I have been talking a lot about how I’m not doing so well lately but I don’t think I really mentioned what the plan is. I heard a quote one time that I couldn’t agree with more and it goes something like this:
“A goal without a plan is just a dream”
I have a goal but I have not had too much of a plan but at this point I think I know what I’m trying to do now. As far as my health is concerned I plan on trying to get my next neurologist to set me up with a plasmapheresis treatment followed by a week of IV steroids to hopefully help clear up some of the symptoms I am currently experiencing. I will then (with the help of some friends I have met on Facebook) find a doctor who will prescribe me LDN which I hope will bring me the same results it has brought so many others. I will of course continue taking Copaxone alongside the LDN because I’ve read that Copaxone is the only disease modifying medication you can take with LDN. This will hopefully be my next course of treatment of course with the help of dieting and exercise. Will this work? Who knows but it’s definitely worth a try! Obviously my current treatment of pharmaceuticals on top of pharmaceuticals is not doing me much good so it’s time to try the route that unfortunately makes our beloved pharmaceutical companies make less money, I mean…. Help… Less… People… Yeah…
I have an appointment with my new neurologist on the 28th of June so hopefully some good will come from this and I won’t drive all the way out to Fontana to hit another roadblock. I know this was kind of a short posting but I will have more content coming soon!