Dear all , Hi I’m new here and newly diagnosed although I’ve personally known for a year that I had Ms . Apart from being angry that maybe the use of my right hand could have been saved if doctors had taken me seriously 2 years ago , I now have several symptoms , heavy legs, feeling of ants crawling over my arm, feeling of burning like nettles on both thighs when I walk, and now a rigid torso and dead spots on my back as well as numbness starting on my left hand. After a brain scan last September , I was given my diagnosis 3 weeks ago ( sorry state of the NHS) and have been offered a choice of two drugs , aubagio or tecfidera.
I currently take a high dose of Vitamin D which this week has been disputed to help and lions mane mushroom powder which aids myelination , as well as sage , vit b and a daily spoonful of sauerkraut .
I m finding my numbness so depressing as I am a musician , or was, as well as not being able to hold a badminton or tennis racquet , anyways I just wanted to know if anyone had any guidance on the drugs I’ve been offered , Aubagio or Tecfidera . Thank you G x
Ps I’m 53 yrs old diagnosed RRMS
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