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What
Can You Do For Me?
Well, I'll Tell You!

by Trisha Tester
I am a metastatic breast cancer patient. Although this means that I
am almost certainly going to die of this disease (barring a miracle),
I am not a victim. I don't like that word, and I would prefer that you
never use that word around me. I am a regular person, who happened to
be standing in the wrong place at the wrong time, and I got whacked with
the cancer stick. I have noticed that people don't always know what to
say to me any more, or what to do to help. Most people are loving, caring
souls who really do want to help, but have no clue what I need. To try
to help you help me, I have made a list. Please keep in mind that this
is purely a subjective list. I have tried to include other viewpoints,
but I don't want you to think that all things work for all people. We
are wonderfully, excitingly unique human beings. And so, of course, our
needs will be different. You will have to judge which suggestions you
feel would be appropriate, and what you would be comfortable with.
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If I want to talk to you about what life will be
like after I am dead, DO NOT under any circumstances give me that
fake, terrified,
cheerful smile and say "Oh don't talk like that. You will be fine." There
is every likelihood that I will not be fine, and it is very comforting
to me to know that you will tell stories of me to your children (and
my children!!), and will always hold me in your heart. It is incredibly
comforting to hear that you will include my children, who are much
too young to lose their mother, in your life in a much greater way
than now, while I am still here for them. You can not depress me, by
acknowledging that death is probable, or even imminent. I am all too
aware of it. As a matter of fact, if you put on that fake cheer, all
you are telling me is that you are not able to be "there" for me
for my needs. If that is the case (and I won't fault you if it is),
don't
even try to pretend. Just give me a quick hug (there is nothing about
me that is contagious), and tell me you care, and skedaddle. I don't
have the time to waste on fair weather friends.
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Don't give me the standard offer, "If there's anything I can do for
you, please don't hesitate to give me a call." Most of us are used
to being strong and capable people, who have taken care of ourselves
(and usually others) for decades. It is very uncomfortable to be
in a position of not being able to do for ourselves. I would suggest
that
you drop in for a visit, pick up a broom, and sweep. Ask me if I
have any plans for dinner, and just start making it. I won't ask
you to
do these things. I am not used to asking for help. I am not good
at it. If it is an emergency, I will call out for help. But if it
is the
little day to day nonsense that piles up until it feels like it is
going to consume me, I will probably not ask for your help (but I
will be eternally grateful if you just come and do it). Be assertive.
(But
never mean!)
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Talk about old times often. This has come as a surprise
to many people when I have suggested it to them. They say "But Aunt Nellie will think
that I think she is about to die if I talk about old times." HELLO!!
She is about to die. I am about to die (although I hope it is prolonged
by long periods of relative wellness). And I love reminiscing. It
helps me to remember fabulous times in my life that I may have forgotten.
It brings me a smile. It helps me to remember that even if my life
is cut much shorter than planned, that it has still been a good life.
It gives me a better sense of wholeness.
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(Actually, corollary to 3.) Take some time to organize the photos
into albums. I don't know a person alive (well, maybe one) who is really
on top of their photos. Put everything else aside, and devote however
much time it takes. Get the photos in albums, with captions, and stories.
If you have a videocam, just set it up and let it go. If you just have
a tape recorder, that would be great too. Not only will your loved
one have a superb walk down memory lane, generations to come will bless
you. If I had only done this with my mother..........
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Don't ever, ever feel guilty for enjoying life. When you find yourself
having a great time, and you happen to think of me, do not feel
bad - not even for a microsecond. Life is short. For all of us, whether
we live to be 10 or 105. Enjoy the hell out of it. I would if I were
in your shoes. Heck, I do now. My favorite cliche du jour: Your
life is a bag of coins to be spent any way you choose. But you can
only spend it once. (Spend it wisely, my friends.)
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Don't be afraid to be afraid. If you are paralyzed with fear (and
believe me, I have been there - as has my family!) it's ok to tell
me that you are afraid that I am going to die. I am afraid too. Sharing
that fear really does in some way make it easier to handle. Denying
it seems very very false. I need real. I have no use for false. Once
we have shared the fear, amazingly enough, we can set it in back of
us again and move on. If we don't do that, it will block our paths
at every turn.
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Chances are that my bills are a pile of unorganized
paperwork in a box somewhere. Cancer is an incredibly overwhelmingly
expensive proposition.
All the charges are mindboggling, and intricate. Insurance companies
(in my experience) are incompetent and potentially fraudulent bozos
who screw up all the time. I don't know if they could really be that
incompetent, or if perhaps they are encouraged to be so, hoping that
you will throw up your hands in confusion and pay some of the things
that they "forgot" to pay. At any rate, I would be enormously grateful
if you would come by some day, without judgement as to what kind
of a mess I have made of the pile, and help me straighten it out.
Maybe
make a few phone calls. Maybe write a few letters. You wouldn't believe
what a difference it would make.
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Say, "I love you" a lot. Depending on who you are, that may come
out as "You are the funniest person I have ever met," or "In the history
of mankind, there will never be another person as __________ as you," or
simply "I love you". But this is your chance. Don't blow it. After
a certain point, there is no going back for makeup credit.
