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.
sending you all the stubbornness, optimism and means for finding joy that I can muster
Thanks, Kate. I love all that you send….XO
Sending healing and peaceful energy your way.
Thank you Susan. It doesn’t have to travel too far either!
Thank you. Keep sharing it all, whether the moment is “that’s better” or “aw shit”.
Thanks Uncle Doug. XO Katherine
i like “victorian and gauzy” quite a bit.
warm and dry here, sending some of that to chilly mass.
ptd
It’s not too cold, just buckets of snow….pretty
This was so beautifully written. I hadn’t been here for a bit and had no idea. Sending you hugs and love.
Thank you! Keep the hugs and love comin’. I love it and will send back…..
Wow! I applause your courage and NO WIMPINESS HERE! I am with you, for you, and hold you in my arms. Laugh, love and live gal!
Sent from my iPhone
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Thank you, Joyce. The reminder to laugh is a good one. Many hours go by without me smiling. It’s hard right now…maybe I will get angry first and then can laugh. I finally feel some anger coming up. It is a strong part of me and has served me well once I’ve learned to allow its power to help me.
I continue to keep you in my prayers Katherine. I’ve heard about and have seen people who seem to be fading, as you say, but then rebound miraculously. It always amazes me how much a body can go through and then recover. Sending you love sister.
Thank you Sandee. I feel it at times, when people are thinking on me.
this is so wonderful of you and I am overcome
Kathy, so sorry to hear you’ve been ill. Please let us know if there is anything we can do to help. Love, Paul and Brigit
Thanks Paul and Brigit. We will let you know. K
Dear Twinkly,
I apologize for not being here for so long. Today I saw your blog in my bloglist and thought “I must stop and read and tell her hello.” And I found this…this shock, this punch in the gut, and now feel I have let you down by not being here, by not being aware of your illness and struggles with pain. I am so sorry. I promise that from today onward I will meditate on this: May Twinkly have exactly what she needs at this very moment.
Soft tears and even softer hugs,
Lydia
Thank you Lydia. So nice to have you stop by and to leave your beautiful words. I can’t keep up with blogs any more, it’s been a while and even the 3 or 4 women whose blogs I used to read regularly, I no longer can. So I try not to judge or pressure myself. I have no thought that you’ve let me down or could ever let me down. I am glad for the small and lovely interactions we’ve had over the last few years.
I love your meditation, selfishly so. I have been asking for so many people to vision me whole, to pray for me, to meditate for me. It is still hard, I still feel I need to justify it or that I am asking too much. But your meditation is such a great teacher. I hope I can carry it and give it away to others in its perfection. YES! I need it, but I know so many of my friends and family need the same thought.
Thank you so much. No worries. I will try to update on my blog. I think about it, about sharing what I’m going through. One thing is that my diagnosis, though it has felt like a hellish eternity sometimes, has gotten easier to digest and my chemo and treatment seem to be working and I am committed to them and to my healing, continually, even when I think I am not.
BEST LOVE TO YOU Lydia! I hope you are well and that the ocean out there is perfectly lovely. I went to Cape Cod for two days this weekend after thinking I may never see it again and in spite of myself, of course, it was perfect.
XO, Katherine