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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>

Sorry long post!! Finally got a diagnosis in March this year. Been a long haul from 2013. In the last 4 days I've had excruciating pain in my face and a banging headache. Back in 2013 it was optic neuritis I was diagnosed with but I ended up with more symptoms and everything got worse over the years...

<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>

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...

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...

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...

<p>Hi guys,<br> As I said in my introduction, passive neurologists and lack of initiative on my part have led me to suffer a severe foot drop (or club foot), which makes me almost drag my right leg. Foot drop has also confused me, because I thought I didn’t have RRMS, but SPMS, but shortened...</p>

This is a long post, so I apologise in advance. I was due to have my first full dose of ocrevus at the end of March. Having made contact with my MS team in the weeks leading up to this to check that I should still go ahead in the current climate (Coronavirus), I repeatedly got the answer back that m...

I am not trying to be a party pooper here. Why would I? I wrote a bit about them here https://shift.ms/topic/doms-covid-diary-sat-25th-apr This is an excellent piece from a pharmaceutical market analyst. These folk really don't care about you or me, they are in it for the money. End of. Have a re...