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For striking up conversation I would say to be yourself, and make some little comment to the other person. Something about how much you enjoy what you are ordering, asking how the other person is doing, comment on the weather (at least a very popular topic of conversation in North Europe where I'm from lol), or any current event. Another way of starting conversation is to ask for suggestions or advice, maybe for a good gym, a nice restaurant, or something practical. Your place of work is, as @suedseefrucht says, a great way to connect and make friends, and here on happiness you can search for friends based on geographic location (we're still a small community though) and through shared interests.

Welcome to happiness! It can be difficult making new friends when you are new in an area; I think most people can relate to that. Although we are still a small community, you can use our search feature to discover other members in your area. I would also say joining a gym, a course or workshop, or any kind of activity where you meet people can be a good way to make friends too. Here on happiness you can also connect with people based on their interests for examples, so this way you know you already have something in common 😊

In connection to my last topic, "To be not neurotypical" I will give you an update. I wrote a blog with over 5000 words and won't translate it manually. This was my first topic: Diagnosis - Dysthymia and APD: what now? sorting and enlightening Important NOTE: I have researched everything to the best of my knowledge and belief and, above all, my own experience has been incorporated. Mental illnesses are as individual as people themselves. I ask you to bear that in mind when reading. I've been reluctant to write a blog about my diagnostic situation lately. The last status for you was that I was looking for a diagnostician. I've written countless emails and also came close to shelling out a lot of money for a private practice. But then a friend came up with “Hey. Look there. Maybe they still have room.” And I also wrote an e-mail there and then waited. A week and I was written to, they called and waited again. Another phone call and then it happened in quick succession. I was immediately given an appointment for the screening and one for the diagnosis and then it was time to wait. I was a total bundle of nerves. As usual for me, I thought everything out. I imagined the worst scenarios. Not about the diagnosis. At least not the actual diagnosis itself. But rather …. that they find nothing and that I remain ignorant. The thought was hell. And at some point the appointment came and unfortunately I had to go there alone, using public transport and was nervous as fuck. And in the end it was all very exhausting. the screening I had to look for the building first. The clinic was huge and the direct route to psychiatric diagnostics was blocked by a construction site (Welcome to Berlin). So I spent 30 minutes looking for it. Luckily I'm so paranoid that I always plan a lot more time for first-time visits. So in the end I was half an hour early. When it was finally my turn, I had to tell almost an hour. And tell. I talked about my childhood, my life, my relationships, jumping back and forth with nervousness. While I lost the thread umpteen times, I watched the psychologist write and write and write and listen. She asked exactly one intermediate question. Then she enlightened me on a thing or two, raised a suspicion that I forgot when I left the room, and basically handed me a laptop on which I had to answer hundreds of questions. The actual screening has started. The questions were strange. Mainly because at first they didn't really match the questions I asked myself. I tried to answer them patiently and then left after three quarters of an hour, totally exhausted. The wait It took 1.5 weeks from the screening to the result. And with each passing day it became somehow harder for me, who is already impatient, to stay patient and strong. Every day I was more exhausted. tired. perplexed? I threw myself into a game, got the job done as best I could, indulged in some beef again. But I wasn't really happy with my overall situation. My husband had to constantly listen to what was going through my head. My friends. Many other people. It helped deflate the head a bit. But the pressure sometimes came back faster than I could talk/write about it. But in the end, and I had to admit it to myself, I had to wait. Whether I like it or not. And then the day came. The diagnosis ... I went with a suspicion (which I will continue to investigate, but only after the move) and this suspicion was ... completely ruled out (I'll get a second opinion there) and I was after I had a few more questions who gave the diagnosis. I suffer from dysthymia (more on that in a moment) and anxious-avoidant personality disorder (AVPD). She tried to explain to me in a very scientific way what it is and my only question was "And this since my earliest childhood?" And she said yes to the dysthymia. My head refused to accept this at first. As I said before, I approached the whole thing with different expectations. After the conversation I went home and talked to my husband. I've exchanged ideas with people a lot and, above all, collected a great deal of information and, now that I've endured the acceptance, I want to start clarifying things immediately. Mainly because I find that important and it also helps me to process things. So let's start with something that hasn't existed since my childhood and that I can even define quite precisely for myself. Avoidant Personality Disorder (APD) Anxious-avoidant personality disorder is characterized primarily by the fact that one feels very inhibited, unattractive and inferior and avoids social contacts for fear of (especially negative) criticism or being ridiculed. They often feel incapable of representing their opinion and very often (as with dysthymia) have the problem that they lose themselves even more in these feelings