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skip to content search for: search call us on 01582 760733 cart (0) donate now about a-t types of a-t how does a-t affect people? a-t and cancer symptom management genetic aspects of a-t the atm gene and protein about a-t ataxia-telangiectasia or a-t, is a rare and complex genetic disorder. it is often referred to as a ‘multi-system’ disorder because it affects a number of different systems within the body. living with a-t a-t stories people like me links to other organisations living with a-t while they may face more challenges than many, people with a-t have lives to live, and the society’s aim is to ensure they have the support they need to live them to the full. how we help getting a diagnosis new diagnosis? a-t specialist clinics local health care advocacy & support support grants meeting others psychological support publications and films how we help our support team, kay and anne, are on hand 5 days a week to help and support families living with a-t. from the shock of the initial diagnosis through to treatment and the challenges of everyday living, we can provide support, advice and advocacy for people with a-t and their family, friends and carers. we also liaise with and offer advice to professionals. kay and anne can be contacted on 01582 760733. support us fundraise for us challenge events our events schools community groups business and corporate in loving memory a lasting legacy shop regular giving inspirational fundraisers support us the a-t society is completely funded by grants and donations, so to keep doing what we do best, we need you to help us. your support means we can continue to raise awareness. be there with emotional and practical assistance for new families, commission more medical research and provide a vital information resource for everyone involved with a-t. shop cards and gifts clothing events and tickets disability access give us a gift shop we have a wide range of gifts and fundraising merchandise in our online shop. every single purchase helps to make a difference to children and their families living with a-t. research about a-t research research we support what’s in the news clinical trials for researchers research into other conditions research research funded and supported by the a-t society has done a lot to advance our understanding of a-t and improve treatments. by bringing top scientists together and exploiting the latest advances in technology we will develop effective ways to treat and ultimately cure a-t. for professionals how we can help you confirming a diagnosis health care in a-t education and a-t what’s happening in research? publications and films for professionals ataxia-telangiectasia (a-t) is a very rare condition with an estimated 200 cases in the uk. most professionals will have limited knowledge or be unaware of the condition when a person is referred to them. about us news meet the team contact us trustees and patrons our story our publications and films about us the a-t society exists to enable people with a-t to make the most of the lives they have. we are unique in that we both support people with a-t and fund research. call us on 01582 760733 about a-t types of a-t how does a-t affect people? a-t and cancer symptom management genetic aspects of a-t the atm gene and protein about a-t ataxia-telangiectasia or a-t, is a rare and complex genetic disorder. it is often referred to as a ‘multi-system’ disorder because it affects a number of different systems within the body. living with a-t a-t stories people like me links to other organisations living with a-t while they may face more challenges than many, people with a-t have lives to live, and the society’s aim is to ensure they have the support they need to live them to the full. how we help getting a diagnosis new diagnosis? a-t specialist clinics local health care advocacy & support support grants meeting others psychological support publications and films how we help our support team, kay and anne, are on hand 5 days a week to help and support families living with a-t. from the shock of the initial diagnosis through to treatment and the challenges of everyday living, we can provide support, advice and advocacy for people with a-t and their family, friends and carers. we also liaise with and offer advice to professionals. kay and anne can be contacted on 01582 760733. support us fundraise for us challenge events our events schools community groups business and corporate in loving memory a lasting legacy shop regular giving inspirational fundraisers support us the a-t society is completely funded by grants and donations, so to keep doing what we do best, we need you to help us. your support means we can continue to raise awareness. be there with emotional and practical assistance for new families, commission more medical research and provide a vital information resource for everyone involved with a-t. shop cards and gifts clothing events and tickets disability access give us a gift shop we have a wide range of gifts and fundraising merchandise in our online shop. every single purchase helps to make a difference to children and their families living with a-t. research about a-t research research we support what’s in the news clinical trials for researchers research into other conditions research research funded and supported by the a-t society has done a lot to advance our understanding of a-t and improve treatments. by bringing top scientists together and exploiting the latest advances in technology we will develop effective ways to treat and ultimately cure a-t. for professionals how we can help you confirming a diagnosis health care in a-t education and a-t what’s happening in research? publications and films for professionals ataxia-telangiectasia (a-t) is a very rare condition with an estimated 200 cases in the uk. most professionals will have limited knowledge or be unaware of the condition when a person is referred to them. about us news meet the team contact us trustees and patrons our story our publications and films about us the a-t society exists to enable people with a-t to make the most of the lives they have. we are unique in that we both support people with a-t and fund research. click here to to find out how to speak to someone click here to read our stories a £20 donation could buy a gift for a child who is seriously ill in hospital. the a-t society supports people living with the disabling and life-limiting condition ataxia-telangiectasia and funds research to find a cure. new diagnosis? how we help living with a-t support us featured news and events tandem skydive thursday 27th september 2018 if you've ever fancied skydiving then now's your chance to join the a-team for a day of fun, laughter and an amazing adrenaline rush. read more about our latest post brighton marathon 14th april 2019 set yourself a challenge and sign up for one of our charity places! read more about our latest post you can make a difference every fundraising event, no matter how big or small, will make a difference to the lives of the people living with a-t. with your help we can continue to raise awareness, be there with emotional and practical support for families, commission more medical research and provide a lifeline for everyone affected by a-t. just £5 pays for an information pack for a family with a new diagnosis of a-t. £5,000 could fund a researcher for a month working on an a-t research project. donate news flu advice for people with a-t 01/05/2018 flu advice for people with a-t flu advisory from dr liz mcdermott (immunologist at our national a-t clinic in... read more > about our latest post delay to the attest trial 01/05/2018 delay to the attest trial as some people will be aware, there has been a delay in recruiting people onto the... read more > about our latest post twitter atsociety @atsociety phones may be answered by miss ebony robinson this afternoon. ebby is here to do a presentation to our corporate s… https://t.

URL analysis for atsociety.org.uk

http://www.atsociety.org.uk/donate/
http://www.atsociety.org.uk/support-us/challenge-events/
http://www.atsociety.org.uk/support-us/inspirational-fundraisers/
http://www.atsociety.org.uk/about-us/our-publications-and-films/
http://www.atsociety.org.uk/about-a-t/symptom-management/
http://www.atsociety.org.uk/how-we-can-help/a-t-specialist-clinics/
http://www.atsociety.org.uk/research/research-into-other-conditions/
http://www.atsociety.org.uk/about-a-t/how-does-a-t-affect-people/
http://www.atsociety.org.uk/research/clinical-trials/
http://www.atsociety.org.uk/events/brighton-marathon-14th-april-2019/
http://www.atsociety.org.uk/about-us/contact-us/
http://www.atsociety.org.uk/about-us/
http://www.atsociety.org.uk/about-a-t/a-t-and-cancer/
http://www.atsociety.org.uk/research/
http://www.atsociety.org.uk/about-a-t/genetic-aspects-of-a-t/

Whois Information

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Error for "atsociety.org.uk".

the WHOIS query quota for 2600:3c03:0000:0000:f03c:91ff:feae:779d has been exceeded
and will be replenished in 158 seconds

WHOIS lookup made at 20:34:49 30-Sep-2017

--
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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 uk.whois-servers.net

  ARGS atsociety.org.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 atsociety.org.uk

NSERVER

  NS3.MEMSET.COM 31.222.188.99

  NS2.MEMSET.COM 78.31.107.87

  NS1.MEMSET.COM 89.200.136.74

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