hissingmeerkat

@hissingmeerkat@sh.itjust.works

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hissingmeerkat,

We haven’t deviated from the 9C path from the now ancient models.

hissingmeerkat,

I’ve eaten on about that before, but decades ago when food was cheaper. Nothing is satisfying, you are hungry all the time, constantly craving some nutrition you no longer even know how to acquire or what it is, but it’s absent from everything you eat.

Peanut butter and bread was too expensive. Peanut butter was a treat. Bread from bakery surplus cost two to three times as much as rice. For your example, at $400 a year you’re looking at $8 a week. If a jar of peanut butter is $3 and has 4800 kCal in it and bread is $1 a loaf and has 24 60kCal slices in it, then a jar of peanut butter and 5 loaves of bread a week only gets you 12000 kCal a week, which isn’t enough for a moderately active adult. And you’re going to be missing out on all sorts of nutrition.

At the time the best things to buy were eggs, beans, rice, and processed dry foods. Then you buy things that make eating them bearable and are also cheap in combination: whole or powdered milk to eat cereals, raw sugar, fat to cook into things, very cheap meats, cheese when it was cheap, and processed frozen foods that are similar in price to their constituents, which at the time were common because they are a way of storing food from a production season to sell in an off season. Then you get a few things to try to stave off cravings, like some long-term storage plastic-packed cuts of meat, or canned vegetables, or concentrated frozen fruit. At a low budget a can of food represents everything you get to eat for a day, or more. Fresh vegetables or fruit were completely unobtainable unless there’s a local surplus.

Now the structure of food markets is different and everything is priced based only on demand and not on supply, so frozen processed foods that were available then due to the product being made to take surplus or trimmings and then store them are now priced based on demand for the product. The only things that have stayed similar are the prices for eggs (usually), the cheapest meats (sometimes), staples (usually), and canned foods which are priced based on the cost of transportation and are still routinely too high for such a low budget.

InternetIsScary, to lemmy French
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  • hissingmeerkat,

    Random word generator

    hissingmeerkat,

    That’s not true.

    It’s not embroidery. It’s cross stitch.

    hissingmeerkat,

    I’m new to magic in this millennia.

    Oh, I thought Outlaws of Thunder Junction was the rotation. I was a bit confused because the crime/etc themes seemed to go with the other current sets and mechanics, and expected a larger reset of mechanics for a new standard. I will definitely “Jump In!” then.

    Two of my children were FINALLY diagnosed, after a long fight.

    It took three years but I finally got them their diagnosis and now I don’t know what to do next. Their school always gave us issues when we held them to the expectation that my kids would get the help they needed from their school. They refused to let my youngest stay a full day last year for his first year of school, and now...

    hissingmeerkat,

    (I’m the spouse of a special ed teacher, but not in Michigan. I’ve just been around this stuff for over a decade hearing it from the grad student/teacher side)

    Getting a diagnosis should make it much easier for you to get appropriate IEPs, 504 plans, and services. I’m surprised they got IEPs without a diagnosis, since there are legal thresholds for a school/states to get federal funding related to IDEA (more on that later)

    It sounds like your local schools and community services are a mixed bag of how well they provide special education services. The positive things to notice are that they have

    • found a way to get IEPs for your kids even without a diagnosis
    • seem to be concerned with making sure they are providing education in the least restrictive environment

    The extremely worrying thing is that they refused to let your youngest stay a full day last year for his first year of school. If this was because it was a kindergarten/pre-school year and the normal school day is a half day I would be less concerned about getting services in the future.

    Federal laws

    There’s two main federal laws that guarantee your kids get an education:

    • Section 504 of the Rehabilitation Act of 1973
    • The Individuals with Disabilities Education Act (IDEA)

    Section 504 of the Rehabilitation Act addresses providing accommodations to students with disabilities, and guarantees they get a free and appropriate public education, and prohibits discrimination based on disabilities.

    IDEA is 3-pronged. It restates a requirement for a free and appropriate public education, requires individualized special education and services for certain disabilities (IEPs), and requires that students receiving special education services do so in the least restrictive environment.

    Your locale seems to be addressing some of these, but not others.

    For a student to be eligible for special education under IDEA they have to qualify under one of 13 categories, one of which is autism spectrum disorder. To qualify under autism spectrum disorder requires a diagnosis, usually an outside medical diagnosis, but occasionally, if a school really cares and tries they can provide (at least here) a school-specific diagnosis based on how it is affecting education. Eligibility for special education is required for an IEP. Since your kids have IEPs the school presumably somehow found a way to qualify them even without a diagnosis. Eligibility for special education has to be reviewed once every 3 years. IEPs have to be updated annually, and they require parental participation, and parental assent (at least initially, they may not for renewals, I’m not sure).

    Special education services and education for students under IDEA have to be provided in the “least restrictive environment”. This means that a student receiving special education must be getting education along with their peers as much as possible. This is supposed to provide a number of benefits like socialization with peers, exposure to grade-level curriculum, and preventing schools from sending all the students to a special ed room and ignoring them all, which is historically how many students with disabilities were treated even after many updates to IDEA. The positive interpretation of CMH saying your youngest son no longer needs their services and should stay in his normal classroom is that they are trying to make sure he gets services in the least restrictive environment.