of incompetence because they feel misunderstood. People with AVPD tend to be quiet and withdrawn, even within groups, and they find it very difficult to say no because it could be interpreted negatively. For people with this diagnosis, social contact is very uncomfortable and eye contact is avoided as much as possible in many cases. When social contacts arise, those affected are usually very careful to keep their distance and tend to torment themselves through the conversation. Above all, they often hold back on the flow of speech in (group) discussions. For me it really depends on the topic. The rest I would say, and I have to admit it to myself, actually fits … like Hati's fist on my eye. Self-assessment APD The origin of an APDcannot be fully deduced. There is a lot of speculation that it can also have genetic causes (which would not surprise me at all). In addition, negative influences play a very important role. But I don't want to rattle down Wikipedia or scientific writings. But one thing in advance: APDoccurs in perhaps one percent of the world population and therefore there is very little therapy evidence. Most therapies manage to bring improvement, but do not really reach a normal level of social skills. Now let's really get to the self-assessment. As a child I liked B. still hugs and physical contact. But that decreased slightly early on because I often felt rejected by my own family. So feelings that I have developed. In the course of my youth, that has already changed. I am still “liked” to go away, e.g. E.g. discos, clubs and such, but with as much freedom as possible for me. In the end I would say that many negative experiences have ensured that the APDhas continued to worsen. It has apparently always been there and would probably be easier to treat if I had been diagnosed as a child. I actually still feel the need to go to a club again. But I hate the crowds that are common in Berlin clubs and I would have to get there drunk to have any "fun". Or I would like to go to a pub or bar again. But the discomfort that this disease brings is like an impassable wall. Movie theater. Cinema always works. I'm someone who distances himself because of this illness. This makes people think I'm arrogant or that I'm talking down to them. Mainly because I often avoid eye contact. But there are other reasons for that. If I do something, I want to do it well. I want to prove to myself and (primarily to others) that I can do things. It's a bit... like a compulsion that you can't escape. Especially at work I was often told (after projects or presentations) that I came across as being condescending. But that is never (!) my intention. And I have often tried to work on it. And now I also know why it never really worked out to work on it. While you can at least try to maintain a certain social level in a normal conversation, it's more difficult (for me) with lectures, because you want to present your work, which you've put a lot of time and effort into, and something switches on in the head around. You get more outspoken and often adopt a tone you don't intend and end up being... the arrogant asshole without even realizing it. I've also forced myself to maintain eye contact for years, no matter how uncomfortable it made me. You know that: "Look at me when I'm talking to you!" And so. In addition, society considers it very impolite not to look the other person in the eye. I don't know why, but Corona made me stop forcing myself. I look at someone for a few seconds and then either look past them or pretend to look for something. Or I would do something “important”. Just so people don't see it as rude. I... just don't like it. In the end, the APDexplains a lot in my life. But how do you explain it to other people? And especially those who come up with sentences like “Just socialize more. You'll get used to it." Corrosive. I hate that. And that in combination with what's coming now, it's like winning the lottery. Only … without a payout. Dysthymia - high-functioning depression Similar to APD, this diagnosis is not very common. Around 1.5% of the world's population are diagnosed with it each year. Approximately 3-15% of this is in the USA alone. Depending on when it is recognized, dysthymia is a largely treatment-resistant psychological disorder. Therapy and medication can bring about an improvement, but this is rarely the case and unfortunately a cure is almost impossible (depending on whether you ask a medical specialist or a homeopath). And the most tragic thing about it: it is chronic. But more on that in a moment. In addition, improvement also depends on when it is diagnosed. It's more successful when it's a kid than it is... my age or even later. The symptoms of dysthymia are seen by those affected as "I'm just like that" and also internalized. Correspondingly, pathways are created in the brain that also store this feeling permanently...? There is also evidence (which unfortunately only takes women into account because the disease occurs more frequently in women than in men) that patients with dysthymia have a different form of certain brain structures than mentally healthy people. In the end that means: an improvement is possible, for a cure I would need a new brain. Exaggerated of course. In the end it's something you live with and have to come to terms with, and you have to appeal to your fellow human beings to accept it. do you know that Especially the bad mood question and that with the smile ensures that at some point it occurs reflexively. You smile because you see someone. You smile because it's expected in certain situations. Similar to eye contact. You force yourself to do it. Dysthymia is... persistent depression. Although it is weaker than most other depressions, the duration is often several years or, in my case... forever. People with dysthymia have very low self-esteem, are often exhausted, have very poor sleep, and very little energy and happiness. Even everyday activities don't make you cheer up or anything. It's like a permanent state of sadness. That would be