Info for future meets...
The meetings will be informal.
With children's groups we provide activities for children (arts and
crafts and some games etc) and get some volunteers on hand to entertain
them. Parents often gather themselves together for more in depth chat!
We will provide teas, coffees, juice and biscuits. Cost:
There is no cost to attend this meeting. But please let Lois know that you will be coming so that we have an idea of numbers.Who is it suitable for:
Children, Teenagers and Parents. We hope to run different sessions for
each but it depends who turns up. Please do register your details with Lois so we can plan effectively.What do I need to do beforehand?
Please email Lois and let her know:
Can I bring my other children?
- how many of you are coming and everyone's names
- the age of any children coming along (making
sure we know which child has alopecia)
- what type of alopecia your child has as well as the extent of the
- any additional needs that we should be aware of (e.g. allergies, medical conditions, disabilities etc)
Yes. Just ensure you let us know how many of you are coming.Finding the venue:
The main pedestrian entrance (Reception) to the Royal Grammar School will be closed. Please enter the school grounds through the gate approximately 100 metres to the left of the Reception entrance (next to Jesmond Church). Cars should be parked on the hard play area (turn immediately left after coming through gate). The meeting will be in the Sixth Form Area - with your back to the gate you will see the Performing Arts Centre in front of you. Please enter the building on your right through the grey door - it will be sign posted.
If you are travelling to Newcastle by train you will need to get a Metro train from Newcastle Central Station to Jesmond travelling north (there are only two platforms). As you exit Jesmond Metro station walk towards the church and through the gates of the school.
Please get in touch with Lois ahead of a meeting and let her know if
you intend to go along so that she can keep track of numbers.
Lois' link with alopecia:
Lois' daughter has had alopecia areata for over sixteen years.From Lois:
"By working with the charity I hope to help kids, their brothers, sisters and parents find a place to meet where they can play games, chat and just generally have a nice time together. Please get in touch if you have any ideas - happy to help!" Need Advice or Support Outside of the Group Meetings?
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:
- [To be completed]
- [To be completed]
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 (or their child) and wanting to reach out and help
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?
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.