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@martin 

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martin

Hello

#hello 🌼 hello hello, as Valerie Cherish once said. It is sometimes okay to be a little anxious and uncertain. When you are bombarded with lots of responsibilities, Its completely natural to get exhausted sometimes. In such a case, take some time out for yourself. Rest, cheer & enjoy!
Mountain Region

Shingles/ mystery flare

Hey everyone, thanks so much for your comments and support on my last post. Really appreciated it! ❤️‍🩹🙏 where I was having a lot of symptoms and weird sensations that had me scared. Since then it all got much worse the past few days where I just had super weak achy limbs, exhaustion and strange n...

@MillarTestAdmin 

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MillarTestAdmin

Sheridan: Coming to terms with my MS diagnosis

I would like to reassure anyone who gets newly diagnosed with MS that it really is not the end.” In a brave fashion, sheridanallison reveals how her recent MS diagnosis affected her mental health and caused her to grow scared of things she usually loved. Welcoming in 2022, she looks ahead to her car...

PPMS

I am new to this site and wondered how many people with PPMS used it? Really interested to hear other people's experience of PPMS. I was diagnosed three year ago after investigations into what was then a mild gait/drop foot problem. Over the past 18 months I have experienced significantly greater...

@dinnerlady 

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dinnerlady

Up all night!!

Just a question for all. Spent another!! sleepless night. For the last 6 months I have been waking in the night 3 or 4 times every night to use the loo checked for UTI all clear so is it the M.s. causing this anyone else got these problems my G.P. s response to most things is it,s probably the M....

@chloec 

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chloec

Managing work

Hello There, Long time no speak. Or type in this case. I just wanted some advice on how to manage work and MS. I have really struggled the past couple of months with my MS and going back to work. I work in hospitality and have been lucky with furlough but also the place I work for has been super bu...

@Shannon_OHara 

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Shannon_OHara

Next drug is cladribine /mavenclad

Hey guys, I've been diagnosed with Ms since I was 13 and had lots of scarring before then, had nearly 10 years of treatment. However, my Ms keeps becoming active. The next and only drug they are suggesting is cladribine /mavenclad. So taking it for the short amount of time over two years. I'd lik...

@fuzzy9 

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fuzzy9

PPMS

Hello! I was recently diagnosed with PPMS. Ever since I have had usually heartburn and swallowing issues. I visited gastroenterologist some months ago and according his review I had no visible problems when swallowing. The question is that can MS cause problems with swallowing? Whenever I try to sw...

@Jill0827 

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Jill0827

High humidity cooler temps

Some of my worst symptoms come during high humidity- regardless if temps are hotter or cooler. It’s a “heavy” feeling in my head that is difficult to describe (not a headache) but leads to nausea, dizziness and overall misery. I see my neuro on Monday so will ask her but I can’t seem to find ways to...

@ZePlanet 

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ZePlanet

Clemastine Fumarate (Tavégyl or Tavegil)

Does anyone has any feedback concerning taking this Anti-histaminic for a remyelination purpose. All the feedback i found in the internet it always someone that started a few days and then stoped cause of the spleepy effect, no feedback on the long run. There is a study that went out this month that...