I’ve always thought this illness (my SCA) has taken away everything in my life, namely; my
- Passion
- Personality
- (Potential) Partner.
My Passion was theatre. It allowed me to express myself with my voice and body; the 2 elements that are now disintegrating everyday due to this horrific illness.
My Personality was that of an extrovert. I liked making nonsensical (but hopefully funny) remarks, joke and “flutter” around during social settings. I enjoyed socialising very much but now I feel repressed, because I’m unable to do what I used to like.
A (Potential) Partner was definitely on my list ‘to get’. Well, I used to be quite the hopeless romantic and it was pretty much impossible for me understand “celibacy” or end up without (the) one.
BUT
God, being God and super great (read: gracious) replaced ALL of the above in my life by knocking His sense into me... His invaluable P!
Yup, His PERSPECTIVE!
My previous Ps, now with this renewed PERSPECTIVE He has granted me have shifted so dramatically:
Firstly my Passion should be for Him and His Plans & Purposes. So, if its not theatre now (or anymore), it must be something else. I’d just have to wait for His leading to find it!
Secondly He is my creator so He definitely knows (& values) my limited Personality. It could now be time to develop the introvert in me - then I’d be perfect! For Him.
Lastly my desire for a Partner has been eliminated & I’m amazed and super thankful for this miracle. Actually it’s very hard to imagine having to manage another relationship in my life given this condition of mine.
While enjoying these new Perspectives I’ve been granted, I’m also delighting in another P of His everyday.. His Power! Yes, I experience this at every moment whenever I ask for help every time I need to overcome any inconvenience this illness brings me. :)
Tuesday, 29 January 2019
Tuesday, 1 January 2019
End of 2018
The year has ended.
But it doesn’t end there for many of us. Things keep rolling on (and on, and on...) especially His blessings!
Many of us must be feeling so blessed at the end of the year (like me!) Idea:
My word for 2018 is LOVED. Here’s just a reminder for everyone (myself included) to keep the blessings flowing on, remember we’re blessed to be a blessing!
Sunday, 9 December 2018
Things I'm too embarrassed to admit I like
- Scrubs
- Harry Potter
- Starbucks Toffeenut Latte
Lets get to the point. So. These are scrubs.
They’re what medical staff wear in surgery. People have fetishes for uniforms etc but mine’s simple scrubs okokok?
The irresistible mystery of those flickering eyelashes plus extremely enchanting eyes behind the surgical mask (often worn together with a scrub) creates such magic for me.. the simple V neckline reveals a glimpse of often well-defined collarbones which are oh-so-charming. Hee hee so me liketh scrubs (very much)!
BUT.
One’s supposed to be unflinchingly serious in that medical context. Who has time for frivolous fetishes or damning desires?? So cannot like.
Ok. Harry Potter. He’s meant for younger folks. JK Rowling must be targeting the lower age group so I am too old. It’s very unbecoming of me to believe in magic too.
Starbucks is just too expensive and commercialised. As a self proclaimed coffee connoisseur, thou shall not enjoy any form of Starbucks.
But I only like Toffeenut Latte that’s only available near Christmas so that’s ok right?
Actually, many might already know that Christmas is not just about Toffeenut Lattes, pretty Christmas trees/lights at Orchard Road or even thoughtful and/or expensive gifts.
IT IS THE DAY JESUS WAS BORN.
That’s the greatest gift ever. As believers, we Christians must always remember why we celebrate Christmas (we can rouse / appeal to others to celebrate with us BUT let us all not be overcome with the festivities or hype of the occasion that we forget the true meaning of Christmas!
Wednesday, 10 October 2018
What good is there in this?
“this” refers to my SCA (Spinocerebellar
Ataxia). I’d never ever wish this horrible disease on anyone (not even my worst
enemy – actually I don’t have one) because its symptoms are really too terrible
to deal with every day, at every moment, every second.
ANYWAY. What good is there in this?
