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Tag: MS

Hot Water helped with Choking

Hot Water helped with Choking

So I took an extra triple magnesium capsule on my way to the bathroom yesterday. I can normally swallow pills without water. Comes from years of taking pills. I wasn’t able to actually swallow the capsule for some reason but I needed to use the bathroom. I left it in my mouth for the second until I could get water from the sink. I just didn’t plan on one of my rock skipping ass off the toilet bowl moves. I…

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My multiple sclerosis spasms

My multiple sclerosis spasms

My spasms have been extremely annoying lately. I have a few different types and it depends what it hitting when. My back has probably been the most frequent. It starts with this warm feeling that spreads across my back and reaches from left to right. It continues to my right hand where it paralyzed it for a second. Then I have the one in right hamstring. This one you can feel building up. It’s like you welcome the spasm when…

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FDA approves Zeposia (Ozanimod) for Multiple Sclerosis

FDA approves Zeposia (Ozanimod) for Multiple Sclerosis

Amidst all that is happening in the world, things are still happening in the world of MS. Another oral medication for the treatment of MS. Read the article here: https://multiplesclerosisnewstoday.com/news-posts/2020/03/26/fda-approves-zeposia-ozanimod-oral-rrms-active-spms-cis-therapy/

When transitioning to a wheelchair be sure to see an OT for evaluation

When transitioning to a wheelchair be sure to see an OT for evaluation

I completely understand why I have the been in the wrong wheelchair all this time. I had a very different experience this morning in preparation for a new wheelchair. I was asked questions to start with. Questions about my home. What accommodations I have done in my home thus far? What is my bathroom shower set up? What is my bed I sleep in? How wide is my kitchen? What difficulties do I have in the bathroom with my current…

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I’m going out…my wheelchair evaluation

I’m going out…my wheelchair evaluation

I’m going out into the zombie apocalypse tomorrow. Wish me luck. It will be my first time out in almost two weeks. I’ve been very good at hiding myself away to keep safe but now I must make an appearance. I finally got an appointment for a wheelchair evaluation at my physical therapy office. I’ve waited four months to be seen. I couldn’t decide to not go. They assured me that the staff is in masks and the gym is…

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A week after Rituxan

A week after Rituxan

I went through my blog posts because I couldn’t remember how many times I’ve done Rituxan. I made the switch from Ocrevus back to Rituxan for the March 2019 infusion. This is my 3rd time. I was on Rituxan at an earlier time but was forced to change when Ocrevus came out. My insurance company, at the time, would not authorize Rituxan because it was not approved for multiple sclerosis. I than changed insurance companies once again and asked to…

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A blister formed after Rituxan infusion again

A blister formed after Rituxan infusion again

On Wednesday I was feeling something itching me under me right breast. I looked many times but didn’t see anything. I was on high alert looking for blister under my breasts. I was very concerned over a repeat episode of the side effects that happened last September. https://multipleexperiences.org/2019/09/17/blisters-on-breast/?preview=true&frame-nonce=b3345af611. When my aid looked on Thursday she was able to see a few little bumps in the area like a rash. We used a little Neosporin on the area. Last night I…

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Welcome to my world

Welcome to my world

Another day at home except this time I’m like many others in the world. Welcome to my life. This is definitely the time to binge TV, read a book or 8 and maybe start a jigsaw puzzle. I’m hanging with my puppies, in my chair, gazing at the water and listening to the construction still going on near my condo. It’s comforting to know that things haven’t stopped completely with this virus. I am still feeling tired from my Rituxan…

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Coronavirus and MS video

Coronavirus and MS video

I watched this video yesterday and wanted to share it with everyone. It discuss relevant information about this virus and MS. It discusses the drugs we take and the possible risk factors involved. I actually learned something about my own drug and how it effects my immune system. Hope you find it helpful Coronavirus and MS:  *THANKING THE MS COMMUNITY FOR SHARING YOUR QUESTIONS AND CONCERNS* with Aaron Boster, MD Neurology-MS SpecialistandDamian Washington, Patient Leader CLICK BELOW TO WATCHSTAY INFORMED- UNDERSTANDING MORE ABOUT…

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Grocery delivery thankfully coming

Grocery delivery thankfully coming

I don’t have much to say. I am home and things are uneventful here. I slept better last night which I think my dogs appreciated. I’m tired from the infusion but that is normal. I have ZERO blisters and that is the main thing. My regular aid has been out the last few days with a cold. She didn’t want to be near me which I am thankful for. I’ve had this nice girl here but there isn’t much to…

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