I have Primary Progressive MS which means there are no disease modifying meds for us. But, I have a super-fine MS specialist and we decided to experiment with Copaxone. If you have any friends using this put them in touch with me as it will be good for me to share experiences with other users. So far, it has had some affect but hard for me to pin down. My thinking is a bit less cloudy, I guess that’s what is making a difference. If it slows down my increasing disability we’ll be ecstatic.
Stay well and as cool as possible as we make our way towards September. I can already feel an Autumn breeze lurking around the corner.
And HEY ! I need Twitter friends ! Find me @MegDavisPrime
Thanks for checking in and be well,