u/Lower-Natural-337

L'ho comprato un anno fa in sostituzione ad un vecchio Samsung (unico Samsung veramente compatto in commercio) che aveva solo 64 GB e, per quanto mi trovassi bene, la memoria era veramente troppo poca. Cercavo altri compatti ma ormai non ne esistono. Recensioni del Motorola Edge 50 neo, che è un po' più "piccolo" tutte perfette, ma ho capito ormai che degli youtuber non posso più fidarmi. Sponsorizzano e basta, non mostrano mai criticità.

1. Come può un telefono medio gamma non avere una galleria incorporata?? Mi sono dovuta scaricare un'app da PlayStore e, non volendo pagare per una a pagamento perché mi sembra assurdo, se riguardo alcune foto, dopo quattro foto scatta pubblicità di Temu o altre assurdità per cui devo chiudere l'applicazione. Questo è un problema delle app gratis, ovvio, ma nel 2025 un telefono senza galleria?

2. Non ha un calendario incorporato. Tant'è che facendo il passaggio ho perso tutte date importanti inserite

3. La fotocamera? A dir poco imbarazzante. Per fare belle foto (e io sono anche fotografa, il telefono ovviamente lo uso come fanno tutti, foto ricordo, foto del gatto, in vacanza) mi porto appresso, udite udite, un Samsung Fame Lite del 2013 che ha 3 pixel e che fa foto portentose. Ma, senza andare di vintage, mi basta riguardare le meravigliose foto, i colori, i bianchi e neri di uno Huawei del 2017 e mi cascano le braccia.

Al di là delle mie fisse, è oggettivo che la modalità base abbia colori così saturati da fare sembrare il mondo sotto psichedelici. Selfie? Faccia rosa e labbra fucsia. Se fotografo una stradina mi applica automaticamente un fastidioso effetto grandangolo terribile da vedere. Modalità pro pietosa. Ormai ci ho rinunciato e non scatto più alcuna foto con questo, ma se non erro non ha nemmeno la modalità notturna.

4. Screenshot? Nel tempo che intercorre tra il cliccare i tasti a lato (perché le tre dita con il touch le prende 1 volta su 3) e la cattura delle immagini, posso tranquillamente farmi un caffè.

Ma c'è davvero qualcuno soddisfatto di questo telefono? Salvo la batteria, nulla da dire, anzi. E l'aspetto estetico (di cui però mi interessa poco). Per il resto è il peggior smartphone che abbia avuto in 12 anni.

As soon as I started playing, I was amazed by the fantastic houses with items and furniture I couldn’t find anywhere else (I wasn’t familiar with the gacha system and thought you could get them by leveling up or through events). Little by little, I realized that, in reality, the most creative homes—both in terms of exterior design and interior decor—are created by players who have NO gacha items at all. And, I’d dare say, very often they have very few pieces of Bob’s furniture, but lots of custom-made furniture (though this is just my personal taste, because Bob only has minimalist or industrial-style items, and I prefer cozier homes). Gacha items, in my opinion, stifle creativity a bit. Unless you design an entire house entirely in the style of that banner (which would cost a fortune), I often find houses that lack taste and have items that don’t match at all. Maybe they look impressive from the outside, but inside it’s just chaos. Sometimes I see real geniuses on YouTube—especially Japanese creators—who build fabulous houses and cottages, and none of them use the gacha system. Maybe it’s different for clothes; it depends on personal taste. But when it comes to building, it really seems to me that, in the end, the houses built by people who spend hundreds of dollars on gacha are often boring and never cozy.

Edit: Given the number of people who downvote every comment that agrees with my post (which I don’t understand—everyone is free to express their own opinion), I feel compelled to offer a further explanation.

