I know how scary it can be to suddenly have blurred vision. After several days I found out that in my case it was a drug side effect, and it went away on its own. But on the day it started I thought I was going to go blind.Hi everyone.
I apologise if this topic has been covered multiple times already.
I was diagnosed with Type 1 a week ago. My levels at time of going to the hospital was 31. I was kept in over night on fluids and insulin and released 24 hours later with instructions to inject 8 units of fast acting insulin before every meal and I now also have a slow release insulin to take at night. I have managed to over the last couple of days keep my BG between 6 and 10, with the odd spike around 13.
I was suffering with slight blurry vision before diagnosis, but over the last 4 days they have gotten much much worse, to the point of not being able to read my phone and computer (my girlfriend is typing this for me!). It is affecting my work.
I am trying to get some answers from the doctors regarding how long this is going to happen, for and reassurance that this isn't going to cause permanent damage and if I am doing anything wrong. However I am not getting this information and care and getting quite frustrated.
Has anyone had the same experience? Does anyone have any advice on how to help this and what to expect?
thank you in advance!
Matt
I know how scary it can be to suddenly have blurred vision. After several days I found out that in my case it was a drug side effect, and it went away on its own. But on the day it started I thought I was going to go blind.
You are not doing anything wrong. As himtoo said, it will most likely improve on its own. The doctors should have told you this.
Just to check, have you recently started any new medication, apart from the insulin? I usually check for known side effects at www.drugs.com
I'm type 2, went into the hospital with BGs of 24.6.... I was having blurry vision, it got worse when my BGs started to come down, and it took a couple of weeks until it got better, over that time I changed my prescription 3 times...
Right now, I'm not wearing any glasses... so yes it can get worse and then better, but I guess everyone is different.
Back then the people at the opticians told me that was normal and to expect changes as my BGs normalized, but at the time it was quite scary to not to be able to read my mobile or my computer, at some point it got really bad.
It was a few days I think.Thank you for your reply, this has helped put my mind at ease a little. How long did your blurry vision last for before it started to improve?
If your boss is accommodating, you might still be able to be at work, and do limited duties.Thanks for your reply. How long were you not able to read your phone for? My job is design so I am a little worried at how much time I may need off work!
Thanks for your reply. How long were you not able to read your phone for? My job is design so I am a little worried at how much time I may need off work!
Hi Matt,
I have the same thing, started treatments 2 weeks ago
I asked the nurse earlier this week and she didn't really answer
So relieved you brought it up and got answers above, puts my mind to rest a little
Cheers
Just to clarify: the worst part of it took a couple of days I can't say exactly how long, is the general normalization that took longer.
For example before diagnosis it was blurry from distance, afterwards diagnosis and as soon as my BG started coming down I couldn't focus, and then it started improving, and by the last time I went to the opticians my eyesight had improved dramatically over the situation before diagnosis...
Thanks for the info. Mine has now been really blurry for 4 days with no sign of improving. I can't read my phone with the font at its largest option, everything is a blur. I am keep my levels pretty steady so I don't understand why it's so bad still.
Hi everyone.
I apologise if this topic has been covered multiple times already.
I was diagnosed with Type 1 a week ago. My levels at time of going to the hospital was 31. I was kept in over night on fluids and insulin and released 24 hours later with instructions to inject 8 units of fast acting insulin before every meal and I now also have a slow release insulin to take at night. I have managed to over the last couple of days keep my BG between 6 and 10, with the odd spike around 13.
I was suffering with slight blurry vision before diagnosis, but over the last 4 days they have gotten much much worse, to the point of not being able to read my phone and computer (my girlfriend is typing this for me!). It is affecting my work.
I am trying to get some answers from the doctors regarding how long this is going to happen, for and reassurance that this isn't going to cause permanent damage and if I am doing anything wrong. However I am not getting this information and care and getting quite frustrated.
Has anyone had the same experience? Does anyone have any advice on how to help this and what to expect?
thank you in advance!
Matt
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