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@DominicS 

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DominicS

Living with/managing MS

Hi all. I have never written about my MS on my blog before. 26y of compartmentalising it. This is about the approach I take to stay sane and manage it. - https://dominicshadbolt.com/2020/05/12/it-is-my-cargo/

MS and assistance dogs

HI, I have just written a piece on MS and assistance dogs on the Barts blog- and how they help hundreds of people with MS lead independent lives:https://multiple-sclerosis-research.org/2020/05/mscovid19-dogs-are-being-trained-to-sniff-out-covid-19/?utm_source=rss&utm_medium=rss&utm_campaign...

@Teide_Barrett 

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Teide_Barrett

Ocrevus infusions

Hi I’m teide I’m 24 and I have RRMS. I was diagnosed in October 2018.. I spent 1 1/2 years on tecfidera but my ms just kept progressing. I started ocrevus last Tuesday and had my first 1/2 dose.. Tuesday I felt ok! I was surprised how well I felt on Wednesday but since then it’s been horrific! Sle...

@Murray 

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Murray

Disclosing MS diagnosis

<p>I have been reading the posts about working as a nurse with MS, and have a quandary – I am a therapist, with RRMS, due to start Ocrevus post-lockdown.</p> <p>The MS does not interfere with my ability to work. A colleague (the only one who knows about the MS) is anxious as to whether my employers ...</p>

@g20-1 

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g20-1

Fatigue with ms

<p>Hi all i find im a morning person with my rr ms, by lunchtime my fatigue starts to set in and i feel like im done the day. Does anyone else feel like this?</p> <div class="i-support-link"> </div>

@Sophietest 

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Sophietest

PPE for the Mind | Ep 1 🧠

<div class="embed-wrapper video-embed-wrapper"></div> <p>L...</p>

@jenny_1 

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jenny_1

Summer Hols

<p>Is it safe for someone with PPMS to holiday in Devon UK this July .. We are prepared to follow all the rules given out by the government. I know MS means a compromised immune system but not sure if MS is on the vulnerable list ?</p> <p>Thank You<br> Jenny </p> <div class="i-support-link"> &lt;...</div>

@thirteen 

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thirteen

Newbie here

<p>Need some advice. I have had health issues half my life. First started when I was about 16. I’ve been trying to find answers for years. Just recently found out that Ms was put in my medical records 2 years ago, although the Dr never verbally told me this. I also have trigeminal, occipital a...</p>

@lemtrada-uk 

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lemtrada-uk

Cycling with compromised balance

<p>I used to be a keen cyclist prior to getting MS. From losing my balance (and ability to walk unaided for long distances) to today, I haven’t rode a bike for 10 years. Now that my young son has learned how to cycle, he wants me to join him on a short bike rides around our block of streets.</p> <p>...</p>

@Browneyedlady 

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Browneyedlady

I need answers

<p>I was diagnosed with MS in 2009. </p> <p>My complaint is my neurologist. She says I have no need for medication at this time and never calls or has me schedule an appointment. She doesn’t listen to my symptoms. I asked many questions and she didn’t answer any.</p> <p>What can I do?...</p>