April 12th,2022 April 12th, 2022
Well. It is 3 weeks since the Botox injection and this what I have
experienced so far. The firs few days there was no noticeable change..Then
change began to take place but not as I had wished or expected.
The spasms began to be more frequent and stronger, more aggressive.
If I had to wee during the night, the spasms accompanied me while I peed
and even sometimes interfered with me while peeing, as the left leg would go
into a spasm lifting the leg up forcefully sometimes causing the urine to go away
from the portable urinal which I have been using because it takes me too long
with the crutches or walker to make it to the toilet on time.
The
portable urinal has been my salvation in my two rooms (office & bedroom).
When I am lying in bed or sitting at my desk, the spasms come about every 20
seconds, small ones, and only every once in a while a bigger one, stronger and
even from the toes all the way up to the hip and across the back. One gets a kind
of signal that it is time to pee and if you don’t move quickly enough your have
a problem. Part of the problem is that just then your leg will go into a spasm
and it won’t let you put your foot down on the floor. ,You may have to try 2 or
3 times before you manage to get the leg from the position that it has brought
the leg up to a 90% spot, and, in the meantime, the urine is not waiting. If you
don’t manage to get the urinal on time, some of the urine is already coming and
sometimes it is a lot and they you have to do some cleaning up and maybe even change
clothing.
I
sometimes complain loudly to God, God says you see that man over there, he can’t
even get out of bed, or that one over there in the wheel chair, with his hands
curled up. He has to be lifted out of his wheelchair. Would you prefer that?
Then I keep my mouth shut.But although I am still not happy, I can still take a
shower (even though even there the spasms come with me there), and I can get dressed
and even put my socks on…and I can still drive since the spasms don’t bother me
while I am driving. (My physiotherapist said that most of his patients can’t
even get out of bed.) I only drive to
the pharmacy to get my meds or to the supermarket to get a few things.A friend
takes me to my doctor’s appointments because it is too far for me to get from
the parking to the office in the hospital. A friend who usually come with him
will find a wheelchair so that I don’t have to walk all that way with crutches
of with the walker.
I was advised to continue my medication and my
physiotherapy (it was too expensive to continue with the professional physiotherapist,
so Brother Albert from the monastery comes to me every day, faithfully, to give
me my physio at 2pm. In the meantime I have been doing a lot of reading and checking
the news on the internet either on my computer or on my cell phone. Sometimes,
like now because of the constant rain, there is no internet.Quite often the
electricity goes off (usually so-called load shedding) but we have a stand by
generator so that we still have our own electrici
The
other day I drove my self to the barber shop for a haircut (it’s not far) and often,
on Sunday for lunch I will go up to the Pillay family (our church leaders) for
lunch and to ask how things are going at Savannah Park. It’s nice to get out of
the house once in a while.
From
time to time a friend will come to visit or to take me out for a lunch and that
also breaks the monotony..
We don’t
do much talking at the table in the dining room mostly because just abut
everyone is deaf and you wind up shouting to be heard, so its better to just
eat and be quiet.
I
thank you for your prayers and ask you to continue as I still have hope that
this Botox will do its thing.
It is very expensive and a cousin in the US has promised to help. The injection is supposed to last for about 4 months and then you need another one. If it gets to be too expensive we just stop. In spite of the spasms that accompany me whereever I go all day long, I am happy to be alive and still of sound mind, more or less. Ha. since the Botox injection and this what I have experienced so far. The firs few days there was no noticeable change..Then change began to take place but not as I had wished or expected.
The spasms began to be more frequent and stronger, more aggressive.
If I had to wee during the night, the spasms accompanied me while I peed
and even sometimes interfered with me while peeing, as the left leg would go
into a spasm lifting the leg up forcefully sometimes causing the urine to go away
from the portable urinal which I have been using because it takes me too long
with the crutches or walker to make it to the toilet on time.
The
portable urinal has been my salvation in my two rooms (office & bedroom).
When I am lying in bed or sitting at my desk, the spasms come about every 20
seconds, small ones, and only every once in a while a bigger one, stronger and
even from the toes all the way up to the hip and across the back. One gets a kind
of signal that it is time to pee and if you don’t move quickly enough your have
a problem. Part of the problem is that just then your leg will go into a spasm
and it won’t let you put your foot down on the floor. ,You may have to try 2 or
3 times before you manage to get the leg from the position that it has brought
the leg up to a 90% spot, and, in the meantime, the urine is not waiting. If you
don’t manage to get the urinal on time, some of the urine is already coming and
sometimes it is a lot and they you have to do some cleaning up and maybe even change
clothing.
I
sometimes complain loudly to God, God says you see that man over there, he can’t
even get out of bed, or that one over there in the wheel chair, with his hands
curled up. He has to be lifted out of his wheelchair. Would you prefer that?
Then I keep my mouth shut.But although I am still not happy, I can still take a
shower (even though even there the spasms come with me there), and I can get dressed
and even put my socks on…and I can still drive since the spasms don’t bother me
while I am driving. (My physiotherapist said that most of his patients can’t
even get out of bed.) I only drive to
the pharmacy to get my meds or to the supermarket to get a few things.A friend
takes me to my doctor’s appointments because it is too far for me to get from
the parking to the office in the hospital. A friend who usually come with him
will find a wheelchair so that I don’t have to walk all that way with crutches
of with the walker.
I was advised to continue my medication and my
physiotherapy (it was too expensive to continue with the professional physiotherapist,
so Brother Albert from the monastery comes to me every day, faithfully, to give
me my physio at 2pm. In the meantime I have been doing a lot of reading and checking
the news on the internet either on my computer or on my cell phone. Sometimes,
like now because of the constant rain, there is no internet.Quite often the
electricity goes off (usually so-called load shedding) but we have a stand by
generator so that we still have our own electrici
The
other day I drove my self to the barber shop for a haircut (it’s not far) and often,
on Sunday for lunch I will go up to the Pillay family (our church leaders) for
lunch and to ask how things are going at Savannah Park. It’s nice to get out of
the house once in a while.
From
time to time a friend will come to visit or to take me out for a lunch and that
also breaks the monotony..
We don’t
do much talking at the table in the dining room mostly because just abut
everyone is deaf and you wind up shouting to be heard, so its better to just
eat and be quiet.
I
thank you for your prayers and ask you to continue as I still have hope that
this Botox will do its thing.
It is very expensive and a cousin in the US has
promised to help. The injection is
supposed to last for about 4 months and then you need another one. If it gets
to be too expensive we just stop. In spite of the spasms that accompany me
whereever I go all day long, I am happy to be alive and still of sound mind,
more or less. Ha.
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