Just some rambling...

I went to the medweb site initially to check into some symptoms we were all having, just cough and cold and allergies and the meds and the contraindication's, etc.  But I have discovered some very good people who want to be a big part in their own "cure" or situation, or possible situation.  It's sad to hear how people run around trying to find out that is wrong with them.  I guess I got lucky with my MS.  It came from -it seemed at the time- nowhere.  Of course the longer I live with my MS (diagnosed in spring 1992) the more tell-tell signs I now see, right their staring at me and I was just ignoring all he signs and flags and whistles my body was sending me.   It is depressing to be sick and know your body isn't as it should be, but no one believes you.  I have read of people looking for answers for years before they finally began to be able o treat their illness.  It is depressing when docs and nurses think someone is crazy or needy or lonely just because they are asking to pay someone to find out what is wrong with their body and can it be fixed or stopped or cured.  My MS came on quick, so I did not have to wonder except for a few weeks about what I might have and how it is treated.  It can be a little depressing to know u have this and always will; but I think it would be worse to not know.  That is depressing.  Be Well.