Please consider helping Debra

Please consider helping Debra of America. Epidermolysis Bullosa EB is a rare genetic connective tissue disorder,. Affecting 1 out of every 20,000 live births. There are many variations of. EB, but all share the prominent symptom of extremely fragile skin that. Blisters and tears from minor friction or trauma. There is no cure.

OVERVIEW

The web page shortfinal.org presently has a traffic classification of zero (the lower the more traffic). We were able to detect two contacts and directions for shortfinal.org to help you contact them. The web page shortfinal.org has been online for nine hundred and thirty-six weeks, eleven days, twenty-two hours, and fifty-five minutes.
Contacts
2
Addresses
2
Online Since
Jul 2006

SHORTFINAL.ORG TRAFFIC

The web page shortfinal.org is seeing fluctuating levels of traffic through the year.
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SHORTFINAL.ORG HISTORY

The web page shortfinal.org was first submitted to the registrar on July 23, 2006. It is currently nine hundred and thirty-six weeks, eleven days, twenty-two hours, and fifty-five minutes young.
REGISTERED
July
2006

BUSINESS PERIOD OF EXISTANCE

17
YEARS
11
MONTHS
10
DAYS

LINKS TO DOMAIN

WHAT DOES SHORTFINAL.ORG LOOK LIKE?

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CONTACTS

NC Consulting Inc.

NC Consulting Inc.

5241 Prairie Dunes Village Circle

Lake Worth, FL, 33463

US

Webstream, Inc.

Host Master

2200 W Commercial Blvd

Fort Lauderdale, FL, 33309

US

SHORTFINAL.ORG SERVER

Our parsers found that the main root page on shortfinal.org took four hundred and thirty-eight milliseconds to load. I could not discover a SSL certificate, so in conclusion our web crawlers consider shortfinal.org not secure.
Load time
0.438 secs
SSL
NOT SECURE
Internet Protocol
64.234.193.80

NAME SERVERS

ns1.securenetsystems.net
ns2.securenetsystems.net

SERVER OS AND ENCODING

We caught that shortfinal.org is weilding the Microsoft-IIS/6.0 os.

HTML TITLE

Please consider helping Debra

DESCRIPTION

Please consider helping Debra of America. Epidermolysis Bullosa EB is a rare genetic connective tissue disorder,. Affecting 1 out of every 20,000 live births. There are many variations of. EB, but all share the prominent symptom of extremely fragile skin that. Blisters and tears from minor friction or trauma. There is no cure.

PARSED CONTENT

The web page had the following in the web site, "Please consider helping Debra of America." We saw that the web site stated " Epidermolysis Bullosa EB is a rare genetic connective tissue disorder,." It also said " Affecting 1 out of every 20,000 live births. There are many variations of. EB, but all share the prominent symptom of extremely fragile skin that. Blisters and tears from minor friction or trauma."

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