to put it very simply. Those affected with dysthymia often have the following characteristics (thanks to Psych2Go DE on YT for a simplified explanation in a video) and unfortunately all of them apply to me. I will also explain my behavior on the individual points: Worries about time My husband can sing a song about how often I complain about not having time and how everything I do ends up being a waste of time. This is very pronounced for me and there is very little that I don't see as a waste of time. This blog e.g. B. I claim that with this content I can contribute to the enlightenment of many people. But in general, no matter what I do, I see it as a waste of time. Even sleeping is a waste of time for me. If not the biggest. Self-criticism Affected people criticize EVERYTHING they do. I'm z. B. a person who tries things out. Again and again. But I criticize myself so harshly that I hardly get anything done. Or even finish it. It comes from the feeling of not being good enough. Not being what you hope/expect of yourself. This drives many of those affected to unhealthy limits. I'm actually one of those people who just drop things (fortunately, let me say this). Thinking everything through . I've been told this so many times and I often say it to others. But in my case it is very, very good: I think about something for so long, no matter how useful it is, or not that it robs me of my sleep. For example, when Hati first came here, I panicked myself so much that I imagined myself barricaded in the bedroom even before he arrived. “What if… and then if…”. These are trains of thought that create a vortex that is almost impossible to get out of. Feelings of misunderstanding In the video by Psych2Go DE, this is broken down very much into the illness. But it is actually a general problem for those affected. One often and quickly feels misunderstood or misunderstood. Be it in conversations or in actions. I have that e.g. B. more often at work. I explain my view of something and run into blocks or I am made to understand (perhaps unintentionally) that my thinking is wrong. That makes you withdraw even further at some point. Especially in connection with the APD. But more on that later. The Sea of Sadness As a dysthymic sufferer, you are sad most of the time, or almost always in severe cases. While with most other types of depression you can say "The last time I was sad was every now and then" it's more like saying "I don't remember being happy" with people with dysthymia. For me, since I can't remember either, it's like "The last time I was happy was on ... because." It is a never-ending sadness, sometimes weaker, sometimes stronger. A .. grumpy mood that won't go away no matter what you do. Unhealthy coping Sick people naturally try to come to terms with their lives and their (often still unconscious) illness. Nevertheless, those affected try to switch off their heads somehow. As a result, many sufferers become addicted to alcohol or drugs. I have a disturbed (but not pathologically disturbed) eating behavior during worse phases. So-called overappetite. I want greasy food and that's what I do. Also in the knowledge that I have a bad conscience afterwards because I ate greasy food again. It has become less. But unfortunately I can't turn it off completely. But the opposite can also be the case. underappetite. Some sick people stop eating. This over a long period of time, which can also be very unhealthy and even lead to worse diseases. Of course, there are more unhealthy coping methods. However, I have limited myself to those that are most common or concern me. Unhealthy pastimes For sufferers, activities such as watching series, burying themselves in games seem perfectly normal. Just like all the other points mentioned. After all, they live their lives like everyone else. It is their flight from reality that makes life so difficult for them. And most importantly, they try to escape the disease a little. It may seem unhealthy to others. For those affected, however, it is a means of not falling into even deeper depressions. It was well described in the video: Sick people often feel numb and sometimes as if they don't fit into the world because others don't. Others laugh, rejoice, fall in love. And in the end, only the veil remains for those affected, which makes us sad. Associated with dysthymia, as previously mentioned, are (everything in my case) increased appetite, trouble sleeping, fatigue and low energy, decreased self-confidence, reduced ability to concentrate (which in my case gets worse the less interested I am), and difficulty making decisions and last but not least often long-lasting hopelessness or pessimism. This is normal … I thought. I really thought what I am was normal. My whole life. And so it is with many sufferers. When it comes to depression, people always thought of these classic descriptions. death unhappy. Often with a tendency to suicide. I hadn't expected that my permanently depressed mood would really be a clinical picture. "I am so." I always thought so, and in the end it is. I am like this and in the end I will stay like this. In the end, Roswitha turned out to be a really existing disease without knowing it beforehand. I also found a few sufferers of dysthymia and I wanted to quote you something that I find very … appropriate in retrospect, especially related to Roswitha. “Yeah, absolutely right…. Dysthymia is a real bitch. Because it's always there, but lets you "Somehow, just about, but never fulfilling or even happy." Additionally, this quote also pretty aptly describes what dysthymia is all about. never to be happy. But what is all this together? I tell you. double depression Dysthymia rarely comes alone. It often occurs together with another psychological clinical picture. The interesting thing is, it can be anything. And that's why every dysthymia is somehow unique. There are days in a year when I can't get up. And even if I make it, I'm then e.g. B. glued to the couch. Nothing could make me do anything these days. I feel weak, useless, unable to do