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@Hayleyp3 

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Hayleyp3

Neuro wants me on Aubagio

Just wondering what peoples experiences are on Aubagio, as a little scared. Copaxone caused a massive allergic reaction and I ended up in hospital, and tecfedira made me feel so ill. Been off meds a few years but need to get back on something. What was your experience on aubagio? Thank you xxx

@Carla_L_Baldwin 

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Carla_L_Baldwin

Service Dogs

My GP and MS neurologist have suggested a dog. I have MS, Anxiety, Depression, Acromegaly and something the doctors are trying to find out why I am falling all the time. My legs stop working and I fall. Most I have to go to hospital because of concussions.

@mikki131 

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mikki131

Thinking in the future

So I was at my Neurologist and her assistant stated to me that I should be a lot worse than what I am! My neurologist agreed.. so this of course got me thinking of the future. I have decided that I do not want to get bad, I know some people r and are happy and that’s their choice and right. I have t...

@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...

@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?

@michael_washburn 

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michael_washburn

Dementia due to MS?

After nearly 3 years of searching for answers to my wife's rapid cognitive decline, multiple tests and MRIs and second opinions it is clear she has a the syndrome of Dementia. Our local neurologist as well as the team at UCLA agree that the cause is MS. Images show significant brain atrophy. I ...

@MikeManc 

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MikeManc

Virtual Neuro / MS Nurse consultations?

Hi everyone, I'm wondering whether anyone on here has had any virtual consultations with their Neurologists or MS Nurses? Either over the phone or even more excitingly over a video call of some sort? I've not had one myself, but I wanted to know what experiences people may have had, positive and or...

Multiple Sclerosis and Turmeric: An Unscientific Trial

Since I've been told by the infamous Dr G (Dr Giavanoni) that it would be too expensive to clinically trial turmeric, I've created this Facebook group to share people's experiences with and document any benefits or side effects that they have after trying half a teaspoon of the stuff after eating