We are increasingly getting to know the Internet using special applications or just social networks. And almost always experience excitement, with hope filling out our profile. But what to do to those who are also worried that its diagnosis can become an obstacle to friendship and love?
We talked with two heroines who are sure: technology helps people with disabilities or severe illness to feel a full -fledged part of this big world.
“I wanted communication”
Natalia (diagnosis: multiple sclerosis)
“Briefly scattered sclerosis can be described as follows: my immunity began to work against me and destroy my cells instead of alien. Therefore, my hands and eyesight refuse, fine motor skills do not work, I do not feel some tastes and smells, sometimes it’s hard for me to talk.
But multiple sclerosis is a “thousand of people’s disease”: in all, it manifests itself in different ways. The only common feature that I know about is that all the sick people walk about equally unevenly.
I would not say that the disease somehow interferes when dating: I myself am quite calm with new people. It is usually not noticeable for me that I’m sick with something. Therefore, when I registered in the application, my profile looked the same as that of millions of other users: several photos, a little about my hobbies and age.
The reason for the registration in the application was completely simple: I wanted communication. Then I lived with my parents outside the city and often could not get out of the house, and online dating gave me the opportunity not to feel insulated. I didn’t even look specifically guys, I just talked with all people.
I talked with my interlocutors as honestly as possible: if I was talking about classes and work, I explained that I was a disabled person of the second group and I couldn’t work much to work. When they asked why, I tried to describe my diagnosis as clearly as possible.
I must say that my attitude towards me has never changed: not with bullying (persecution. – approx. Ed.), neither with happic (hatred in messages. – approx. Ed.) I have not encountered. Rather, on the contrary – people offered help. For example, when I needed to go for the documents, they drove up and really helped. There were, of course, those with whom communication quickly stopped: they regretted me, but I do not like pity.
Once I met one girl. She is at that time the future doctor-neurologist, and it was quite interesting for us with her. I know a lot due to my neurological disease, and it is as a professional. Later it turned out that we have common topics for conversation besides medicine.
My illness did not scare her away, rather the opposite – she was as attentive to me as much as possible. We moved to social networks and soon made friends. But over time, disagreements began, and our communication gradually ceased.
I can advise people with the same diagnosis not to despair, try and look for: find a https://alkhaleej-medical.com/2023/09/05/follando-en-directo/ couple or people to communicate in applications quite real. It is important to clearly indicate what you are looking for and why: if you are looking for communication or friendship, and write. Often it is even more important to know what you want from them than what kind of person you are. “.
“Honesty is important”
Elena (diagnosis: SMA-spinal-muscular atrophy)
“SMA is a genetic disease that affects the motor neurons of the brain and as a result leads to muscle atrophy. In simple words, motor development is delayed, the volume of the lungs is reduced. Any cold or mild disease of the respiratory system can bake into pneumonia and end in deplorable.
But I do not think that SMA is something that I should hate. Because this disease is part of me, and to hate it means to hate yourself first. It does not bother me in social life. I think that if it is difficult for a person with a diagnosis to get acquainted with people, then most likely the matter is not in illness.
Eight years ago, I registered on a dating site from pure curiosity. On the profile, I put several photos with an open smile and with a stroller, and in the profile described myself as “a girl in a stroller, frankly wanting to dump to the sea”.
Then I thought that it is not worth hiding features in editing services, because you can’t build relationships on the Internet anyway. Real contact in real life is important, but without honesty it cannot happen. Over time, I began to receive response.
The diagnosis did not interfere: indeed, several men stopped communication, learning that I was moving in a stroller. But I did not focus on this: it means that they were not my people. I also did not have to face bullying – I have long abandoned the role of the victim, so it is difficult to hurt me.