anything. Then one speaks of a double depression. The APDcan indeed be episodic and at the end and in connection with the dysthymia can cause a total knockout. There are years when this happens more often and then there are years when it only happens once or maybe twice. This is also a time when one feels infinitely empty. Not the emptiness I usually wish for because my head is overloaded. But an uncomfortable emptiness. Helplessness hits me pretty well, I think. Rarely, at least for me, does it happen that it takes a longer period of time. My husband also struggles a bit with me because I'm generally listless. And I'm always particularly sorry when we then e.g. B. do something, and I'm rather unsympathetic. And I'm always afraid that this will change something. job loss e.g. B., or that my partner(s) turn away from me. It ends up being a flood of all the fears I've talked about before. I also took the trouble once and created a graphic, which was also shown to me in a less beautiful way, to clarify the whole thing for you: thegreen: The line represents the mood of a mentally healthy person. Sometimes you're in a good mood, sometimes you're not. An up and down with no significant peaks down. theRedLine is the average depression, as it is often described. You have a course like that of a mentally healthy person, but it goes down episodically. As mentioned above, these people can often pinpoint when they have been depressed. theblue-turquoiseLine would be a dysthymia sufferer. A permanent gloomy mood with no upward improvement. And thepurpleLine is... Gerry. This is then a double depression as described above. You always move in the depression and fall into a hole episodically, only to end up in the permanent depression again at the end. There's no way straight up. while e.g. B. Jokes ensure that people can be amused by them for a while, it is a little different with dysthymia sufferers (especially from my own experience): I z. B. can laugh me to death. I can find things hilarious. But that doesn't cheer me up at all. I'm back in my gloom within moments of laughter. And from experience I can say... it's hell. This combination also ensures that small changes in familiar situations throw me off track. I have a small example for this: At work, we work with so-called backends. So desktops where we can do many things. Once an input window was moved. To the right edge of the screen. It blew my mind one day (and I tried my best not to show it). And it took me over a week to get used to it. And it was exhausting. And in the end there is no way out. My combination in particular is really … bad (personal feeling). Both are difficult to treat and cannot be cured. This means …. oh I'll get to that later. But please believe me when I say I hit the jackpot. But I'm sure others fare even worse. But there is more. The samples I once got a funny saying in a different context. But I convert it a bit and pass it on to you. “It's like this with the special issues: It's like being in a perfumery. You buy your depression illnesses and get other little problems as samples in the bag.” At the end, the following flows into the dysthymia. I have increased impulsiveness compared to the average human. This ensures, among other things, that I quickly get upset and mentally get up to 180 very quickly. This is (for me) very difficult to control. In addition, it also takes a lot of strength to keep this impulsiveness in check. Especially when I feel misunderstood and people don't make an effort to understand me. I think I've philosophized enough about my fears and even made huge projects out of them, so I'll just skip that part. A great deal of insecurity in social contact is also one of these little tests. There are actually moments for me where I think, “Are you really texting this person? Would she even be interested in a conversation?”. And only digitally. In real life it's even worse. Other problems such as B. understanding other people (especially facial expressions and gestures) are also present. Or the rendering of one's own inner being to third parties. This also applies to communicating in an understandable way. I'm often bold, forward-thinking and, at least I'm often given the feeling, ambiguous. In the end... I could have done without these samples. How does it go from here? After the diagnosis I was advised to see a therapist. With emphasis on the fact that this / r has a license to practice medicine. Funny. I almost had to laugh. It's hard to find therapists at all. Finding a therapist is more like looking for a needle... in 20 haystacks. At least in Berlin. But I know that I won't do that again in Berlin. We have decided to move this year. And I don't want to put myself through the stress of searching and any therapy per se and having to move with me. Afterwards the boys have to do everything themselves because I can't get up. I'm so scared of this exact situation. In addition, it would be pointless to start therapy here and then start all over again in six months. It's already... very stressful. If it was up to me, I would take some time off. Sleep in (although it's a waste of time, I seem to need it). My energy balance is currently absolutely in the basement. It all cost a lot. The dysthymia is already very energy gluttonous (she is an energy whore). The last few weeks have been exhausting. And the last few days have sucked me dry. And I also dedicated myself to the beef and now this blog with thousands of words. I'm just done. But I'll see if I'm more motivated to draw. Because when I was actively drawing, everything was a little better. I'm trying to optimize my setting a bit to counteract the displeasure and my own laziness. I'll definitely see a therapist at some point, but I've planned other paths for now. The positive side of the coin Much of what is bad often comes with a positive side, which comes to light when you network with people who have similar or even deeper problems. Especially with diagnoses. I have a very strong sense of justice (which sometimes kicks a little...too