People with alopecia invited to take part in ground-breaking research study Read more
10-year-old Cameron Eiko Scott and family feature in this new short film directed by Sian Reeves Read more
Can you offer a listening ear to people affected by alopecia? Read more
Following a committee meeting in September, NICE has published its draft guidance for ritlecitinib Read more
Simon Ray is leaving the Alopecia UK Trustee Board Read more
Caroline Ward has published a new story book designed to help children affected by alopecia Read more
Alopecia UK is currently recruiting a Treasurer to join our Trustee Board Read more
Alopecia UK is looking for new Trustees to join our Board Read more
NICE continue to not recommend baricitinib, currently the only licensed treatment in the UK, for the treatment of severe alopecia areata. Read more
Alopecia UK says goodbye to Kerry Montgomery as she embarks on the next step in her career.. Read more
We are looking for more sessional workers to support our regional events delivery for children, young people and their families. Read more
We take a look back on Alopecia Awareness Month 2023.. Read more
We’re looking for people or businesses (alopecia related or not) to sponsor free tickets for children with alopecia to attend our Alton Towers event. Could you help? Read more
Family festival fundraising event Elizachella is a big success! Read more
11-year-old Cameron Eiko Scott has been awarded the 2023 Hannah Dennis Alopecia Awareness Award Read more
Alopecia UK CEO welcomes you to Alopecia Awareness Month 2023 Read more
Two ten year olds are raising awareness and funds for Alopecia UK this September Read more
Simon Ray has stepped down as Chair of the Board of Trustees for Alopecia UK. Simon is succeeded by Chris Philipsborn as Chair from August 2023. Read more
Alopecia UK and the Centre for Appearance Research have published their study exploring the socioeconomic burden of alopecia areata Read more
NICE has confirmed that it will not recommend baricitinib for routine commissioning on the NHS for severe alopecia areata Read more
We provide a summary of the results of our recent Support survey.. Read more
We are looking for Charity Champions to raise awareness and funds this September! Read more
Last month, Team AUK attended the EHRS conference in Sheffield. Read about how we got on... Read more
Alopecia UK is looking for feedback about the work we do under our Support aim via a short survey to our community Read more
On 23 June 2023, the US Food and Drug Administration (FDA) approved ritlecitinib (brand name Litfulo) for the treatment of severe alopecia areata, marking the second FDA-approved treatment for the condition in adults, and the first for children ages 12 and up. Read more
In collaboration with the College of Trichological Science and Practice (CTSP), Alopecia UK is delighted to announce the launch of a new online course ‘Introduction to the Psychology of Hair Loss and Scalp Conditions’. Read more
Linzi Brack of Diamond Wig Bank North East tells us about her recent landmark fundraising total.. Read more