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.
my blog

Monday, April 2, 2012

swimming with your head above water

When I first started this blog I must admit that I had some delusions of grandeur. I figured everyone I know would be reading this and become instantly inspired. Well that certainly had not been the case at all. I can't even get my own family members to read it so I have just decided to let it be what it has evolved into, an online journal.

For the first time in many many months, I have been feeling good. I went from using a walker in January walking only a few feet to not needing a cane in the house. My cane is still my companion once I leave my front door, but my stamina has improved so much. I am or as tired as I have been, still have to be careful about doing too many tasks. I tire very easily. The hot season is near by and I don't need any setbacks.

It is so weird to think that a few years ago I would never have thought about these things. My walk was alerts brisk and I rarely sat still. I was a working machine and nothing could stop me. That was until multiple sclerosis started to rear its ugly head.

I have decided to do a little more for my body. My biggest fear is to end up in that wheelchair or worse. I am back in the gym swimming. It is such a strange sensation because there are parts of my body that I have no control over. My left foot for example just kind of flops around and does it's own thing. My left hand, I can't control some of the fingers and the spread apart when I am swimming. This is the nerve damage that I may never regain but I am going to do my best to prevent what I can. I can tell that my left side is so much weaker as it tires out so much faster, but slowly but surely I hope to regain that strength. For now I am a work in progress and I hope that this disease will leave me alone for awhile, actually forever sounds good to me! The other thing I hope for is the courage and mindset to keep going to the gym. It's hard and I dont want to give up.