actsma.co.uk Report : Visit Site


  • Server:Microsoft-IIS/10.0...
    X-Powered-By:ASP.NET

    The main IP address: 217.160.0.180,Your server Germany,Karlsruhe ISP:1&1 Internet AG  TLD:uk CountryCode:DE

    The description :act for sma, the ally cadence trust for spinal muscular atrophy, uk charity giving support to families affected by sma type 1...

    This report updates in 23-Aug-2018

Technical data of the actsma.co.uk


Geo IP provides you such as latitude, longitude and ISP (Internet Service Provider) etc. informations. Our GeoIP service found where is host actsma.co.uk. Currently, hosted in Germany and its service provider is 1&1 Internet AG .

Latitude: 49.004718780518
Longitude: 8.3858299255371
Country: Germany (DE)
City: Karlsruhe
Region: Baden-Wurttemberg
ISP: 1&1 Internet AG
    moneyobserver.com 

HTTP Header Analysis


HTTP Header information is a part of HTTP protocol that a user's browser sends to called Microsoft-IIS/10.0 containing the details of what the browser wants and will accept back from the web server.

Content-Length:9432
Content-Encoding:gzip
X-AspNetMvc-Version:3.0
X-AspNet-Version:4.0.30319
Vary:Accept-Encoding
Keep-Alive:timeout=15
Server:Microsoft-IIS/10.0
Connection:keep-alive
X-Powered-By:ASP.NET
Cache-Control:private
Date:Thu, 23 Aug 2018 09:14:04 GMT
Content-Type:text/html; charset=utf-8

DNS

soa:ns1093.ui-dns.biz. hostmaster.1and1.com. 2017072901 28800 7200 604800 300
ns:ns1093.ui-dns.org.
ns1093.ui-dns.de.
ns1093.ui-dns.biz.
ns1093.ui-dns.com.
mx:MX preference = 10, mail exchanger = mx01.1and1.co.uk.
MX preference = 10, mail exchanger = mx00.1and1.co.uk.
ipv4:IP:217.160.0.180
ASN:8560
OWNER:ONEANDONE-AS Brauerstrasse 48, DE
Country:DE
ipv6:2001:8d8:100f:f000::273//8560//ONEANDONE-AS Brauerstrasse 48, DE//DE

HtmlToText

-- -- 0800 23 43 762 0333 44 43 762 " supporting families affected by sma type 1 " " supporting families affected by sma type 1 " 0800 23 43 762 0333 44 43 762 0800 23 43 762 0333 44 43 762 " supporting families affected by sma type 1 " about us about sma what is sma? sma type 1 other types of sma available help act faq's other help bereavement news & events news & events justgiving pages butterfly ball 2018 casino & karaoke butterfly ball 2019 donate make a donation butterfly funds justgiving funds donate by text how you can help fundraising ideas ebay just text giving online shopping how your money helps shop tributes poems alex camwell ally cadence humphries andy butler corben kemp eilys elisabeth hartley ella sergiew harry fish jaiden dale maddison sherwood rowan poole supporters blog contact us about us about sma what is sma? sma type 1 other types of sma available help act faq's other help bereavement news & events news & events justgiving pages butterfly ball 2018 casino & karaoke butterfly ball 2019 donate make a donation butterfly funds justgiving funds donate by text how you can help fundraising ideas ebay just text giving online shopping how your money helps shop tributes poems alex camwell ally cadence humphries andy butler corben kemp eilys elisabeth hartley ella sergiew harry fish jaiden dale maddison sherwood rowan poole supporters blog contact us ally cadence trust the ally cadence trust is a uk registered charity, committed to supporting families affected by spinal muscular atrophy, also known as sma, type 1. spinal muscular atrophy is a neuromuscular genetic disease that results in progressive muscle weakness. click here to read more. mission statement: "the ally cadence trust for spinal muscular atrophy aim to protect and promote the physical and mental health of sufferers of spinal muscular atrophy and their families across the united kingdom, through the provision of support, education and practical advice and funding into research into the condition. also to advance the education of the general public in all areas relating to spinal muscular atrophy." the history behind the ally cadence trust ally cadence was the daughter of emma & karl, the founders of the ally cadence trust for spinal muscular atrophy (act for sma). she died aged six months, just twelve days after being diagnosed with spinal muscular atrophy (sma) type 1. her family hadn't heard of sma until a few weeks before she was diagnosed, and after the diagnosis they were told about support families that would contact them. these families are people who have been affected by sma in the past and, while not qualified in any particular field, they can answer basic questions that arise on a daily basis. in the twelve short days after ally's diagnosis, her family had a lot of support from the nhs, but they never got to meet their allocated sma support family. they would have been the one point of contact that could see things from a parents point of view and it was mainly this that inspired ally's parents to set up act for sma. they felt that parents with recently diagnosed children deserved a quick response to a request for support and information on spinal muscular atrophy, should it be requested. the answer was the ally cadence trust for spinal muscular atrophy, a way to provide others with a simple, yet highly important, level of support that is often underestimated. ally was a very happy little girl who never stopped smiling, she loved life and would be proud to have played her small part towards helping others love life too. having read a lot of misleading information online regarding support from other charities and organisations, ally's family were dissapointed to discover that very little of the specialised equipment was actually available. this was simply due to a lack of funding and so the ally cadence trust for sma was set up to try and generate a new line of funding and raise awareness of spinal muscular atrophy nationwide, and to provide sma support to affected families. to read ally's story in full, please visit www.allycadence.co.uk sign up for our newsletter... first name: last name: e-mail: we will not share your e-mail address with anyone make a monthly donation i would like to donate £ per month, to act for sma. please gift aid my donation. facebook sma what is sma? sma type 1 sma type 2 sma type 3 sma type 4 smard useful links about us faq supporters privacy policy help act for sma other help bereavement fundraising online shopping ebay how your money helps shop shop online donate make a donation butterfly funds just text giving news news and events butterfly ball contact contact us facebook twitter instagram registered charity no. 1133272 copyright © 2009 - 2018 ally cadence trust for spinal muscular atrophy, all rights reserved

