Welcome to the Sheffield Alopecia UK support group!

What happens at the group?

We welcome adults affected by any type of alopecia. The group provides is a safe place to meet others affected by alopecia and to share experiences. There is no pressure, it is a relaxed and informal group, we have a chat and a cuppa.

First time coming along to a meeting and unsure what to expect?

Please have a read of our Support Group Guidelines for an overview of how our support groups run as well as our Frequently Asked Questions for more helpful information.

Group Meeting Details

Date:  Time: Location: Extra meeting details:
Saturday 4th July 2026 10:30am - 12:30pm The Burton Street Foundation, 57 Burton St, Hillsborough, Sheffield S6 2HH
Saturday 12th September 2026 10:30am - 12:30pm The Burton Street Foundation, 57 Burton St, Hillsborough, Sheffield S6 2HH

Please contact the group lead prior to attending a meeting so they can plan accordingly. 


Who can attend:

    This group is designed for any adult living with or affected by alopecia from the ages of 18 and above. 

    Contact details:

    Gemma & Natasha
    Email: [email protected] 
    Gemma and Natasha are happy to answer any questions about the group via email. Please be aware that any questions they are unable to answer will be sent on to staff at Alopecia UK.
    Support group leads are not professional counsellors but people who have personal experiences with alopecia and, along with members of the support group can help to give insight and advice on living and dealing with alopecia on a day to day basis. 
    Please note that our Support Group Leads are volunteers and do this in their spare time, as such please allow up to a week for replies to emails. Support group leads also cannot give 1:1 support.

    Gemma's link with alopecia: 

    I’m Gemma, and I’m delighted to be stepping into the role of chair for our Sheffield meetings, having previously supported the online groups.

    My own hair loss journey began in August 2023, when I noticed my first patches. Within just a few months, my alopecia progressed to Alopecia Universalis. Those early months were terrifying , but the support  I found through Alopecia UK made all the difference. Connecting with others who understand allowed me to gain the confidence to go out bald, share my journey and to eventually have fun with wigs. That’s why I’m so passionate about creating that community and safe place to help others navigate their own journey. 

    In September 2024, I began taking Ritlecitinib and have experienced some regrowth- it’s still patchy, but I’m grateful for every step forward. Like many of us, I don’t know what the future holds, but whether I have hair or no hair, I carry a deep understanding of the challenges and emotions that come with hair loss.

    I’m here to listen, to share, and to support you- wherever you are on your journey.

    Profile picture of group leader Gemma


    If you have any feedback on this support group please consider leaving it here.

    Alternatively, if you have any Suggestions, Comments, Compliments or Complaints for the charity please do so here.