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Joined 9 months ago
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Cake day: September 30th, 2023

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  • In Australia we call this “skimpflation” because they aren’t shrinking the final product, they’re skimping on ingredients to lower production costs.

    It’s the bane of my existence because brands I know and love will change their ingredients without warning and without changing anything on the packaging (sometimes not even changing the ingredients list! If the ingredients list has always just said “starch” they don’t have to change anything going from arrowroot starch to cheaper potato starch)

    I have allergies and I’ve bought two boxes of the same product at the same time, and had an allergic reaction to one, but not the other.

    I used to always blame it on my housemates not washing the cooking utensils properly, but I now use separate cooking equipment and I clean down the kitchen before I start and cook at odd times so I’m the only one using the kitchen.

    I’ve started emailing companies after my allergic reactions to determine if they have changed an ingredient, and 90% of the time they confirm they have changed the ingredients. Usually they put some PR spin on it about the new ingredient being more allergy friendly or sustainable (they don’t clarify “environmentally” so I assume they mean “financially sustainable for the profits of our company”)


  • Again, it depends on the purpose of the group you’re creating, does this person in question face discrimination for their perceived race? Then a support group for people who have faced discrimination for their race may be the right place for them, assuming the intersection of having “chosen” to present as a race they’re not doesn’t create an unsafe space for the other group participants.

    However if your group is for people who have grown up POC or been raised in a non-dominant cultural group to discuss shared experiences, then obviously someone who identifies as POC later in life would not be served by that group, so would not be eligibile to join that group.

    There are circumstances when even if you fit the criteria of the group, you may still be excluded due to the way various identities and experiences intersect, or because your personal actions are not serving the group.

    It’s not discrimination to be told you can’t use a private service because the service can’t serve your specific needs, and your personal circumstances reduce the groups ability to serve its other members.



  • If you’re a private entity and there is a specific reason that having non-black people in the group would be detrimental to the purpose of the group, yes, in Australia you can make a black only space.

    For example, if you want to create a support group for POC to discuss trauma around being subjected to racism, to ensure you create a safe space, making the space POC only is not only legal, but often the more ethical choice for this group.

    Want to create a social and dating app for queer women to meet other queer women? What purpose would it serve to let straight people into that group?

    There is difference between public spaces, that must allow access and entry to all, and a private organisation that caters to specific demographics, and being freely open would completely defeat the purpose of the private organisations goals.

    I’m not an alcoholic, I don’t personally know anyone who has struggled with alcoholism. Why can’t I go to an AA meeting to talk about my feelings on alcoholism? Obviously, Because that’s not helpful, it has the potential to be harmful to the people who attend because they have lived experiences with alcoholism. I could argue I’m being discriminated against because of my medical history, but I’m not being discriminated against, I’m just not being catered to, because I don’t have an unmet need in this specific situation.





  • Depending on the time of year, produce is what I splurge on.

    In winter, I get sick of apples and satsumas, I could spend $4 on a highly processed snack that is tasty but doesn’t offer much else, I could $8 on a relatively “healthy” sweet snack (compared to the cheap snack), or I could spend $8 on small scale greenhouse grown strawberries.

    Given my options, if I’ve got money, I’m going to buy the strawberries, which is a splurge considering apples were $3 and there’s nothing wrong with apples other than “I’m bored of them”


  • I do understand your point, but as a layperson there is no real way to single out your protest impact to only effect those directly responsible, especially when, in most cases, those directly responsible are removed from the community to a degree that there is little you could do to impact them without also impacting their innocent underpaid intern who’s just trying to do their job.

    Yes, protesting impacts a bunch of people that can’t individually do anything and are therefore being inconvenienced (mildly or substantially, depending on the individual) for something they have no control over that is someone else’s fault.

    But I think part of the reason you see it this way is due to a general a lack of solidarity. If I’m inconvenienced because my bus is stuck behind a protest, that sucks, but I’m not going to blame the protesters (unless I genuinely disagree with their requests/what they’re protesting) I’m going to blame the very same people the protesters are trying to reach, because they are the reason that petitions, inquires, public outcry and lobbying hasn’t worked and now we’re at a stage of protest.

    It might push a few of us to get off the bus and join the protest because what else can we do. It might prompt someone to write into their local representatives to push them to hurry up and sign negotiations so the protest can end because they’re sick of the slow bus.

    There’s no such thing as someone that has “nothing to do with the issue” when the issue impacts us as a society. If you feel like a social issue has nothing to do with you, but the protests around it are impacting you, you have to ask yourself what you’re gaining from the current system, and what stands to be gained from the changes demanded by the protesters. If you genuinely think you have nothing to do with it, you might be a true hermit.


