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@Isa_Elfers 

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Isa_Elfers

Cymbalta

Hi all, first post. I'm 22 and slogging through the long and troublesome diagnostic process to figure out what's going on. My strong suspicion is MS, but my objective clinical indicators are either barely there or nonexistent ⁠— I have small demyelinated lesions and speckled ANA blood titer, but tha...

@Adele_Barrow 

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Adele_Barrow

hi

hi guys I've been diagnosed for many years thinking they were wrong , but over the last 2 years o.m.g I should of listened ive gone from rrms to spms since I lost my dad and anti social behaviour from my neighbours ive had to give in and think shit they was right ive 4 kids 3 under the age of 7 and ...

@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...

@dalebrooks 

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dalebrooks

Symptoms before diagnosis how long?

My doctor told me that I have dormant multiple sclerosis meaning that I have the gray areas in my head and most of the symptoms but not the bands in my spine. My question is : is it normal to have symptoms for years before a real diagnosis? My dr told me that dormant ms isn’t a real diagnosis. So as...

@ciara1982 

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ciara1982

Diagnosis

Hi I have had a recent mri identifying inflammation on both spinal cord and brain. I’m seeing neurologist on Friday. Did anyone get a diagnosis with the same mri result? My symptoms are weak left leg, tingling in right hand and poor balance. I also tend to be very sensitive to alcohol.

@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...

@Stephen_Williams 

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Stephen_Williams

Hi to my old friend!

Hi to my old friend! That is SHIFT MS! - Not you, well it could be? I guess a stranger is a friend you just haven't met just yet! I was speaking to my OT via video call at hospital during this crazy and unusual time. She suggested going on SHIFT MS and it is a website I joined several years ago and...

@jennymay1548 

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jennymay1548

Introduction

Hi! I’m Jenny-May,I’m 21 and I’ve recently been diagnosed with relapsing remitting MS. I’ve been advised to join because I’m quite ‘lonely’ as my therapist says 🤦🏼

@nicole_kelly 

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nicole_kelly

Allergies

Has anyone else had issues with dairy, I realized a few months before getting diagnosed that dairy was making me very sick. I just want to know if it could be related or?