Hello, While I am in an online class, I am having a hard time enjoying this particular class, so I found myself searching the web. Here I am ..
I was diagnosed in November 2012 with Probable MS. I have had only one Neuro attack where I had about a two week period where my right arm would spasam, and my lower right lip would go numb. I have no residual issues.
My MRI at the time had several lesions, and flares. The Neuroligist told me to take a month and look at the different options of medications. I was leaning on Tysabri, but my blood work came back that I was a carrier of the JC virus, so I elected to not do the Tysabri.
I start a titrated dose this Friday of Avonex.
My Neurologist has told me that he does not believe that I will have any lasting disabilities from my MS, because after my first attack I returned to normal. He believes that with medication it will be something that causes me minor inconviences in my life. Is this Normal??
I am planning on getting a second opinion, but is anyone else being told that? I have not seen a whole lot of people reporting this.
I am also wondering about carreers. I am a paramedic. I work 24 hours shift, often going on little sleep.. I was already in the process of changing carreers, but I wonder how many others in EMS are challenged with MS
This diagnoses has been really hard on me emotionally. I feel betrayed, I feel lost, I feel alone. I cry a lot about it. It has been a rough few months!
Thanks for reading
** Moderator's note - Post broken into paragraphs for easier reading. Many people with MS have visual difficulties that prevent them from reading large blocks of print. **
I was diagnosed in November 2012 with Probable MS. I have had only one Neuro attack where I had about a two week period where my right arm would spasam, and my lower right lip would go numb. I have no residual issues.
My MRI at the time had several lesions, and flares. The Neuroligist told me to take a month and look at the different options of medications. I was leaning on Tysabri, but my blood work came back that I was a carrier of the JC virus, so I elected to not do the Tysabri.
I start a titrated dose this Friday of Avonex.
My Neurologist has told me that he does not believe that I will have any lasting disabilities from my MS, because after my first attack I returned to normal. He believes that with medication it will be something that causes me minor inconviences in my life. Is this Normal??
I am planning on getting a second opinion, but is anyone else being told that? I have not seen a whole lot of people reporting this.
I am also wondering about carreers. I am a paramedic. I work 24 hours shift, often going on little sleep.. I was already in the process of changing carreers, but I wonder how many others in EMS are challenged with MS
This diagnoses has been really hard on me emotionally. I feel betrayed, I feel lost, I feel alone. I cry a lot about it. It has been a rough few months!
Thanks for reading
** Moderator's note - Post broken into paragraphs for easier reading. Many people with MS have visual difficulties that prevent them from reading large blocks of print. **
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