"Welcome to the Bath, Bristol and Wiltshire support group.  We cover a wide geographical area from North Somerset, across Bristol and Bath and into Wiltshire, so we alternate meetings between Bristol/Bath and Swindon. Members say the best thing about the group is meeting people who know exactly how they feel and understand what they are going through.  I hope to see you at a meeting soon."

What happens at the group?

Meetings are informal and new members are always given the chance to tell us their story, if they want to, or to just listen if they prefer.  The Swindon meetings are supported by a Trichologist who gives members free advice and cakes! Bristol/Bath meetings are held in a variety of different locations.

Group dates:

Date: Time: Location:
Saturday 11th January 2020 2-4pm Downend Folk House, Overndale Road, Bristol BS16 2RW
Saturday 8th February 2020 2.30-4.30pm Hair and Trichology Clinic, High Street, Chiseldon, SN4 0NQ

CANCELLED

Saturday 7th March 2020

CANCELLED

2-4pm

CANCELLED DUE TO CURRENT NEWS EVENTS.

 SEE HERE FOR MORE DETAILS 

CANCELLED

Saturday 18th April 2020

CANCELLED

2-4pm

CANCELLED DUE TO CURRENT NEWS EVENTS.

 SEE HERE FOR MORE DETAILS 

Saturday 9th May 2020 2.30-4.30pm Hair and Trichology Clinic, High Street, Chiseldon, SN4 0NQ
Saturday 13th June 2020 2-4pm Percy Community Centre, New King Street, Bath BS1 2BN

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 15 and above. 

Contact details:

Sally Smith
Email: [email protected] 
Sally is happy to answer any questions about the group and provide a listening ear at a time arranged by email. Please be aware that any questions Sally is unable to answer will be sent on to staff at Alopecia UK.

The group leads are not professional counsellors but people who have personal experiences with alopecia and, along with member 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

Sally's link with alopecia: 

Sally first started losing her hair 22 years ago with a small patch that grew back.  Gradually over the next 15 years, patches came and went, but hair reduced overall.  Then in 2010, her hair stopped growing and the bald patches became greater than ever.  In December 2010, a photo taken at a colleagues retirement "do" made her realise that she could no longer cover up the bare patch and she got her first wig. It took 6 months to get her first NHS wig, but in the meantime she struck lucky with a wig consultant in Cardiff who helped her initially and found the "right one" at the first meeting. Sally now has alopecia universalis.


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