//Norsk versjon lenger ned// Today I had my 12th Tysabri infusion. Oh well, time flies when you’re having fun. Just kidding, Tyabri is no fun, but it’s kind of necessary. I though I could write about the process (or what you would call it) of receiving Tysabri. Every disease-modifying drug is kind of different and… Continue reading My Life on Tysabri
//Norsk versjon lenger ned// It was October the 20th last year when Selma Blair, the famous Hollywood actress posted a picture on Instagram with a caption revealing she had MS. And at the end of February ABC News aired an extremely raw interview with Selma Blair, which was filmed a few days before her first public… Continue reading MS Awareness Month
//Norsk versjon lenger ned// Yesterday I had my 9th Tysabri infusion and I was thinking about this blog post. It’s kind of the part 2 of the last one I wrote: How I got my MS Diagnosis. When I was at the hospital and they told about what they had seen on the CT scan, I… Continue reading You have MS!
//Norsk versjon lenger ned // This is the story about how I found out I have MS. I’m not exactly sure when it started, but in February 2018 I was so tired, the fatigue was worse than ever before. We were going on a round trip in Asia for three weeks, and for the very… Continue reading How I got my MS Diagnosis
// Norsk versjon lenger ned // The Christmas vacation is over and a new year is already here, but I just want to write about the Christmas week. I’ve spent 12 days at a cabin up in the mountains with family, wanting to relax and be spoiled a bit by my parents. Some will say… Continue reading My Christmas Week