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@Henrietta 

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Henrietta

Diagnosis - the long and winding road

2001 Optic neuritis. Go blind suddenly - and fortunately temporarily - in one eye. Ophthalmologist sends me to neurologist. The neurologist tells me in a jovial tone to say that I have had optic neuropathy to insurers - if I say optic neuritis they’d put me down as having MS. MRI done. No follow up...

@Sophietest 

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Sophietest

VOTE for Shift.ms - pls 🙂

Please VOTE for Shift.ms to win ➡️ https://buff.ly/2CcRgUc ⬅️ 'Best non-fiction' at Webfest Berlin. The 'Animated Symptoms' series has been nominated - a series that shows real stories & experiences told by people living with symptoms of MS. You can watch it here: https://www.youtube.com/playli...

@queenbuffy 

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queenbuffy

New to the ms community by way of Feb

I'm going to be on ocrevus in a few weeks, what are the best options for treatment so far?

@Henrietta 

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Henrietta

Newly diagnosed - which DMD?

Diagnosed yesterday (by phone of course, thanks COVID) with RRMS. Was expecting it so not surprised. Now have to decide between Aubagio and Tecfidera. I’m tending towards Tecfidera but would welcome feedback / opinions / advice. Thanks 😊

@Rachel_Hilton_1 

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Rachel_Hilton_1

Starting anew?

I’m struggling at the moment. As we went into lockdown, my partner of 11 years decided to tell me he effing hates living with me and dumped me, the same week as I had to have my 19 year old dog put to sleep. He knew from the outset of the relationship that I had ms and it is a degenerative disease...

@Will_Berard 

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Will_Berard

Live Standup Comedy - tonight

Hello Shifters, I will performing some standup comedy "live" over the internet, as per the New Normal. Starts tonight at 8:20 (20:20 - get it? Cause it's the year? see what they did there? ) FB: https://www.facebook.com/events/306540333735425/ YT: https://www.youtube.com/watch?v=7RsMJtmmqOI Tha...

@Aimee 

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Aimee

Hobbies & Interests

I’d love to hear about everyone’s hobbies and interests- whether it’s something you were into pre-diagnosis that you’ve adapted to work around your MS symptoms, or if it’s something completely new to you that you wouldn’t have discovered without your MS. You never know when someone might need an u...

@watsoncraig 

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watsoncraig

Facemasks

Facemasks are not for me, they are for YOU should be the new slogan

@BeeFirefly 

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BeeFirefly

Seeking advice

Hi there im just wanting some advice and help really. In a nut shell I am 25 years old and had this illness since just shy of my 16th birthday (great gift that was) anyway last year after my birthday i suffered a miscarried (first time pregnant as well) and that sent me down a dark dark hole anyway ...

@SBGill91 

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SBGill91

Tyasbri

Just back from infusion #5 of tysabri and doesn’t seem to be making any difference at all...... Still original symptoms and new symptoms Anyone In same boat...? Also whilst I’m on, anyone got recommendations on CPD vapes?