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Archive for February, 2014

If you have been a reader here for a while, this piece may not be particularly different or surprising; but maybe somewhat so. In any case, I am not writing to panic you or make you think I am not going to come out on the other side of my multiple myeloma treatment with anything but my life intact. I expect a full remission. On the other hand, I try not to project too much about particulars at this time. I don’t expect to know a lot of things, and I am learning not to be too cocky any more. I was really cocky, thinking I’d never get cancer: that will never be me. It had no place in my vision for myself or my life force. Now I won’t show such hubris as to project ages and dates because I think they will not have the same meaning to me that they used to. Now I don’t get too far ahead of myself. This is a piece about just what it is. If if helps, think of it as fantasy.

Also:

If you are going to comment, please do not put forth your own beliefs about how I am doing or whether I am doing the right or wrong thing. That is not what this writing is about. You may send your love and light and wholeness, your chi, your prana, your aligned and lit-up chakra energy. I know you are sending images and colors and calm and I love it all. I am filled with love for you and from you. You may pray to Jesus for me, to God, to Buddha, to a tiny pea seed hiding in the darkness, waiting for spring. You may bless me and love me. But I do not want your judgment, for that belongs to you alone.

♥ ♥ ♥

I lie on the table, looking out the window into winter. I am weak. The room is warm, too warm, making me give in further to my weakness. The effort to shift my bones is too much so I don’t move. I sink. To smile at the male cardinal cracking seeds in his beak is too much. I feel Victorian and gauzy. I am the weight of a square of gauze. If I had to wear anything but a silk gown next to my skin, I would surely break into pieces.

I want to fade away, but I would fade into misery. Do they talk about the pain? The exhaustion of hauling around a shell, the ghost of my formerly strong body. When was the last time I could take a deep breath without it getting caught at the sides of my ribs? When didn’t I gasp for air to come in or to wince in slight pain when it went out?

Now I know that lo these 9 months (and then some!) I was never being dramatic. I never had a low pain threshold. Au contraire. I wish I had listened with a non-judgmental ear to that pain. I never thought of myself as stoic, I thought I was whining. I thought my pain was a bore to those around me. I popped ibuprofen like it was candy. Ibuprofen and ice, sometimes dancing or vigorous hiking would give relief. So it must not have been that bad.

I birthed two babies, hard labors, at home. Especially my first birth was long and hard—21 hours of active labor on top of 2 days of early labor and I started out with a flu which had left me sleep-deprived and dehydrated. Baby had the cord wrapped around her body 4 times and was born with a compound presentation (her tiny perfect arm wedged up against her head). I did that without pain medication. Still I’ve thought of myself as weak in the face of pain.

Yet here I am and here I have lived for over 9 months, painful fractures throughout my bones.

Time is not time. Time is weariness is pain is too much. Time has to end now. Time is too much for me to bear. How can I stay alive through this? What if I get worse tomorrow? Surely I don’t have the reserves of strength this will take. Surely I need a pillow to be carried on, a sedan chair, does no one see this? Why aren’t the hospitals equipped with silken pillows and nursemaids who will bathe and oil and dress me. They have to carry my arms, move my fingers for me, lift water to my mouth. I am too weak to manage my own body. I am fading but no one sees.

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So. Damn. My computer screen is going crazy—for about 4 days now, it periodically goes to diagonal static lines. My computer, how old is it? I can’t remember, not too old. I know I need to get a diagnostic on this, but this is not gonna be the week.

I may be out of a computer for a few days if my screen goes dead. Sucks because it is my lifeline right now. I can’t drive and Hubby will be away for a few days. I am covered for people helping and schlepping and bringing food and carting kids, but the computer is how I can ask for more help…ah well, ’twill work out.

Here:

IMG_1704Annie made this little guy the other morning. He was quite tiny—maybe 8″ high. Annie thought he looked evil with his red berry eyes so she gave him a sword. Later I think the dog knocked him off the railing. Silly dog.

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The hard truth of bone

embryonic cells swirling

differentiating into

nuclei

osteoblasts

blood

Dear readers:

As you well know, I have been struggling with pain in my upper body since April 2013 and before that with a couple of rib injuries in 2012.

Last December, things got worse—more pain and a sudden, painful protrusion on my L clavicle.

I started to feel really crappy, said to Hubby, “I am not myself; something’s wrong.”

I have been seeking help and answers the whole time—blood tests, lyme tests, RA tests, lupus tests. X rays; physical therapy, acupuncture, doctors. Everything I had been tested for came back negative—I’m strong and healthy by all appearances.

In January, I had a CT scan because of a concern my doctor had. Lo and behold, my ribs, sternum, clavicles, and spine are full of tiny fractures, ones that never showed up on 3 different x-rays over the last 2 years. These indicate multiple myeloma, a cancer of the blood.

More markers have come back which show certain proteins in my blood, further narrowing it down to multiple myeloma.

I need to use my blog again. Perhaps I will start slowly, perhaps I won’t use it much, but I need to refill my creative outlet here. I am steeping myself in a helpful, loving community and I ask for healing thoughts and visualizations and meditations. I ask you to see my ribcage and bones in white light, in liquid gold, healing, healed. Maybe you see violet, maybe you see the cool blue of water. Anything healing that you see when you think of me, send it.

Not only do I believe that my bones will be cleared of this after chemo, but I want the faulty signals causing the cells to have the wrong kind of party to be reconfigured so the right messages are sent to the marrow.

I ask you to chant and meditate and breathe for me and my family, for peace, for calm. It is hard for me to ask for these things, but I am learning, humbling. I know that quieting the mind and lighting up the chakras works, the visualizations help tremendously. I hope they help us all, givers and receivers alike.

I am on a healing journey and I am using the full force of what Western medicine has to offer. My adjuncts will be my acupuncture and my imagination and any healing thoughts and incantations you can send. I am smart and I will be with some of the best doctors around who treat mm. A world-class specialist at Dana Farber in Boston will likely coordinate with my local oncologist and I can still get chemo and day-to-day care locally.

I will allow comments here, but I may shut them down if I find it too difficult to field and manage input.

I do not want information that you have from the internet. I do not want questions. I do not need new information about alternate therapies at this time.

On the other hand, if you have a delicious recipe for a high-protein smoothie, I say AMEN!

In other support places, I am emphasizing being honest with my emotions, not matter how yucky they may be, but also I’m trying to remain positive and open. The use of my blog, my writing, may be slightly different. This is my space. You are guests.

My blog is sacred to me and I will be using it as a creative outlet and force, a place where I will allow myself to go into the dark if my soul needs it. If you judge me for this, I will block you from my blog.

That is all for now. Send love and light and thoughts of calm sleep and freedom from fear.

Peace.

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