Hi to all of you who read this. I am a Canadian who lives with MS now for just over a year. I live in an area of Canada that they tell me has a very high concentration of MS. I am a very optimistic person and it is very hard to get me down but I have to say lately I have never felt more alone in all of this. I find that the people who should have the best understanding about this can’t seem to tell me anything and have now pretty much wiped their hands clean of me (meaning doctors of course). I refuse to take pharmaceuticals b/c i just don’t trust them and because of that the doctors have pretty much dropped me. Until i have a relapse. So where i stand now is with one leg that doesn’t want to function properly a tremendous amount of pain constantly unable to work and living in a country with a government that will only pay me for 15 weeks to be “sick” a disability program offered through this government that is substandard b/c the application process takes 6 months. And no guarantee that i will get accepted b/c my MS is relapsing remitting. Does anyone else seem to have the same problems as me or am i really just that alone? It is more the frustration with my own countries governing bodies that seem to be making my MS react worse than anything else.
Well after all of hat i thank you for bearing with me through this to the bitter end and that you for wasting a part of your day to read it. I guess i feel a bit better now.
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