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Berkshire Teens

This is a completely new group for 2018 and aims to cover Berkshire and Buckinghamshire.  It is also Alopecia UK's first group specifically for teenagers.

The following are welcome to attend the Berkshire Teens Support meeting:
  • Young people with all types of alopecia age 11 - 17 years (male and female)
  • Parents of children with all types of alopecia
  • Siblings (age 11-17 years) 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.

Meetings

Date Time Location
Friday 23rd February 2018 7pm Bowling Alley (contact for details)
Friday 23rd February 2018 - Bowling Alley
The current group members have decided to have the first meet up at the Bowling Alley.  Please ensure you get in touch with the group leads so that they can book enough lanes.  They will also then give you exact meet up details including location.

Although Sheila and Clare are down as group leads it will actually be Amaliah that will take the lead at the meetings with the other young people.

Support group contacts

Sheila (and Amaliah) Knight

Phone: 07912 983229

Email:

Clare Meldrum

Phone: 07767 268008

Email:

Please get in touch with Sheila and Clare ahead of a meeting and let them know if you intend to go along so that they can keep track of numbers.

From Sheila:

Sheila's daughter, Amaliah, has Alopecia Universalis.  Amaliah has had alopecia areata for nine years, since she was five years old.  Three years ago this developed in to alopecia universalis.  Sheila says, "Although I will be running the group my daughter will be taking more of the charge roll.  We have both grown in understanding alopecia and already talk to other parents and newly diagnosed young people and feel we have a lot to offer".

From Clare:
Clare's daughter has alopecia.  Clare says, "When my daughter first developed alopecia, we tried to support her as much as possible but she found it very difficult to come to terms with her hair loss.  The turning point for her was when she attended the Alopecia UK event at Alton Towers and was able to spend time with other young people who were going through the same experiences as her.  This group will allow teenagers to meet regularly and talk about the things that matter to them.

Need Advice or Support Outside of the Group Meetings?
The main role of support group leads is to facilitate, and answer questions about, the group meetings.  Some may offer additional support and you can see what is on offer from both below:
  • Sheila and Clare both have their telephone number advertised and are happy to provide a listening ear via telephone call if someone phones (between the hours of 3pm-8pm for Sheila and 6pm-9pm for Clare).
  • Both are happy to receive support questions via email from those in their local area and will answer to the best of their ability based on their own knowledge and experiences.  Please be aware that any questions Sheila and Clare are unable to answer will be sent on to staff at Alopecia UK.
Please note that all of 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.  The majority of group leads are not trained health professionals and will be helping from the standpoint of being someone who is affected by alopecia themselves and wanting to reach out and help others.

You can always contact Alopecia UK head office direct during office hours should you have any queries that need a more urgent response.

Suggestions, Comments, Compliments, Complaints?
If you have any 'Suggestions, Comments, Compliments or Complaints' about any of the Support Groups listed on the Alopecia UK website then you can let us know by clicking here.  Feedback is always appreciated.  The information will be used by Alopecia UK to help us understand what works and what doesn't in order that we can support and advise group leads more effectively and develop the Alopecia UK support group network.




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Alopecia UK is a registered charity number 1111304 and Scottish registered charity SCO44702
All content is © Alopecia UK 2018

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