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...
<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>
<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>
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<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>
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<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>
<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>
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<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>