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@Jem_Carter 

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Jem_Carter

Can you change your neurologist?

Please let me start off by saying I'm not whining or being ungrateful...my current neurologist has been very efficient in organising scans and treatment over the years. But...I am wondering if I can change my neurologist. When I saw him about a year ago he encouraged me to get back with my ex husban...

@Alessa_Bless 

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Alessa_Bless

The natural route

Hey there... New to this... I’m wanting to hear feed back from folks who have opted out of DMT... I was diagnosed 7 months after my son was born in 2010. I am currently having my 3rd relapse, though this one has required a 3 day dose of solumedrol. I completely changed my lifestyle after diagnosis, ...

@schulz_alice 

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schulz_alice

Multiple Sclerosis cure

My name is SCHULZ ALICE and i am 46 years old . I was born on 19/01/1974 in Carinthia (Klagenfurt)Austria . I grew up there till the age of 20 when i started having Vision problems,Fatigue and weakness,Bladder and bowel dysfunction,Sexual dysfunction,Cognitive problems. Since i was still young i nev...

@Fiona1992 

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Fiona1992

Newly Diagnosed

I was diagnosed with RRMS mid May 2020 at the age of 28. All rather shocking because the only symptom I've experienced is optic neuritis. It has been said that I need to start on Tecfidera next week. I'm feeling pretty anxious about this. More so because all my neurologist seems to say is 'No-one ha...

@Cooper 

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Cooper

Cognitive issues............

I was diagnosed last year, i thought I was lucky with relatively light physical symptoms. Balance, some pain but cognitive problems are really starting again.............. Does anyone have issues of trying to make simple calculations work in your head? I find it difficult at the moment. I'm trying t...

@Debbie_Titley 

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Debbie_Titley

Newbie

Hi i am new to this site i am 53 and was diagnosed with RR ms when i was 19 only got told about this site recently nice to find people in the same situation and now what its like hope everyone is fine and safe at this unsure time. I am at the moment ok just sat waiting like some of you to start new ...

@Thorpee 

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Thorpee

Hello, I'm new here..

Hello everyone, as the title suggests I'm new here. Although, I've been lurking for some time. I got diagnosed with MS last week after a lot of barking up the wrong tree. I'm a Police Officer and in 2016 I decided to apply to transfer to firearms. The fitness test is a bit harder for this but didn't...

@ncm22 

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ncm22

Started dmds 8 years after diagnosed hel

Hi, I have rrms, diagnosed in 2010, symptoms since 2007. I started copaxone in 2018, had MRI new lesions. So started tecfidera in February this year. I just wondered as i have not been on dmds for 8 years after being diagnosed. Whether the dmds would be less effective going forward, I know t...

@carolelawrence 

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carolelawrence

Not happy!

Long story..had mri Feb 2 non specific liasions on my brain and 2 non specific liasions on spine. My left leg and foot numb since Jan. My right leg and foot and my right toes numb last 4 weeks..so my mobilty gradually deteriorating last 14months..dreadful burning night pain in legs and feet burning ...

@ColettePage 

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ColettePage

Stairlifts

Hi all, what’s the lowdown on stairlifts? Is the consensus to get one? I am very fortunate to have enough rooms in my house to make a bedroom downstairs & we are having our large utility/ cloakroom converted into a wetroom. I’m undecided whether to get a stairlift as well to prolong my sleeping ...