Okay, so guess what? Yours truly has been on a winning streak lately. Not in monetary terms, but in terms of being sick. I’ve been diagnosed with a disease that is usually apparent in children, & yes you’re right, it’s HFMD.
LIKE WTF?! SERIOUSLY?! How in the blue world did i get that?! Must be from one of the kids that i came in contact with at work. Considering the fact that my work area is pretty open and exposed, makes me more susceptible to all these viruses. First was H1N1 last time, and now this? Le sigh. i think i need to build up on my immunity. Gonna battle all these flu bugs and viruses with a Redoxon a day!
Oh and i must express my unhappiness on the treatment that i received at CGH. To begin with, my impression of CGH has never been under the favourable light. Reason being, i’ve heard far too many stories on the poor services provided to the patients and how the doctors and nurses there seem to be uncertain of their job scope or even giving proper diagnosis.
& so on thurs i went to my GP and was referred to CGH A&E because the GP felt like it wasn’t the usual HFMD and wanted me to seek a second opinion, preferably from a skin specialist. But unfortunately it was fully booked, but i still decide to make my way to CGH to see if they could squeeze me in a slot. As usual, A&E makes you wait for hours , & i waited for a good 1 and a half hours before consulting the doctor.
The first thing the doctor asked me was ” So what’s wrong with you?” & his tone wasn’t even empathetic. It felt like he was asking for the sake of asking and seemed completely uninterested in the patients. & so i went on telling him i had suspected HFMD. He then began to ask me a few questions then went off without excusing himself. So i was left sitting there for 5 minutes before he came back with another female doctor. Had to repeat my whole story AGAIN and then the doctors just did some checks on my mouth and said “okay, yes this is HFMD. There is no medicine so you just need to go home and rest, we will give you one week of MC”.
I was like okayyyyyy, so is there even any painkillers to help ease the pain because the blisters on my feet are hurting to badly and it doesn’t even look like the ones a typical HFMD patient should be getting? It felt like i had to keep asking before they would actually give me something to ease my discomfort. But all i got was just paracetamols, calamine lotion & bonjela. With that, i slowly made my way home, limping.
4 days later, my blisters on my feet got worst. It was so bad to the extent i couldn’t even set foot on the ground. Or if i really needed to, i had to tip-toe. So my folks decided i should seek a second opinion again since it doesn’t seem to be getting well although the spots on my hands were fading and the ulcers in my throat were almost gone. This time we went to NUH A&E. & i should have gone there straight in the first place.
The doctors and nurses there were very professional. The way they speak and analysed my situation, you know that they are not just bullshitting you and trying to get you out of the place asap just to clear the queue. They gave me a jab on the butt to ease the pain for my blisters , did a blood test and gave me oral medication for my blisters. & i felt much better almost immediately after the jab. The pain was minimal and i could walk, although i still had to be careful not to burst the blister.
NUH is still the best. Even though it’s far, i think in future i’d just head straight there instead of going to any other A&E. Besides, they’ve got all my records stored. Lesson learnt – Never go to CGH.
Keeping my fingers crossed. Really hope the blister will subside after 5 days. I’ve my exams on sunday and i’ve a trip to HK next wednesday! I can’t afford to miss it 😦 have been anticipating it for so longggggggggg.
Okay, back to the books. Enough time wasted ranting.