Brief background- I was diagnosed in November with RRMS. Been on Tecfidera since the start of Jan.
I’m a doctor (hospital medicine), currently on a phased return to work. Occupational health have advised I don’t do any long days or night shifts until august. I’m trying at the moment to think through what my future career might look like- I realise this is a fairly impossible task as I have no idea how things will progress!
Just wondering if anyone here works night shifts? How do you find it affects your MS? Do you get an increase in symptoms? How do you manage your fatigue?
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