One day earlier this week, I was
on the way into church on the bus. On the journey I found myself standing, as
the seats downstairs were mostly taken. Standing can sometimes be a problem for
me because of my MS. It is difficult to explain (or even understand… for me
too!) but the experience of standing can be debilitating and result in energy
depletion, heavy limbs and muscle aches.
Although most of the seats
were occupied, there was one seat… one of the ones for those who are elderly or
disabled… I kept standing.
Was it pride? Well, perhaps…
But I think it was also
because I do not APPEAR ‘disabled’. I did not have a walking stick that day (although
I do occasionally use one) nor any other outward indication that I am ’disabled’.
And yet I AM ‘disabled’. In fact, one recent (and rather surprising) discovery has been that the very fact
that I have MS categorises me as ‘disabled’ in the provisions of the 2010
Equality Act. But even forgetting all
that, I know that standing for long periods is a problem, energy depletion is a
BIG problem, cognitive function can sometimes be a problem and so on and on.
(I will spare you some of the
further symptomatic details which restrict but which are not visible)
And, as if that were not
enough, I also have a second chronic condition more recently diagnosed and rather
more difficult to talk about. Three months ago I was diagnosed with Ulcerative
Colitis.
Once again, I will not go
into all the gruesome details except to say that there are very real
restrictions caused by both my conditions, that they both are causes of fatigue
and energy depletion and that neither of them
looks as though they are doing anything other than getting worse!
But, to the outward observer,
I seem to be the picture of health!
Which is, of course, why I
find it is difficult to choose to sit on these disabled seats on the bus!!
And so back to that morning a
few days ago… After the bus journey for which I stood all the way, when I
reached St Cuthbert’s we were about to begin our monthly lunchtime Bible Study
based on the passages for the next Sunday’ services… and if you have looked
ahead, then you will know that the Gospel passage on Sunday is about the
daughter of Jairus and the woman who had been bleeding for 12 years.
We cannot be sure, but I
think we may assume, that the woman who touched Jesus’ robes would not have
been obviously ‘disabled’. Her condition and its symptoms would likely have
been ‘invisible’ to others.
I saw the connection.
But I was not just thinking
of myself, but of the many (very many!) friends, family members, congregational
members (past and present) and pastoral contacts who have conditions (physical,
mental or emotional) that are not outwardly ‘visible’.
Let me be quick to say that
those of us who have less visible disabilities often do not face the challenges
of those who are more ‘obviously’ disabled. The very invisibility tends to
mean (in most cases at least) that we do not face the same physical challenges.
And we are not generally subject to such discrimination and prejudices as still
exist in our society with regard to the ‘disabled’.
While for many people with
MS, the effects of the condition are very evident and visible, for me and
others they are not. And there are many others who have disabilities that may
not be visible, but are nonetheless debilitating, challenging and awkward to
cope with, and which put real (and often permanent) restrictions on life. I am thinking
of the likes of dyslexia, inflammatory bowel disease, autism/Aspergers,
depression, anxiety, and so very many more…
Both the Church and society
have moved far in terms of support, inclusion and attitudes to those who have disabilities.
But there is still a distance to travel.
Perhaps one thing we could still try
to do is find an alternative description to ‘disability’ (and please not ‘differently
abled’!) And another is to work harder at ensuring that being ‘disabled’ does not
automatically imply that we are also considered as ‘disqualified’ from certain
jobs, positions or roles.
After all, in the ‘West Wing’,
President Bartlett seemed to do a pretty decent job in spite of his MS! Just a
pity he had to start off hiding it!
But none of all these musings
resolve my problem with taking a disabled seat on the bus! Perhaps I should just
carry a walking stick as a matter of course…