Support & Advice Support Groups Birmingham Children Welcome to Birmingham kids group! We welcome children and families affected by alopecia to meet in a relaxed atmosphere. It’s a great chance for children to meet others with alopecia, and for parents to chat as we know things can be tough on parents too. What happens at a Group? Our meetings are relaxed and informal. We bring along things to keep the children entertained, including crafts and games. We also do some group activities which are a lot of fun and a big hit with the children. Group dates: Date: Time: Location: Extra Meeting Details: 2021 Due to the current pandemic, all of our face-to-face support groups are currently cancelled until further notice. READ OUR FULL CHARITY UPDATE HERE To remain up to date on support and resources available for young people, please join our mailing list. Please contact the group lead prior to attending a meeting so they can plan accordingly. Who can attend: Children and young people with all types of alopecia up to the age of sixteen (male and female) Parents of children with all types of alopecia Siblings of those with all types of alopecia (accompanying someone with alopecia) Please note that those age under 18 must be accompanied by someone age 18 or over Contact details: Gosia FederowiczEmail: [email protected]Gosia is happy to answer any questions about the group and provide a listening ear at a time arranged by email. Please be aware, any questions Gosia 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 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 leaders are volunteers and do this in their space time, as such please allow up to one week for replies to emails. Gosia's link with alopecia: Welcome to the Birmingham Kids group! My name is Gosia, and I am the mum of 3-year-old Sophia, who has Alopecia Universalis. I hope that this group will provide support, a safe space, and a place to meet up for children and parents alike. I look forward to hearing from you soon! 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.