One of my first ‘funhouse’ memories was the Canadian PNE (a travelling summer fair), where I did everything really well, including the spinning optical tunnel with wind until it came to leave. There was a tumbling barrel, like a dryer, and no matter what I did, the thing just kept flipping me over, I tried to escape by reaching out in hopes of grabbing a handrail to pull myself out. But no go. There was much amusement from people waiting in line.
I go to Wales, there is a carnival faire that comes at Xmas and they have a fun house. In the UK, or in Cardiff at least, there are two amusements: one is to GO on a ride, and the other is to hang around with drunk friends and laugh at and harass people on the rides. So each ride has a crowd of about 40 people + in front of it just watching. And Linda and I decide to go on the fun house. Same thing, I am stuck in the barrel, luckily Linda pulls me free, to much laughter from crowd. I am mortified and disappear until the New Year approaches when we are approached by a guy who wants us to say hi to his girl friend on the phone...then he wants to kiss us. This random kissing thing from guys is a reason we stopped going downtown on New Years Eve. But help yourself to 'random drunk kissing' if you are in the area.
Sorry, beyond memory lane, I wanted to show you the edema, which is the pooling of blood/liquids in the arms and legs and sometimes torso. The day after the pain drain, I was on the edge with my body in shock almost constantly, shivering, and overheating at the same time. I slept most of the day woke up and my legs were like this. As you can see, one is THIN (thinner than I have seen in a long time) while the other is twice the size (with some very large and odd bruising).

Also, the hands. This is within three to five minutes of waking up, and though the camera has ‘intellegent auto adjusting’ which is to make people’s skin and body look…well skin color: you can still see some wacky Reynaud’s in my hands and on my left hand, in the finger cuticles, you can see the purple/blue, while the right hand is pink.

BUT, I went to sleep again and if I woke up the same I figured, “well, it has been a good run”, but I was able to not superheat, and got a bit more of endurance. I am still too weak to shower, but I am breathing, and not hallucinating quite as much: I was apparently frequently saying, “I am not an octopus, don’t make me into little balls and eat me!” (a treat at Japanese Festivals).

While in recovery Linda has been helping me (watching episodes of 'Psych'), like here where we are playing cards.

The goodish news is that we have contacted the makers of one of my nighttime painkillers and they have faxed a sheet to one of the doctors who agreed to fill it out. Once they send it back, I get three months of compassionate medication. Which is WAY better than the 6 days of samples I have right now. So hope is on the way.
Also, thanks to some surprise donations (really, thank you!) we priced up Lyrica and the alternatives for nerve pain online. The problem is, we know the reactions to the other medications, and only Lyrica and one other can be used as a single pill for an anti-seizure medication AND a nerve pain medication. While two other popular nerve pain meds have seizures as a common side effect. Which means I would need a nerve pain pill and then two anti-seizure pills.
So a couple hours of research and options later and It turns out, eliminating the drugs I have bad side effects with, that Lyrica is the still best option. We found that the price is the same whether you get 84 of 25 mg or 300 mg pills. So we are going to order from a company we already use online (I am supposed to be 300mg+ a day). There is no generic for Lyrica (and won’t be until 2013), but the amazing display of kindness with surprise donations will cover an order for three months worth of the medication at the level I am on (plus we eliminate the $30 per month ‘filling fee’) - making it almost half price of what we pay now. So that is another week or two away, to survive, but we found six more pills, so now I am on 35% of the doctor recommended dose, which covers about 50% of my pain.
So the hope is to keep working towards a Fentynal patch, as the pharmacist says they can start at a very, very small dose and the patch can be applied even when I can’t move or the pain is so bad that I am not making sense or with diaphram problems and unable to swallow. Plus they last up to three days per patch. So, we have hope that, thanks to the kindness shown, we will have three months to work out getting the pain problem addressed with, and Linda some temp work to help income.
For me, I am ‘making money’ by reading manga. Yes, I am having a sort of final manga sale, which has me reading what I have so that I can sell a host of sets, many of them out of print. We will do that the end of the month, I am also selling my books at the Book and Paper show in a week. So as I say, it is what it is.
I plan and hope to go to Sakura-con this spring.

Because I was too sick to go to boxing this week, I need to get strong enough to go and sweat and get my circulation in action to keep me alive. Alive is good. And as someone pointed out to me, Hope is the key. To look at a future filled only with stop-gap issues where I am constantly in terrible pain until I eventually die is NOT something that I can keep doing, or something I think anyone can keep doing. For me, the mental refusal to stop, to quit, as evidenced by boxing, by trying to wheel outside 2-3 times a week and by getting out of bed every day, is critical to avoid quick deterioration. So though this MINUTE, Sakura-con looks a long way away and has a lot of things in my life to stabilize, I believe I am going to go, and with Linda and Cheryl. This year we can see the Cos-play chess!
There is now, which is important to live in, but there is also the future, and if there isn’t much hope NOW, then I need to find a future and what needs to be done to find that hope. Back to work at the ‘manga mines’
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