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Joined 1 year ago
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Cake day: June 10th, 2023

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  • I live in a country with socialised healthcare.

    I am at the point that I am looking into diagnosis mainly to be able to get meds because just living is hard. I remember being diagnosed as kid, but I might have a mixed up memory with my brother getting diagnosed and the IQ assessment I had.

    I walked into my GP, who is usually very compassionate and even understanding of mental health things telling them that, speaking about what I struggle with and they go „it is a trend diagnosis too and I personally know a man that says he doesn’t feel a difference with meds“ and give me a referral for a neuropsychologist. No expedited, no like guaranteed thing (there are a kind of slots for that). Tbf they named two good options they can recommend even if they aren’t allowed to show bias. My first „checking if we can help you“ date is on the 8th of August, and I filled their entry questionnaire over two weeks ago. Mind that is a first date, nothing in the way of diagnosis and they might say they can’t help me.

    The only other option is to either pay out of pocket for it (there are loads of private only doctors for it, in fact I did accounting for one of them), which I don’t want for two reasons: not having money laying around and not wanting to just walk out with a predetermined diagnosis. I am pretty sure I have ADHD, but autism plays a role as does childhood trauma and other things. So just treating the ADHD part could be detrimental. Or go call some helpline/emergency line and tell them I am suicidal and getting institutionalised. Judging by the treatment my childhood best friend got for that, I‘ld rather not.

    I am female and females present differently, so that plays a role too.

    My brother didn’t get treated btw, because my mother believed the stories about ADHD vanishing with puberty and that not happening when people get meds. He is also seeking diagnosis currently.



  • When I started my apprenticeship as assistant tax adviser in 2016, I used the fax regularly to send stuff to the IRS equivalent. I was also in charge of printing certain thing because the setup for those to come out right was unholy. In the company I am in now, we are pushing for digital solutions but still have a lot of clients with a listed fax number. One of our digital partners had fax: we don’t do that here written in their signature.

    It is a thing still sadly.



  • Largely owned by tencent afaik, putting things that are QoL and somewhat accessibility behind paywalls (like themes are a nitro only thing), do nothing against the spam bot malware thing (and they can scan the messages, since you can set the nsfw filter on them), not searchable outside of the app so things can get lost easily, their audio function is somewhat known to be problematic (for me it „catches“ the full audio out without software in between, so game sound or Netflix or whatever gets cut off completely). Those are what I can think of quickly. I am also not knowledgeable enough to accurately judge their software in terms of performance, but it feels very bad to me.


  • I also unticked the two things below, which told me I can’t get experimental features if I do so. Who knows how they label stuff internally, maybe they have something new in regards to contact scanning and we got „volunteered for testing“?

    Am also with you in the situation that discord isn’t my first choice, but one big community I engage in is there.






  • I am across the pond from you and as far as my knowledge goes laws are even more strict here.

    I am not a medical professional, but I did accounting for a lot of them and from what I have seen them pay for the relevant authentication hardware and software it seems to be nightmarish to navigate.

    While I am very pro data security and people being the owners of their own data, this goes the other way for me too. I own the data about my health, so I should be able to decide that I am fine with having it on my phone.

    The medication rollback I mentioned would have been completely unnecessary if that option existed. It was Ibuprofen, which my SO shouldn’t due to an already stressed kidney. Now that I know that I can look out for it too, provided I am allowed to go with.


  • This sounds great in a bubble where it works.

    Over here there is no standardised way of sharing such info between doctors/hospital/care givers. I have been through multiple GPs because some stopped working, some where to far away after a move and so on. I had to bring my data to them and good luck to me if I hadn’t gotten a copy of something when it happened. I had to stop medical personnel from giving me paracetamol (I have asthma and shouldn’t take any of that or anything like aspirin), the GP of my SO had to basically partly roll back a medication plan he had gotten from the hospital after being in the ER and those are mild cases where nothing did actually go horribly wrong. My SO got two incompatible medications about two years ago because the tool that crosschecks the database did not throw the relevant warning correctly. It messed with his brain chemistry a lot. His GP wrote the programs makers to have them remedy that asap, since it was pretty bad.

    I actually use the health app medication reminder/tracking now and have seen that the app can theoretically store data from health professionals about me. It looks like it is completely unused in the country I am in and I can’t manually add in data at all. This would be super helpful in some cases where I could use it to quickly convey key points about my health, especially when I am not as present (high fever, accident or some such).