Lockdown is taking it's toll with dire consequences leading to unimaginable fatigue and pain. I can't wait to be making appointments again with the freedom of attending them without the thought of Covid-19 in the background.
I've been on Tech for 4 years and I recently had a MRI scan which showed new lesions (sad and disappointed).
Yesterday My Neurologist called to formal tell me of the results. However my brain switched off and I didn't fully listen to what the next step is.
<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!</p>
<p>Welcome to our wee friendly group! </p>
<p>We’re having a virtual meet up tomorrow on Houseparty from 12pm. </p>
<p>We usually meet up in either an ice cream parlour, pub / restaurant or tearoom locally and have either brunch or lunch or afternoon tea, depending on the time of da...</p>
<p>So after alot of thinking, weighing up the pros and cons, I’ve gone back to work this week. Was I nervous at first, yes because I work in a school but mentally and emotionally it was the right decision for me. I checked with my doctor, I’m 9 months post year 2 of Cladribine so my risk...</p>
Hi
After 4 years on alemtuzumab I was due to move to Ocrevus (following breakthrough activity) in April. Bad timing. I'm treated at the National Hospital for Neurology and Neurosurgery, and was told yesterday that infusions the new patients might not be available until September/October. A huge cau...