A Patients and Families Support Group

A UK website about atypical Haemolytic Uraemic Syndrome (aHUS)

IN THE CENTRE OF THE CENTRE

IN THE CENTRE OF THE CENTRE

From the moment it was formed, aHUSUK supported the setting up an aHUS Expert Centre for aHUS. Indeed one has existed, albeit as a temporary arrangement within NHS England since the time that AGNSS recommended it should be created. AGNSS was not just about evaluating eculizumab. In May this year NHS England finally chose theContinue Reading

Answers for aHUS gets going

Answers for aHUS gets going

A member of each of four of the two hundred or so families affected by aHUS in the UK attended ,in person or by teleconference,  the first meeting of Answers for aHUS. Along with representatives from  the “expert centre” in Newcastle and Kidney Research UK  the meeting discussed what might be needed to continue theContinue Reading

OPT OUT ORGAN DONOR PETITION RESPONSE

OPT OUT ORGAN DONOR PETITION RESPONSE

A petition seeking an opt out organ donor system in England, as has been adopted in Wales, has reached sufficient numbers to warrant a Government response. Below is a copy of that response sent to petitioners: The Government has responded to the petition you signed – “All UK residents to be placed on the OrganContinue Reading

A UK  PATIENT’s AGENDA FOR aHUS RESEARCH

A UK PATIENT’s AGENDA FOR aHUS RESEARCH

In the 2016 aHUS Global Survey undertaken earlier this year there were 42  UK aHUS patients or carers participants out of a total of 233. UK replies far exceeded the rest of European countries replies combined with  42 out  72 coming from UK respondents, which demonstrates the interest and willingness of the UK aHUS communityContinue Reading

HELLO FROM “Answers for aHUS”-  FOR THE FEW BY THE FEW

HELLO FROM “Answers for aHUS”- FOR THE FEW BY THE FEW

From today this website* belongs to Answers for aHUS . Answers for aHUS is a aHUS community group for all affected by aHUS in the UK . Not a charity in itself, and not a registered membership based organisation. It will have a “committee” to steer this project for the four years agreed with KidneyContinue Reading

That was the aHUSUK that was

That was the aHUSUK that was

Today Monday 3 October 2016 is the day that aHUSUK ceases to be . For over five years it has worked for aHUS patients and families doing what it said it would do when a group of aHUS patient families came together in Wimpole Street London on 10 September 2011. It became a registered charity.Continue Reading

3 October is the date for aHUSUK to bow out

3 October is the date for aHUSUK to bow out

The date has been set for aHUSUK dissolution. It will be on 3 October 2016. There will be some paperwork to conclude and then the charity  will be removed from the registers in England & Wales and Scotland. It is now just over five years since aHUSUK was formed and much has been achieved inContinue Reading

Syndromes involving Haemolysis and Uremia come in many forms

Syndromes involving Haemolysis and Uremia come in many forms

On Tuesday 20th September, sixty one years ago, the  term Haemolytic Uremic Syndrome first appeared  in public; and  it is worth remembering that the person who coined the term, Conrad von Gasser, saw HUS as syndromes not one disease. This summer another  e coli outbreak occurred in Scotland and another child died from HUS asContinue Reading

The transition has begun to Answers for aHUS

The transition has begun to Answers for aHUS

In the midst of all the Awareness Day and other activities changes are taking place to move from aHUSUK to Answers for aHUS. As part of this the website is to be re structured with new content for Answers for aHUS and to keep some of the aHUSUK archive available and visible. It will takeContinue Reading

24 September 2016 aHUS Awareness Day -Some aHUS facts

24 September 2016 aHUS Awareness Day -Some aHUS facts

Click on fact image in ascending order:              Continue Reading