Skip to main content

July 18, 2021 - Confirmed Relapse MRI Images

My symptoms keep getting worse. Yesterday I could barely walk. I told my husband yesterday that I was seriously considering going to the hospital in Oregon. I don't trust the doctors here, especially after one told me she couldn't treat me. 

So today Kurt took me to the hospital. We didn't have a wheelchair and I couldn't walk so Kurt wheeled to the car in my office chair. Along the way I tried to keep upright in the car which was difficult because my right side was so weak and I kept falling toward the door. I used my left hand to hold onto the seat belt to keep me upright when we hit bumps or when we turned. 

When we got to the hospital Kurt got a wheel chair and took me inside. They brought us back and we waited for the doctor. All the staff were extremely professional and nice. They got ahold of neurologists and sent me off to get an MRI right away. Finally a doctor came in and told us that I had a large exasperation and they admitted me.

The took me to another room and we were informed that I would be admitted for 5 days. They got me all set up and brought me a bed side commode. Kurt stayed with me. 

I had never stayed overnight in the hospital before except when my mom passed away but never because of a personal injury or illness. They are going to start me on IV steriods to prevent further progression of inflammation from the lesion. Hopefully I can get back to normal soon! 


This lesion is measured as 4.0 X 2.6 CM which is considered large. It caused right-sided paralysis. It is the large white circle on the right in each image. 













 













Comments

Popular posts from this blog

September 1, 2021 - Tummy Trouble

     So this morning I was able to get out of bed and use the bathroom before the spasm hit. It was a nice change of pace. I am praying that this means things are getting better but if they are it means the muscle spasms were influenced by my menstrual cycle.      I am glad in the sense that this would mean that I wouldn't have them as often but I am disappointed that I will dread my period even more now. Only time will tell for sure.      I stopped taking the baclofen. I didn't take it at all yesterday which proves that it wasn't doing anything.       I have been working to improve enough to return to work. I miss being independent as well as not having to rest like an 80-year-old. In fact, I think an 80-year-old would have more stamina.       Having MS isn't fair. I pray the Tecfidera is working. If not, it would mean my MS is aggressive and that I would need to take some serious measures because I do...

September 16, 2021 - Prednisone 50 Pills Per Day, 20MG for 3 Days , Update

     Today is the last day of oral steroids. I think they are helping because it doesn't seem like my symptoms have gotten worse however my left leg is weak, my left arm is recovering, my right side is recovering and movement or change in position is exhausting. I just keep hoping I will wake up and have all functions back but that is unfortunately not how this disease works.      Do you know how older people say they need to stop and rest? I now know exactly how that feels and it sucks! In my mind, everything seems normal but when it comes to the task itself my body refuses to accept the messages sent by my brain. My left leg refuses to move and it takes time for it to finally receive the message.      I like the steroids because I feel like they help so much except for some side effects. Heart racing, shortness of breath, darker facial hair, and brain fog/confusion are just to name a few. They're not so bad but do catch you off guard. I won...

September 17, 2021 - Embarrassing and Uncomfortable Moments

One wonderful thing about having MS is that you never know what to expect. Symptoms can come out of nowhere at any time, for any reason. That's why it is so important to keep your spirits high and to have a good sense of humor. Today I will share some of my own special moments. Hopefully, you find the humor in them as I do. I have to pee. Of course, urination is normal but because of all the fun medications I take, I pee about once or twice an hour. The medication makes me thirsty so I drink water all day. Also because of the relapses, I am unable to hold it in. My husband hurries me to the bathroom as fast as I will go, we struggle to pull down my underwear, and as soon as my butt hits the toilet I already have a study flow streaming. In the event I don't make it totally in time, I manage to leak a tiny bit. I won't complain. I could have no control and rely on depends. I could only imagine my husband and me dealing with that. Sometimes while I pee I try to look him in the...