Sort 34 results by

Page 2

@Henrietta 

Last reply

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...

@xhulia 

Last reply

xhulia

MRI is the same

Hi guys, please help. I did an MRI today and my result is no active lesions neither enhanced or added. So from November 2019(my last MRI) according to the radiology examination nothing is changed. But in reality I feel so much worse. I used to walk miles on november and now I cant walk even 100 mete...

Another Major Event

I apologize in advance for the long post. I know MS is different from Person to person, My ms consists of numbness in my right hand and neurological pain in my abdomen and fatigue and I experience these symptoms on the daily. When I 1st knew something was wrong was my 1st clinical event that happe...

@Laaa 

Last reply

Laaa

Do emotions effect symptoms ?

Hi, first time I have posted but am having tough day. Am 50 but don’t like to think I look it or feel it, in my head at least. Diagnosed rrms in Jan this year (2020). It was actually good to have reason for so many things gone wrong with my health over many years. Am generally not too bad, bladder ...

@Tania_Pilz 

Last reply

Tania_Pilz

Waking up with numb hands

Hello MSers! I was wondering if you have ever woken up with numb hands and if this could be related to MS or medication (Tecfidera)? This sensation is different, is just like when you sleep in a weird position and your arm or legs fall asleep, very different from the normal MS numbness and tingling...

@ncm22 

Last reply

ncm22

RRMS TO SPMS

Hi, I was just thinking they say rrms progresses to spms. And it usually is 10 to 15 years after being diagnosed. I would like to know other peoples experiences, if they would like to share. I have been diagnosed since 2010 with rrms, but had symptoms since 2007. Main symptoms numbness from wais...

@KaijuRising 

Last reply

KaijuRising

Other specialists you may have seen?

I am wondering if anyone has seen either a geneticist or immunologist in the context of your MS. My brother is encouraging me to go, and he is also encouraging me to eat a keto diet. He doesn't quite articulate what he thinks these other doctors can do for me. My brother reads a lot of books about h...

@Andraz 

Last reply

Andraz

Multiple Sclerosis symptoms appearing

Over the last 2 weeks i've started to notice a lot of MS symptoms, like muscle twitching, spasms, weakness, fatigue, pins and needles, numbness. Most of them appeared in the first week and are now slowly getting a bit worse. I wanna know what was your experience of first getting MS symptoms and in w...

@Claire_Juliet_Woon 

Last reply

Claire_Juliet_Woon

Advise on Exercise

Hi I have RRMS, diagnosed September last year and been on Tec since May this year. Anyway to cut long story short started weight training again after a period of not doing anything, the issue I have is after lifting weights I have had NO arm/muscle ache at all the day after, it is like I have not ...

@Rosie_Paolo 

Last reply

Rosie_Paolo

Feel a bit deflated and stupid

So I’m waiting for a diagnosis of various symptoms. I had an appointment via video link at home with a neurologist and I just feel like I messed it up. I’ve been waiting for 6 months , in pain , and I couldn’t articulate my symptoms . He asked me if it’s there all the time or now and again - I an...