URL analysis for actsma.co.uk


http://www.actsma.co.uk/page/what-is-sma
http://www.actsma.co.uk/page/act#faq
http://www.actsma.co.uk/page/just-text-giving
http://www.actsma.co.uk/page/other-help
http://www.actsma.co.uk/page/maddison-sherwood
http://www.actsma.co.uk/page/ebay
http://www.actsma.co.uk/news
http://www.actsma.co.uk/page/ella-sergiew
http://www.actsma.co.uk/page/other-types-of-sma
http://www.actsma.co.uk/page/jaiden-dale
http://www.actsma.co.uk/page/sma-type-1
http://www.actsma.co.uk/page/act-for-sma
http://www.actsma.co.uk/page/other-types-of-sma#type3
http://www.actsma.co.uk/page/other-types-of-sma#type2
http://www.actsma.co.uk/page/other-types-of-sma#type4
allycadence.co.uk
butterflyball.co.uk

Whois Information


Whois is a protocol that is access to registering information. You can reach when the website was registered, when it will be expire, what is contact details of the site with the following informations. In a nutshell, it includes these informations;

Error for "actsma.co.uk".

the WHOIS query quota for 2600:3c03:0000:0000:f03c:91ff:feae:779d has been exceeded
and will be replenished in 21797 seconds

WHOIS lookup made at 20:13:44 07-Sep-2017

--
This WHOIS information is provided for free by Nominet UK the central registry
for .uk domain names. This information and the .uk WHOIS are:

Copyright Nominet UK 1996 - 2017.

You may not access the .uk WHOIS or use any data from it except as permitted
by the terms of use available in full at http://www.nominet.uk/whoisterms,
which includes restrictions on: (A) use of the data for advertising, or its
repackaging, recompilation, redistribution or reuse (B) obscuring, removing
or hiding any or all of this notice and (C) exceeding query rate or volume
limits. The data is provided on an 'as-is' basis and may lag behind the
register. Access may be withdrawn or restricted at any time.

  REFERRER http://www.nominet.org.uk

  REGISTRAR Nominet UK

SERVERS

  SERVER co.uk.whois-servers.net

  ARGS actsma.co.uk

  PORT 43

  TYPE domain

DISCLAIMER
This WHOIS information is provided for free by Nominet UK the central registry
for .uk domain names. This information and the .uk WHOIS are:
Copyright Nominet UK 1996 - 2017.
You may not access the .uk WHOIS or use any data from it except as permitted
by the terms of use available in full at http://www.nominet.uk/whoisterms,
which includes restrictions on: (A) use of the data for advertising, or its
repackaging, recompilation, redistribution or reuse (B) obscuring, removing
or hiding any or all of this notice and (C) exceeding query rate or volume
limits. The data is provided on an 'as-is' basis and may lag behind the
register. Access may be withdrawn or restricted at any time.

  REGISTERED no

DOMAIN

  NAME actsma.co.uk

NSERVER

  NS-UK.1AND1-DNS.BIZ 217.160.81.3

  NS-UK.1AND1-DNS.ORG 217.160.83.3

  NS-UK.1AND1-DNS.COM 217.160.82.3

  NS-UK.1AND1-DNS.CO.UK 217.160.80.3

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Mistakes


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