intensely). Discrimination, disadvantage and such are a red rag for me, which I jump at in 99% of all cases. Like an angry bull. I no longer have to be ashamed of being "ungrateful," "rude," or "antisocial." In the end (and while that sounds like a cheap excuse), it's not my fault. And I've now taken two days to understand that. Of course, the shame will never end. But it doesn't have to make me feel any worse than I already feel. I had given the monster a name in my head. Roswitha. And now the monster has a shape too. And that's reassuring. I finally have a tool to educate people who have issues with me. I can say “Hey. This is due to the following reason…”. Of course, that doesn't make things any easier. I will have the same problems and challenges in the future as I do now. But I can work better with it now. And I solidified other choices. Met new ones and I hope my own urge to drift off into doing nothing doesn't get in the way. It has been very… present in recent years. And what is perhaps also important … Due to the illness, of course I (was) the perfect victim of bullying. I was also able to recognize a lot for myself. However, that does not justify bullying. And never will. But... let's be honest: I was easy prey. But still … past contacts First of all: You don't need to have a guilty conscience. You didn't know. I did not know it. Nobody knew. But I can close some "files" now. I've often asked myself why people left my life. Especially the APDexplains a lot. There are two subtypes in the APD. And I've done both. I used to be pliable-exploitable. I felt taken advantage of by others or was even taken advantage of, which explains the current problem. Because I was blind to those signs. I think it has accompanied me for 25 years to belong to exactly this type. By now I would say I've become the "cool-aloof" subtype. I've become very suspicious. Especially if you want things from me. I don't know if it's common to iterate over both subtypes. That's the way it is with me. People (including very important people who I somehow even still miss) have often turned their backs on me because I'm always so negative. Because I tend to look at everything grey-black instead of white. Because I push forward with my negative thoughts. Because people couldn't accept that dark spot called Gerry in their lives anymore. I even understand that now. Although I continue to believe that toxic positivity is a big problem. There are one or two contacts that I think it would be nice to re-establish and maybe people understand that that's who I am and that can't be changed in the blink of an eye, and maybe never. But I don't believe in it. In addition, the wrong people will also feel addressed by it. So if I don't answer you... you don't belong. What doesn't help? Now how do we deal with this? "I'm sorry for you" ... It's allowed. But... it doesn't help. Expressing sympathy when you don't understand something only serves to make you feel better. It doesn't help those affected at all and in the end you feel bad (in my case at least) because you might have even made someone sad. Also, trying to impose things like positivity or hope is totally unhelpful. This combination of diseases almost does not allow you to absorb hope and positivity. Or even perceive. And no matter how hard a person tries to instill confidence in a hopeful future, it's more likely to result in... reducing and ending the conversation, or in the case of sustained PA, the contact. I've always tried to avoid that. So cut off contact. This often took care of itself (see last section). As hard as it sounds: In view of the facts regarding treatability, let alone a cure, there is no hope. Or I don't see them and I can't either. You're welcome to have hope. Nobody forbids you that. But don't force it on me (and possibly other sufferers you meet). This is a waste of time and energy. Mutually. Also, forcing someone to do something (for example, saying that you should seek treatment immediately) is counterproductive. I have my pace. I want to set my own pace. The "readiness" to do something has to come from me. I have to make the decision to start therapy. to practice a sport. to find a hobby. And and and. I must not be denied the right to make my own decisions on this particular issue. And now? I've done a lot now. In recent years I have tackled many things that were put off for years. I've built up a small but fine group of friends. I changed my name. Official with certificate. And now I have a diagnosis. But now... I'm tired. And somehow I have to manage to gather enough energy in my head for what's still to come. The move first. I would like to let myself rest for now. Spending time with my family and friends. The subject itself will come up many more times in these contacts. And I hope that you all understand that. But I don't want to press any further for changes. i need a break I will read more about the two diseases. Educate myself to maybe find ways to explain it more easily. I'll learn to deal with it. And above all, I will try to approach those around me in a reasonable manner in order to explain and clarify this. I have two diseases that cannot be seen. Externally I am healthy (perhaps a bit too fat). Oh well. Except for little things like my acne or my eczema. But you'll never see my head. The chaos. The fears. The perpetual darkness. I will keep getting up. Carry on doing my steps. No matter how many times I fall. I will live with the diseases and continue to fight my life until maybe one day I can't anymore. And I should be aware of that, and so should my family: it can happen at some point. And it's up to my family and friends if they want to continue with me. You see a Gerry who is grumpy. You like (or hate) him. And now you also know that I'm sick. In the head. With ailments that many people think a little sunshine could cure. Or even refuse to accept them. If you have questions: ask. If you want to talk to me about it, talk to me. Thanks. Thank you to everyone who has been there for me so much over the past few weeks. Gerry

