#blurred-vision - Shift.ms

21 Feb 2021 14:03Last reply 22 Feb 2021 06:28

Blurred vision

Has anyone experienced blurred vision? When I put my hand over on each eye I see clearly. I can't drive at the moment. I vape and have had to stop just in case it was that causing it,however I've had it before I vaped. I'm calling my doctors in the morning. Any advice would be appreciated.

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@laurasavage567

4 Jun 2018 09:34Last reply 15 Nov 2020 14:40

Blurred vision in both eyes

Hi everyone, I’ve had optic neuritis for the past 4ish months now just affecting my right eye, I had gotten used to it! However this morning I have woken up and instantly noticed my eyesight has worsened in my left eye now. Really speckled and blurry in both eyes now 😪 Does anyone know if MS can...

18

@Marmizuko

3 Jan 2017 23:48Last reply 7 Jun 2018 21:44

Gilenya and blurred vision - new here :)

Hi everyone, I was recently diagnosed after 8 years of denial (CIS but not started on treatment as wanted children then ignored multiple attacks over the last 4 years, very good at coming up with alternative explanations such as migratory disc prolapse!). I started on Gilenya 4 weeks ago and hav...

5

@Chazwick

20 May 2016 14:41Last reply 21 May 2016 17:09

Blurred vision in Right Eye

So I'm in a difficult situation and I'm just wanting to know how seriously I should take this. I have RRMS and was put on Gilenya (Fingolimod) over a year ago now. I am currently in Finland on an Erasmus exchange and in my last week. Yesterday I suddenly had a slight blurriness in my right eye. It's...

7

@beccygreeneyes

30 Sep 2012 05:53Last reply 1 Oct 2012 09:21

Blurred vision?

Heyyy. How are u all? So u know i had optic neuritis in may which has still not recovered fully. Is there a reason why i randomnly get blurred vision in both eyes. I have woken up with it today and had it yesterday as i was driving home. Whyyyyy is this happening? xx

6

@Loves

21 May 2022 17:22Last reply 4 Jun 2022 23:22

I was feeling kinda normal

Nothing but headaches, but yay no migraines till it started day before yesterday. Fatigue, hoping it was just from the heat or extra activity I went to bed earlier and rested more. To wake up with blurred vision right eye looking puffy around it. Right side of my head hurting, feeling nauseous. For ...

6

@ERLCA92

1 Jun 2022 11:14Last reply 1 Jun 2022 13:40

Neurology report

I’ve had the report from the neurologist that ran the brain scans. To summarise: I have typical lesions of MS in the periventricular region but also In the Infratentorial area of my brain with brain stem involvement. I have other smaller lesions in other parts but these are the main 2 he is discuss...

2

@watsoncraig

25 Feb 2020 23:00Last reply 21 May 2022 16:22

A friend posted this

Hi everyone hope this helps explain MS a bit better and what most of us suffer lots if not daily. Onwards and upwards MS and b12 deficiency symptoms, and explanations to help with BRAIN -COGNITIVE ISSUES Memory loss. Loss of concentration. Difficulty of keeping track of conversations, processing i...

13

@Minnie_xo

19 May 2022 18:21 EditedLast reply 19 May 2022 22:09

Never ending trauma

Hi guys I was advised by my MS advisor to join this app today because I wanted to share my endless trauma regarding my RRMS. I was diagnosed last year with RRMS - it felt like an intensive rollercoaster ride that wouldn’t end and I’m finding it difficult to accept my diagnosis. I was only 21 when...

8

@B_The_Travelling_MS

16 Apr 2022 16:24 EditedLast reply 16 Apr 2022 21:33

Work, stress, MS

Work has been busy lately! I'm grateful outdoor event gigs have been more consistent but it's the out of the blue, brain fog, blurred vision, trouble with speech days that still give me the fear of relapse. My Glasgow neuro said anything could've triggered my last relapse but my strongest pre-relaps...

2

@Loves

13 Mar 2022 12:49

To start off...no ms diagnosis

So I've been trying to advocate for my own health. Why do I feel so guilty, for trying to be the best me? I've prompted more visits to the local sliding scale Dr. Office. Bc of migraines, that every MRI has said my brain in fine. Made an eye appointment bc honestly I don't remember ever having an ey...

@Kanga

26 Jan 2022 11:09Last reply 26 Jan 2022 17:52

Managing ongoing optic neuritis symptoms

Hi I am looking for some advice on how to manage my ON symptoms when I return to work. I had iv steroids at the end of November and most of my vision has returned in the right eye but using electronic devices/screens can cause the blurred vision, Fogginess and pain to return temporarily. Occ he...

6

@Nicb

8 Nov 2021 11:54Last reply 10 Nov 2021 15:32

Optic neuritis

Hi, I'm new to this site and have not been diagnosed with MS yet. I have suspected for 7 years now that I have it. I am 50 years old and live in the North West of England with my husband and 14 year old son and 11 year old daughter. 7 year ago I was very ill and bilateral optic neuritus was diagnos...

3

@Nicb

8 Nov 2021 11:54

Optic neuritis

Hi, I'm new to this site and have not been diagnosed with MS yet. I have suspected for 7 years now that I have it. I am 50 years old and live in the North West of England with my husband and 14 year old son and 11 year old daughter. 7 year ago I was very ill and bilateral optic neuritus was diagnos...

@Nzkiwi

7 Sep 2021 07:06Last reply 12 Sep 2021 23:43

New Kid 🙋🏽‍♀️

Hi Everyone, I am awaiting my 1st Neuro appt. I have had problems with my left side for soooooo long! From the top of my head to the tip of my toes, I have weakness, numbness, it’s not pain but I wouldn’t describe as pleasant. I have blurred vision and a feeling of pressure behind my left eye and ...

Taupo, New Zealand

2

@Hollyp

17 Aug 2021 19:20

Advancing symptoms, no new relapses?

Hi, I was diagnosed with MS summer 2019. At that point I had had some minor symptoms such as numbness in my hands and feet and some blurred vision. Optic neuritis led to my diagnosis. Since then my day to day experience has got progressively worse. I have struggled to walk any distance at times and ...

@StaceyM

31 May 2021 15:12

MS treatment vs Covid Vaccine

Hi all! Hoping gather some input as doctors all say there is not enough data to share with us. My wife has been taking tecfidera for the past 5+years and is working great with the right diet and exercise. Doctors have been pushing her to switch to a once/ twice a year. infusions. As she had a few ...

San Diego, California, United States of America

@sriram

20 May 2021 02:59Last reply 21 May 2021 13:56

Recently Diagnosed

Hi All, I am caregiver for my wife who has been recently diagnosed with ms. She is 36 year old from India. One of the hardest part for both of us is coping up with the uncertainty. 1. Wife has lesions in spine and brain - does it mean an aggressive form? 2. Wife has had 3 relapses since onset of sy...

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@Cony77

26 Mar 2021 14:12 EditedLast reply 26 Mar 2021 17:28

Stroke vs ms

Went to A an E a few weeks ago with usual symptoms numbness down left side ! blurred vision in left eye and a few other things Im already waiting for a neurogy appointment before this visit .they were treating me for a stoke had ct scan and other test ect and let me go home because bloods were ...

6

@Stephanie

6 Feb 2021 22:12Last reply 7 Feb 2021 10:27

DMD’s for new diagnosis & mental health

Hello, I am newly diagnosed with MS & would like some perspective on treatments & mental health resources. Some background: I’ve been incredibly fortunate that from contacting my GP about symptoms and being admitted to hospital for tests (incl MRI & lumbar) then discharged from hospital with stero...

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