I am good at advocating for myself and getting my needs met,
in all venues of my life. I knew that
travelling would exercise those skills, but I honestly didn’t worry about it
very much. I am very, very familiar with
FAA and TSA regulations and how they apply to someone travelling with a chronic
illness/ medical device/ lots of medication.
The bottom line is that they are required to accommodate you provided
you have the appropriate documentation. Which
I have. In spades.
I called my airline last month and explained that I had mast
cell disease and required several accommodations. These accommodations included a wheelchair
from ticketing to the gate, gate checking my larger suitcase (which also
contained medical supplies), boarding early so that I could administer IV meds
and set up my infusion, and that I needed to infuse for the duration of the
flight. The person I spoke with was
extremely helpful. She asked some questions
about my infusion pump and the volumes and types of medications I would be
bringing. She asked that I bring a
letter from my treating physician stating that these medications needed to be
with me while travelling and that I needed to infuse for the duration of the
flight. No problem.
I arrived at Logan Airport and had a very painless
experience. They opened up all my bags
and swabbed my hands and my meds for explosives. They patted me down. They were very courteous and helpful. When it came time to board, I was the first
one on the plane and was happily infusing fluids when we took off. It was really easy.
Then I arrived a week later for my return flight and it was
a mess. It made me really mad, especially in light of
my previous positive experience.
The first problem was with gate checking my bag. I explained to the agent that it had medical
supplies and she tagged it appropriately and said it was all set. Then another agent came up to me and told me
that I couldn’t gate check my bag because it was too big. I told her it contained medical
supplies. She argued with me. After about two minutes, I told her again
that it contained medical supplies. “Oh,
well you didn’t tell me that!” she exclaimed, rolling her eyes. Whatever, lady. Gate check my bag.
I got on the plane and pulled out my stuff to give IV
meds. A flight attendant came over and
told me to put my backpack containing my infusion pump and meds under the
seat. I told her that I couldn’t because
it was going to be attached to my body and I didn’t want there to be tension on
the IV line. I told her that I had
spoken with the airline and that the infusion pump/meds are not considered
luggage and can be with the passenger in their seat. “The FAA isn’t going to let you do that,” she
said. I explained that I had infused on
the flight from Boston to Seattle. I offered her documentation and she talked over me. “Well,
you can let me know when you’re done and we’ll take off then,” she told
me. “It’s an eight hour infusion,”
I told her. She shrugged and walked
away.
A few minutes later she came back
and told me that “the FAA sees things like this in black and white, and [I] can’t
expect them to see things in grey because of people like [me.]” I didn’t reply and she said, “I’m trying to
be sensitive here.” I do not think that
word means what she thinks it means.
So I didn’t start infusing until I was flying. This is important to the story. When I started infusing, I noticed there were
a lot of bubbles in the PICC line extension.
I realized that the extension was cracked and air was getting into the
line. This is very bad. I stopped the infusion and had to trouble
shoot the situation at 30,000 feet where I couldn’t just call my IV service and
ask. The fact that I couldn’t start
infusing while on the ground turned a manageable situation into something very
scary.
While I was trying to identify the best course of action,
the lady came over and asked if I felt okay.
I told her that I feel like I always feel. “Do you need help?” she asked pointedly. I just looked away. Her behavior was making me mad, which was
causing me to react while I was managing this situation. I was really not amused.
I ended up disconnecting my extension and connecting the infusion
directly to the PICC line without a clave to keep the end of my PICC line
sterile. This required some changing of
hardware in the obviously less than sterile environment of an airplane. I kept the clamps on the line and did not
infuse fluids, which guarantees me a bowel obstruction in the next day or two, which guarantees me anaphylaxis. I bought Wifi and
messaged all of my PICC knowledgable friends because I didn’t know what else to
do.
I’m now going to have to have a conversation with my doctor
about this in the morning and the line will almost certainly be pulled and a
new line put in because of infection concerns.
After I had to have IV meds administered to me by my friend (since I can’t
access my PICC line without an extension), I put the cap directly on the
line. It is unusable until I get someone
to come out to my apartment and fix it. Thanks,
airline lady! I was so hoping to have
more surgery this summer. I also really
enjoy having a line for emergency meds that I can’t use.
The really unfortunate part of travelling while you’re sick
is that it doesn’t matter if you know your rights if everyone else doesn’t know
them too. This woman’s behavior put me
in danger. It remains to be seen if I
get a central line infection, but at the very least, she made it a serious
possibility. I am going to get a bowel obstruction because of this situation, which is massively painful and causes anaphylaxis. This is unacceptable. I don’t want this experience for anyone
else.
I am reaching out to the airline and hope they will do
something about this. I will keep you
all posted.
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