Let the summer begin...Please!
Tomorrow AM I will be attending a Focus Group for MS patients that are taking Copaxone for less then 2 years.
I have been asked to attend. For 60 minutes I will sit with a few others and discuss the side effects of Copaxone. They will film our little chat and I presume use it for research.
The good part...I will get paid for my time!
That...that is always nice!
I am still doing very well health wise. Having been so busy I am tired but hanging in there!
I have no symptoms at the present time and am loving it!
I wish all fellow MS'ers could be healthy.
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