Take charge of your life with these easy and comprehensive classes taught by teachers with years of meditation experience. The Foundations of Mindfulness. I am here to take more ideas to make yourself happy , i will be happy to hear some good things from anyone who is already doing 🙂 thanks for your support and help.

For me, this music is a yoga. Music is really the best way to relieve stress, and yoga is a great skill but it's hard to find the right video, but you can easily find it on your mobile so you can try it too.

For me it's music and yoga. Music is indeed the best way to relieve stress, and for me, listening to playlists from youtube is the best way to cope with anxiety and so on. But it's hard to find the right video, but with services like mp3 juice, it's easy to get everything on your phone and listen to it. So I don't have any problems finding the right music and coping with stress that way, so I think you can try it as well.

First of all, thanks for sharing your story. I'm an engineer too and it can be stressful sometimes. Fortunately, I found a job where quality is more important than speed, so there is not too much stress. I guess, there is a "not" missing? There where internships attached to your diploma studies, right? So did you try to work as an engineer yet, so you can tell if it is too much stress for you? If not, you should try an internship first, just to get to know the work. Also, you don't have to go the way, people expect you to go. If you figure, you can't work as an engineer, you are free to do something else. Yes, you might not need your diploma anymore, but you gained experience. I don't know if you studied mechanical, electrical or some other kind of engineering, but you could just become a mechanic or electronics technician, if you like. To me, a good work life balance is more important than a high salary job anyway. If you earn enough money to get by, everything above is just a bonus.

I used to be a strong boy who could broke coconut by punch. When I turn 20 (in 2018) from then misery in life started. Middle of 2018 Just finished my diploma engineering degree and it was time for me to start a new life, a new career. But in that time I fell sick so bad for 6 months I couldn't do a thing. Went to few doctors they couldn't help much. Finally found a doctor who could really diagnosed my problem, and it is a bad DNA related rare disease. No I won't die quick but will suffer for rest of my life. Last quarter of 2018 I was getting a little better and felt the same young energy again, I decided to go Russia for higher studies. Did as thought, February 2019 I went to Russia, things were good but for only a little while. I got sick again but this time problem was much worse because I wasn't good at Russian language to explain what was really going on with me and couldn't understand words from my doctor basically lost in translation. I was taking too much pain killer everyday that my condition was getting more bad. Took a leave from university and flee back home for treatment. Good thing I did that if not I could've risk my life. Get treated, get good and get back to Russia again in February 2020. And not long after that corona virus pandemic broke out. I was studying on self finance, but during that time my father's business was at stop, I have a big family so things were little out of control. And things kept getting worse, my father had a brain stroke and got half paralyzed. I was so depressed at that moment I couldn't even came back to see him because of flight restrictions. In August 2020 I quit my studies and came back for good. I stayed almost 18 months in Russia, went to study but couldn't study at all because of all the hardships I was having, wasted time and money. As of today I not fully healthy as I said I'll suffer rest of life, I can't do stressful works, I'm educated enough to do high salary desk jobs either. I'm enduring the pain, the stress but don't know how long I can take it all.

