It’s a dreary day today. It’s raining outside. My apartments all dark except for the light of my iPad. That’s OK, I don’t have much going on except for packing. I’ve been talking so much about my new place I haven’t talked much about MS. I finally was able to see my physical therapist to get some exercises for when I fall and there’s nothing around me to help me get up. I’m on the physical therapy maintenance program so…
I’m so excited to finally write this post. I’m moving!!! After 11 years in this apartment, 21 years in the same town, I’m leaving. My mom and step dad bought me a condo in a neighboring town. It has two bedrooms and two bathrooms. For the first time ever in my life I will have my own bathroom. I will have no more stairs. I am located right off the elevator. I have a pool, fitness room, and tennis court….
When I was at my doctor the other day, I was explaining some of my symptoms. I thought I possibly my optic neuritis was acting up. My very first MS symptoms was optic neuritis. It was in my right eye and it was like a huge sunspot in my field of vision. I had it once very mildly in my left eye, same thing but much less intense. I believe I had one other issue in my right eye over the…
If you’ve never read my blog before, I invite you to look through the search box and find my numerous posts on biotin. If you don’t want to take my word, this is an article from the web with the doctor who has been conducting the clinical studies on high dose biotin in multiple sclerosis. https://multiplesclerosisnewstoday.com/2017/05/09/medday-new-phase-3-trial-and-belief-in-biotin-potential-to-treat-progressive-ms-interview-with-frederic-sedel/ My MS doctor had read the notes on the clinical studies and started me on biotin back in December of 2016. With biotin being a…
Going to the neurologist are usually a bittersweet day. I really like my neurologist in the city, she is a wonderful doctor. I honestly couldn’t ask for more compassionate, caring and understanding for MS. That being said, there’s limits to what could be done for me. Since seeing her regularly I’m on my third MS drug that I started back in September, which is Ocrevus. I can say that I was on Rituxan prior to this and the changes only…
This will mark my 11 th month being vegan. December is my year anniversary. I went vegan for health reasons, not for the animal cruelty reason. HOWEVER, the only reason I didn’t go because of animal cruelty is because I could NEVER watch something like that and eat again and I know it. I love animals and if that makes me sound foolish or ignorant to the vegan world, I’m sorry. Anyway, vegan opinions set aside, I made the rash…
I’m very chipper this morning. I slept in. Both dogs let me sleep until 8:00. However, most importantly, my leg strength, or I should say what normal strength they have, came back. I stopped using the bathroom a million times throughout the night and I haven’t had any accidents since Thursday. The chances that I really did have a UTI and needed the antibiotics are pretty good. The doctor even said in two days you’ll know because your MS symptoms…
I’m wearing shorts on October 25th in New York. My windows are open in my house but there is no such thing as global warming. Oh please. This is crazy. https://www.accuweather.com/en/us/new-york-ny/10007/october-weather/349727. In case you actually care, everyday it’s been higher than normal this October. I always said I wanted weather like San Francisco 70 degrees and beautiful each day, guess I’m getting it except we get humidity. Yesterday was so humid and MS doesn’t like humid. It’s like starting five steps…
Good morning. I am not sure where my post is going to go today because I have no idea what I want to say. I have a headache again. I’ve been getting them more and more frequently. Luckily they have been going away with ibuprofen but I’m on medicine everyday for headache/migraines, why am I getting them? They were really bad when I was sick last week but I had one yesterday and now I have one today. I guess…
I am finally feeling a little better. I got some Musinex yesterday which helped but the pounding in my head finally stopped too. I still don’t feel great but the fog that swept over my head and body has mostly lifted. I must again say with warning to anyone on an immunosuppressive drug be smart around others with any kind of sickness. I’ve was on Tysabri for almost two years and Rituxan for over a year and a half and…
