#blurred-vision - Shift.ms

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...

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@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...

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@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

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@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...

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@AndyTurner

12 Jul 2018 13:18Last reply 15 Jul 2018 19:38

Flare up

I been having double vision, blurred vision and pain behind left eye. Managed to get a cancelation at opticians. Optical neurtis has popped its head up again. Now have to wait for appointment at the eye pavilion. This is the sexond time this year.

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@mattbr

23 Jul 2012 14:59Last reply 25 Jul 2012 12:03

Greetings from Brazil!!!

Hi there everyone!!! Kind of new here, although í´ve been reading your chating for the last few weeks. As the title says, i´m from Brazil (it´s not a problem, is it?) and still don´t have my dx. Actually, i don´t have almost any of those "classic" symptoms of MS (by classic i mean fatigue, blurre...

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@HayleyCousins94

10 Jul 2016 17:06Last reply 19 Aug 2016 05:21

Newbie

Hey (: My names Hayley, completely new here and not really sure how this all works but thought I'd give it a go I'm 22 years old and from Cambridge I got diagnosed with MS on the 17th of June 2016 after having tingly/numb hands and legs and blurred vision I was given steroids for the first 5 days ...

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@Teide_Barrett

19 May 2020 16:38Last reply 23 May 2020 11:42

Ocrevus infusions

Hi I’m teide I’m 24 and I have RRMS. I was diagnosed in October 2018.. I spent 1 1/2 years on tecfidera but my ms just kept progressing. I started ocrevus last Tuesday and had my first 1/2 dose.. Tuesday I felt ok! I was surprised how well I felt on Wednesday but since then it’s been horrific! Sle...

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@boodle06

6 Jul 2012 18:30Last reply 9 Jul 2012 18:38

New & undiagnosed

Hi, I've been looking at all of your comments on this site for a couple of weeks and have finally been brave enough to post. You all seem so helpful. I'm 30 yrs old & it all began last November, I had a virus then my right hand & wrist became completely disabled, my speech was not right ...

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@kerrylousie

4 Dec 2012 20:59Last reply 6 Dec 2012 11:36

Eyesight

The last 2 days i have been having strange blurred vision that comes and goes randomly. Has anyone else experienced this and is it a fatigue thing?

13

@maura

15 Jul 2018 11:55Last reply 16 Jul 2018 20:16

Limbo land and scared

Hi guys My name is Maura up until April I was very fit active 37yr old working long hours in a very physical job.In April I started getting abnormal sensations in my right foot Foot mainly felt numb and heavy by end of May both feet were like that all the time.I presented to A&e twice but as I c...

13

@abikeride

20 Sep 2017 21:05Last reply 23 Sep 2017 22:52

Noob question

Hey hey hello. I've been lurking around for a while and I'm very grateful for everyone who shares their experience. First off, I was diagnosed with ms four months ago and I started taking avonex. The first symptom was double vision on my left eye, and I received no treatment for this and it simply g...

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@JessGibs25

21 Feb 2019 16:54Last reply 2 Mar 2019 14:18

How it all started. Who have I become?

I’ve always felt off balance ot had little to no balance. As a young child/teen I suffered from clustered mirgarines which had symptoms of blurred vision, numbness, impaired speech, even paralzation on the left side. The “episiodes” got better once I got glasses but I was always afraid of getting he...

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@squishedmish81

15 Jul 2013 15:16Last reply 19 Jul 2013 14:07

Am I the only person between diagnosis and and an MRI?

Hello, So I got diagnosed with MS is April by a very good Neurologist based on a fairly nasty attack which left me numb/very very weak on my right side and unable to walk in February. He ruled everything else out with all of the other tests and while he couldn't find lesions on a standard MRI, he is...

12

@feeblefee

27 Sep 2016 14:35Last reply 2 Oct 2016 12:05

The long wait

Hi guys! I'm new to this ?. I have yet to receive a diagnosis of ms I am waiting on a neurologist appointment (hopefully coming soon) ill give u a brief back story on how I ended up here. For the last 3 yrs I had been consistently going to my GP with pins&needles along with sharp pain in my fore...

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@ruggermad

26 Aug 2014 09:02Last reply 27 Aug 2014 17:19

Anxiety and paranoia..........

Hi everyone, just posting here to see if anybody can help give me any tips or experiences on trying to deal with anxiety which I believe has been brought on by my situation of being in limbo. I unfortunately do not have a definitive MS diagnosis yet (if ever I do get one) and the two neuros who I ha...

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@watsoncraig

25 Feb 2020 23:00Last reply 14 Mar 2020 06:24

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...

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@Lou1666

5 May 2017 05:26Last reply 5 May 2017 18:25

Ideas to help daughter with MS

Hi All, I am new on here, I have been looking for a support group to help give me ideas to provide support to my daughter who was diagnosed with MS two years ago. She had several attacks in the early days and now receives treatment (Tysabri) which does seem to have slowed down the attacks. However e...

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@Zak783

11 Jun 2017 13:02Last reply 12 Jun 2017 14:14

Frightened..... not sure what to do.

Hi everyone, I'm hoping by registering on here that people will put my fears at ease. About 5 years ago I had tingling in my right hand on the tips of my fingers. I went and had nerve tests which showed nothing.... and over time it disappeared. Then about 18 months ago I had the same sensation in m...

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@Kimberleylouise627

7 Oct 2013 09:12Last reply 11 Oct 2013 06:09

Newly diagnosed.. Just finished steroids feeling rough and confused!

Hi, I was recently diagnosed in July I'm only 27 and have been on a roller coaster of emotions over the last few months from denial to anger and now just completely hopeless! My nurses put me on a 5 day 500mg a day course of steroids which I finished yesterday but I am feeling worse than ever, very...

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