
From Multiple Sclerosis Caregiver
To Multiple Sclerosis Patient
To Health & Life Coach
I have two autoimmune diseases myself. I also have a couple other chronic diseases, but I’d like to talk about Multiple Sclerosis here, about how it’s impacted my life, and how what I’ve learned can improve the lives of other MS patients and anyone else with an autoimmune disease, or other chronic illness. I was diagnosed with MS in 1987 after the birth of my second child and I had two more children after that. There were no drugs for MS back then, only cortisone for acute relapses to counteract inflammation. But cortisone has many terrible side effects. There were some drugs for certain MS-related symptoms too, as there are now.
I started with Relapsing-Remitting MS, which converted to Secondary Progressive MS after 20 years, as it usually does. Since my diagnosis all those years ago, I’ve experienced many of the typical MS symptoms — visual problems (I was blind in my right eye for 5 months), strange sensations throughout my body, pain, dizziness/vertigo and balance problems, major fatigue, brain fog, muscle spasms and excruciating contractions.