Problems challenged kids and their
parents face in Egypt
This
article is not only about us and Tala, these are problems that I heard from
other parents as well. They are not in order of importance as I believe they
are all equally important.
A) I
believe that one of the biggest problems we face in Egypt is the lack of information,
starting from doctors, schools, nurseries, rehabilitation centers until the
parents themselves. There’s no one to tell you or guide you where to start or
what to do or where to go. It’s like a mission impossible in Egypt to get
proper information that can draw even a rough map to help you on your journey.
It’s a
trial and error, you try this doctor and you follow your gut.. taking an
informative decision from someone you trust is extremely rare.
There are
no support groups, no TV shows, no parents training centers that provide
parents with the tools they need to help their kids.. Challenged kids need
parents who understand their limitations and know how to deal with it.. parents
who know that a tantrum is not misbehaving it’s just that the child can’t
tolerate that kind of noise, for example. When we don’t know what’s going on in
our child’s mind or body, how can we help him develop?
There are a
million TV shows about health and they invite doctors to talk about how to stay
healthy and how to lose weight and how to lift your face, not ONE show about
challenged kids..
We need to
know a lot of things, I will list a view just to make my point a little more
clear..
1- How to identify our child’s
disability
2- What’s the first thing to do when
you find out
3- What are the different kinds of
behavior to expect and how to deal with it?
4- Are there special tests we should
run periodically?
5- Where are good rehabilitation
centers and how can I decide that they are really good
6- What should I observe in my child?
7- What’s the normal development pace
so I can compare and find out what my child needs to work on?
And it goes
on and on and on and no one is there is no one to answer you..
B) I
noticed something that really gets on my nerves. Apparently rehabilitation
centers don’t like each other and if a therapist used to work somewhere and
left, then it’s war between him and the center.. Our kids are the ones who pay
the price for this ridiculous behavior.. So if I say in one place that I take
Tala to X, they start telling me how horrible they are and they will do no
progress with my child and vice versa.. and they put me in a whirlpool that I
can’t get out of because the thought will always haunt me “what if they are
right? What if the other place is better?” Again, the lack of knowledge will
put you under the mercy of these people..
C) Finding
all therapies your child needs in the same place or at least close to each
other.. A child with chromosomal issue
will probably need the following therapies:
1- Physical
Therapy
2- Speech
therapy
3-
Occupational therapy
4- Oral
motor therapy
5-
Cognitive skills development
6- Sensory
processing
7- Vision
therapy and much more than that
Imagine
that every facility provides some of these therapies but not the rest, so now
you have to take your child to several places, they aren’t close to each other
and most probably not all of them will be close to where you live.. you will
find yourself wasting all day in traffic and in therapies..
You won’t
have time for yourself, your other children, your husband and you won’t find
time to spend normal quality time with your child who needs to feel that he’s a
kid.. instead of running and playing and spending time lazy on the couch watching
TV, he’s spending his time with total strangers or in the car..
There
aren’t enough facilities in different areas.. I saw parents who used to come
all the way form south of Egypt just to attend a therapy session that lasts two
hours.. they wake up 4 am, take the train for 6 hours to attend a session, then
take the train again for another 6 hours and do it all over again in a couple
of days.. because where they live there’s no help. How are they supposed to be
productive people.. a mom told me once “I feel that all the therapy my son does
here goes to waste in the train ride, I’m the normal adult and I go back home
all my muscles aching and can’t get out of bed, what about him?”
D) Support
groups and training centers
I’m
stressing again on this point because it’s nerve wrecking for the parents to
have a challenged kid. It can get the worst out of you if it’s not handled
correctly.. It can destroy families, it can affect the siblings.. parents need
to know how to deal with the child, how to deal with the brothers and sisters,
how to channel their frustration to productive solutions instead of taking out
on the child or on themselves.. if the parent is unhappy and stressed, the
child is unhappy and stressed..
Support
groups allow the parents to release the pressure they’re under, talk about
their feelings with someone they can relate to.. someone who understands
perfectly what they’re talking about, not just sympathizing with them. It
gives us a chance to share experiences
and compare notes..
It’s the
parents who spend most of their time with the child, it’s the parents who KNOW
what their child likes and dislikes.. this is a very powerful tool, why not
train the parent to do activities that will help the child’s development.. as
long as it’s not a medical or technical activity that needs a specialist, a
parent will be able to do it much better than the therapist.. Because I can
pick the time when my child is in a good mood and ready to work.. Some times I
used to take Tala to therapy and she was in no mood to work and this session
was gone to waste..