I have absolutely not criticized anyone who spends money on gacha; everyone is free to spend their money however they want (and I’ve tried the gacha twice myself with the previous banner, so I’m not passing judgment). What I said is that I’ve found more creativity and ingenuity in the construction and furnishing of houses that weren’t built using gacha banners. It may well be that I’ve seen more attractive F2P houses purely by chance. But it’s also true that—to give a simple example—if you want to build something cool as a free-to-play player, you have to get really creative, as I’ve seen some YouTubers do. With gacha items, you have a lot of things ready-made. It’s clear that there are gacha players with great creativity and free-to-play players with little creativity. What I think, though, is that to create a beautiful build while playing F2P, you have to come up with unique solutions. There are people who’ve created fantastic kitchens or libraries using free-to-play options that I would never have thought of. With gacha items, it’s clear that you have a lot of cool furniture and don’t have to get creative to build them. During the group house-building event, I saw some WONDERFUL gacha-based builds—and some that were incredibly creative, too. But generally speaking, I find it more challenging to build a house using basic furniture.

There's only one thing I don't like about the gacha system in Hearthopia: it's too expensive and can be addictive, just like any gambling game. But that's another matter, and it's up to the developers.

To give some background, I had my second bout of Long COVID (the first one was in 2020) starting in September 2025, and it lasted a full seven months. I was completely debilitated. I’m doing a little better now, but I spent exactly seven months in bed. I also developed POTS this time.

Since then, I’ve also developed all, or at least many, of the symptoms of MCAS. Not only did the allergist dismiss the existence of Long COVID, even though I was diagnosed with it in December, but he immediately concluded that my symptoms were due to gut microbiota affecting my reactions to histamine-rich foods or foods that trigger histamine release, as well as things like thermal water, friction, or insect bites.

For almost a year now, I’ve been having frequent, extremely severe migraines after eating or drinking certain things, as well as bloating and pain in my stomach and intestines, severe itching, and huge welts from mosquito or insect bites that start at the bite site and then spread over my entire body.

I also have extreme fatigue, although that may still be due to Long COVID, even though my Long COVID symptoms are improving. I also have constipation or diarrhea, and other symptoms.

Has anyone ever been told that everything was caused by dysbiosis (and therefore that there are no tests to do) and that MCAS had nothing to do with it?

He didn’t even mention MCAS, but I don’t even know whether he knows what it is. He spent two hours talking nonstop about his research on the gut microbiota and prescribed a treatment with probiotics.

I absolutely don’t want to deny that I could have dysbiosis, but how am I supposed to know whether it could also be MCAS? In fact, my symptoms only seem to improve with cetirizine. He told me to take it whenever I want.

I honestly don’t know anymore. I’m completely confused.

All I know is that the Long COVID–POTS–MCAS triad has been studied and is real.

I have a chronic delayed swelling (edema) under my left eye that first appeared in 2024 after receiving a hyaluronic acid (HA) filler in the upper cheekbone/zygomatic area (not the lateral cheek) in 2022.

A high-frequency ultrasound performed in 2024 did not detect any remaining filler, but it showed tissue changes both above and below the muscle, thought to be consistent with a possible inflammatory aftermath. However, high-dose corticosteroids and bromelain had no effect, so it does not seem to be inflammation.

I would like to see a doctor who specializes in filler complications and who performs a high-frequency ultrasound before deciding on any treatment. However, after reading about the possible risks and complications, I am quite worried about hyaluronidase.

Are there any alternatives to hyaluronidase? Would it be better to "simply live" with the swelling?

The swelling fluctuates. It is always present, but sometimes it becomes worse depending on what I eat or drink, how I sleep, or during periods of significant stress. I also had long COVID this year, which lasted for six months.

In 2022, a doctor who was clearly neither honest nor transparent told me that I needed filler in the front part of my cheeks (not the lateral cheek area). I trusted him. He used a cannula and injected the filler, but I wasn't given any real explanation. He gave me the product label, and since I had no experience with fillers, I didn't know what questions to ask.Immediately afterward, I noticed irregularities on the left side. I was told to massage the area. Within a few months, the irregularities disappeared, but from time to time I still noticed something "strange" under my left eye—very subtle, almost imperceptible.

Then, in the summer of 2024, I woke up one morning with a swollen lower eyelid. The swelling has never gone away since.I had a high-frequency ultrasound performed by an experienced physician who specializes in both ultrasound-guided filler injections and ultrasound-guided hyaluronidase treatments. He told me there was no residual filler visible, but the ultrasound showed "alteration of the tissue planes above and below the muscle, more pronounced on the left side, possibly representing the aftermath of an inflammatory process." He advised me to be patient, take bromelain, and possibly use corticosteroids if necessary.

