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  From judyz July 31

  It has nothing to do with MS, just men and their remotes. We have 3 and I have NO idea how to use them all because my husband has them all programmed differently. When my son goes to college I think I will be relegated to the small 19 inch flat screen in my office without the digital TV or TiVo if the main TV is not on the right setting when I turn it on. Keep the faith, perhaps 1 main controller which is easy to understand is coming!

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  From threed June 28

  Hello,I have MS and I am sending out hugs today

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  From EczemaParent June 24

  THANK YOU for the gastro info!! ( :

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  From lottery46 June 11

  you are not alone! i use to feel like a babbling idiot, the brain and mouth were not insync. i was so relieved when i joined support groups and found so many struggling with the same issues. i learned it's the ms but most importantly how to laugh at myself and with others as well!

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  From trufaith777 May 28

  Jan, beleive me i do understand how you feel. i took avonex for my first medicine. and after having my "2%" seizure i quit altogether. i got on a totally veggie diet and for 8 months i didn't have any symptoms at all. then i started getting bad again so i got on...lets see where to start. :) avonex first, then copaxone, then betaseron: which i thought was woking for me and i felt better before having my doctor tell me i had two new lesions and i needed to yet once again get on a new medicine...again he thinks tysabri is the one i need. i am a little scared about the whole death aspect of it. so i guess i have a decision to make. i will pray about it. just keep fighting.

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