After I saw this short but intense interviews, I think you are the best MS Ambassador the world could get. Really a living experience of resilience and strong and focused mind. You are really a wonderwoman, believe me🙏
A close family member of mine has MS, its great seeing someone continue to do what they love in spite of this condition. All the best to Lina and her family
MS and any other related neurological degenerative conditions are horrific. The pain is unbearable. Lina is incredibly young like so many people. Nobody should be living with it. I hope someday, treatments are found to help slow down, help reduce symptoms or help reverse them. More needs to be done for early detection. More has to be done so access to scans and neurologists are done almost immediately.
I have a friend who has MS that has gotten progressively worse over the years. We looked into Stem Cell therapy and believe it may give him 30-40% of his mobility and bodily control back. 🤞🏾
My understanding of MS today: combination of a generic risk factor and a virus (Epstein-Barr ? ). Northern Europeans have a higher risk to get it (genes, diet, exposure to pathogens, ...) ? Some diet adjustments may improve your quality of life e.g. the Terry Walsh diet.
