treatments through science-driven public policy.

OVERVIEW

This domain everylifefoundation.org presently has an average traffic ranking of zero (the smaller the more users). We have audited nineteen pages within the web site everylifefoundation.org and found eighty-two websites associating themselves with everylifefoundation.org. There is one contacts and locations for everylifefoundation.org to help you communicate with them. There is two public communication sites possessed by this website. This domain everylifefoundation.org has been online for six hundred and ninety-eight weeks, nineteen days, three hours, and fifty-eight minutes.
Pages Analyzed
19
Links to this site
82
Contacts
1
Locations
1
Social Links
2
Online Since
Jul 2011

EVERYLIFEFOUNDATION.ORG RANKINGS

This domain everylifefoundation.org is seeing diverging quantities of traffic all through the year.
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EVERYLIFEFOUNDATION.ORG HISTORY

This domain everylifefoundation.org was first submitted to the registrar on July 13, 2011. As of today, it is six hundred and ninety-eight weeks, nineteen days, three hours, and fifty-eight minutes old.
REGISTERED
July
2011

MATURITY

13
YEARS
4
MONTHS
16
DAYS

LINKS TO WEB PAGE

essential behcets

Information that impacts your life. Wednesday, November 16, 2016. In the 2016 Rare Artist Contest. Sponsored by the EveryLife Foundation for Rare Diseases. Winning artwork will be displayed on Capitol Hill. Feb 27 through March 3. PLEASE VOTE BY CLICKING ON THE PICTURE BELOW; it will take you to the voting site. The Rare Artist Contest is ded.

CADASIL Together We Have Hope Non-Profit - Official Site

These are families who has shared their experiences with how they deal with CADASIL. Since CADASIL has so many different symptoms, it is impossible to find a caregivers group just for CADASIL.

CheckOrphan

Tamoxifen and raloxifene slow down the progression of muscular dystrophy. Expert Discusses Potential Combos With Ruxolitinib in Myelofibrosis. Huntsman Cancer Institute joins study aimed at improving leukemia screening, treatment. Community prays for star athlete. Naperville Mom, Former Librarian Fighting Leukemia. FDA Grants Rare Pediatric Disease Designation to ABO-202 for Infantile Batten Disease.

Home - Chelseas Hope Lafora Children Research Fund

Lafora body disease is a metabolic storage disease. The Lafora bodies are the purple blobs in the neurons. Recurrent, Increasingly Intractable Seizures. Sign Up For Our E-Mail Newsletter. A condition that affects fewer than 20.

EURORDIS - The Voice of Rare Disease Patients in Europe

What is a rare disease? Find information or help. What is an orphan drug? Improve the safety of your medicines. List of the latest marketing authorisations and orphan medicinal products designations. Living with a Rare Disease. Rare diseases in the arts.

Fibromuscular Dysplasia

An informal place to help support people afflicted with FMD. Sunday, October 8, 2017. Dr W Park, Chief of Vascular Surgery at Cleveland Clinic Abu Dhabi.

Insmed Powered by Purpose

Every pharmaceutical company has the ability to develop medicines, but not all have the entrepreneurial spirit for truly innovative treatments. 10 Finderne Ave, Building 10.

Home - Italian Street Painting Marin

Wonders of Space and Time. Wonders of Space and Time.

WHAT DOES EVERYLIFEFOUNDATION.ORG LOOK LIKE?

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CONTACTS

Domains By Proxy, LLC

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Scottsdale, Arizona, 85260

US

EVERYLIFEFOUNDATION.ORG HOST

We found that a single page on everylifefoundation.org took three thousand and fifty-two milliseconds to download. I found a SSL certificate, so therefore our crawlers consider this site secure.
Load time
3.052 seconds
SSL
SECURE
Internet Address
192.124.249.159

NAME SERVERS

ns1.secure.net
ns2.secure.net

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SERVER OPERATING SYSTEM

I observed that everylifefoundation.org is utilizing the Sucuri/Cloudproxy operating system.

TITLE

EveryLife Foundation for Rare Diseases

DESCRIPTION

The EveryLife Foundation for Rare Diseases is dedicated to accelerating biotech innovation for rare disease treatments through science-driven public policy.

CONTENT

This domain has the following on the homepage, "Dedicated to accelerating biotech innovation for rare disease treatments through science-driven public policy." Our analyzers observed that the web site also said " We are a science-based advocacy organization that works to bring lifesaving treatments to the 30 million Americans with rare diseases." The Website also stated " We focus on educating and activating the patient community to ensure they are heard by policy makers in government and by industry developing the treatments. Affecting 1 in 10 Americans. Have no FDA approved treatments. Sign Up for Our Newsletter."

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