cystinosisfoundation.org valuation and analysis

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Title In Memorial Jean
Description "With great love and sadness, the family of Jean Hobbs Hotz shares her passing into eternity on 18 November, 2020. Jean established the Cystinosis Foundat
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WebSite cystinosisfoundation faviconcystinosisfoundation.org
Host IP 107.180.46.218
Location United States
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cystinosisfoundation.org Valuation
US$1,820,170
Last updated: 2023-05-13 09:02:14

cystinosisfoundation.org has Semrush global rank of 5,815,008. cystinosisfoundation.org has an estimated worth of US$ 1,820,170, based on its estimated Ads revenue. cystinosisfoundation.org receives approximately 210,020 unique visitors each day. Its web server is located in United States, with IP address 107.180.46.218. According to SiteAdvisor, cystinosisfoundation.org is safe to visit.

Traffic & Worth Estimates
Purchase/Sale Value US$1,820,170
Daily Ads Revenue US$1,681
Monthly Ads Revenue US$50,405
Yearly Ads Revenue US$604,857
Daily Unique Visitors 14,002
Note: All traffic and earnings values are estimates.
DNS Records
Host Type TTL Data
cystinosisfoundation.org. 599 A cystinosisfoundation.org. 599 IP: 107.180.46.218
cystinosisfoundation.org. 3600 NS cystinosisfoundation.org. 3600 NS Record: pdns14.domaincontrol.com.
cystinosisfoundation.org. 3600 NS cystinosisfoundation.org. 3600 NS Record: pdns13.domaincontrol.com.
cystinosisfoundation.org. 3600 MX cystinosisfoundation.org. 3600 MX Record: 10 mailstore1.secureserver.net.
cystinosisfoundation.org. 3600 MX cystinosisfoundation.org. 3600 MX Record: 0 smtp.secureserver.net.
HtmlToTextCheckTime:2023-05-13 09:02:14
"With great love and sadness, the family of Jean Hobbs Hotz shares her passing into eternity on 18 November, 2020. Jean established the Cystinosis Foundation in 1983. She saw suffering and tried to heal it. Her legacy of kindness and unselfishness endures. We are forever grateful to her for sharing her many gifts including great compassion, understanding and peace." Karen Ritchie, U.S.: Many will remember this Cystinosis pioneer, and those who don’t, should. When Jean’s grandson, Josh, was diagnosed with cystinosis in the early 80’s, she saw a great need to bring other families suffering the same disease to come together. Those were the days before the internet, social media, or information on Cystinosis. It was almost impossible for a group so small to raise any meaningful funds. She turned "impossible" into "I’m possible" . There was virtually no treatment and most of us were told our children would die before 10 years, and sadly many did. For this reason, Jean created the first
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Date: Tue, 21 Dec 2021 02:44:38 GMT
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