| my mom never posted on her blog except for one time:
March 10
Dear Family and Friends,
I
know I don’t usually give the updates myself, but this week I was
reminded at my treatment again what a difficult thing cancer (or any
life threatening disease) can be. For those of
you who haven’t been in the typical chemo room at a cancer center, they
usually consist of six to as many as thirty big recliners each equipped
with a blanket (chemo often makes you cold – being overly thin just
accentuates the shivers), a pillow, and the ever present infusion pole
with multiple towers. My family has referred to these as ‘Fred’ since
my surgery in 2002. I honestly can’t remember why now. So if you are having treatment and you need to use the ladies’ room, Fred has to go, too. I can drive quite well now, maneuvering around all the other people and their poles. The Rocky Mountain Cancer Centers have several locations around the Denver
area. I have elected to go to the one that is the smallest. The
doctors’ suite is in a medical building attached to a hospital.
However, there are only six big chairs, so it is a less depressing
atmosphere to me than the others which look like chemo factories. This
past Thursday, there was just one other woman and me. She had the
completely bald head that says her hair fell out, rather than just got
thin, so she shaved it. Her husband was with
her, but could have been taken for her son. That is one of the
byproducts I have observed in myself and in others. Disease
ages you in a way you cannot imagine. When you lose a lot of weight,
your teeth even crowd each other, so that with the skin changes of
different chemicals, and the hair changes, you often wonder, “Who IS
that woman staring back at me? I didn’t expect to see anyone like her
for at least 30 years!” Speaking
of thin, or rather SKINNY, there are two types of people who are
unnaturally thin – overpaid models (and the young girls trying to be
like them) and the chronically ill. For all of you who bewail those
10-15 extra pounds, just think, “Curvy is cool!” Anyway,
there becomes an instant bond in chemo centers. (Similar, but not fun
and exciting, like women at a birthing class) So this woman’s husband
is describing how she lost 27 pounds in eleven days, etc. when a
husband, wife, and their daughter came in. I knew as soon as they came in that the woman was getting ready to join ‘our club.’ She
had that overwhelmed look on her face. Actually, they all did. This was
a lovely African-American woman, who looked to be in her 40’s. This ‘club’ is one that
you do not elect to join, but are rather forced to join.. No welcoming
handshake, but a reaching out to squeeze their hands – to somehow
communicate that we hurt with her. The
nurse began giving her the prep talk for chemo. One of the most common
confusions is that all the people in a treatment area have the same
cancer and the same drugs. Usually a newcomer
wants to know first off, “How sick do you get?” It takes some time to
keep gently saying that everyone is different – everyone gets different
drugs in varying doses. The next question (And I have observed men ask
this as much as women), “Will I lose my hair?” Sure
enough, she was very anxious about this. (She has beautiful, perfectly
groomed hair). Yes, says the nurse, you will lose it all by the second
treatment. She looked at the other patient and I
– we were not reassuring in appearance. The other lady clearly bald
under her cute hat, and me whose hair looks like a grandpa who is
trying to keep what little hair he has. Then the questions began in earnest. Newcomer:
I want a wig and I want it as soon as possible. (So conversation ensues
to give her the best resources for a soft, reasonably priced wig.
Cancer patients can get really good prices. My sweet mother has wanted
me to get a wig from the beginning of all of this. I can’t go there. I
couldn’t tell you why.) Nurse: (Laughing) Oh, you won’t care about your hair before long. (This
is a great nurse who gives us great care, plus stand-up comedy she
should be paid for, but here she is wrong. No matter how sick you get,
you still care. A woman does that. When we come in stooped over and
looking like a train wreck, it isn‘t because we suddenly no longer care. It is because we don’t have the strength to do anything about it. There is an important difference.) Newcomer: How sick do you get? How long does it last? (We answer) Then we all converse about the difference between PIC lines (which I have) and PORTS (which the other lady had). Mine require daily flushing; PORTS usually do not. If
you watched Meredith draw the saline solution from a small bottle with
an ultra thin needle and “burp” it, then add Hepron, you would think
she was a nurse of longstanding Then we get into harder questions. Newcomer:
Do you cry, I mean do you cry a lot. (Yes, we both cry – sometimes a
lot) I cry all the time. (Looking at her hurting husband and daughter,
you know they all do or want to.) Are you scared? I
mean really scared? (Yes, we both are scared – sometimes really scared)
Can I talk to other cancer patients like this? (Yes, most are more than
happy to share help of any kind with another) If
you read the literature on cancer, there is a lot there that is
encouraging. Lance Armstrong’s Foundation has some excellent resources.
It is interesting to me as a Christian how much of the secular input is
how the medical profession encourages patients to become ‘spiritually
connected”. They aren’t quite sure how or where for you to do this, but
doing it gives you a definite edge, so say the statistics. That, and
forgiveness are the hot topics. No real surprise here for those who
take Scripture seriously. But back to my sweet
newcomer. She is not ready for the strong medicine yet. Will she get to
the place where she puts all of her energy into the fight? Probably.
But before she can get there, she must have hands to hold, and she must
let the tears come, and she must admit her fears before she can fight
those as well. And she will learn that for every
PETscan or MRI or even bloodwork, she will face questions all over
again. This isn’t a fight that you complete one day, never to waiver
again. It is like climbing one of the beautiful ‘Fourteener’ mountains
that grace Colorado.
One tackles the climb bit by bit. The people that I hurt most for in
these battles are those who have no family or no friends, and even
worse, no comfort in God. I have been blessed with family and friends
who have reached out to me in amazing ways – ways that bring me to my
knees. And I would say that before all of this, if you asked me about
God, I could have told you many, many things. And if you asked me now I would say, “God is good and God is real.” As many of you know, I just celebrated by 56th
birthday. I am grateful that I am alive to do that. Without the help of
my ‘Dream Team’ (here and other places), I would never have made it to
this birthday. My oncologist called my Hospice doctor recently and
said, “Hey, guess who is still alive?” They both tell me that they
can’t believe I am still here. On many days, neither can I. Thank you
all for the cards, emails, and prayers that mean more than I can say.
Meredith planned a surprise party for some of my gal friends here. It
was a special day. The Barnes family engineers a
very labor intensive juicing/food program that surely is helping me. We
are attempting for me to gain weight – always a challenge when food
choices are limited. Oh,
and just so I clarify, besides the bittersweet scenarios that take
place around cancer, there are some times that are incredibly funny –
you can’t get that many people with ‘chemo’ brain together and not have
some humorous moments. Anyway, sorry for this
longwinded epistle. Blessings to you and your families. And, hey Adam,
I love you. Thanks for our long, and sometimes hilarious, talks. You
are a champ! Love, Judi
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