Welcome to Essex Kids group. We meet twice a year and welcome children and families affected by alopecia.

What happens at the group?

In 2019 we did different activities including a tennis coaching session and a bouncy castle/ fun day. In 2020 we are looking forward to doing more – in April we may have a picnic – watch this space. While the kids have fun parents are welcome to chat and have tea and cake


Group dates: 

Date: Time: Location: Extra Meeting Details:
    2020 dates TBC  

Please contact the group lead prior to attending a meeting so they can plan accordingly. 


Extra meeting details:

Who can attend:

    This group is designed for any child and their family living with or affected by alopecia from the ages of 12 and under.

    • Please note that children must be accompanied by someone age 18 or over. 

    Contact details:

    Gemma Hurry
    Email: [email protected]
    Gemma 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 Gemma 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

    Gemma's link with alopecia: 

    "I became a group leader in 2018 after my daughter was diagnosed with Alopecia at the age of 4, now 8, I realised that there was very little local support. With the knowledge I gained, and my amazing inspirational daughter, I started the first kids Essex support group for children with Alopecia and their families. We can now share our knowledge and support, and learn more from all the others that we meet on this journey."


    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.