13. Meeting My New Neurologist

As most of you know, my beloved neurologist who diagnosed me with relapsing-remitting ms on March 14, 2018 retired at the end of the year.  He saw me one last time in December 2020 to see me off properly and set up me up with another neurologist at UCLA with whom he thought my family

03. Vitamin D3

After I was diagnosed and we discussed the main medications for treating my MS, my neurologist told me that I need to take Vitamin D3 in large amounts.  Many studies suggest that there is a connection between Vitamin D3 deficiencies and MS—meaning those with Vitamin D3 deficiencies are significantly more likely to acquire and be