New for me
Hello
This whole message board and chatting thing is new to me. I've been encouraged by my physio to connect with others who are in the same situation.
I have not contacted the local chapter of the ms society - i thought i would this could be just as beneficial.
I have had relapsing remitting ms since 1983. In 2000 the disease progressed to secondary progressive. Was on rebif for 1 1/2 years. Now nothing. Wear an AFO. is there anything better out there? Anyone know about the walk-aide or the dorsi strap? Anyone on the bioms drug that is in clinical trial right now.
I'm from Windsor ON. Open to suggestions.
***Post split into paragraphs for easier reading!***
Hello
This whole message board and chatting thing is new to me. I've been encouraged by my physio to connect with others who are in the same situation.
I have not contacted the local chapter of the ms society - i thought i would this could be just as beneficial.
I have had relapsing remitting ms since 1983. In 2000 the disease progressed to secondary progressive. Was on rebif for 1 1/2 years. Now nothing. Wear an AFO. is there anything better out there? Anyone know about the walk-aide or the dorsi strap? Anyone on the bioms drug that is in clinical trial right now.
I'm from Windsor ON. Open to suggestions.
***Post split into paragraphs for easier reading!***
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