Monday, January 16, 2006

Strange how quickly

one gets used to change. I remember only three months ago being distraught at the lack of hair on my head, at the handfuls coming out around myself, and now? Now I put my hand constantly up to my scalp to feel my baby fuzz. The only drawback is that I do feel, how shall I put this...vaguely related to King Kong when I do. I feel that I should be picking nits out of the person next door to me, jumping up and down and grunting with hands locked under my arms like all the best imitations that we used to do at school.

But things are changing... I have become used to the feeling of fuzz on my head, but notice, as the days pass, that my scalp is itself not so exposed..that beneath that level of spiky, very short hair, is another layer, a layer of very soft fuzz, an undercoat almost and I hardly dare to hope, hardly dare to even put into words that I think this is my hair growing back... It is so soft, so shallow a layer that I couldn't even try to put a colour onto it. No, because it is almost only by touch that I can feel it, this soft, downy mattress beneath my spiky clumps.

And there, there, in that tiny, personal fact lies one of the eternal dichotomies surrounding cancer.

Yes, I am thrilled it is growing back, I am so pleased that my few months of complete poison have resulted only in temporary hair loss, that I am lucky enough to have it grow back but does that mean that the chemo isn't working? Does the fact that I am not being so sick, that my hair is growing back mean that the effect upon that evil traitor above my heart is diminished? Because, if it is, bring on the sick bowl, fire up the steroids, and get the ulcer cream out again. And that, as I understand so many survivors' writings, is one of the ways cancer changes your life. You are never so blithe, so innocent about the effects of your life again. When you get a pain in your back, you don't ever just think 'too much gardening yesterday', but worry about bone cancer. When you get a cough, it is never a possible cold, your mind leaps into the world of lung cancer.

Once in your life, it changes you, it changes those around you and it changes the world that one looks at too.. Certainly, this means that that state of young innocence is gone, and gone forever. Once you have felt the breath of Cancer down your neck, close enough that all the little hairs go up, you do not forget his shadow.

But it isn't all bad. You remember the fragility of life, you see the value of gesture, of touch and of words, and you see that all the events that normally punctuate a winter's weekend in London are put in a spotlight of appreciation. My nephews' red cheeks as they came in from football, my brother's hug, my sister in law's laughter as we cleared up a mountain of children's clothes, my friends' delicious lunch, all become part of a snapped collage to take out and treasure on monotonous days where the four antiseptic walls and anonymous faces of a hospital become our temporary normality...

Minerva

13 comments:

amanda said...

Woo-Hoo, Minerva's hair is coming back!!!!

Our doctors have told us that in time, we'll be able to get over some of the fear and apprehension that goes along with cancer treatment.

I hope that all continues to go well with you, and that you reach the twin goals of happiness and confidence in your health in no time at all.

Thinking about you...

Suburban Turmoil said...

I can't even imagine what you're going through, but I'm so grateful that you're sharing it with the rest of us. Because you help me make each moment count, too.

cmhl said...

that is exciting about the hair.... yay!!!

and, what you said about being concerned.. my mother had breat cancer nad went through the chemo and radiation, and her hair behaved really strangely, really. I specifically remember her being worried that since it was growing back, it meant that her body was USED to the chemo, and it wasn't working.

but it did work, for her. and it will work for you.

her hair grew back in a totally different color, and texture.

Anonymous said...

I meant to say to you that you were looking particularly jowelly on Sunday. Could it be fatty chin cancer?

Oh, and you know who posted this one baby!

x

Raehan said...

I have nothing helpful to say, not having had anyone close to me go through chemotherapy.

Only, "Thank you" for sharing the experience with us.

And yay for hair. I interpret it as a sign that your body is as resilient as your spirit.

tablefor4 said...

I'm so glad that I found your blog. Weird to see others who I've come across also and added them to my links section. (amanda). I hope that it's o.k. for me to add you to my links section also.
My dad is going through chemo, and having a very difficult time of it. His hair hasn't fallen out, but he keeps getting reactions to the chemo that's given. He's now in the hospital and getting better with each day. I'm glad that he is there, even though he just called me YESTERDAY to tell me that that's where he is.and has been there for two days now.
I can't imagine what it would be like to have it myself, but I know what it's like sitting on the sidelines, and watching the pain and feeling the aftermath of it all. It truly puts life into perspective for our family. I think we took things for granted quit a bit before my dad was diagnosed.
I hope your feeling better, and I'm glad that your hair is coming back in. I hear that when your hair grows back in, it's a million times more beautiful than it was before. :-)

Minerva said...

Amanda - As always, you are so much the unselfish one delighting in other's joy..Thank you...

Lucinda - And you make me LAUGH every minute...*grin*

CMHL - You have no idea how reassuring your comment was as it is a worry, that even though the body does get through and survive, that it means the cancer might be getting through too..Thank you!

Anon - You are a very NOSY character..*satisfied grin*
Does that show I know who you are?

Raehan - You are lovely.. To all who read this blog, please go over and read Raehan at Agog and Aghast. She is also a competitor at most inspirational blogs and a worthy one.. Her posts inspired by motherhood are really moving...

Tablefor4 - It is so hard to be on the outside as well as close to someone going through it... I do think of you and wish you the best of luck.. Please, don't hesitate to email me if you need any more support or check out some of the heroines list on the left to find people going through the same thing...

kenju said...

I think before the CA, that "snapped collage" would not have been snapped. So it is the silver lining to the clouds, as I see it. Good luck with the downy fuzz....

Evil Minx said...

I can't help feeling that it is far more likely to be because the chemo is working than it's not.

I base this on the not-exactly-scientific theories of Dr. E. Minx, of course.

Seriously, though, the poison is doing it's work, the cancer is reducing (long may it continue!) and now you have downy fuzz. New life sprouts, new growth... it's good, it's all good.

The lion's mane will return, my sweet, i have faith.

Your

Minxxxxx

/A. said...

Thinking of you every day - even from the other side of the world. Look forwars to seeing you again soon if you want. *hug*

Rainypete said...

I think the capacity to adapt to changes is one of the most amazing things about the human animal. We are always seeking atability and contentment, but can adapt to almost any situation anyways.

May you and that fuzzy head of your never lose their appreciation for the real tresures in life.

Deadly Female said...

I recall one woman I worked with for a year, while she went through her personal journey of chemo and surgery. Her hair started to grow back around the time of her 7th chemo and I recall her feelings back then. Your words are like an echo of hers.

She is now well, getting on with everyday life, and her experience has also become a station in the journey of her life.

xx

Anonymous said...

hope you get better soon..totally got here by accident ....take care

alec@e-mile.co.uk