Of course
you might think that the internet is available so why not use it to educate
yourself? Well, not everyone has access to the internet and every child is
unique with his own set of symptoms and you will have a million questions on
your mind as you’re reading or watching a video and no one will answer them..
Of course
it helps a lot but I’m not talking here about myself only, I’m talking about
every mother in Egypt. Every social class, every level of education.. you can’t
ask someone who doesn’t even have water in their homes to search the internet!!
E) Finding
a place to take your child to play
As much as
our children need the tons of therapies they do every day, they need play time.
Play time helps a lot in development.. it helps also the psychological aspect..
Playtime
makes you feel human again, makes your heart melt when you see your child
laughing and having a good time, it gives you energy to start another day of
fighting, makes you survive through all the fear you have every second.
There are
no places that have swings specially designed for challenged kids, or have
ramps, at least..
There are
very little number of places that will even allow a challenged kid to enter..
This again
goes back to problem number 1, nobody knows how to handle a challenged kid..
simply because we never hear anything about them, we never see them so why
bother and do anything for them?
F) finding
a nursery or school..
This is one
of my biggest problems so far.. I want my child to be accepted.. Every time I
went to a nursery and they told me they
can’t accept Tala, my heart was broken.. feeling that your child is being
rejected over and over again for no fault of hers or yours is devastating..
I felt like
I’m pushing a wall.. These were some of the reasons I heard why they can’t
accept Tala:
1- If she can’t walk, other kids will
ask why? And we don’t know what to tell them.. (go back to problem 1)
2- We can’t take the responsibility of
any injuries because she can’t walk or talk..
3- There’s no one to carry her around.
4- We don’t have chairs or swings with
belts to help support her..
To me, these are all ridiculous reasons.. and I still blame
it on illiteracy..
As for
schools,
You will
pay double or triple what a normal child will pay but you have to provide a
shadow teacher, and your child must talk first..
What if my
child never talks, but she can excel in other aspects?
What if she
learnt how to write and can express herself then through writing? What does it
mean that you are a school that has a disabled section but you can’t take a
child who doesn’t talk? Isn’t this a kind of disability? And if I’m paying
triple what other parents are, why am I the one providing the shadow teacher?
And there
was another school, they said ok we will take her but you have to accept that
she will not meet all of the objectives.. if we have this understanding, then
ok we will take her..
I felt that
they won’t fight for my daughter, they will use her disability as an excuse for
their failure.. they won’t advocate for her..
G) Sports,
art, music, crafts and other activities..
Is there a
sporting club that provides trainers who can work with challenged kids? Are there
places that provide other activities for those kids? I guess you know the
answer by now.. NO
Or to be
fair, very limited..
To me, and
I’m a teacher, I believe that excelling in education is not the only form of
success.. more importantly I believe that sports and art and music and other
forms of activities is part of education.
If my child
can’t workout a mathematical equation but plays the piano, she’s successful..
God creates
a person to LIVE… we are built to survive.. every cell in our body is
programmed to keep us alive as much as possible.. and yet we insist on burying
these kids alive.. nothing is worse than living like the dead.. we provide
nothing for these kids.. there’s no outlet for them.. there’s no where to go..
they have a lot of energy and love and they’re still breathing for God’s sake
and we decide that they just stay at home cause they’re a waste of space.. They
stay at home because we don’t want to take an extra step to provide for them..
Doctors around the world are finding cures for deadly diseases to keep people
alive and breathing and we are failing to simply make ramps in malls and in the
street.. we are failing to make campaigns to spread awareness about these
kids.. we are failing them every day in every aspect..
I’m sure if
these kids can speak, they will say things that will makes us all ashamed of
ourselves..
A mother
told me once her child went back home from physical therapy and he was in his room
looking at his legs and talking to them.. he said the following “ I’m mad at
you cause you are there and you refuse to work, if you exist then you have to
do something” an 8 year old child said it all in a very simple sentence.. “ if you exist then you have to do something”
We are here
and we are refusing to work.. we are consciously making a decision everyday to
do nothing for these children..
We are not
teaching our kids compassion, and tolerating differences and helping a person
who might be weaker than us in some aspects but nonetheless learning from
them..
We should do
a lot more to integrate these kids on our society and trust me, it’s us who
will benefit from this inclusion.. we will learn a lot from them..