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It sounds as if many Sll/Cllers travel. When I was

diagnosed in Jan 2011, one of my assumptions was I couldn't

get on a plane to travel d/t a compromised immune system. I

used to get sick sometimes when I flew with a healthy immune

system. Anyone have advice for traveling with SLL/CLL?

Thanks,

Peggy

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Peggy,

Since I am post-treatment and still very immunosuppressed,

my hematologist provided ongoing prescriptions for

acyclovir, fluconazole, and SMZ-TMP. These 3 medications,

taken prophylactically, provide (likely) protection against

viral, fungal, and bacterial infections to which CLLers are

vulnerable. I also travel with a 5-day dose of Tamiflu.

Regards,

Tim Klug

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Peggy

This topic is well covered in the archives and others have

their personal tips

A well fitting N95 mask, hand sanitizer, and a seat in first

class (or at least away from cougher) is your best

protection. Some like an antibiotic ointment at the entrance

to the nasal passages. The only one that I believe that has

been proven to help in a controlled study was the first

class seat.

I and many other CLLers travel all around the world. I

always take Levaquin and Tamiflu and a note from my doc

about my CLL and my meds

Be well

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I always wear a mask. The N95 masks can be uncomfortable,

so one tends not to wear one. Stanford's BMT patients wear

a double filter respirator like this:

http://tinyurl.com/6cghgql

3M makes it. It is very comfortable for long-term use, but

everyone will stare at you. So what!

I wear a mask every time I fly. The worst I've ever gotten

sick was on a full Southwest flight from San Diego to

Sacramento. I ended up in the hospital for five days.

It's the mask from now on. I feel vulnerable without it.

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