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@Kevin_Jackson 

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Kevin_Jackson

Grateful to join this community page.

Hi everyone. My name is Kevin, and I was diagnosed with MS about a year and a half ago. What a whirlwind journey so far. I actually have a question for anyone thats felt this...i had a very serious bout of anxiety and stress in mid July; I've started yet another drug for that but does anyone have re...

@Scott_Alderson 

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Scott_Alderson

Greetings and salutations!

Hello from Calgary,Alberta ,Canada. I am Scott, diagnosed May 10/2012 Primary Progressive Multiple Sclerosis. Poet with 8 books in print(2017 release "Imaginative Spasms". 5 YouTube videos(Scott Alderson Poetry). Life is good, just different. Still human, simply modified. Hope for today is that y...

@Allan_Harrison 

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Allan_Harrison

New to MS, and to this group

Hi all, I'm a 52 year old male just diagnosed with Primary Progressive MS. It's mostly affecting my left leg so far, with foot drop, altered gait and weakness. I can no longer stand up from a squat on that leg, which is scary for a guy who's been healthy, strong and physically active his whole life....

@MattW 

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MattW

Sildenafil thoughts please

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

@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...

@Clary 

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Clary

Hi

Hi all, I am new to this site. I am currently in limbo. I do not have a diagnosis, although the neurologist felt it probably is MS. Limbo is difficult because I do not fit in with any group. One minute I am up, and then I am down. This is uncertainty. I guess a lot of people out there have experienc...

@AdiWood 

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AdiWood

Does it get better?

Hi Everyone - I am newly diagnosed. I go in next week for my prescription. I am curious...is this it? My memory and brain are not functioning very well...is it just always going to be like this? I don’t think working anymore will be an option for me if I am unable to improve. My physical abilities h...

@DRUMmondBASS 

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DRUMmondBASS

Potential redundancy

Hope everyone is doing well! Tough time but we've made it this far. I have been furloghed sinced the end of March, my job isn't technically allowed to be open until the 1st of October. It would seem there's a high chance they won't open until next year. This would mean I will have to find a new j...

@laurenlucyjane 

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laurenlucyjane

Super fun new symptoms!!

Hey guys, So I was diagnosed in January and after recovering mostly from my first noticeable relapse I thought I was doing just fine. In the last month or so I've been having some bowel and bladder problems such as urgency and hesitation etc it's making me scared to leave my house or walk far or go ...

@LadyLaura 

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LadyLaura

New member

Hi all, I'm new to this site. I feel a slight veteran as I was diagnosed in 1992 aged 20 ( 1st episode aged 15) so have lived with it all my adult life, I'm now 48! so if I can help with anything please ask!