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Graham Barker, director of services and development at the Haemophilia Society, wrote a letter to Alf Morris MP indicating that some health authorities were refusing to pay the additional costs associated with recombinant Factor 8.

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Graham Barker wrote to Liz Lynne MP drawing attention to the Government's reluctance to adopt the UKHCDO guidelines and highlighting the difference in approach in Scotland where all children with Haemophilia A had been transferred to recombinant plans, by 1997.

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Jan Wallace described her involvement in Haemophilia Wales' campaign in 1997 which aimed to "ensure all haemophiliacs in Wales received the safest treatment known as Recombinant".

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Dr Ludlum raised concerns about the inequality of haemophilia care across the UK, in particular that of the very uneven availability of recombinant factor VIII.

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Concerns were raised at a meeting between the Haemophilia Society and Department of Health that access to recombinant Factor 8 was not equal.

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Beverley Tumelty set out the role her late brother, Gareth Lewis, played in campaigning for recombinant treatment for haemophiliacs in Wales. He was Chairman of the South Wales Haemophilia Group during this period.

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An Information Pack produced by the South Wales Haemophilia Group referred to their success in campaigning for Recombinant treatment for all haemophiliacs in Wales.

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Dr Graham Winyard and Dr Metters sent a memo to Baroness Jay regarding New Variant CJD and Blood.

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Carol Grayson wrote to Frank Dobson to enquire about plans to roll out recombinant to all patients, but was told in reply that "there are no plans to arrange this centrally" and that "the Department of Health does not accept that the clinical case has been made for the general use of the recombinant product".

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One man wrote to Tony Blair expressing his concern that his son's haemophilia treatment might revert to human-derived plasma after he reached the age threshold, as well as expressing further concerns about the affordability of recombinant Factor 8.

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A Health Services Circular (HSC 1998/999) was published. This promulgated the announcement that central funding would be provided to health authorities in order to provide recombinant Factor 8 to new patients as well as patients under the age of 16.

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The Department of Health published a further Health Services Circular (HSC 1998/147). This document considered specific arrangements for health authorities to submit claims for additional funding to provide recombinant Factor 8.

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The Secretary of State agreed to the central funding for 1998/1999 of recombinant Factor VIII for new patients and those under 16. This was on what were described as humanitarian (rather than effectiveness grounds).

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At a meeting of the UKHCDO Executive Committee Dr Ludlam said that Charles Lister had "again informally indicated that funding for [Factor 8] should continue beyond the 16th birthday."

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Bruce Norval described writing to the Secretary of State "to try and make sure that kids got on to recombinant products as early as possible".

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Pete Longstaff refused human derived Factor 8 products in a treatment strike which lasted until his death.

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Recombinant Factor 9 was licensed and the funding arrangements in England mirrored those for Factor 8.

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Charles Lister wrote to Nick Raisen regarding synthetic blood products.

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By this date all patients with Haemophilia in Scotland were being treated with recombinant Factor 8 or 9.

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By this date it had been confirmed that in Northern Ireland recombinant Factor 8 would be funded for all patients.

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