My first words
I was diagnosed with MS in 2009 and so far I got relapses only thank god for that, they thought it was a stroke at the start and after staying at home due to the cortisone effect in my blood I decided to see a Consultant instead of the surgeon who said that I had a stroke, and that’s when my new doctor made the MRI for my spine and knew that was MS.
I was hopeless when I knew that only 300 people are infected in my country, I started looking for some people, who were diagnosed with MS to help me with my condition, couldn’t find someone around me, so that’s when I met some wonderful people through facebook who really encouraged me through whatever is going on with me.
I am using Vitamins for my condition (calcium, D, B12 & Magnesium), and didn’t use the Beta interferon yet as my Dr is always advising me to do so, Thank god I started to control my emotions more than ever which helped me going through whatever can cause me a relapse (emotional damage triggers it for me).
I experienced the optic neuritis last year when I was released for no reason from my previous company; I restored 97% of my vision so far.
Today I still take my vitamins and nothing else, thank god
I was hopeless when I knew that only 300 people are infected in my country, I started looking for some people, who were diagnosed with MS to help me with my condition, couldn’t find someone around me, so that’s when I met some wonderful people through facebook who really encouraged me through whatever is going on with me.
I am using Vitamins for my condition (calcium, D, B12 & Magnesium), and didn’t use the Beta interferon yet as my Dr is always advising me to do so, Thank god I started to control my emotions more than ever which helped me going through whatever can cause me a relapse (emotional damage triggers it for me).
I experienced the optic neuritis last year when I was released for no reason from my previous company; I restored 97% of my vision so far.
Today I still take my vitamins and nothing else, thank god
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