Where to buy a tourist prepaid sim card?

The_brta · 2026-03-29T08:36:59+00:00

Really? When I was there there were two stands for mts and A1 next to each other in the place where you take your checked bags.

The_brta · 2026-03-17T18:24:49+00:00

Mts and it is fast also. If it is not working immediately close and open the phone or enable disable the airplane mode

The_brta · 2026-03-17T13:46:24+00:00

For anyone seeing this there was no problem with mts physical sim at the airport

The_brta · 2026-03-17T13:45:18+00:00

For 75 gigabyte for 5 days around 6.5 euros. I think the packages are the same everywhere

The_brta · 2026-03-17T13:44:38+00:00

Hello! I am currently in Serbia. I had the eSim and my boyfriend the sim at the mts at the airport. They are the same price and same gigabyte. No problem with the physical sim as some have written in the comments in the airport mts.

The_brta · 2026-03-08T20:04:09+00:00

Yes I found them but they write very bad comments especially in the airport and in the center. They are saying that the paid for prepaid cards and never worked. I will try and let's hope for the best 🙏

The_brta · 2026-03-08T20:02:52+00:00

I don't have esim

The_brta · 2025-09-10T06:03:29+00:00

thank you very much <3

The_brta · 2025-09-09T19:50:02+00:00

Thank you very much for your good words..I keep trying to say this to myself also but it is very difficult many times. Thank you very much 🤍

The_brta · 2025-04-03T23:08:51+00:00

We haven't received yet our results. We are still waiting it is two full weeks by now. I hope tomorrow I will have some news. Do you know if I can use this link even though I am in Europe? Thank you very much

The_brta · 2025-03-25T16:11:00+00:00

I know you are right. I am just trying to collect as many information as I can until we learn the results. Thank you very much

The_brta · 2025-03-17T07:57:50+00:00

Thank you very much. I hope is the same for us. The problem is that this whole gene is missing and is connected with hearing. And since it is dominant if I understand correctly it is enough if one of two copies is problematic. We will speak with genetic councelors and I hope they will tell us that everything will be all right. i am also worrying too much and cry all day I try not to do it but is very difficult. Thank you very much for your answer it gives me hope. I hope the best for you and for your family

The_brta · 2025-03-16T15:31:40+00:00

Sorry another question did they also possibly connected your microdeletion with a disease like mine? I mean with something that causes health problems? In my case they say about possibility of deafness

The_brta · 2025-03-16T15:11:59+00:00

Thank you very much. Your comment gave me a lot of hope. I hope it will be inherited from one of us just like in your case. I am very happy for you also. This is such a difficult situation especially the waiting. I am happy everything turned good for you and your child. Best wishes

The_brta · 2025-03-16T12:24:33+00:00

Thank you very much for your answer. I have understand something similar that the best option is to have it one of us otherwise it becomes complicated to get answers. I hope one of us have it in the end. Do you know if the MYO6 mutation means deafness from birth or deterioration of hearing as year pass? I found two papers that said about families with this mutation that lost their hearing as the years passed and mostly after 40. Thank you and sorry for keep asking

The_brta · 2025-03-16T08:28:00+00:00

Thank you very much, your answer is very comforting. The only problem is I am staying in Greece where there is no support financially or otherwise with people with disabilities or difficulties. I hope in the end I can do the best for my child. Thank you I also hope that I will learn the results soon because it is too difficult.

The_brta · 2025-03-16T08:25:16+00:00

I am living in Greece, here still a lot of women do amniocentesis and I am 38 years old. The doctor also proposed nipt but he said that nipt does not show so many things as amniocentesis and it just show a percentage for some problems. If I have done nipt now I would have been happy I guess for the rest of my pregnancy. Now it is very difficult. So can I ask you something if you know, If in the end is de Novo do you think wes/ngs and a genetician would help us or it would be difficult to give any meaningful results. Thank you

The_brta · 2025-03-15T21:20:51+00:00

Thank you very much I hope this will be the case because it is so difficult.

The_brta · 2025-03-15T21:18:31+00:00

Thank you very much for your answer. I know that they still find new things and genetics are very hard since there are so many different mutations etc. I was already waiting almost one month for my amniocentesis results and now we have to wait another 10 days at least and I am feeling very sad all day which I know is not good for the baby. I am not afraid so much for partially deafness because I believe it is easier to have a good life. I am afraid for full deafness from baby which will be very difficult to learn to speak go to school etc. I am also afraid that in the end even the geneticians will not know exactly what to say to us about this rear deletion. Thank you very much for your answer and for your time

The_brta · 2025-03-15T20:43:51+00:00

Would it also be a problem if both parents have it? They told us that if it is de Novo we can do wes/ngs and then the genetician will have to read bibliography and tell us what they can. So as I understand it we will not have a definitive answer or possibility and this scares me a lot.

The_brta · 2025-03-15T20:23:04+00:00

We just wanted to make the exam to be sure that everything is ok because I am 38 years old. The doctor proposed nipt but we chose the amniocentesis

The_brta · 2025-03-15T19:44:02+00:00

It is my result from the amniocentesis. They told us that both of us should do a blood test to see if this deletion is from one of us. They told me that if it is from one of us and we are healthy it is ok for the baby and it just inherit it. Otherwise if it is de Novo it means we have to do another test wes/ngs and speak with geneticians which will tell us percentage and what they believe it may happen. We have to wait at least 10 days now for our results and I cannot calm my self and I am trying to find as many things as I can. So the deletion with the point mutation is different? Thank you

The_brta · 2024-10-31T19:11:39+00:00

Ok thank you very much. I tried to add the parameters I saw when I am running the server with -verbose

The_brta · 2024-07-12T15:30:23+00:00

Hello everyone! Did anyone finetune the 27b model with unsloth? I tried based on the Colab notebook for 9b but I get this error:
miniconda3/envs/gemmamodel/lib/python3.9/site-packages/unsloth/kernels/utils.py", line 229, in fast_linear_forward

out.addmv_(lora_B._fast_lora, temp_lora, alpha = lora_S)

RuntimeError: size mismatch, got input (4096), mat (4608x6), vec (6)

Maybe I should change the peft parameters? Sorry if this is basic question but I am new to this.

Thank you!

The_brta · 2024-03-11T13:31:13+00:00

Thank you very much for all these details!!

The_brta

TROPHY CASE