11 Tips For Traveling With ME/CFS or FM

Traveling long distances with ME/CFS or FM -process adequately. This is especially true when
most of us avoid it at all costs! It's just too muchyou're traveling...
for our bodies to handle!... the noise of the train, bus or plane, the chatting
I had the very same opinion because I was (andpeople, the fast moving countryside outside, the
still am) largely housebound due to Post Viralthrong of other travelers...
Fatigue Syndrome (also known as ME/CFS). ButAll of this can play havoc with your brain and can
as a result, I had forfeited seeing my belovedend up making you feel even *more* exhausted,
family (who live abroad) for four long years. Soand your brain even *more* foggy!
recently, I decided to 'bite the bullet' and go. PostThere's not much you can do about this. But say
Viral Fatigue Syndrome or not.you're on a train for example - if the fast moving
I had a lovely time there, but the voyage therecountryside is making you feel dizzy, then try to
and back raised quite a few issues for me as aavoid looking out the window. Close your eyes if
sufferer of Post Viral Fatigue Syndrome.you have to, or wear a sleep mask. If you find
When it comes to ME/CFS no one sufferer hasthat you're getting dizzy and tired when you're in
the same experience as the next. For a start,a busy corridor full of commuters in the subway
you may suffer from this condition less or morefor example, stop and face the wall for a few
severely than I do. You probably also experienceseconds to regroup and regain your clarity and
a different mix of symptoms. But there are abalance.
few things you can bear in mind if you do plan on10) Wear some magnetic insoles.
making a long trip:I had made it a point to see my Nutritionist/
1) Rest adequately beforehand.Kinesiologist before I left for my trip abroad. She
This might mean not exerting yourself mentally ortested me with all the supplements I took daily,
physically for a number of days or even weeksand found that the 'Pure Synergy' superfood
beforehand - easier said than done, I know. Butpowder really raised my vital force (see point 11
bear in mind that resting is a BIG priority PRE-trip.below).
2) Plan your trip.But perhaps even more astounding was the
Leave LOTS of time in-between train, bus ormagnetic insoles she gave me - they raised my
plane times so that you don't have to rush.vital force so much that at first, it literally felt like
**Over-estimate** the amount of time it will takeI was standing on a power pod! I could even feel
you. That way, if you get there early you cana subtle tingling sensation in my legs!
just sit and rest instead of rushing and stressing,I wore my magnetic insoles on the trip and I
which will only make you feel more weak and ill.have to say that I *did* feel more energized! It's
3) Get help.a very subtle feeling and after an hour or so of
If you're making a long trip then it's advisable thatusing them the tingling went away. You may or
you ask someone (like a relative or friend) tomay not have the same sensations when you
accompany you there and back. Ideally this wouldfirst try them - depending on how severe your
be someone who understands your condition andME/CFS is and how susceptible you are to
how it affects you. If you have trouble walkingexternal forces. But they're well worth a try. I
(or if this wears you out too much usually) thennow make it a point to wear my magnetic insoles
consider asking someone from the train or planewhenever I have to venture outside and now
company to meet you with a wheelchair. Mostthat I know how much they help me, I most
large commercial companies seem to offer thiscertainly wouldn't be without them.
service, but you usually have to tell them in---------- SIDE NOTE ----------
advance. You might also consider using a walkingYou can check out my full review of wearing
stick. Anything to help you get there in one piece,magnetic insoles here:
right?---------- SIDE NOTE ----------
4) Don't rush.11) Perhaps most importantly, pack some
Pack slowly. Don't leave it until the last minute! Inourishing food and supplements specifically for
had an open suitcase in my bedroom in which Iyour voyage.
put things as I thought of them. I also made aIt's important to eat small amounts regularly
check list for the morning of the trip, so that Iespecially when you travel. It's not a good idea to
didn't forget the things that I needed to packeat sugary foods or anything containing caffeine
after using them that morning (like toothbrush,(including coffee, tea, sweets or chocolate)
toothpaste, tablets etc).because although that may pep you up for the
5) Pack light!first few minutes, they are likely to make you
If you're going on a short trip, then maybe youfeel a lot worse in the long term.
can get away with not packing any luggage at all?I took a few of Dr Gillian McKeith's 'Living Food
----- SIDE NOTE ----- If you're traveling to aEnergy Bars' with me - I always keep a spare
different time zone, consider taking some earone in my handbag for emergencies anyway. Nuts
plugs and a light-blocking sleep mask with you,are also a great idea when you're traveling (if
just in case you need to sleep during the day. -----you're not allergic to them that is).
SIDE NOTE -----I also took some of that amazing 'Pure Synergy'
6) Don't forget to pack your medicines, vitamins,superfood powder, and mixed it in with some
and supplements!cooled herbal tea in a small bottle. No sugar. No
Don't make the mistake of not packing enough.caffeine.
Count out how many tablets you'll need just toIt was my energy pep-up drink - and I swigged it
make sure.all the way back on my voyage. It did the trick.
7) Warn the people you're going to be staying---------- SIDE NOTE ----------
with about your needs.You can read my in-depth review of Pure
This may be your family, friends or the hotelSynergy here:
manager. Let them know about your sleeping---------- SIDE NOTE ----------
habits and your dietary needs. Is there anythingSo there you go - eleven things that will help to
you *can't* eat or drink? Caffeine or dairy, formake any long trip less stressful and exhausting.
example? Should they get some special food orBon voyage!
drink in like say, soya milk?Copyright, Claire Williams, 2003-2005. All Rights
8) Bring a book on ME/CFS with you just in caseReserved.
the people you stay with are interested in your** Publication Guidelines **
condition.The article above may be freely reproduced
If you have ME/CFS then I really recommendprovided that:
Lynn Michell's book 'Shattered', because it really(1) you only mail to a 100% opt-in list; (2) ALL
explains what it's like to live with the condition.links are LIVE hyperlinks (3) the article is published
AND it packs a punch - just in case you face anyin its entirety including the title, copyright notice, &
skepticism while you're there! No need to startthe author's bio & resource box (which must be
explaining yourself - just hand them the book. ;)placed directly below the article).
---------- SIDE NOTE ----------Claire Williams is editor of sleepydust.net and has
To read a complete review about Lynn Michell'ssuffered from Post Viral Fatigue Syndrome since
book, visit:1995.
---------- SIDE NOTE ----------She created sleepydust.net to help ME / Chronic
9) Sensory overload.Fatigue Syndrome and Fibromyalgia sufferers deal
When you suffer from ME/CFS, visual and auralwith their condition - from handling their money
stimuli can be too overwhelming for your brain toworries, to recovering from their illness...