Robot | Path | Permission |
GoogleBot | / | ✔ |
BingBot | / | ✔ |
BaiduSpider | / | ✔ |
YandexBot | / | ✔ |
Title | FA Parents’ |
Description | Home About FA Mailing List Living with FA Our Families Medical Research Fundraising Links Search Members FA Parents Group History and Introduction In Sept |
Keywords | N/A |
WebSite | faparents.org |
Host IP | 208.106.244.221 |
Location | United States |
Site | Rank |
US$1,470
Last updated: 2023-05-20 00:14:40
faparents.org has Semrush global rank of 0. faparents.org has an estimated worth of US$ 1,470, based on its estimated Ads revenue. faparents.org receives approximately 169 unique visitors each day. Its web server is located in United States, with IP address 208.106.244.221. According to SiteAdvisor, faparents.org is safe to visit. |
Purchase/Sale Value | US$1,470 |
Daily Ads Revenue | US$1 |
Monthly Ads Revenue | US$40 |
Yearly Ads Revenue | US$488 |
Daily Unique Visitors | 11 |
Note: All traffic and earnings values are estimates. |
Host | Type | TTL | Data |
faparents.org. | A | 3600 | IP: 208.106.244.221 |
faparents.org. | NS | 3600 | NS Record: ns1.newtekdns.com. |
faparents.org. | NS | 3600 | NS Record: ns2.newtekdns.com. |
faparents.org. | MX | 3600 | MX Record: 10 MailA5.newtekwebhosting.com. |
faparents.org. | TXT | 3600 | TXT Record: v=spf1 a mx/24 ip4:63.134.207.1/24 ip4:216.119.125.66 ?all |
Home About FA Mailing List Living with FA Our Families Medical Research Fundraising Links Search Members FA Parents Group History and Introduction In September of 1997, a small group of FA parents had been coming together via email to share questions, support and information about Friedreich’s Ataxia. Since then, our online support group, FAPG, has grown to an international group that now includes parents and guardians of children with other childhood-onset ataxias. Email is a great forum for support and has remedied the isolation and loneliness many of us feel dealing with the challenges of raising children with these degenerative diseases. This website provides another forum for us to share our unique experiences and knowledge of how we’ve learned to cope with ataxia in our family. If you are the parent of a child with FA or an undiagnosed ataxia, we invite you to join our free email support group. Fill out and submit the form on the membership request page. We welcome you to |
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