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@Adele_Barrow 

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Adele_Barrow

determination

I've secondary progressive ms , I went from rrms about a year ago as me and my family were suffering really bad with the neighbours anti social behaviour I mean bad , no help from police or any other authority, I went to my doctor and cried, I felt so low I couldn't see away out plus ide just had ...

@Bobbij 

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Bobbij

Keeping positive

Hi was just diagnosed with MS, but going back on the last few years it has affected much longer than just finding out now. My brother has lived with MS for over 40 years. So MS is nothing new to me except learning to live with it myself now, one day at a time. Thanks and take care folks

@Peter_Bishop 

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Peter_Bishop

Welcome

Hi All. Just wanted to say Hi I'm new to this site and hope to meet like minded people that i can talk about my MS too. Hope to meet some MS warriors on here 👍

@angieH 

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angieH

Eye symptoms

So basically I know it’s going to be a bad day when I wake up with what I call heavy eyes. Has anyone had this symptom with MS? My eyelids feel weighted and so I have to struggle to keep them open. This will last all day. I do some eye movement exercises like moving my eyeballs in all directions,...

@David_Elliott 

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David_Elliott

Questions

What is MS hug? What is drop foot?

@Dalex 

Last reply

Dalex

please HELP!

Hi my name is Dominique. I went into the hospital last week because I had some type of stiffness, weakness on my left side. I instantly thought it was side effects to my medication, but long behold, after a MRI, they found lesions in my brain and spinal cord. Being diagnosed with RRMS and being a ...

Have you been a PPI rep on a project?

Hi all I'm hoping you can help. I am speaking about 'Patient and Public Involvement' (PPI) at the MS Frontiers conference in Bath, UK on the 5th July. I'm keen to speak with MSers who have been a PPI representative on research projects... is this you? Are you happy to share your experiences? If s...

@RitaM 

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RitaM

Thank you for all the insights

Hello this is my first post, although I have been following the forum for several months. I was diagnosed in January and my MS nurse recommended the site. I want to say thank you to you all for all the support you give to each other and new people like me and loads of information that I have picked ...

@David_Elliott 

Last reply

David_Elliott

Do people really understand the symptoms

Hi folks. I was diagnosed with MS 2018. I've recently retired on health grounds and have just been granted PIP which is a great help. I'm very reluctant to visit anywhere where I dont know where the nearest loo is. Nightmare in the current climate !!! (covid19) Mobility is a problem re walking and b...

@ryba 

Last reply

ryba

Glaucoma and MS

Hello! I think I need advice from someone a bit more experienced than me. Does any of you have both glaucoma and MS? How do you get it diagnosed? After my recent optic neuritis (in march) my optician suggested a week ago that I might have glaucoma, but that she is not certain, as it damages nerves i...