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Sept. 18, 2020 – it was surreal , but also good to have a diagnosis
Not applicable yet as I was diagnosed 4 months ago and thankfully feel really good. I am absolutely petrified of not being able to work.
I was immediately put on 5,000 Vitamin D and plasma transfusions. I was then given 2 transfusions of Ritaximub, my next is Feb. 2021 and every 6 months.
I completely lost eyesight in right eye, I would say thankfully I got about 90 % back, still a bit blurry. I struggle most now knowing I have brain lesions and really wanting to know how old they are, how long have I actually had this ? Why 2020, I’m 54, so I’m a little older than most to get diagnosed. I’m for now struggling with all of the unknowns.
Not to my knowledge.
Not to my knowledge. I’m just more aware now of sleep, stress, eating , etc.
Not applicable
Not applicable yet, no current symptoms
Breathe, have faith, reach out to support groups
I’M ALISSA!
I help women who have also been diagnosed with Multiple Sclerosis make specific and personalized diet, lifestyle & subconscious changes so that they can begin to heal their body, reduce disease symptoms, and return to a life they love.hey there,
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