CHANGING FACES
WORKSHOP, September
2003
Shortly
after our summer holiday this year I was contacted by Karen Stewart
asking if I thought Mitchell (who is aged 11 and has Apert Syndrome)
might benefit from a workshop she was organising with Changing Faces
about children who look ‘different’ making the transition to
Senior School.

Ryan, Mitchell, Zoe, Jay and
Laura
Mitchell
is currently in Year 6 and so will make this ‘leap into the
unknown’ in September 2004. He has been extremely happy in his
Primary school, where he has been since he was 4, and is fully
accepted as one of the boys. I believe that he was almost totally
unaware that children could be unkind to each other, as he has
suffered none of this during his school life so far.


This
said, Mitchell was keen to attend the workshop and we travelled to
London on the Saturday morning a little unsure what to expect. We
couldn’t have been made more welcome and Mitchell was immediately
introduced to the four other children and taken off to his workshop
– we had little idea of what was to happen in his room! The
parents (myself included) were taken by Angie Lawrence to discuss
the more technical details of transferring to Secondary School with
Special Educational Needs. All the parents at the meeting that day
had children with Apert Syndrome and it was refreshing to see that
they shared many of the same difficulties in learning although all
had had different experiences at Primary school.



Lunch
was a trip to the local MacDonald’s, where everyone was extremely
helpful, and which the children (and adults) enjoyed enormously!

After
lunch the children returned to the workshop and we were later given
the chance to view the ‘work’ that they had done. The children
had a great time and it was useful for us to see what had been
discussed and the child friendly way it had been presented to the
children. This enabled them to understand and participate in the
message that was being put across about the different types of
people one encounters during a lifetime (aptly named the Sharks, the
Fish and the Dolphins!).

As
Mitchell's Mum, I want to spend my life protecting him from the
hurtful people out there who find it hard to accept our children for
the wonderful individuals that they each are. Unfortunately I
realise that that isn’t always possible, so a day given up for
this workshop, where Mitch could learn some skills to deal with
situations when I won’t be able to protect him, we both found
invaluable. I hope that Mitchell will have no need to use these
skills when he transfers but at least I know they are there if he
does! Thanks to all those involved in the day.
by
Sarah
Green – Mum of Mitchell (who has Apert Syndrome)
If
you would like details on how to contact Sarah
please telephone Gil Ruff – Group Administrator, Headlines –
Craniofacial Support on 01454 850557