Why alternatives are not researched baffles me. The MS Society raises money for research, but only medical related, what!!!!!! no alternative research, why not. To me it makes no logical sense at all. Why isnt any one brave enough to look outside the box.
It has cost me a mear 1,000 pounds so far to find out exactly what my problems now are. My Atlas, I now think that my spine misalignments may have happened due to me adapting my stance to avoid pain and falling over. Thats why you and me cant, walk for different reasons, but at the same time have one important factor in common, an iffy Atlas.
So my conclusions are we are all here for different reasons and factors, many many crossovers Atlas, Lymes, Candida, Lupus, CFS bung in stress or a traum either physical or psychological and what do you get a cocktail of a mess not ms a mess, then chuck in various drug side affects which also can mimic symptoms classed as ms. and there are other factors Epstein Barr link. You and I are not Doctors, Scientists or Neurologists, but we know our own bodies and its reactions better than any of them. They can tell me nothing except perhaps, maybe, possibly, its very unpredictable. What a load of utter rubbish. I dont work for a reason, I have now found what that reason is.
I wont sit down and be quiet like a good girl. I do not stand alone, I've got you, its a start just watch us finish!!!!
I do my own research, and find my own answers Its good to talk