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7th Anniversary - 10
October 2007
My dear friends
Friday 5 October marked the 7th
Anniversary of the day I was diagnosed with Motor Neuron Disease. Back then, who would
have thought that seven years later I would be retelling the story this side of the
sunset? Indeed, God's ways are unsearchable!
My thoughts took me back to that morning at
St Augustine's Hospital in Durban when the neurologist sat me down in a private room and
broke the news to me. It was more of a confirmation of bad news than a surprise since
there were indications along the way that the symptoms I had pointed to some serious
disease.
The previous day I had taken time to talk to the
Lord and I pleaded for the grace to accept the outcome of the extensive tests I had
gone through. I must admit that the difficult part for me was to be told that there was no
medical cure for MND and whatever else I tried would be to no avail.
In the early days of my illness a friend who like
many others could not bear to see what MND was doing to my body told me that she had
prayed, "Lord, heal him or take him." Well, seven years down the line God has
taken neither of the two options.
Truth be told, many of us would like to see the
miracle of restoration but so far it has pleased the Lord to grant us the miracle of
sustenance in an impossible situation.
During my last visit to Europe in May 2001 a
sister in Germany made an interesting comment about my size. To her I was a 'halbe
Portion' (half portion) of the Fano she knew. I guess that today she would most probably
rate me at 25%.
Yes friends, MND has played havoc with my body.
There is nothing exciting about living in a totally paralysed body, incapable of making
any movement or sound. Who would choose to be pinned down to a bed, fixed to a ventilator
and under intensive care for 24 hours a day?
On the other hand, MND has come with invaluable spiritual blessings that sometimes I
wonder if I would have received them in any other way. Our finite human mind would never
fully grasp God's mysteries but when He in His grace gives us a glimpse of some of His
treasures our hearts are filled to overflowing.
One of the convictions that was impressed on me
in the early days of my illness was that 'it ain't o'er till it's o'er.' I have
to keep going, I have to press on till it is over. Somehow I believe that the
Lord is writing a book about my life; only He knows what and when the last chapter will
be.
At this late stage of MND I am learning to live
one day at a time. With my daily long list of things that I would like to share
I have had to accept that my health condition places severe limits on my activities.
Some days at the end of the day I look back and
marvel at how much I could tick off my list. Then there are days that would
cause some people to say, "This was not my day." Days when I am extra weak, the
computer refuses to co-operate or I am delayed by too many interruptions (or, are they
interruptions?) When clouds of frustration threaten to darken my soul I remind myself of
what a late senior colleague said to me next to my hospital bed one day, "Izinsuku
azifani mntanami" (Days are not the same my child).
When during late evening hours health and time
constrains overtake me I am forced to call it a day. As my carers pack away my computer I
am often reminded of the last verse of a song that we sang at Dlangezwa High School
and later with the KwaSizabantu Men's Choir:
"When from earth, Thou,
Lord, shalt call me,
Calm Ill lay my burden down;
For I know, whateer befall me,
Thou remainest, Christ, my crown."
When I wake up in the morning the enemy strikes
by reminding me of my physical condition. I respond by acknowledging that I face a big
challenge but add that there is nothing new about that. What is new is that I am being
given yet another day.
Yet another day to walk on.
Yet another day to toil on.
Yet another day to press on.
"I press on towards the goal to win the prize for which God has called me
heavenwards in Christ Jesus." (Philippians 3:14)
Have a blessed week further.
Pressing on!
In His love
Fano Sibisi
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