My First MS Symptoms and How I’m Helping Others

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This is my first video interview about this site and why I set it up. I’ve been told that “First is Worst” and it can only get better from here, so I’m hopeful! It was recently pointed out to me that many people with MS develop issues with their vision, so I thought a videoblog would be a better medium of communication (I can’t believe I didn’t think of that, since Optic Neuritis was my first and is one of my recurring symptoms) so I’m going to make an effort to do more videoblogs or at least add audio to the articles.

What’s your opinion? Please share! Click on “comments” link below.

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Early Symptoms of Multiple Sclerosis

I came across another great article on the topic of early symptoms of MS. Here it is for your reading enjoyment, and I’ll comment on it afterwards.

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The Early Signs of Multiple Sclerosis

There are several early signs of multiple sclerosis. Have you ever experienced tingling, numbness, loss of balance, weakness in one or more limbs, blurred or double vision? These are some of the most typical signs or symptoms that might suggest to a doctor that you have multiple sclerosis.

The signs may come on so gradually that you may not even know you’re having any symptoms until you look back years later. The signs can range from very mild to very severe. When mild, the signs may be barely noticeable. When severe, you may end up in the hospital wondering what is going on. The doctors may have to put you through several tests to find out the cause of your symptoms. Continue reading

Typical MS Symptoms – Early Signs

Before I was diagnosed with MS, I had no idea what was going on with my body. In my left eye, my colour vision was fading and I was light sensitive to the point of constant nausea. I actually went out and bought an eyepatch – and then drew a skull and crossbones on it with a white-out pen. Aaarrr Matie! As long as my eyes were open I had a headache so bad it bought tears to my eyes, and I felt this bizarre pressure, like there was an ice pick tearing into the back of my eye from inside my head. I found out later this is called “Optic Neuritis.” Continue reading

Talk to me about Multiple Sclerosis

 

After my initial diagnosis I felt … shocked and isolated and VERY glad I didn’t have a brain tumor. I was told MS was an autoimmune deficiency that is different for every person. Can you imagine my surprise when I came across this video with another lady describing MY LIFE?

Please leave me comments on how you reacted to your initial diagnosis, and what you think of this video. I was terrified at first because I didn’t know what to expect, and I don’t want you to feel like that – you’re NOT ALONE in this, there are other people who have been where you are and WANT TO TALK ABOUT IT!

So please share.