How do people with schizophrenia live?

Is different? For what reason? Here we tell you with the help of an expert.

Let’s start from the fact that the outcome of schizophrenia is to be a little abstracted from reality. Now, exactly how they see it and how they experience it depends a lot on each person’s particular case.

There is presence of these , So it is very possible that they live in scenarios very different from what is happening in reality. There are hallucinations of people or objects that are not here, but there is no single way in which they see and experience it, and not all of them have the same manifestations.

Finally, many times it is also difficult for them to express clearly what is happening. So the information we have is what is seen from the outside of people who live with this condition, but it is very complex to understand exactly how they are experiencing the world or how they are living their reality with the disease.

If a close person says that they are seeing and hearing voices or things, how can you understand it so as not to say something that is more negative?

The first thing is that If a person is stating that they see, hear or feel situations different from what is really happening and does not have a diagnosis, it is a giant red flag. So it is very important that you visit a professional and undergo the appropriate evaluation to define what may be happening.

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If you already have an established diagnosis of schizophrenia, it is necessary to understand that this is a health condition and that you are not doing it to attract attention, the person is really immersed in a series of things that are true for him or her.

The role of caregivers

It is difficult and very complex to be the main caregiver of a person with schizophrenia, which is why it is important to educate ourselves about it: better understand how the disease truly works, accompany the person to their check-ups and medical follow-ups, know very well how the diagnosis has evolved.or, but above all, It is very useful for the caregiver themselves to have their own therapeutic process.

Many times it can be very useful because you will eventually get tired, feel frustrated, sad, hopeless, and it is It is very important that they can also externalize everything they are feeling and thinking.even that they know how to handle and manage it so that they don’t end up at the end of the day perhaps taking it out on the person who has the condition.

There is no blame for feeling tired and overwhelmed. He or she is going through their own process and we must look for tools that allow us not to explore, not question, invalidate and hurt the other.