O.K we are back to continue were we left off...I think...
So we have been living & struggling with the day to day reality of MS...and honestly there is no way to adequately put into words what that is like, cause it is different for everyone.
Fred spent hours on the computer researching MS seeing what was out there and at the beginning of his journey there wasn't much hope!
After a rather nasty relapse he went on Copaxone a drug that is suppose to help the time between relapses...and costs alot of money each month...but there is some financial help from Trillium (thank you Trillium) and from the makers of the drug (thank you drug makers ??:{. For Fred the drug has helped we think, but how do you really know if it is just the natural progression or if it is doing what it is suppose to do ? Fred has had a major relapse on the drug but they (his relapses) are a few years apart and that is what Copaxaone claims to do...but his body & its capacity are still gradually getting worse.
Sooo to sum it all up MS sucks...we were going to name the blog that but thought it might be a little rude for some.
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