Right now, I can think of 3 things:
1)
CLOSER TO GOD
2)
CLOSER TO FAMILY
3)
CLOSER TO FRIENDS
They happen to be all Cs’!!! Recently I’ve
also been thinking about the essential Cs’ in my life (quite far from the
typical Singaporean’s Cash, Car, Condominium, Credit Card, Country Club – think
maybe it should be a Career and/or Clever Children nowadays hahaha).
So, my five Cs’ are
Christ
Coffee
Curry/Chili
Chocolate
Connections (to people)
As I was saying (before I rudely
interrupted myself), I’m definitely
1)
CLOSER TO GOD
There are a lot more pockets of free time
where I can seek God, find Him & talk with Him. It’s certainly easier for
me to fit God into an emptier schedule; daily bible reading combined with a
regular feeding of Christian literature becomes very unrushed, ‘second-nature’
and comfortable. Not to mention it is often very enlightening, an encouragement
to the heart and soul. This two-way relationship where He speaks to me as I listen & talk back
is certainly being strengthened day after day.
is certainly being strengthened day after day.
2)
CLOSER TO FAMILY
I have two older brothers; my eldest
brother is also struck with this disease and is currently living in a nursing
home, my second brother is married to a very virtuous, respectable & nice
woman I’d affectionately term as my SIL (sister-in-law). Oh, my father passed
away when I was 10, my mother brought 3 of us up single-handedly.
I thought I was already very close to my
Mom, at least that was years ago… 2009 to be exact, when we went on a family
trip to Hong Kong (was together with my second brother & a pregnant SIL).
See Mom & I:
Then my niece was born. Things changed. At
least, that was how everything appeared to me. I found myself trying so hard to
please Mom & earn her approval or gain some acknowledgement/recognition…
But as nothing seemed to be working, I
began to accept that it would probably be impossible for me to regain my
previous favoured position as her ONLY daughter and I backed away.
Fast forward years later, now with my SCA.
Niece is much older (more matured, less affectionate).
I think Mom and I are still figuring out
our roles (mother-daughter, caretaker-patient, fellow believers) and our daily
interactions with each other on a 24-hour basis but I must say that we are
currently building a well-weathered relationship through this ‘storm’.
3)
CLOSER TO FRIENDS
I believe it’s the same idea as having more
time now to focus on building closer relationships. With this SCA, it becomes
so much easier for me to discern who has been/will be a waste of my efforts and
energy at strengthening our bonds and who will certainly stick around and be
TOTALLY WORTH IT.
You’d know who you are if I’ve been “a bother”
or I’ve bothered to be in your life (texting you quite a bit, be it serious
conversations or random riddles/jokes/pun-ny stuff that classify as rubbish, sharing my favourite food, celebrating
your birthdays, buying you gifts, inviting you over to my humble abode…)
YEAH YOU ARE IN MY INNER CIRCLE :)
YEAH YOU ARE IN MY INNER CIRCLE :)
Wednesday, 12 September 2018
The 'Tyranny of Normality'
‘NORMAL’ was something I kind of despised
when I was younger (& undiagnosed). I’d always remember this conversation I
had with my student(s):
A student(s): Miss Lee, you are so…
hmm… (uncertain) strange!
Me: THANKS FOR SAYING THAT! I hate
being just ‘normal’. (big grin)
Well I certainly enjoyed being different! It
was not just my dress sense I suppose, think it was everything else I could
manage then – even my fingernails & toe nails! I remember doing a lot of my
own prettifying (read: Sally Hansen ‘Salon Effects’). See some of my DIYs
below:
So in terms of my dressing, I was also into
wearing neon colours, bold prints, asymmetrical designs featuring cut-outs and
extra layers with “cool’ looking folds etc. Yes, I was vain. VERY VAIN.
Therefore, in conjunction with that, my attitude
and behaviour in/outside of the classroom as a teacher must duly be LOUD &
PROUD. Ha ha~
But now, I work SO VERY hard everyday to be
‘normal’.
I’d like to appear as normal as possible
despite my ataxia. However, it’s not easy for me not to draw attention to myself
with my wheelchair, incomprehensible speech, incontrollably loud choking (on
top of my retarded eating) and occasional breathlessness.. oh there are other
countless symptoms regarding this ataxia but I shall not elaborate on them yet.
I might do so later…
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