Hi all, I'm a new member and I am glad to be here. Since the recent lockdowns prompted by the pandemic in UK and around the world I have been exploring the idea of alternative health in combating stress and anxiety and their immediate effects such as tiredness, insomnia, eating disorder and other mental health issues. I find that meditation is an excellent alternative health method and that I don't have to keep taking prescription medicine for common stress and anxiety. I am currently considering the self hypnosis techniques using positive affirmations. Any recommendations from the forum on books or audios on self hypnosis is appreciated and I will keep the forum updated on my journey into guided meditation and hypnosis.

Work can be stressful, but if you don't want to burn out, what you really need is a better attitude about stress. The approach I find most useful, and the one I recommend in these pages, is a practice called mindfulness. Mindfulness is paying attention on purpose, in the present moment, and nonjudgementally to the unfolding of experience moment to moment.

@Sorai Until now I didn't know that it was based on a book - I was only aware of the anime by Miyazaki. Which brings me to what I'd like to watch. I rarely watch anything and most definitely not twice - only for Miyazaki I'd make an exception because in each phase of my life his films touched a different part in me.

That would only apply if it's fully automated based on simple output and there isn't the human touch like the nominations in the forum. The Happy token for examplestrives to make valuable contributions tangible in a a bit more refined way. 🙂

In this 1971 Center For Disease Control handout photo, monkeypox-like lesions are shown on the arm and leg of a female child in Bondua, Liberia. CDC | Getty Images Belgium has become the first country to introduce a mandatory 21-day quarantine for monkeypox patients as cases of the disease — typically endemic to Africa — spread across the globe. Health authorities in Belgium introduced the measures Friday after the country reported its third case of the virus. As of Monday, the country has recorded four local cases; confirmed global infections currently number around 100. Belgium’s compulsory measures apply only to patients with a confirmed infection. Close contacts are not required to self-isolate but are encouraged to remain vigilant, especially if in contact with vulnerable people. “Infected persons will have to go into contact isolation until the injuries have healed (they will receive concrete instructions about this from the treating doctor),” a version of the government announcement translated from Dutch said. The UK meanwhile has said those who have a high risk of catching the disease should self-isolate for 21 days. That includes household contacts or medical professionals who may have come into contact with an infected patient. What is monkeypox? Monkeypox is a rare disease caused by the monkeypox virus — part of the smallpox family — with symptoms including rashes, fever, headaches, muscle ache, swelling and backpain. Though typically less severe than smallpox, health experts are growing concerned about the genesis of a recent outbreak, starting in early May, in countries beyond Central and West Africa. Health authorities, including the US Centers for Disease Control and infection and the UK’s Health Security Agency, said they have noted a particular concentration of cases among men who have sex with men, and urged gay and bisexual men in particular to be aware of any unusual rashes or lesions. As of Saturday, the World Health Organization reported there were 92 cases in 12 countries, and a further 28 suspected cases under investigation. The US, UK, Canada, Australia, Germany, France, Italy, Spain, Sweden, Belgium, Portugal and Netherlands have all confirmed cases. In this Centers for Disease Control and Prevention handout graphic, symptoms of one of the first known cases of the monkeypox virus are shown on a patient?s hand May 27, 2003. CDC | Getty Images The public health body said recent reported cases had no links to travel from endemic African countries, which is unusual for the disease. It usually spreads via human-to-human or human-to-animal contact. “Epidemiological investigations are ongoing, however, reported cases thus far have no established travel links to endemic areas,” the WHO said in a statement posted on its website Saturday. “Based on currently available information, cases have mainly but not exclusively been identified amongst men who have sex with men (MSM) seeking care in primary care and sexual health clinics,” it added. More monkeypox cases likely The recent surge in community cases, particularly within urban areas, is now raising concerns of a wider outbreak. “To have it appear now — more than 100 cases in 12 different countries with no obvious connection — means we have to figure out exactly what’s happening,” Seth Berkley, CEO of global vaccine alliance Gavi, told CNBC Monday. “The truth is we don’t know what that is and therefore how severe it’s going to be. But it’s likely that we’re going to see more cases,” he said. Though most cases of monkeypox are mild and typically resolve within two to four weeks, there is currently no proven vaccine. The smallpox vaccine has proven 85% effective in preventing infection, and some countries have already begun stockpiling doses. Berkley cautioned that the new outbreak, occurring even as the existing coronavirus pandemic is “not over yet,” was a warning to authorities to invest more resources into infectious diseases. He was speaking at the World Economic Forum in Davos, Switzerland, where political and business leaders have gathered this week to discuss key global issues, including pandemic preparedness. “This is evolutionarily certain that we’re going to see more outbreaks,” he said. “That’s why pandemic preparedness is so important. Look at what it can do economically when you have a pandemic hit” CNBC Health & Science Read CNBC’s latest global coverage of the Covid pandemic: #Belgium #country #introduce #mandatory #monkeypox #quarantine #global #cases #rise Belgium becomes first country to introduce mandatory monkeypox quarantine as global cases rise;