Well, I've been patient for two years, and nothing has changed. That's why I don't think ongoing inflammation is the explanation anymore. I believe the migrated filler may have obstructed the lymphatic vessels around the eye area. I find it very difficult to live with the way I look now. In my country, an oculoplastic surgeon has described this condition as late-onset chronic edema, which, according to him, can appear even up to ten years after filler treatment. He treats it with hyaluronidase, but in his published articles he also states that about 60% of patients are dissatisfied afterward because of volume loss. For those patients, he reinjects a filler specifically designed for the under-eye area using a particular technique called the G-Point technique. However, after reading so many stories about complications from hyaluronidase, I simply can't bring myself to trust it.

The swelling is not severely disfiguring, which makes me wonder: if I do nothing, is there a risk that it will get worse, as this surgeon suggests?Has anyone experienced filler migration causing swelling years after the original treatment? I'm considering getting another high-frequency ultrasound from a physician who specializes in filler complications. The ultrasound costs $300, and the consultation is another $200. But I keep wondering: what if the only treatment she recommends is hyaluronidase?

I've also had COVID-19 four times since 2020 and suffered from long COVID twice—once in 2020 and again this year, lasting about six months. I wonder whether this could make adverse reactions more likely. I'm feeling better now, but I believe my immune system has been very fragile since 2020. This year has been especially devastating. Are there really no alternatives to reduce the swelling besides hyaluronidase?

I haven’t read Lacan’s seminars yet, but for now I’ve read books on Lacan’s thought. What strikes me deeply—and what I find absolutely pertinent—is that Lacan places somatic delusion at the center of schizophrenia, placing specific emphasis on the body. I find this pertinent because I have, in fact, known people with schizophrenia for whom the body was indeed the site of the most terrifying suffering. Not just fragmentation, but invasion, movements, co-sensory disturbances, “too much skin,” bodies being punched, bodies that don’t belong, bodies without boundaries, bodies felt to be deformed, bodies in excess—and I could go on. Yet, in the classic definitions of schizophrenia, (in psychiatry but in other psychoanalitic schools) very little is said about somatic delusions in favor of visual or auditory hallucinations. Why, in your opinion?

This is my first time playing a gacha game, and I don't really want to spend a lot of money. I really loved the Eastern-themed banner, so I bought a first €4.99 pack (it gave me 6 items, including the carpets, and there were no duplicates). Then today I bought another €4.99 pack. It gave me the carpets again, along with the tickets/currency you get when you receive duplicate items, but... I can't find the carpets anywhere in the whorehouse! Shouldn't I have a duplicate copy of them? Please help me, I am new

There is little material available on the psychoanalytic approach to patients with psychotic features. Lacan was very clear on what “should not be done” and what “should be done,” even if he perhaps never explains it entirely well (but basically not the direction of the cure but a treatment with a warmer setting, no cut of the session, and attempting to construct a symptom/sinthome if one is absent). For Freud, it was simply impossible to do so, and he also considered transference impossible with a psychotic. Although he later believed that what destabilized Schreber was precisely the transference with his psychiatrist, so who knows. Regarding Winnicott, Bion, Klein, and the others, I have many more gaps in my knowledge. But if I’m not mistaken, Winnicott believed that in the case of psychotic patients, there had been even less holding and also severe traumas (I can confirm this). I know that—perhaps a legend—he had kept a very seriously ill patient at home to protect her during a phase of extreme vulnerability. So more warmth, as Lacan believed?That said, questions remain: on the one hand, many psychotic subjects are referred to other forms of therapy, so there is less experience in the field. On the other hand, it seems to me there are very different approaches to managing the setting. Personally, I believe the setting should be more flexible and warm. The distance from the analyst acts as a “driving force” in neurosis, but in psychosis? I have the feeling that a worsening of the condition is more likely, and (on the post-traumatic side) symptoms of retraumatization. Furthermore, if there is a significant psychosis (such as melancholic psychosis or others), or if there is a bipolar pattern with a risk of self arm attempt —in this regard, I have never understood how psychoanalysis would interpret bipolar disorder; perhaps by considering *Mourning and Melancholia*, likely specifically in terms of the melancholic psychotic aspect. But It Is not the point. But I’m also thinking of patients who are “on the edge,” considered borderline, or patients with a history of suicide attempts? Don’t you think that in these cases the analyst’s role should be more one of “containment,” perhaps even ensuring the possibility of contact between sessions, provided it is agreed upon? Or do you think that, in reality, an even more regulated and rigid setting is needed? If you have any articles or references, I would appreciate it if you could point them out to me.

