Robot | Path | Permission |
GoogleBot | / | ✔ |
BingBot | / | ✔ |
BaiduSpider | / | ✔ |
YandexBot | / | ✔ |
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 |
Keywords | N/A |
WebSite | cystinosisfoundation.org |
Host IP | 107.180.46.218 |
Location | United States |
Site | Rank |
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. |
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. |
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. |
"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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