Team Sanfillipo Parents united to find a cure

Cure Sanfilippo, Gene therapy, Get help for Sanfilippo, MPS, MPS III, Rare diseases, lysosomal disease, and Fundraising

OVERVIEW

This website teamsanfilippo.org presently has a traffic ranking of zero (the smaller the more traffic). We have sifted twenty pages inside the web page teamsanfilippo.org and found one hundred and twelve websites referencing teamsanfilippo.org. I noted two contacts and addresses for teamsanfilippo.org to help you correspond with them. I noted three social networking sites possessed by this website. This website teamsanfilippo.org has been online for seven hundred and sixty-seven weeks, fourteen days, seventeen hours, and thirty-two minutes.
Pages Analyzed
20
Links to this site
112
Contacts
2
Locations
2
Social Links
3
Online Since
Oct 2009

TEAMSANFILIPPO.ORG RANKINGS

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TEAMSANFILIPPO.ORG HISTORY

This website teamsanfilippo.org was first filed on October 23, 2009. It is currently seven hundred and sixty-seven weeks, fourteen days, seventeen hours, and thirty-two minutes old.
REGISTERED
October
2009

COMPANY MATURITY

14
YEARS
8
MONTHS
14
DAYS

LINKS TO WEB PAGE

Abby Grace Foundation - Helping Find a Cure for Sanfilippo Syndrome

Helping Find a Cure for Sanfilippo Syndrome. The body uses the . About the Abby Grace Foundation. We feel a sense of urgency to get a treatment or cure for children affected with Sanfilippo Syndrome. Each day that goes by is a day of more progressive brain damage.

Mały Maciek i Wielcy Czarodzieje

8221; he wrote to Jenkins Hernandez. The Bills could ask Clay to restructure that bonus, spacing out the cap hit over the remaining four years of his deal. It To submit your questions or ideas, or to simply learn more about CareerTrend, contact us.

Life with Emily

The adventures of living with a little girl who just happens to have Sanfilippo Syndrome. The challenges are great, but the adventures are many! Saturday, June 4, 2011. Things to do with Emily on a rainy day. I think this is a problem most mothers of toddlers face. Only now, you, the parent get to play too! Just as soon as you vacuum t.

WHAT DOES TEAMSANFILIPPO.ORG LOOK LIKE?

Desktop Screenshot of teamsanfilippo.org Mobile Screenshot of teamsanfilippo.org Tablet Screenshot of teamsanfilippo.org

CONTACTS

Interactive Media Consulting, LLC

Beth Moeller

480 Broadway, Suite 220

Saratoga Springs, NY, 12866

US

Interactive Media Consulting, LLC

Beth Moeller

480 Broadway, Suite 220

Saratoga Springs, NY, 12866

US

TEAMSANFILIPPO.ORG HOST

I caught that the main page on teamsanfilippo.org took two thousand four hundred and seventy-four milliseconds to stream. I could not find a SSL certificate, so therefore we consider teamsanfilippo.org not secure.
Load time
2.474 seconds
SSL
NOT SECURE
Internet Address
65.38.104.133

NAME SERVERS

ns2.1stpeople.net
ns1.1stpeople.net

FAVORITE ICON

SERVER OPERATING SYSTEM AND ENCODING

I diagnosed that teamsanfilippo.org is implementing the nginx server.

TITLE

Team Sanfillipo Parents united to find a cure

DESCRIPTION

Cure Sanfilippo, Gene therapy, Get help for Sanfilippo, MPS, MPS III, Rare diseases, lysosomal disease, and Fundraising

CONTENT

This website had the following on the site, "Parents united to find a cure." Our analyzers viewed that the web page said " Parents united to find a cure." The Website also said " Scientific and Research Advisory Board. What is Sanfilippo Syndrome? How You Can Help. Host or Attend an Event. Become a Hero Among Us. Research France and Netherlands. Gene Therapy Coming 2014! What is Sanfilippo Syndrome? How You Can Help Team Sanfilippo." The website's header had Sanfilippo as the most important search term. It is followed by MPS, MPS III, and Rare diseases which isn't as highly ranked as Sanfilippo. The next words they uses is lysosomal disease. Fundraising Sanfiliippo was included and could not be viewed by web engines.

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