MS and COVID 19
I was diagnosed with MS in 2016 but I had the first signs in 1996 overseas. In spite of these signs, I had a normal life, thank God. I started having more serious signs again in 2012.
I struggled after the diagnosis to accept the disease, the MS drug, and the new MS challenge. I was doing ok in general till the apparition of this monster / COVID-19 virus. I have been saying: we do not need another enemy in life. We fight MS and this is enough. I say, Beat it COVID-19. We deserve a better quality of life.
How many specialists did you see before finding "The One"?