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I have had MS for years -diagnosed 1999. My husband has Parkinsons Disease. It’s so hard to cope - I try to be positive - he is always negative! Any advice?

I've had depression since I was a teenager. Now, finally diagnosed with MS, last year, I will get to look forward to when I can no longer fend for myself. Hasn't happened yet. Fortunately, I have worked since I was in highschool. I know that after 35+ years of taxes paid, I am now an elder. I deserv...

Sorry if this is against the rules guys but some help is needed!!!! My story... My name is Adam Dawar and I have Secondary Progressive MS. I was diagnosed about 7/8 years ago. Like many of you, I went to bed one night and when I woke up - life as I knew it had changed forever and my journey into M...

The government paid $6,000 on repairs and I'm still not getting it used and I was prescribed an electric wheelchair with the automatic legs and backing all three different prescriptions I was diagnosed with secondary Progressive. Don't understand Ontario Health Care coverage ODSP?

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...

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...

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 ...

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 😊

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...

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...