That is indeed part of the charm. The people who like swing lens panoramic cameras like the Widelux like that look. The alternative is something like the Hasselblad Xpan, or even just a panoramic crop from a regular camera. A swing lens does something unique.
I'm curious, is it generally used hand-held, as in the website's pics? I would guess that it adds wobbling on top of the distortion (maybe a less desirable feat).
Yeah, I've been waiting for it for years too. I thought it was going to be substantially more than $4400 (more like $6-7K). Under $1,000 is unfortunately simply impossible. Used Wideluxes go for a fair bit more than $1K.
That said, too much for me right now. Maybe someday.
Eddie Rocket's is an Irish chain of American diners. I've eaten there in Dublin. Although at least that location is downtown, and in a bigger building, not a classic diner style building. The inside is very much American Diner themed with vinyl seats, chrome, jukebox controls at the table, and of course the menu of burgers, fries, shakes, etc.
Many of the film cameras that people 3D print essentially outsource that stuff to off-the-shelf focusing helicoids which are readily available, along with medium or large format lenses which are traditionally mounted in a leaf shutter anyway. So the hard parts (lens, aperture, focusing mechanism, shutter) are not part of the 3D print itself. You're right that 3D printing a serious shutter mechanism for anything other than a pinhole camera isn't really feasible (yet?). It's the light tight box and the film transport that are completely reasonable to print.
Yeah, it’s really starting to depress me how much text published to the web is written using an LLM now. Things that seem interesting at first glance become much less appealing when they have that telltale LLM quality to them, and I also start questioning whether they’re full of factual errors (“hallucinations”). I don’t know why I should spend my time reading something the author couldn’t even be bothered to spend time writing.
Spina Bifida is not primarily a genetic disease. It's caused by a failure of the neural tube in the developing embryo to close fully. No one knows the exact causes, but folic acid deficiency in the mother before and during pregnancy makes it more likely. It also seems to run in families a little, but only weakly, and we haven't identified any specific genetic cause. This treatment is very promising, but it's not a cure, just a (hopefully) even better treatment than the existing in-utero surgery that doesn't include stem cells.
Thanks for sharing about your daughter. It's good to hear from other parents dealing with it. My daughter with spina bifida is only 18 months. It's early of course, but so far she's right on track cognitively and socially. I expect she'll be in a wheelchair full time, but don't know for sure yet. She's also just the most joyful, loving, social, happy toddler.
I know what you mean about elevating otherwise normal kid illness. She had her first shunt failure in January. It was pretty stressful going from "hmm, she's fussy" to surgery within less than 24 hours. But she was back to her happy self with hours of the surgery too, which was a pretty stark indicator of how much the shunt is doing for her.
One of the nicest things anyone ever did for me was the day after she was born, when I had just started at a new job, an older dev asked if he could talk to me and pulled me into a meeting room. I didn’t know anyone there and was confused. He’d overheard me talking about my daughter just being born, and said “I’m nearly 60, I have spina bifida, and I want you to know it’s going to be alright.” He stressed how important doing a regular catheter routine is, as the most likely thing to kill him in the next 10 years is kidney failure due to bad catheter habits as a kid and young adult. Also, overnight foley catheters with a bag has been a lifesaver, and gave us our sleep back. The doctors often just won’t mention these things, and the quality of care can vary greatly depending on your care team, as I’m sure you’re well aware. At least the doctors seem to have some respect for us as caregivers to a medically complicated child and they often trust our judgment.
Hopefully it’ll make you feel better, but the shunt revisions became far less common for us as her growth slowed down. She had one around a year old, but they put a good amount of tubing in there, and they haven’t had to go do a revision in the past 6 years.
The main goal of physical repair of the defect in utero is actually to reduce the incidence of hydrocephalus and hindbrain herniation, which are very common in people with Spina Bifida. The existing fetal surgery reduces the incidence of hydrocephalus from about 80% to about 40%. The improvement in leg and bowel/bladder function is actually a secondary benefit.
My understanding is that the hindbrain herniation (aka Chiari Malformation Type II) is the main cause of cognitive trouble in people with SB. But it's worth noting that it's very far from universal in causing that. Most people with SB are basically normal cognitively assuming they get good early intervention (VP shunt, PT, OT, etc.). Some early cognitive development can be slower as a knock on effect of not being able to move around as much as a baby and toddler, and thus less able to explore the environment, etc.
Source: I'm the parent of a toddler with spina bifida. She's completely on track cognitively and with fine motor skills so far. She's way behind with gross motor skills due to her inability to move her legs very much.
Another sb parent here, my kid is seven now, she’s also on track intellectually. We got the decompression surgery for the Chiari II a few months after she was born, and the VP shunt even earlier than that. Aside from some stammering (which her non SB sister also has, so I suspect it’s hereditary), and weirdness with foods (OT has helped a lot) she’s totally on track intellectually.
Our daughter was a particularly severe case too, and these interventions seem to have helped a lot. For the first four years she’d hold her breath every time she was upset, and need CPR, but we got her breathing again every time, so we don’t think there’s any brain damage. If we’d missed once, maybe I’d be telling a different story now. Thank goodness her head grew!
reply