Support & Advice Support Groups Anglesey & Gwynedd “Welcome to the Anglesey & Gwynedd group. This is a new group set up at the end of 2019 and we had our first meeting in December. I am really looking forward to welcoming you all in 2020 and supporting people in the area” What happens at the group? We are a new group and started in December 2019. We have only had one meeting so far where we had a chat about what we would like to do at group meetings. We look forward to welcoming more people along in 2020! Group dates: Date: Time: Location: Extra Meeting Details: Saturday 22nd February 2020 TBC Quakers Meeting House Bangor (North Wales), Dean Street, Bangor, LL57 1UR Saturday 25th April 2020 TBC Quakers Meeting House Bangor (North Wales), Dean Street, Bangor, LL57 1UR Saturday 13th June 2020 TBC Quakers Meeting House Bangor (North Wales), Dean Street, Bangor, LL57 1UR Saturday 22nd August 2020 TBC Quakers Meeting House Bangor (North Wales), Dean Street, Bangor, LL57 1UR 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. Please note that those age 15-17 must be accompanied by someone age 18 or over. If under the age of 14 and looking for your closest support group please see here for a list of our children and teen groups. Contact details: Vicki Hennesey-JonesEmail: [email protected] Vicki 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 Vicki is 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 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 Vicki's link with alopecia: My name is Vicki, I have had Alopecia Areata since I was 11. I want to run a support group to hopefully offer the same support that I received from friends in Alopecia UK and provide a comfortable platform to others with hair loss to chat and maybe meet up. 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.