Meeting dates:





Who can attend:

  • Those with all types of alopecia age 14 and over (male and female)
  • Friends/Partners of those with all types of alopecia (accompanying someone with alopecia)
  • Parents of children with all types of alopecia

Please note that those age 14-17 must be accompanied by someone age 18 or over.  This group is not suitable for those under 14.  If you have a child under 14 and are looking for support please contact the separate Yorkshire Children Support Group.

Contact details:

Email: [email protected]
Daisy does not have her telephone number advertised but is happy to provide a listening ear via telephone call at a time arranged via email. She is also happy to receive support questions from those in her local area and will answer to the best of her ability based on her own knowledge and experiences. 
Please be aware that any questions Daisy is unable to answer will be sent on to staff at Alopecia UK.

Daisy's link with alopecia: 

Daisy was diagnosed with alopecia areata at age 11 and has had it for fifteen years.  Daisy also experienced alopecia universalis in her teenage years, experiencing full regrowth and then losing it all again a short time later. 

From Daisy:
"I am 26 years old and have had alopecia since I was 11 - ranging from alopecia areata to alopecia universalis.  I would love to create a warm and welcoming group to enable myself and others to discuss alopecia freely, including the thoughts and feelings that go with it, and help others on their alopecia journey."

Need Advice or Support Outside of the Group Meetings?
The main role of support group leads is to facilitate, and answer questions about, the group meetings.  Some may offer additional support and you can see what is on offer from Daisy in her contact details.

Please note that all of 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.  The majority of group leads are not trained health professionals and will be helping from the standpoint of being someone who is affected by alopecia themselves and wanting to reach out and help others.

You can always contact Alopecia UK head office direct during office hours should you have any queries that need a more urgent response.

Suggestions, Comments, Compliments, Complaints?

If you have any 'Suggestions, Comments, Compliments or Complaints' about any of the Support Groups listed on the Alopecia UK website then you can let us know by clicking here. The information will be used by Alopecia UK to to help us understand what works and what doesn't in order that we can support and advise group leads more effectively and develop the Alopecia UK support group network.