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Member
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Join Date: Jan 2015
Location: IL
Posts: 279
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Member
Join Date: Jan 2015
Location: IL
Posts: 279
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I have traveled by air a lot (before CRPS but with a quadriplegic child as well as 4 'normal
children)...only twice since the CRPS (and both were before I was diagnosed)
I agree, pre-boarding is important. Also, a lot of airlines and/or airports will provide assistance transporting you (and any carry on) to the gate.
With my son, we always sat in the bulkhead...mostly because he was a spastic quad and would kick...constantly. But it was also easier because we didn't have far to get on/off the plane.
Going through security can be an issue if you have any pain pump/SCS, so make sure you bring the device card and show the TSA agents. My son always bypassed the scanner & went to a screening room.
As for the flight: my carry on's have always been a small bag with my purse and medication in it and a pillow with a throw blanket in the pillow case. Most airlines allow an additional carry on for medication/equipment. You can also request medication bags be inspected rather than x-ray'd and are allowed more than the '3 oz' of liquid medication (& don't have to baggie it), Make sure to let TSA know about it before going through the scanner.
I wear comfortable slippers and make sure to do as much ROM and small movements in your seat as possible. I also sit in a window seat, but that's because I like to plan which trees to fall on.
I am not sure if it was my first flare or if the air travel affected the swelling/discoloration when I flew before diagnosis. I was very apprehensive flying back but all went without any further problems. As a matter of fact, I experienced more pain traveling by car from LA to Reno.
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Believe in the Strength of Faith and Hope, within there is Peace and Love...Always ~pe
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