I’ll try to explain this clearly since I’m not a native speaker. I’m relatively new to Hearthopia, but my language isn’t available in the game, and there aren’t any videos or tutorials in my country, so there are a lot of things I haven’t understood.

As I built, I realized I could save my “current home” to a slot, and then eventually move it using the Blueprint. Every time I made changes, I saved another “current home,” and yesterday, after spending a whole day building my dream house—starting from an empty slot and clicking “Edit”—I built it and then saved it for the first time at some point. By then, I only had 3 empty slots left, all filled with old saves of previous houses. Then today I did other things, created greenhouses and rooms, and spent many hours furnishing them. At one point I wanted to save the new changes, and not knowing how to do it without taking up yet another slot, I clicked on Blueprint, and when I exited, the house was still a work in progress. I’m on edge, but I want to ask you guys before I do something else stupid and get back to work.

1. Can I delete previous houses from the saved blueprint slots? I can’t find any options, but many of them are really useless. It would be enough for me to keep the second-to-last one. If so, how?

2. If I go back to working on the house now, do I have to save the changes in a new slot in “Current Home,” or is there a way to save/overwrite it?

Please help me!

*I report this because redditt blocked me the previous post I don't know why. I also Say that I am in major depression from months with hypersomnia. After a thing happened with my therapist, fram 3 days I have switch in a completly insonnia: I can be awake till 7 am. Then I take some meds tò sleep. I am not switch ed in mania because my mood Is totally the same. But I am a bit worried.

The post:

Am I the only one who doesn’t experience psychosis during hypomania but only during depressive episodes?

When I broke down and lost control, I actually felt unworthy and guilty for simply existing—to the point of thinking I deserved to be in prison—and I was hospitalized for the first time after and episod like this one. My analysts diagnosed me with melancholic psychosis (which emerged right in the middle of analysis, due to a “misguided approach,” believing my symptom was neurotic in nature; instead, I was pre-psychotic, and that very symptom allowed me to lead a fairly normal life, despite having experienced phases since childhood that I would now describe as mildly depressive and mildly hypomanic). I then experienced alternating long phases of major depression—though often bordering on delusions—and genuine hypomanic phases; but in reality, during those I had no psychotic symptoms. On the contrary, I seemed almost more normal, even if accelerated, hypersexual, self-assured, hypercreative, etc., and then I’d switch and reconnect. Here I see almost everyone talking about psychosis in mania and never the opposite.

Is there anyone here like me?

Am I the only one who doesn’t experience psychosis during hypomania but only during depressive episodes?

When I broke down and lost control, I actually felt unworthy and guilty for simply existing—to the point of thinking I deserved to be in prison—and I was hospitalized for the first time after a suicide attempt. My analysts diagnosed me with melancholic psychosis (which emerged right in the middle of analysis, due to a “misguided approach,” believing my symptom was neurotic in nature; instead, I was pre-psychotic, and that very symptom allowed me to lead a fairly normal life, despite having experienced phases since childhood that I would now describe as mildly depressive and mildly hypomanic). I then experienced alternating long phases of major depression—though often bordering on delusion—and genuine hypomanic phases; but in reality, during those I had no psychotic symptoms. On the contrary, I seemed almost more normal, even if accelerated, hypersexual, self-assured, hypercreative, etc., and then I’d switch and reconnect. Here I see almost everyone talking about psychosis in mania and never the opposite.

Is there anyone here like me?

Why is it that the more plots you have and the further back your house is, the further away your pets stay and the more they stay indoors?

