So now you know you have MS, but what exactly is MS. You probably have figured out that it has something to do with the nerves and the brain, hence the neurologist. The following is based on my understanding of MS through the research I have done. I encourage you to visit the links on this blog to further your understanding. I am not a physician and I do not play one on T.V. Knowledge is power, your research may yield a different perspective.
MS stands for Multiple Sclerosis, meaning many scars. These scars are called lesions when they are seen on a MRI machine. What causes these scars is still a source of great debate, which is why there is no cure yet. These scars are seen in the central nervous system which consist of the brain, brain stem and spinal cord.
The most popular theory is that MS is caused by an over active immune system. Something has triggered your body to see the myelin sheath (the nerves of the central nervous system protective cover) as foreign. The protein in myelin is essential for the transmission of nerve impulses. Without this protein, signals are not reaching its destination so to speak, which is what causes difficulty walking, numbness and tingling along with other neurological impairments.
In the beginning stages of MS, your body has the ability to repair the myelin if not too severely damaged which is why it is so hard to detect on an MRI. But after repetitive damage to the same area, the body loses its ability to repair leading to scarring of the area, this is when it becomes harder to recover from relapses. At this point you are left with permanent deficits, for example, foot drop.
There are other theories out there, but the thing that every theory has in common as of this point, is no one knows why MS happens or what triggers it. If they figure that out, then it would help them figure out how to cure it.
That's all for now folks, this chickadee is a little tired.
http://www.nationalmssociety.org/about-multiple-sclerosis/what-we-know-about-ms/what-is-ms/index.aspx
Title pretty much says it all. Journal of dealing with this very confusing condition on a daily/weekly basis. Sharing laughter, frustrations, and all the emotions that come with Multiple Sclerosis.
Welcome
Welcome to all who visit this Blog whether you suffer from Multiple Sclerosis or have a loved one who does. Hopefully this will help all who read understand that they are not alone even though MS affects us all in very different ways. Maybe it can help open eyes of those around who do not know the unpredictability of daily life with MS.
The purpose of this blog is to offer support and inspiration. Please feel free to share any useful information that you have gathered along your journey and words of inspiration. It is hard to overcome all the obstacles we must face and it is nice to hear ways people have adapted. Inspirational stories and anectedotes are especially sought after.
If you post and suffer from Vision disabilities you are welcome to post in all capitals and no one will think that you are shouting.
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