wehaveaface.org valuation and analysis

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Meta Tags
Title Huntington’s Disease | WeHaveAFace Global HUBS | United
Description Press WeHaveAFace.org Global HUBS - Choose your destination: USA, England,
Keywords WeHaveAFace, HDSA, CHDI, HD, JHD, Huntington’s disease, disease, Huntington, HSG, Huntington Study Group, Neurology, HD organizations, Huntington’s disease organization, Huntington’s disease support groups, HD support groups
Server Information
WebSite wehaveaface faviconwehaveaface.org
Host IP 185.230.63.171
Location -
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wehaveaface.org Valuation
US$1,662,963
Last updated: 2023-05-14 12:44:08

wehaveaface.org has Semrush global rank of 6,364,727. wehaveaface.org has an estimated worth of US$ 1,662,963, based on its estimated Ads revenue. wehaveaface.org receives approximately 191,881 unique visitors each day. Its web server is located in -, with IP address 185.230.63.171. According to SiteAdvisor, wehaveaface.org is safe to visit.

Traffic & Worth Estimates
Purchase/Sale Value US$1,662,963
Daily Ads Revenue US$1,536
Monthly Ads Revenue US$46,052
Yearly Ads Revenue US$552,616
Daily Unique Visitors 12,793
Note: All traffic and earnings values are estimates.
DNS Records
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HtmlToTextCheckTime:2023-05-14 12:44:08
top of page WHAF HD/JHD? What is HD/JHD PROJECT CHANGE PROGRAM SUITE STUDIES / TRIALS RESOURCES UNITY PROJECT Press Release WeHaveAFace USA and WeHaveAFace England and Wales Retires Charities ​ Florida, January 16, 2023 – After almost fourteen years of providing services, supports, and recourses for the International Huntington’s community, WeHaveAFace.org USA and England and Wales, will be closing on March 1, 2023. WeHaveAFace Canada, and support chapters: WeHaveAFace New Zealand and Germany, will remain open to provide services and supports to the Huntington’s and Juvenile Huntington’s community. WeHaveAFace.org was created by Huntington’s disease patients and families in 2009. At that time in history, a small group of individuals decided to make a difference in the lives of their peers to find a viable treatment or a cure for Huntington’s disease. After two years of advocacy, the team grew into a diverse international family and maintained the same mission – to broaden
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