When I had a house that was “closer to the street,” my cats and my dog would stay inside, climb onto the beds—the dog would even follow me up to the third floor if I went there (he’s clingy). Now that I’ve created a large front yard, not only do they no longer come inside, but they’re always out on the street.

I know it sounds silly because it’s just a game, but I’ve grown attached to my little pets, and now it’s practically as if they weren’t there :(

Two months ago, I wrote here that Latuda, which I had been taking for 3 years, had made me incapable of crying, laughing, or feeling any emotions. I was taking 20 mg, but on an empty stomach with just a coffee (no one had ever told me that it must be taken with 350 calories). Even though I had already been in a major depression since October, my psychiatrist suggested a 50% taper. However, scared by such a drastic reduction and having just found out it needed to be taken with 350 calories, I cut the dose in half but moved it to after lunch. Ten days later, I experienced a week of severe irritability, which eventually subsided, but at this point, I don’t know if it was caused by that shift.

At the next appointment, she told me to taper another 50%, essentially down to zero. That seemed like too much of a risk to me, so I did this instead: I take half the dose, but with just coffee again. Therefore, I believe the real withdrawal/taper is happening right now. I am crashing even further, with thoughts that I am now at the end of the line. I even asked my partner—who since October had been doing all the cooking just by himself—to go back to his own place, just so he wouldn't have to see me in this state.

Despite suffering from Bipolar 2 and CPTSD, or affective/melancholic psychosis, I wasn't taking Latuda (of which I was clearly absorbing only 10 mg) for depressive relapses, but rather for post-traumatic anxiety. However, I’m not experiencing a rebound of that anxiety, but a worsening of the major depression. In fact, I haven't been able to get out of bed since October, but right now I feel absolutely zero instinct for self-preservation. And yet, I have been taking 300 mg of Lamotrigina for years, and it’s doing absolutely nothing.

Has anyone else experienced such a severe crash during discontinuation? These feel like withdrawal symptoms to me, not a rebound, because I wasn't taking it for the depressive component. I don't understand anything anymore, but I am all alone, shut inside the house, and I can barely manage to eat. Not a single friend has said 'I'm coming over to visit you,' even among those who know I'm struggling to eat. Living like this, I just don't see what the point is anymore.

Basically, that’s it. I had started because in other forms of therapy (psychoanalysis) I felt “alive” and like myself—and, incidentally, as a recognized artist, I worked in a state of semi-trance (not pathological! It was my “method”), but I felt I was continuing to destroy myself because of the severe trauma I had suffered. I kept repeating the pattern in abusive relationships. A past of childhood sexual abuse, violence, psychological abuse, a rape, and toxic relationships as an adult. And I thought: I’ll try CBT with this doctor who claims to be an expert in trauma. I felt safe with her, and it’s certainly true that she didn’t trigger any post-traumatic reactions in me. She certainly didn’t have an abusive personality and was supportive. But year after year I lost pieces of my personality, and whenever I mentioned a trauma, she seemed completely taken aback. “Your mom did that? How strange, and why?” Damn it, because she was a psychopath! “I don’t understand why you’re afraid of your brother; you hardly ever see him.” Christ, he threatened to kill me, sexually abused me, and is a severe pathological narcissist! During a relationship with a manipulator, I had her read some messages, and all she could say was, “My goodness, what a heavy-handed man!” I could list many more; these mostly sound like the words of an ignorant therapist. But everything I felt was, in fact, exaggerated.Or, under psychological abuse. “Why don't you just leave? It's not like you have a gun to your head.” Jesus, do you even know what emotional dependency is? And yet I only saw his kind, motherly side, and I let myself be fooled by this stupid need of mine for love, for being looked after like a little girl.

