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New Online Support Group Meetings

The Alopecia UK team are now offering online peer support group meetings for both people with alopecia and parents of children with alopecia.
Jen and Amy reflect on film and TV representation of baldness

With the recent adaptation of The Witches gaining some attention, charity managers Jen and Amy reflect on their different experiences with the original film...
Caring in a time of coronavirus

Operations Manager Amy explains the current challenges the charity is facing and explains ways that you can still support Alopecia UK whilst continuing to social distance
AUK is recruiting two new Trustees!

Alopecia UK is looking for two new Trustees to join the Board

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A Guide to Wigs

Links to our downloaded PDF wig guide, and information on the NHS England wig report.
The ups and the downs

My story includes a brief summary of my alopecia journey. The main focus of my story is about self-acceptance and becoming your own best friend though-out hair loss.
Alopecia UK Support Groups

Find out exactly what a support group is, where your nearest AUK group is and how to start your own support group.
Online Groups

Links to our online support platforms (Facebook / Healthunlocked) where you can meet and talk to others in a similar situation
Advice for children and young people with alopecia

Including fact sheets for varying age groups and helpful links
What we do

Alopecia UK works to improve the lives of those affected by alopecia through aims of support, awareness, research and fundraising.
Alopecia UK Shop
Service Directory

Find useful products and services from the many businesses listed in our Service Directory
NHS England Wig Report

Alopecia UK has published its report examining wig provision from organisations within NHS England.
London

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#lichenplanopilaris #hairloss #realisation #supportdiagnosis