    If your school is not letting your youngest son stay for a full day they are not providing a free and appropriate education and are discriminating on the basis of disability. You are going to need to advocate for him or dispute with the school district, and are probably going to need help from an advocacy group, mediation, or lawyer. In some states the state will provide a mediator to make sure school districts comply with the special education rules, but that does not seem to be the case for Michigan.

    504 plans

    Section 504 is the easier of the two for a school to use to provide accommodations. For a 504 plan they only need to document two things:

    1. That the student has a disability that limits a major life activity
    2. That it is interfering with their education

    (the second of those might not even be required)

    There are many accommodations that a school can provide for autism besides individualized education, and these can be called out in a 504 plan instead of an IEP if for some reason you can’t get an IEP modified in a timely manner. Example accommodations include:

    • Speech and language services
    • occupational/sensory therapy
    • social/time management/educational skill services (though these are more often part of an IEP)
    • behavioral intervention
    • Extra time on tests/homework
    • Break times to unwind from sensory overload
    • Noise cancelling headphones
    • stress relief/fidget/sensory toys
    • Quiet areas
    • Anything else that would help your child that isn’t getting individualized instruction

    IEPs

    Individualized education plans require eligibility under one of 13 disability categories. This requires 3 things:

    1. An identified disability (this can be identified as part of the eligibility process)
    2. The disability must have an adverse effect on their education
    3. The student must show a need for specially designed instruction

    The major difference between a 504 plan and an IEP is specially designed instruction. If the student’s getting specially designed instruction, it needs to be an IEP (from the school’s point of view). This means school districts might only provide speech and language services/sensory therapy/social skills/study skills/etc. under an IEP and not under a 504 plan. An IEP can include any of the services that could also be provided under a 504 plan.

    An IEP is where you are going to get help with any academic area your kid is struggling with due to a disability. For autism spectrum disorder this varies greatly between students, but that’s the point of an IEP, that it be individually designed for the student.

    IEPs require an annual review and parents are entitled to participate in that process. The annual review involves updating goals and progress and what services are appropriate/need to be provided and in general modifying the plan. This means you should get to participate in what services your kids are getting in no more than a year, but there should be nothing that prevents a school from updating these at some other time if it’s appropriate and they include you/their IEP team (see the parts of the pages I linked below about “Prior Written Notice”) and learn who should be on your student’s IEP team)

    Eligibility for an IEP must be re-evaluated once every 3 years. With a diagnosis for autism your kids will only need to show an adverse effect on their education and a need for specially designed instruction to remain eligible.

    Michigan

    I’d check out Michigan Alliance for Families for information that’s more specific to Michigan. In particular their pages on Parental Advocacy and Dispute Resolution

    Other options

    If your school district simply won’t provide appropriate special education services, many parents will seek out a different source of education than the school district. This can be a local charter school, an online charter school, or some other school of choice system. Beware that not every charter/school of choice system is required to provide special education services at all. Online charter schools with good special education programs get a lot of students enrolling in the school, getting evaluation, eligibility, and IEP plans, and 504 plans, and then transferring back to a brick and mortar school with documents in hand. A 504 plan from an online school will not address many in-classroom accommodations because there isn’t a physical classroom, but might still include accommodations that can be adapted to a physical classroom like being allowed to use stress relief toys during class.

    hissingmeerkat,

    Do you have a medical diagnosis for autism or ADHD or just school diagnosis?

    A “developmental delay” is only eligible for special ed under that category until a kid’s 10th birthday.

    If you can, getting a medical diagnosis for autism makes other services available even outside school (see kidswaivers.org). Doing so can be difficult both in cost and in the backlog of neurobehavioral health clinics that do autism diagnosis. You would probably need a referral from the kid’s GP/pediatrician.

    You can get more services on an IEP than a 504. If your kid needs individualized instruction they need an IEP. Either way your kid will have special protections when it comes to disciplinary action. A school can not academically disciple (suspend, expell, ot remove from the classroom, or e.g. not allow to attend full day vs half day) a disabled student for more than 10 school days in total over the course of a school year without holding a “manifestation to termination meeting” to determine if the behavior is a manifestation of the disability. If it is the school has to implement behavior intervention programs instead of disciplinary action.

    If they ask you to come pick up your kid early that constitutes “suspension or removal from the classroom”. If that happens keep track of the number of days, and use those words talking to administrators.

    I don’t know if those rules apply to preschool and kindergarten, but they should if kindergarten is mandatory in your state.

    School district are also required to attempt to identify children with disabilities living in their district prior to enrollment in a process called “child find”. This is to provide early intervention programs, like developmental preschool.

    It’s extremely distribing that your son was excluded from preschool due to a disability. I would be considering talking to a lawyer if I were in your place, at least seeking out the advice of a Michigan specific advocacy group.

    hissingmeerkat,

    I actually know none of that. I was eating dinner with my spouse.