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Be very conservative in what perfumes/colognes you wear. Chemotherapy
often makes for incredibly sensitive olfactory senses. Perfumes can
be overwhelming and nauseating. And by the same token, be especially
sensitive if you are a smoker. (Unless the patient is a smoker - I
wouldn't know about that situation.) If you do have to smoke, please
go outside. Even if I say it is OK. And hang out outside for an extra
5 or 10 minutes to air out. You wouldn't believe how much vile aroma
clings to you.
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Make plans, not offers. Instead of asking if I want
to do lunch sometime, ask me if next Tuesday is free. Then tell me, "Great! I will be by
to pick you up at 11 so we can go out to lunch. Maybe we could do a
little window-shopping if you are up to it." Of course, you will
have to be flexible, in case Tuesday is one of those days that I
feel like
I have been run over by a Mack truck...
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When you ask me how I am, please remember that I am much more than
my disease. I know that people ask out of concern, but I get a little
tired of reciting disease progression/regression, treatment updates,
symptoms, etc. Remember that we really did have things we used to talk
about BEFORE I got whacked. Those things are still important to me.
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Please be aware that "looking good" has NOTHING TO
DO WITH IT. Don't worry - I even do it myself - tell my friends how
good they look as
if it meant that the cancer must be under control... No such luck.
Until the very very end stages, cancer itself frequently doesn't
cause any distress at all. Usually doesn't hurt. Often you can't
even feel
it (which is why so many of them go undetected for so long.) The
treatments, on the other hand, can make you want to die, even when
they are saving
or (at least prolonging) your life. This doesn't mean I want you
to stop telling me I look good. I just want you to realize that it
really
doesn't mean diddly-squat.
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I need you to realize that this experience has changed
me in several ways. I am still the person I have always been, but
I am different,
too. For one thing, I am tired. You know how tired you are
when you are sick? Imagine having that be your new "normal".
Be sensitive to my need to rest often. And don't expect me to be
able to go as
long or as fast as I used to do. I also don't have the memory I used
to.
Treatment has taken things from me that I will never get back. Now
I feel like I am slogging through marshmallow goop, both physically
AND mentally. Another change is in attitude. Some things just don't
seem important to me any more. (Hopefully, I don't yell at my kids
quite as much.) And other things have become more important. For
example, I talk to strangers more often now. When I have something
to say, I
say it! Don't be surprised if I start dancing in the aisle at the
grocery store. It can be a little disconcerting. If I embarrass you,
you are
free to walk away and pretend you don't know me. But please don't
try to limit me. Let me spend the rest of my life doing exactly what
I
want to do!
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Don't edit me. Yes, it's true - I do have "a lot on my plate".
But it is not your job to withhold bad news from me. I'm an adult.
I don't
expect the bad stuff in the world to stop because I am fighting the
cancer war. I don't want to be left out of the loop. As long as I
am alive, I deserve - and need - to live a full life, which includes
knowing
even the bad news, being able to share your pains as well as your
joys. My body is failing me, but my spirit needs to support YOU in
whatever
way I can, for as long as I can. I don't need protection from truth.
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Go to the doctor's appointments with me. Sometimes
my poor "chemo
brain" drops important information. It is very companionable to have
someone with me in the various waiting rooms (maybe someday doctors
will operate in a timely fashion.......nah, never mind - it'll never
happen!). And it's great to have someone to talk to during an infusion
drip. It is a good idea to have a pre-written list of questions.
Again, a tape recorder can come in handy. And if the doctor is a
little short
or brusque, dig your heels in and be assertive. Help me to remember
that although I am but one file in the doctor's toppling stack of
workload, I am the single most qualified protector of MY LIFE. I
have every right
to as much of the doctor's time as I need. He (in my case she) certainly
keeps me waiting long enough!
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(Actually, corollary to 14.) If I don't like the
doctor's advice, or manner, remind me that there are plenty of doctors
out there, and
I deserve a second (or third....) opinion. Cancer treatment - especially
for metastatic disease, is not even close to refined yet. There is
so much "art" and doctor's judgement to it, that I should never be
coerced into a treatment I don't feel right about.
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Respect my decision. There may come a time in this journey that I
decide to lay down beside the road and stop fighting. If I make this
choice, I know that you will be disappointed and dismayed. Maybe even
furious. Please remember that it is my battle, and my decision. I know
that you love me. I know that you want me to fight. But if that day
ever comes, please understand that there is simply no more fight left.
I promise you that I will never ever make that decision lightly.
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If I am walking around bald from chemo, take the
plunge. Shave your head! You would be surprised how refreshing it
is to stick your head
under a faucet on a hot summer day... Don't worry. I will not be
in the least surprised if you "pass" on this suggestion. I can say
in all honesty, I doubt if I would do it for you!
I hope that these suggestions help you to understand what is TRULY helpful,
in dealing with a friend or loved one who is battling a life-threatening
illness. Of course, the most important thing you can do is to just be
there. Listen. Perhaps your heart will hear what needs to be said
or done. Bless you for caring, and may there be miracles enough for all
of us!

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