  • But what if your message is “can we all get along together please?” the other persons message is litteraly “you don’t deserve a vote, you don’t deserve equal rights, you don’t even deserve to drink the same water as me, you are not even legally a person, this is the law, get out of my face nigge* before the lynch mob arrives, because I won’t stop them”

    How are you supposed to remove yourself from that situation when that situation is brought onto you, and there’s no way to simply negotiate or compromise because the two “opinions” are diametrically opposed.

    If someone’s boot is on another person’s throat, I honestly don’t care if I sound like an asshole as I tell them to move their fucking boot. I’d rather be an asshole on the right side of history than a coward who was just following orders.



  • That feels like a large payout for that type of injury, but that’s not my business.

    Everytime I hear news like this, or stories of people who “receive support for xyz injury, but can still do abc activity so must be cheating the system” I can’t help but think how brightly it highlights that the author has never had to experience chronic pain and dynamic disability.

    Anyone who has ever injured anything knows, some days it just randomly hurts more than others, and you have very little control over predicting or changing that randomness other than through avoiding certain activities when you can to preserve your health and energy for days and times when you don’t have a choice and have to perform that action.

    It’s also about balance.

    Because of my wrists I can’t do the dishes and do latch hooking on the same day. I have to do the dishes, I can’t just live in squalor. But some days I also “need” to take some time for latch hooking because it’s a mindful hobby I find enjoyable and it’s so good for my mental health.

    Now is it wrong of me to tell my OT that my wrists mean I struggle to do the dishes and latch key, so I’d like support with the dishes - maybe I get a dishwasher, or a helper twice a week to come in and do the heavy dishes for me.

    If I’m sat on the couch doing my latch hooking putting pressure on my wrists “just for a hobby” while the dishwasher runs in the background - was I lying about my injury? Was I being a cheat? Do I no longer deserve the dishwasher because I’m “abusing it just so I can run off and have fun latch hooking”

    She tossed one Christmas tree at a one off event.

    How does that change the pain it is causes to play with her kids or carry groceries every single day that she wants and needs to do those tasks?


  • If she loves organisation, “A Little to the Left” and “Unpacking” are cute.

    Stardew Valley is being mentioned a lot and with good reason, there are a lot of elements to that game and you can choose which activities you like most - farming, mining, fighting monsters, foraging, interacting with villagers.

    From there you can get a really good idea of what other games could be even better. For example if she loves the social side of Stardew Valley a Japanese Social Sim game might be fun too.






  • Hmm, should I try getting it a fourth time? 😂

    I managed to avoid it until Jan 2023 when I was hit the first time. Completely asymptomatic, I would have had no idea I was infected if it wasn’t for the fact I RAT/lat flow tested twice weekly because of my job.

    Recovered fine, didn’t have any lingering symptoms.

    Then in May I started getting a bit run down, my lymphnodes around my neck and jaw were really swollen and inflamed, and I was chronically congested, but not with any mucus or anything, just felt like my sinuses were swollen shut, and in the first week of June I had my second covid infection, still mostly asymptomatic, no cough or anything, just fatigue and headaches.

    The headache never really went away. I’ve had chronic headaches my whole life due to arthritis in my neck, but this was different, more pressure and in a different location.

    In September I got Covid again, and since then I have felt so crook. Migraines almost every week, moderate headaches every day from the moment I’ve wake up to the moment I pass out from exhaustion. The fatigue never went away but I can’t sleep anymore. I’ll lie in bed for hours but only get ~4 hours sleep a day, sometimes I’ll get 8 hours but in multiple naps. I’m thirsty all the time and can’t quench it, but I’m not really peeing at all, even less than usual despite drinking more water. Some days I can’t keep food down, some days food goes straight through me, there’s no middle ground. My lymphnodes are still swollen and now it’s all over my body, not just in my jaw and neck. I’ve had sinus bradycardia since September and dyspnoea (feeling like I need to yawn but can’t, like the air in my lungs isn’t getting in deep enough), and my nose bleeds every morning.

    I’ve seen my doctor 8 times since June, basic tests have been run and all they can say is “it’s stress and long covid”

    Im fucking sick of it. I’ve had to drastically reduce my hours (and pay) at work, and I miss my friends and all the fun active things I used to do.

    I’m still managing to get by, but I wish I had a better understanding of why I feel the way I feel. “long covid” feels just as useless as no diagnosis at all.