    Border Patrol must care for migrant children who wait in camps for processing, a judge says (www.pbs.org)

    Migrant children who wait in makeshift camps along the U.S.-Mexico border for the Border Patrol to process them are in the agency’s custody and are subject to a long-standing court-supervised agreement that set standards for their treatment, a judge ruled....

    hissingmeerkat,

    This is the Biden administration. On immigration the US is now more xenophobic than the Republican primary between Reagan and Bush in 1980.

    hissingmeerkat,

    No. This is the alternate history of energy. We could have been building primarily molten salt solar plants for the last 40 years. They had similar costs to coal, fuel plants, could be built with no semiconductor manufacturing bottlenecks, provided more consistent base generation than wind, had no fuel dependencies, combustion emissions. Now photovoltaics and battery storage are cheaper, more efficient, don’t require water and cooling, and work with wind as well as solar, and aren’t really bottlenecked by manufacturing.

    hissingmeerkat,

    That makes as much sense as saying trans, non-binary people only need to have a satisfying, meaningful life without a vision of masculinity, femininity, or gender Identity.

    hissingmeerkat,

    No. Gender Identity isn’t zero sum. Things can be positive without other things being negative.

    hissingmeerkat,

    I hate gender roles and assigning anything to them. But everybody deserves a positive view of the traits and ideals they identify with and everybody deserves positive examples of how to express/demonstrate the traits and ideals they identify with.

    Noticing more smells and colors and flavors and sounds and being able to listen to more complicated music are all skills that we gain over our life. Identifying and identifying with traits you have or aspire to is almost certainly the same, and even if it isn’t I have no place to say that someone else shouldn’t think about themselves primarily as being a reproductive male (which may be devastating if that’s not something they can do), and since that is a common way to see oneself, due to the importance of reproduction or due to culture or due to some aesthetic like which flavors go together, then people identifying with masculinity deserve positive views of it, and positive examples of how to express it.

    hissingmeerkat,

    Silly. The limit should be 0. You can take no gas that you don’t pay for. You can vent/leak no methane except for emergencies, some tiny fraction of leak/well or pipe distance. If you flare gas you have to pay for both the gas you took and the lost utility of the gas to other users.

    And that’s not even getting to addressing climate issues.

    hissingmeerkat,

    Before you drive up to Minneapolis, there’s nothing to do there either. Walk/bike along/over the river is probably the best thing, and you can do that in Rochester too.

    hissingmeerkat,

    He was one month shy of his 16th birthday when he died. Now he’d have to wait a month or get his learner’s permit before being allowed to get killed by a car on an e-bike.

    hissingmeerkat,

    It’s not a literature review. It’s a case report on a specific patient. It’s impossible to imagine writing a discussion of your own patient in this way, or to accept an approximately 5 page article without reading it.

    The journal https://www.sciencedirect.com/journal/radiology-case-reports is refereed by an editorial board led by University of Washington professors, associate professors, and doctors of medicine.

    Radiology Case Reports is an open-access journal publishing exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women’s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.

    $550 - Article publishing charge for open access

    10 days - Time to first decision

    18 days - Review time

    19 days - Submission to acceptance

    80% - Acceptance rate

    hissingmeerkat,

    I don’t think HIPPA applies in Jerusalem.

    hissingmeerkat,

    Everyone I’ve ever seen open carry a handgun has been publically abusive of the people they were with (spouse/children) and it was obvious that the open carry handgun was to make sure nobody intervened in their abuse.

    Wanting to do things and having ideas is painful

    The last couple days I’ve finally been able to work on some of the big projects I care about and have wanted to do for months. But wanting to do all the things I want to do and having lots of ideas is painful, like before I got anxiety, ADHD treatment (which my doctor interpreted as being more of an anxiety thing) but also...

    hissingmeerkat,

    I started doing that last year with Joplin on my computer and it’s a big help.

    I also keep big notes to just dump everything I’m working on into - websites, pdfs, screenshots, screen video captures with no commitment to organization except I can add things in chronological order. A lot of it is initiated by showing it to someone else and then realizing I should have a note for myself too.

    I really should start doing the same with personal stuff and random observations. If something is important enough to tell (or what to tell) other people about it should be important enough to tell my future self about.

    It’s crazy how much not experiencing rewards yourself/the inability to do things for yourself influences things I wouldn’t even imagine before understating what ADHD is/does and consciously examining them.

    hissingmeerkat, (edited )

    Based on what they’ve done in the past, they’re going to write it off on their taxes when though the titles aren’t even games that they own.

    hissingmeerkat,

    That’s heartachingly alienating, I’m so sorry. I hope you find safe places to make friends both online and irl, where everything that you are now, have experienced, and want to be are valid and prominently welcome.

    hissingmeerkat,

    I’m terms of abilities, there’s problems other people can solve that I never will even with years of study and training, and there are problems I can solve that my immediate peers never would, even with years of study and training.

    I’m terms off knowledge, everybody you meet knows something you don’t. (They might not have the ability to help you find what it is though)

    In terms of skills, behaviors it seems like nobody ever considers trying and finding out for themselves, which is endemic across all levels of academia, government, business, and profession, and in that matter they are all as dumb as a bunch of rocks.

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