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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Wednesday, November 3, 2010

??????

Today, my daughter comes home from school saying that she was really tired and she doesn't know why.  No big deal right????  Then she tells me that her legs are heavy, she has been very clumsy and that she kept falling down today.  Alarm bells are going off in my head.  She has a neuro appointment in January, I hope that I didn't pass this on to her. She is so young and I don't wish this on my worst enemy, let alone my beautiful daughter.  I pray to the good Lord that she doesn't have this problem.
Been a little over a month since started back on the Copaxone.  Still taking "research  drug or placebo".
I felt better the last couple days, getting a little more energy, my balance is better, my walking is better,  my talking is better.  MS is such a weird disease.  Literally, one minute your good, then the next minute you are not.  That's why it's so important not to make hasty decisions in the midst of a relapse.  It's hard to predict where you will be at the end.  However, it is important to plan.
God Bless.

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