Has anyone tried "ecstatic dance"? Or at least that the trend in Europe where you dance sober, wild and expressive. The music at those events doesn't really do it for me but generally speaking some free, wild, ecstatic dancing really has a stress releasing and freeing quality.

When I want to make a project, I plan it a lot and sometimes I plan to much and it never gets done or it turns out it doesn't work as planned. Here is an example: About 17 months ago, I wanted to build a wooden box. Sure, you can buy a wooden box for like 5 bucks, but it would probably be some kind of spruce wood and it wouldn't be anything special. So I wanted to make a box from some nice wood like oak with hand stitched paddings and a hidden second chamber for a music box in the bottom. I could have started simple by nailing some planks together, but then I would not really like it and build a better box anyway. So why not build the better box now? I spent a year deciding for the right wood, deciding for the right connection so you wouldn't see any end grain, I got to know all kinds of oiling, varnishing, staining and so on. Then I splitted the first plank in half and noticed, 10 mm thick wood would bend by itself because of stress in the material and so the whole project didn't work. Since I don't have any kind of wood plane or CNC machine, there was no way to get the wooden planks in shape for the project. It was very frustrating to get this result after all the planning, especially because a wooden box is available for just 5 bucks. Do you guys have some advice, how to learn things like building a box without this kind of overthinking? I would still like to do it, just don't really know, where to start

"People like me (maybe I explained more what "people like me" are in a seperate topic) can't reduce the mental stress with meditation or similar directly. we need an outlet to relieve stress." When the ego cannot be eliminated in meditation, it is difficult to reduce mental stress with meditation. So a guided meditation connecting you with your I AM Presence could help.

When you start feeling restricted by the mental stress and you don't know a way out, yes. Unfortunately, this year there are long waiting times, because a lot of people suffer from depression because of the pandemic. Yes. In the past it was a lot more common to be married, to have a family and people around you. Nowadays there are more single people and most people want to be independent. That makes it harder to find people to talk to about this stuff.

I experienced by myself that mental stress can be very dangerous. And if the mental stress is too heavy it affects my whole energylevel and at a mental breakdown I won't get up from bed. People like me (maybe I explained more what "people like me" are in a seperate topic) can't reduce the mental stress with meditation or similar directly. we need an outlet to relieve stress. In my case it's blogging. And our societies should be more serious with mental stress and health.

I'm not sure if I understand the question correctly. So let me know if you meant something different. There are different opinions about mental stress. Some people say: "Be a man, be strong, don't show weakness", some other people say: "A real man shows feelings.". In my opinion, everyone has problems or stressing periods in life. Some are smaller, some are bigger, but we all have some. We can't avoid them completely, so it's even more important, how we handle them. Repressing these feelings may help in the moment, but all the problems will accumulate over time until you get a mental breakdown. So my way is to have one best friend to share these things with, to get a second opinion, to solve these problems from the root and to move on. If you feel like you would like to talk about it and you dont know, who to talk to, you can text me if you want.

@TajAgha123 With mental stress, do you mean stress caused by your mind? As stress is the body's response to a stressor such as an environmental condition or thoughts. Stress is the body's method of reacting to a condition such as a threat, challenge or physical and psychological barrier. A quick first help is conscious, long and deep breathing for a couple of minutes. If you have chronic stress it can cause severe bodily problems. In that case I recommend a more thorough intervention - for example MBSR (meditation-based stress reduction).