πŸ”΄ MARCH LIVE STREAM RIGHT NOW: ASK ME ANYTHING MULTIPLE SCLEROSIS



Join me LIVE right now! Ask Me Anything Multiple Sclerosis! ********************************************************** The Boster …

32 Comments

  1. πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯πŸ”₯❀Happy Doctor’s Day❀️

  2. Howdy! What's your take on plasmapherasis as a stopgap measure for deterioration between Ocravus treatments? My new and industrious neurologist is pushing me, but it sounds too severe for my taste. Happy Pesach from Jerusalem! πŸ€—

  3. Thank you SO much for your very informative vlogs. I wish there was someone, medically trained, in the UK who would speak up for MS patients . I was diagnosed with PPMS in September of '22, I'm coming up 59. I have been 'thrown in at the deep end' with virtually no support or even facts. ☹️ I have subscribed and watch all your videos, thank you .

  4. Thank you for doing your videos, I unfortunately missed the live show but if you do get a chance to answer my question I would appreciate it

    As my psoriasis has flared a lot and just getting worse my dermatologist has said I need immunosuppressant meds to stop the psoriasis but as I am on ocrevus I’m not sure if I can, so my question is would you be comfortable with immunosuppressants for psoriasis whilst on ocrevus?

    I am currently waiting for my next appointment with dermatologist to discuss

  5. Regarding supplements for spastticity, you forgot to mention GABA. It works better (and is safer for the kidneys) than any of the drugs you mentioned, and works better for spasticity than magnesium, in my opinion. I take magnesium as well, though. And regarding magnesium, they are not all the same. You should spoecify which type/form.

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