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@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,...

@Amy_Hauber 

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Amy_Hauber

Fecal urgency

Hi there! First time posting here. I was diagnosed with RRMS 8 years ago and am recently experiencing major fecal urgency. It’s scaring me. Does anyone have any insight or advice? I’m terrified that I’ll be out and the urge will hit me and there won’t be a bathroom nearby.

@Dalex 

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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 ...

@David_Elliott 

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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 

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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...

@JayJay10 

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JayJay10

In need of treatment.

Hey guys, it’s been a while since I’ve come here and hope you are all doing well. I have been suffering quite a lot of late due to the immobility of my legs and the constant pains below the waist. Does anyone recommend any treatment to take or maybe some advice to treat spasticity and prolonged ag...

@keld 

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keld

Sweating and spasticity

I cant take the hell of constant sweating and how bad the spasticity is in my legs and arms , 😔 is anyone else dealing with these constant issues to and if so how do you manage to cope with them ?

@WendyHills 

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WendyHills

Working towards yr2 cladribine

I saw my consultant today and finally feel like she’s listening to me. My lymphocytes are back to normal levels six months after cladribine just need more bloods in October and I’m ready for year two. As I failed in my attempt at my MRI in June not sure how effective the tablets have been for me ...

@lemtrada-uk 

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lemtrada-uk

Lost ability to urinate

Need some advice please guys. Has anyone else lost their ability to urinate following an excessive hospital stay due to a physical trauma. Recently I broke my femur so was hospitalised. Whilst in hospital, I was urinating via a long term catheter. My bladder had gone into retention caused by the tra...

@ItsMewithMS 

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ItsMewithMS

Vestibular Issues and PT options

Hi- with Covid really just passing through my area I have restarted my PT. I left off in December when they shut down. He left me with some good exercise options and I tried some of the other options so readily available on-line. The good news is that I think I have been able to maintain strength p...