Support & Advice Support Groups Anglesey & Gwynedd “Welcome to the Anglesey & Gwynedd group. I am really looking forward to supporting you all in 2021 and helping people in the area” What happens at the group? Meetings are informal, just a chance to have a panad (cuppa!) a chat and meet new people in a similar situation to your own. New members are always welcome so please feel free to come along and either share your story or just listen to others. No pressure! I also welcome any ideas/suggestions about what you would like to see in the group. Group dates: Date: Time: Location: Extra Meeting Details: We have now tentatively re-opened our support groups, however, it is at the discretion of individual group leads to decide what they feel comfortable delivering in the community, in addition to local COVID-19 guidance given in your area. If you are interested in attending a future group meeting, please contact Vicki directly for more information on upcoming meetings. 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.