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@Sarah12 

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Sarah12

Weak legs

Hi I am Sarah. Diagnosed with ms in 2012. Over the past few weeks I seem to have got really weak legs that has starting going heavy and giving way after about 5 minutes of walking. I was wondering if anyone had any advice on the best way to tackle this as I want to be able to live my normal life....

@apop 

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apop

Always relapsing no remmition ...

My name is Ana. I was diagnosed with MS relapsing remmiting type in 2015. The onset of my MS started in 2011 but I didn't know it. I was diagnosed first with severe Anxiety/Depressive disorder with Panic attacks. I am in constant nerve pain, numbness, spascisity and other symptoms. The evenings are...

@EmilyMac 

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EmilyMac

Treatment advice

Hello! I’ve been told today how amazingly positive this site is and I can already see from just having a little nose it’s just what I need! I was diagnosed 3 weeks ago, shock probably was an understatement. I haven’t googled anything really, just had conversations with the Neurologist and my nurse. ...

@NicolaJinks 

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NicolaJinks

Life insurance

Hey all, I have just been diagnosed with very early RRMS. It hasn't really affected me physically as of yet but I keep getting adverts on my social media about thinking about life insurance. It is also all targeted at MS. My question to all of you is do you think it is something I should look int...
Lincoln, United Kingdom

@Sim1211 

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Sim1211

How To Cope?

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?

@GG_Alexander 

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GG_Alexander

Suicide

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...

RAW ORANGE

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...

@Andre_Cyr 

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Andre_Cyr

Wheelchair access

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?

@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...