Home - Rare Disease Foundation

Skip to main content. Guest Sign In. Family and Patient Support. The Health Ministers of Québec, Ontario, Alberta and BC Put Kids Before Bureaucracy - Turn Heartbreak to Hope. Medical research is offering new hope to more than half a million kids who suffer from rare genetic diseases. Our provincial governments need to step up to the plate and make. Rare Disease Foundation - Genetic Testing Petition. From Rare Disease Foundation. Dear Caring Canadians,. The Face of Rare Diseases. July 21, 2015. Washin.

OVERVIEW

The web site rarediseasefoundation.org currently has a traffic ranking of zero (the smaller the better). We have examined zero pages inside the site rarediseasefoundation.org and found seventy-one websites referring to rarediseasefoundation.org. We were able to discover one contacts and addresses for rarediseasefoundation.org to help you correspond with them. We were able to discover three social networking accounts acquired by this website. The web site rarediseasefoundation.org has been on the internet for eight hundred and forty-six weeks, twenty-one days, sixteen hours, and sixteen minutes.
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71
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3
Online Since
Sep 2008

RAREDISEASEFOUNDATION.ORG TRAFFIC

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RAREDISEASEFOUNDATION.ORG HISTORY

The web site rarediseasefoundation.org was registered on September 24, 2008. It is currently eight hundred and forty-six weeks, twenty-one days, sixteen hours, and sixteen minutes old.
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September
2008

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16
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WHAT DOES RAREDISEASEFOUNDATION.ORG LOOK LIKE?

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CONTACTS

Millan Patel

C234, 4500 Oak St

Vancouver, British Columbia, V6H 3N1

CA

RAREDISEASEFOUNDATION.ORG SERVER

Our parsers discovered that the main page on rarediseasefoundation.org took five hundred and sixteen milliseconds to stream. I could not find a SSL certificate, so in conclusion we consider this site not secure.
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72.35.20.201

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ns1.cfri.ca
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We revealed that this website is weilding the Microsoft-IIS/8.5 server.

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Home - Rare Disease Foundation

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Skip to main content. Guest Sign In. Family and Patient Support. The Health Ministers of Québec, Ontario, Alberta and BC Put Kids Before Bureaucracy - Turn Heartbreak to Hope. Medical research is offering new hope to more than half a million kids who suffer from rare genetic diseases. Our provincial governments need to step up to the plate and make. Rare Disease Foundation - Genetic Testing Petition. From Rare Disease Foundation. Dear Caring Canadians,. The Face of Rare Diseases. July 21, 2015. Washin.

PARSED CONTENT

The web site rarediseasefoundation.org states the following, "The Health Ministers of Québec, Ontario, Alberta and BC Put Kids Before Bureaucracy - Turn Heartbreak to Hope." We noticed that the website said " Medical research is offering new hope to more than half a million kids who suffer from rare genetic diseases." It also said " Our provincial governments need to step up to the plate and make. Rare Disease Foundation - Genetic Testing Petition. The Face of Rare Diseases."

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