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skip to content ukts menu about us agm 2018 our team ambassador’s programme board members patrons ukts documents vacancies at the ukts login about thalassaemia inheriting thalassaemia living with thalassaemia treatment networks newsletter library calendar donate welcome to ukts parents stories in march 2015 the sickle cell and thalassaemia screening programme advisory group set up a sub group to focus on the timeliness of antenatal screening and prenatal diagnosis. the subgroup included parents of children with sickle cell disease and thalassaemia, representatives from ukts and the sickle cell society and representatives from midwifery, obstetric and genetic counselling professional organisations. read the parents’ stories sickle cell and thalassaemia screening screening is the process of identifying people who appear healthy but may be at increased risk of a disease or condition. healthcare professionals will offer information, further tests and appropriate treatment to reduce their risk or any complications arising from the disease or condition. the nhs sickle cell and thalassaemia ( sct ) screening programme is a genetic screening programme. this means that it also identifies people who are genetic carriers for sickle cell, thalassaemia and other haemoglobin disorders. continue reading “sickle cell and thalassaemia screening” → panel 1 placeholder panel 2 latest news infected blood inquiry posted on december 21, 2018 december 21, 2018 by hasomeri in heads up we encourage you to share your story with the infected blood inquiry. it is essential that those infected have their voices heard in this inquiry. prescription charge posted on october 11, 2018 november 30, 2018 by hasomeri in heads up the ukts is a member of the prescription charges coalition, an alliance of charities campaigning to abolish prescription charges for all people living with long term medical conditions. nhs blood donation posted on july 7, 2018 november 30, 2018 by hasomeri in heads up we provide a blood and transplantation service to the nhs, looking after blood donation services in england and transplant services across the uk. panel 3 latest event the hepatitis c coalition is a group of leading clinicians, patient organisations and other interested parties committed to the reduction of morbidity and mortality resulting from hepatitis c, and the eventual elimination of the virus. some 214,000 people in the uk are thought to be living with chronic hcv. many of these do not know that they have the virus and at present only 4% of those chronically infected receive treatment each year – an unacceptably low number. yet with the right diagnosis and treatment, hcv is curable, thanks to new therapies that are now available. research from the london joint working group on substance use & hepatitis c (ljwg) found it was cheaper to treat chronic hepatitis c virus (chcv) than to allow the disease to progress, and that treating just 10% of those people with hcv could save £200 million in london alone. a vision for hepatitis c: test, treat, cure a vision for hepatitis c – infographic letter to nice regarding evaluation of new drugs to combat hepatitis c virus tif’s position paper on viral hepatitis c in thalassaemia – final 2015 panel 4 social facebook twitter vimeo stay in touch subscribe to the ukts and stay updated! your email address will only be used to send you information from the ukts. leave this field empty if you're human: resources infected blood inquiry december 21, 2018 prescription charge october 11, 2018 nhs blood donation july 7, 2018 donate with paypal privacy policy © copyright pmg creative 2018 for the uk thalassaemia society charity reg no 275107

URL analysis for ukts.org

https://www.ukts.org/patrons/
https://www.ukts.org/agm-2018/
https://www.ukts.org/heads-up/
https://www.ukts.org/livingwith/
https://www.ukts.org/board/
https://www.ukts.org/networks/
https://www.ukts.org/home/nhs-screening/#more-3424
https://www.ukts.org/pdfs/hepatitis/vision_for_hepatitis_c_infographic.pdf
https://www.ukts.org/heads-up/infected-blood-inquiry/
https://www.ukts.org/privacy-policy/
https://www.ukts.org/heads-up/nhs-blood/
https://www.ukts.org/heads-up/prescription-charge/
https://www.ukts.org/wp-content/uploads/2018/11/parents-stories-publication.pdf
https://www.ukts.org/calendar/
https://www.ukts.org/

Whois Information

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WHOIS LIMIT EXCEEDED - SEE WWW.PIR.ORG/WHOIS FOR DETAILS

  REFERRER http://www.pir.org/

  REGISTRAR Public Interest Registry

SERVERS

  SERVER org.whois-servers.net

  ARGS ukts.org

  PORT 43

  TYPE domain

  REGISTERED unknown

DOMAIN

  NAME ukts.org

NSERVER

  NS1.LIVEDNS.CO.UK 213.171.192.250

  NS3.LIVEDNS.CO.UK 213.171.192.254

  NS2.LIVEDNS.CO.UK 213.171.193.250

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