
So I try to not REACT, though when I got the ‘nasty’ EEG tech on Wednesday, I couldn’t help do a little debate to wind her up, which she got revenge on by having ‘the last word’ while telling me I had to stay still or ruin the test. Then when removing the 12 electrodes stuck in my hair and scalp, the hair that is thinning even more, she ‘saved time’ by simply grabbing the cord they all connected to and YANKED, ripping all the electrodes (and bits, and chunks of hair) off of my head with force. She also came over when I could not move, and kept raising my arm and dropping it to see the dead weight. We COULD have used that data to compare how I am sending OUT the signal to move but nothing is happening IF she had made a note, but she was sort of annoyed at me because I wasn’t moving and came over and played with different body parts. Professional? Um, I thought morticians had more respect for the body.
I have a favor and something of interest to ask you to take a bit of time to look at. The first is my Postcard Project. I know, Elizabeth and her Postcard Project.

I ended up talking today in an interview about accessibility in Victoria about the Postcard Project. Because I said that for me, accessibility is making sure that everyone is included, that everyone is having the same good time, the same standard of experience. I told the reporter that I realized that I was privileged before, sure I had tried to eliminate any discrimination on race, and worked toward gender and sexual orientation equality (sigh, but if only those heterosexuals would just, you know, not BROADCAST the orientation SO much with kisses on TV, and that! Sorry, still working on that one). But I never looked at people using walkers or those using a cane, or a wheelchair or any assistive device or brace and thought ‘that could be me’. No, that was THEM and I was me, and so when I fenced or I did sports or taught or was in church or participated in society, I would make some accommodation IF TOLD TO. But I never looked around and said to myself, “All of us, we will have the same level of experience.” And worked toward that. Because they (a wheelchair, for goodness sakes) weren’t like ME.
I’m ashamed of that.
So when the reporter asked about the Postcard Project I told him that is was my attempt at postal accommodation. That with impediment or not, that stuck inside due to snow or ill health or not, lonely or not, healthy or not ALL would be equal in The Postcard Project. That is why I would ask for a favor and have if possible that people list about the Postcard Project, and link to it in boards or with people, or on forums that I DO want to send people postcards, very much. This isn’t my penance, this is my progress.
The second thing is that a man named David Wybenga in Japan is helping me find some postcards. He and his wife run a program in Kyoto called The Japan Cat Network, because in Japan, problems (like disabled people for example), are not talked about and pretended not to be seen. Stray cats is one of these problems, here is an English article from The Japan Times on it. Very few stray cats are neutered, many cats are simply abandoned in ill health.

This of course, in true anime style got me to thinking of cat girls (a common anime theme! What is better than a cat, and a girl? So first I had to find the ‘Linda’ catgirl. Here she is:



Just as I know there are many cat owners out there (and I would love to be one of them!), and cat lovers, that this might be a project you would find of interest. Since this is a very global blog. Knitters please wait, I WILL have a knitting themed blog post in the near future, yes, be still all of our beating hearts.
Thank you for reading and for checking out the sites and if possible for passing on info about the postcard project. I have met some wonderful people and friends through the last time, and yes, I have a lot of people I send postcards to that I haven’t heard back from but that isn’t the point. That the postcards went out and they got them is the point!
The question for me, which I don’t know if I have faced is, who am I going to be in the future. We don’t talk about the future except for dying. Well, there is a space of time between NOW and dying and that is the future.

Okay, I am not the same Elizabeth who wrote Zed, which is a good book (oh and on sale at Linda's website again, we got a shipment from the publisher!), not my BEST novel, but a good book. I have realized I am not going to be the person who I dream, or dreamt of being, or who I liked being in my casual moments (this picture is for Cheryl)


I have good memories but I am never again going to be what I trained to be, no matter how many fencing and epee books I have. No matter how many dreams I have where I am fencing or have a sword in my hand again.

A great deal of my life, when I am not in my hospital bed, or at the computer is spent like this

See, honesty. I wake up horny some days, I just can’t seem to do anything about it – but with some tips from the MS society, I am trying (but oh GOD is it frustrating to get so CLOSE!). I have created myself a few jobs: the postcard project is a big one and I am going slowly through and editing some of the essays to try and make a book about degenerative and chronic disabilities. About the real stuff, which does yes, include the days you are high as a kite because they got the pain meds a little wrong (but in a GOOD WAY!). But also the days of crying, and of feeling that as a person, I can’t go on, that I was permantly BROKEN. But humans are unique and resilient. We do go on.
One thing I forgot for a while, because I was so worried about the pain, and that I was dying was about my future. I have an outline of a plan. Money from publisher is not coming, so I will work on another book. Because I want to be in Hawaii in the spring with Linda, Cheryl and anyone else that wants to join us – lets go to the Onsen! I will sell anime, I will sell books, I will sell things of the past, the life that I do not have. Because I will, yes, with some emotional pain, look to the future.

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