Hearing the voice of Moses
Maya mentioned in her dvar torah that she has special needs –though
I would argue her sense of an inability to sing is only a disability if Maya
believes it is! It’s often said that we in fact all have special needs of one
sort or another, we are just affected by them in different ways. Our
limitations are often placed on us by the world we live in, but it is not
uncommon for us to place limitations on ourselves, through our own fear and
doubt. Moses demonstrates this perfectly in this weeks Torah portion, trying to
convince God (not just his parents or a teacher) that he really can’t do the
task he has been called to. He has a speech impediment, which midrash tells us
was caused when Moses had placed hot coals in his mouth as a child[1]. But
we can learn a huge amount from Shemot about supporting those who may need more
support to achieve their full potential than others. If we are all given the
right encouragement and guidelines, and perhaps more importantly resources, just
as Moses is by God, we can overcome much that life has thrown at us.
And of course it isn’t just this week’s portion which tells
us of the Jewish imperative to support the vulnerable in our society, there’s
the obvious quote from Leviticus: “You shall not insult the deaf or place a
stumbling block before the blind” (19:14). But there are other imperatives too;
one of my favourites comes from Isaiah (56:5) talking about the Temple: “For my
house shall be a house of prayer for all people”. We need to not
just enable, but ensure our houses of worship, and the world around us, is open
to all, not just those we see.
In starting to think about these issues I sent a twitter
message on Thursday to a tweeter known as @BendyGirl who I follow and have
learnt a huge amount from. She suffers from a condition called Ehlers Danlos
Syndrome and blogs, in her words “about the highs & lows of life lived with
joints that dislocate as frequently as the British weather changes”. To leave
the house she needs an electric wheelchair, however to qualify for one on the
NHS you have to be wheelchair bound in your own home for 6 months. At home it
is good for her health to move as much as possible, so in walking at home, she
is precluding her opportunity to leave the house. She was incredibly helpful
and suggested in response to my unsolicited online message that I just give her
a call. Which I did.
It is clear that our responsibility, Jewish or otherwise, to
support the vulnerable in our society is not going well. You might even be
surprised to know that members of our own congregation are struggling through
the benefits system, and despite already living hand to mouth, are facing cuts
in Disability Living Allowance and Employment and support allowance. Proving
you need the benefits is becoming harder and harder, with those who are
wheelchair bound, likely in the new benefits which will replace the DLA to be qualified
as able to work as well as you or me, as long as they can propel the chair
themselves.
We all know cuts and savings need to be found, and it’s
important to note this is not a coalition problem, these cuts began to be made
under the previous government. But I was struck by something BendyGirl (whose
real name is Kaliya) made. In Nazi Germany, well before there were Jewish
pogroms and camps, disabled and mentally ill German citizens were rounded up,
and it was for them that camps were initially developed. And how were the rest
of the population convinced this was ok? They were told that these people were
an economic drain on the nation. Increasingly, as Kaliya sees it, our media has
been spearheading a campaign to convince us that the disabled are work shy
benefit cheats. In the last 18 months campaigners have noticed a significant
increase in hate crimes towards the disabled, and they are no longer referred
to as ‘spaz’ when attacked, but as ‘benefit scrounging scum’. In fact, only
half a percent of all disability claimants have been found to be fraudulent,
and yet to combat these false claims, benefits are being cut by, at the most
optimistic estimate, 20%. Deuteronomy (15:7) says “If there be among you a
needy person, you shall not harden your heart, but you shall surely open your
hand”. We need to start hearing not only the encouragement of Deuteronomy, and
indeed of today’s portion, but the voice of those like Kaliya, who feel
invisible (especially if they don’t have a wheelchair or white stick) and
incredibly vulnerable.
Disability campaigners are, on the whole, themselves
physically struggling, sick, and isolated. Moses’ inability to express himself
clearly is a useful metaphor for this, he had his brother, Aaron, to help him
along the way, and he became the greatest leader of the Israelites. With this
kind of support, three defeats against the welfare reform bill were achieved
this week in the house of Lords (cavod to my senior colleague in the
corner). Yet these cuts have been happening for a while, and will continue if
more isn’t said and done.
Maya, I know you are an incredible ally and support to your
mum, and many in the community are carers and supporters just like you. I have
seen and worked with some of you here as you struggled with eviction because
benefits couldn’t be processed when they were needed. As a community we have
felt the cuts in social care and allowances biting, and have this month been joined
in our professional team by a Social Care worker – Jo, who is helping us deal
with the sheer volume of work that is coming our way now that social services
are not doing their bit, or at least helping us to navigate the incredibly time
consuming beurocracy. What I hear from Kaliya, and from many other voices,
particularly on the web, where the housebound often have their only outlet, is
that people aren’t making enough noise about this. As part of her condition,
Kaliya’s larynx had collapsed when we spoke, making the parallel between her
and Moses even more stark – she, and so many others, need our voices, so that
they can cling onto the meagre benefits they have now. We need to support those
that we can, and be the voice for those who can’t raise theirs up loud enough.
Even if this doesn’t affect you directly, it is still our responsibility to
speak up for others.
And as a community we are also being given the chance to come
together to work to change how accessible we are through the Judith Trusts
Inclusion Campaign which is working with us to ensure we can reach out and
include, and I hope more of you will want to become involved in this training
as well.
Mishnah Sanhedrin (4:5) says that humans make coins, all from
the same mould, and they all come out the same. God, however, makes humans each
from the same mould as the first human, yet each of us is unique. We all have
unique skills and abilities, as well as challenges and disabilities. Maya, you
confessed to us what you struggle with, but you also demonstrated what you are
fantastic at. Everyone wants to contribute, but not everyone can do so in the
same way or to the same extent. I hope we can all learn from you about how to
be a support and a friend. I must confess, as a sister of someone with special
needs, I’m angry at what is potentially being lost both in care and in human
dignity, but as a Jew, and as a British citizen, who knows we can do better, I
am angrier, and I want us all to lift up our voices, in remembrance of Moses
who couldn’t.
Cain Yehi Ratzon
May this be God’s will
Venomar Amen.
4 comments:
What a wonderful sermon. Can you thank him from me? :)
today i wrote a song:
we would like to show the world an echo,
of things replacing strife,
alchemy heart and nourished soul,
and safecare for all.
sitting on a form singing for all,
to etcho a memory,
changing power hunger all the while,
instilling thoughtfulness.
could we get along and understand,
each others difference,
respect and care so others can,
believe in giving well.
Thank you so much for publishing this. The Rabbi has reminded me that many in our society do genuinely care about our predicaments. She has raised my spirits a little.
All we seem to get from the press and parliament feels like verbal abuse to me!
"All we seem to get from the press and parliament feels like verbal abuse to me!"
They are struggling to contain their hatred of the disabled and none more so than Cameron. Cameron's hatred of the disabled is so vitriolic that he even hated and resented his own son for being disabled because in his mind it was a disgrace to his own genes. The only use he got out of that kid was for PR purposes but I guarantee you, he was DELIGHTED when he died.
Post a Comment