My experience of MRIs... | ryuuzaki's Blog


This is my experience of having my first (and, hopefully, only) MRI scan.  It was not greatly pleasant...

 

I was sent a leaflet in the post that told me what to expect.  I was to arrive at the hospital at 9.50am where I would sign consent forms and be told about the proceedure.  I would be made to change into a gown and possibly injected with something that would show up better on the scan.  I would then undergo a 20-45 minute scan.  Finally, I would be allowed to change and receive another little pep-talk before I went home.  The proceedure would take about an hour and a half in total.

 

Here's what really happened.

 

I reached the X-Ray ward at 9.50am.  I signed some consent forms.  Then I sat in a waiting room for 10 minutes.  I was taken to a cubical and given a gown to change into and told the nurse would be with me in about 5 more minutes.  I was alone in the cubical for an hour because the MRI scanner broke down and they kind of forgot about me.  Then I was taken to the scanner and given a 30 minute scan with no prior talk or explanation.  I was then given my clothes and told that I could go home because I wouldn't get any results for about two weeks.

 

The scan itself was singulary unpleasant.  Calling the scan claustrophobic was an understatement.  My nose was about three inches from the ceiling of the tunnel and my elbows easily touched either wall.  It made very loud mechanical noises that made me feel as though I was trapped in a dot-matrix printer.  They tried to cover these noises by piping in rubbish pop music, so honestly I would have preffered the mechanical noises...

 

I was pretty unimpressed by their whole treatment of me.  I even told the nurse that I was very scared by the thought of the machine when I was going in, but they didn't seem to care.  Here's hoping that I never have to have another one...

My mood: extremely morose
My health: been better

This Blog Entry's Comment Board (4 comments)
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Posted on 08:15AM on May 20th, 2009
At least this is now behind you. Bit sad so many things went wrong or at least not according to plan. And can imagine how you must have felt inside a mechanical and noisy machine that's doing invisible things to your body. Wonder why they don't give people a choice of music? And what's wrong with just relative "silence" as you say? Having to wait 2 weeks for the report also seems rather rich. Makes me glad to be in Oz - my experience in recent years with several medical "procedures" has been very straightforward and uneventful. But that doesn't help you. Again, best wishes, hang in there, and I hope it's much ado about nothing - or very little.
Posted on 05:37PM on May 20th, 2009
The time is the thing that annoys me most. Doctor D said that if I wasn't treated quickly, I'd run the risk of damaging my vision permanently, yet it will have been almost eight weeks since I was diagnosed by the time my test results come back. I wouldn't really call that quick. Especially as I've already lost some depth perception and I'm hoping that isn't permanent...
Posted on 10:18PM on May 20th, 2009
Have you checked on the web abt the urgency? I've found that doctors often say something is urgent, but it ain't necessarily so. Genarally (and again in the Aust health system) when something is really urgent (eg cancer diagnosis) the system moves people through quite quickly. But I realise that with what you've been told it must be very annoying.
Posted on 05:40AM on May 21st, 2009
I'm not sure how "urgent" urgent is. On the net, all I've found out is that papilledema is usually without symptoms in its early stages, but as it progresses it leads to the blurring and blind spotting that's permanent if untreated. I guess it will be fine unless I suddenly develop these symptoms. It was just lucky that my optician spotted the swelling when he did as it looks like papilledema is a fairly rare condition...
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