Sort 453 results by

Page 15

@Sarah12 

Last reply

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 

Last reply

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 

Last reply

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. ...

Would I be changing meds?

Hi all. So, I know, a couple of weeks ago, I had an MDT DMT meeting, discussing my medication and recent relapses and new lesions. Still not received a letter from them, but I know that it can take a couple of weeks. However, a nurse from my MS team called me today, telling me that they'll be booki...

@LaFeeVerte 

Last reply

LaFeeVerte

Learning to drive

Hi I'm learning to drive and my instructor keeps asking me if I'm allowed to drive. I've informed the dvla etc. I don't need adaptions but I keep taking too long to check my mirrors and I steer slightly off course . I'm not sure if this is normal nerves or ms related. I will be driving my kids ar...

@NicolaJinks 

Last reply

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...

@VanBax 

Last reply

VanBax

Negativity

Hi Everyone I’ve had MS a while now but have recently noticed (probably as I’ve recently been walking slower and with a slight limp and have probably been looking more fatigued than usual) that people, who do know me, talk to me in the same way as they would a child and/or can be very patronising....

@voltanne 

Last reply

voltanne

Pain

I woke up on saturday morning at 5am and have the most dreadful pain which seems to be radiating from my hip through to my knee. I have been taking painkillers since on phoning the doctor this morning said it was probably soft tissue damage, keep taking the pain killers. I am really worried as I am ...

@Sim1211 

Last reply

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?