My art? The first time she asked me, “What’s one thing that makes you feel safe?” I said, “When I go into a trance and paint.” Her response was, “You mustn’t dissociate.” I haven’t painted since. It was my work, my life—perhaps the only thing that gave me a reason to live. When I told her I felt that something had broken with the therapy and that phrase, she told me it was impossible and that it couldn’t have anything to do with it. (But it did; I did a lot of research.) She strongly convinced me to get institutionalized, pushing me to apply for disability, so now I have a label my abusive family can use against me: “She’s the sick one, she’s a psychiatric patient” (these idiots have confused my terrified withdrawal from the world while I was in a retraumatizing relationship with negative symptoms of schizophrenia...) . I think I’ve racked up at least 15 diagnoses in my entire life. The therapist had figured out it was C-PTSD, but geez, did she really know how to work with it? Her first sentence, knowing I’d had self-harm issues, was “let’s make a deal: I don’t know how to make it hurt because you can’t do therapy with a dead person.” Without considering that this line was cookie-cutter and could be found in a manual, the paradoxical thing is that yes, I didn’t hurt myself anymore. But in the end, she did therapy with a dead person: a living dead person.

Maybe I was a little strange, but I was alive. Now, for years, and getting worse year after year, I live in bed, shut away in my house, incapacitated. Was this the price I had to pay for trying to become “normal”?

Cognitive behavioral therapy can really reduce a person to a machine that needs fixing. And in the attempt to do so, it takes the machine apart and leaves it that way, destroyed. I hate all of this. I can’t go back. I was a good little girl, adapting to her when she told me to speak “down-to-earth” instead of in my own way. But it was my way! I hate myself for letting myself be reduced to simply nothing. And I’ve also been left alone.

I gain as a reward in Gourmet life the receipe of restaurant servono cart. I had the backpack full, ok. So I found in the mailbox as usually if it happens, I claimed but there is not! There is not in the fornitures receipes, no in building modality, nore in kitchen receipes (it should be very strange but I tried all I could try). What can J do?

The extreme ME-like fatigue has decreased significantly; I only experience crashes every now and then. Even the constant fever now only returns occasionally. POTS, however, is still present. I’ve had alopecia since my first bout of COVID in 2020. For some time now, however, gastrointestinal symptoms have also appeared. Foods that didn’t bother me at all before now trigger either severe nausea and headaches, or vomiting (this recently happened with game: after a dinner, my stomach was swollen as if I were six months pregnant, and at 3 a.m. I woke up vomiting everything up), or intestinal pain and alternating constipation and diarrhea. I get gastritis if I drink wine or coffee. I’m almost certain this is another symptom of long COVID. As soon as one symptom goes away, another one starts. It’s as if my body has become extremely fragile. Do you think it makes more sense to see an allergist to see if histamine is involved, or to see a gastroenterologist?

This. More, I fell so flat, with anedhonia and most of the time depressed, no emotions, no even capability of crying. Neither in a funeral. Neither in Major depressione, and I am in It from october.

So I asked to get out of this med. My doctor say ok (I take 300 mg of a mood regulator too), and She told me: you are on 20 mg, you can stop cold Turkey. WTF. I answered that I was scared, She told me One day yes One day off. I also asked her: but, Is It true that I have tò take Latuda with 350 kcal? No, Is not important. Because I have take It every morning from 3 years with a coffee only. It's ok, She said.

I asked her if I could cut the pill in 2 part instead of one day yes one day not, because of scare of mood disregulation (documented). She said ok.

It seem that she says ok to everything I say, so I wonder why I spend 80 dollars for 15 minutes of "ok". Is It more competent IA?

God, I read here that Is strictly recomended tò assume Latuda with 350 kcal! So the amount of Latuda I was takin for last 3 years was like 10 mg??

My doctor lives me alone in this tapering. I have decided to cut the pill in two part, but I started to take It after lunch. So...Am I taking the same amount of before now? I mean: for 3 years Latuda with a coffee only, now half of It but 350 kcal.

I am really confused. I have had withdrawal symptoms the second week, irritability, mentali acatisia and rage, then like normality (=Major depression that maybe Is worsening but I am not sure).

I am wondering now if It was Latuda that made/makes me without emotions or if It Is the High dose of Lamotrigine or of It Is my cptsd worsen or the wrong psychoterapy.

I am really confused now. I am on bed. The only sign I have received from my psychiatrist in this month of tapering has been, yesterday, the Bill.

I would like to come back in 2019 when I took only 5 drops of a sedative, 100 mg of Lamotrigine and klnopin. Now I am a zombie.