LAL Solace Patient Community - LAL Deficiency Lysosomal Acid Lipase Disease Wolman Disease patient support
LAL Solace is an online support group to help patients with LAL Deficiency Lysosomal Acid Lipase Disease and Wolman Disease.
OVERVIEW
The domain lalsolace.org currently has a traffic ranking of zero (the lower the higher page views). We have downloaded twenty pages within the site lalsolace.org and found nineteen websites interfacing with lalsolace.org. We were able to precure one contacts and locations for lalsolace.org to help you reach them. We were able to precure one public web platforms linked to lalsolace.org. The domain lalsolace.org has been on the internet for seven hundred and thirty weeks, two days, fifteen hours, and forty-three minutes.
Pages Parsed
20Links to this site
19Contacts
1Addresses
1Social Links
1Online Since
Feb 2011LALSOLACE.ORG TRAFFIC
The domain lalsolace.org has seen diverging levels of traffic within the past the year.
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LALSOLACE.ORG HISTORY
The domain lalsolace.org was registered on February 08, 2011. It is now seven hundred and thirty weeks, two days, fifteen hours, and forty-three minutes old.
REGISTERED
February
2011
SITE AGE
14
YEARS
0
MONTHS
2
DAYS
LINKS TO LALSOLACE.ORG
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WHAT DOES LALSOLACE.ORG LOOK LIKE?
CONTACTS
LaL Solace, Inc.
Mary Pruitt
191 Barnstable Court
Harvest, Alabama, 35749
US
LALSOLACE.ORG SERVER
We discovered that a lone page on lalsolace.org took one hundred and seventy-one milliseconds to come up. We could not discover a SSL certificate, so our crawlers consider this site not secure.
Load time
0.171 sec
SSL
NOT SECURE
IP
208.82.16.68
NAME SERVERS
ns67.domaincontrol.com
ns68.domaincontrol.com
SERVER SOFTWARE
We observed that this website is operating the nginx/1.12.1 operating system.SITE TITLE
LAL Solace Patient Community - LAL Deficiency Lysosomal Acid Lipase Disease Wolman Disease patient supportDESCRIPTION
LAL Solace is an online support group to help patients with LAL Deficiency Lysosomal Acid Lipase Disease and Wolman Disease.PARSED CONTENT
The domain lalsolace.org states the following, "LAL Deficiency Lysosomal Acid Lipase Disease and Wolman Disease patient support." I observed that the website said " Support Organization for Lysosomal Acid Lipase Deficiency - Advocacy, Care and Expertise was created to bring LAL Deficiency patients and families together to share experiences, knowledge and compassion." They also stated " Dear Gabi,Thanks for your words of encouragement. We will continue to have patience and hope. Is now friends with Tatyana." The meta header had Disorder as the first keyword. This keyword was followed by Ester, help, and Lipase which isn't as important as Disorder. The other words the site used was Deficiency. Disease is also included but will not be seen by search engines.SEE OTHER WEBSITES
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